https://cellbio.subwiki.org/w/index.php?action=history&feed=atom&title=Organelle
Organelle - Revision history
2026-06-08T11:20:23Z
Revision history for this page on the wiki
MediaWiki 1.41.2
https://cellbio.subwiki.org/w/index.php?title=Organelle&diff=169&oldid=prev
Sebastian at 20:28, 25 November 2017
2017-11-25T20:28:57Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:28, 25 November 2017</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td></tr>
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<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || 20 nm –200 nm[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/] || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian Camillo Golgi)[https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false][https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/]<del style="font-weight: bold; text-decoration: none;">)</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || 20 nm –200 nm[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/] || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian Camillo Golgi)[https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false][https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td></tr>
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Sebastian
https://cellbio.subwiki.org/w/index.php?title=Organelle&diff=168&oldid=prev
Sebastian at 20:27, 25 November 2017
2017-11-25T20:27:54Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:27, 25 November 2017</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l8">Line 8:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || 20 nm –200 nm[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/]<del style="font-weight: bold; text-decoration: none;"><ref name="The Asymmetrical Structure of Golgi Apparatus Membranes Revealed by In situ Atomic Force Microscope">{{cite web|title=The Asymmetrical Structure of Golgi Apparatus Membranes Revealed by In situ Atomic Force Microscope|url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/}}</ref> </del>|| || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian Camillo Golgi)[https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false][https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/])</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || 20 nm –200 nm[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/] || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian Camillo Golgi)[https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false][https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/])</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td></tr>
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Sebastian
https://cellbio.subwiki.org/w/index.php?title=Organelle&diff=167&oldid=prev
Sebastian at 20:27, 25 November 2017
2017-11-25T20:27:07Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:27, 25 November 2017</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || 20 nm –200 nm[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/] || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian Camillo Golgi)[https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false][https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/])</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || 20 nm –200 nm[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/]<ins style="font-weight: bold; text-decoration: none;"><ref name="The Asymmetrical Structure of Golgi Apparatus Membranes Revealed by In situ Atomic Force Microscope">{{cite web|title=The Asymmetrical Structure of Golgi Apparatus Membranes Revealed by In situ Atomic Force Microscope|url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/}}</ref> </ins>|| || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian Camillo Golgi)[https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false][https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/])</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
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Sebastian
https://cellbio.subwiki.org/w/index.php?title=Organelle&diff=166&oldid=prev
Sebastian at 20:25, 25 November 2017
2017-11-25T20:25:33Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:25, 25 November 2017</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian Camillo Golgi)[https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false])</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || <ins style="font-weight: bold; text-decoration: none;">20 nm –200 nm[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/] </ins>|| || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian Camillo Golgi)[https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false<ins style="font-weight: bold; text-decoration: none;">][https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628984/</ins>])</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td></tr>
</table>
Sebastian
https://cellbio.subwiki.org/w/index.php?title=Organelle&diff=165&oldid=prev
Sebastian at 20:22, 25 November 2017
2017-11-25T20:22:46Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:22, 25 November 2017</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l8">Line 8:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian <del style="font-weight: bold; text-decoration: none;">[[w:</del>Camillo Golgi<del style="font-weight: bold; text-decoration: none;">|Camillo Golgi]]</del>[https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false])</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian Camillo Golgi<ins style="font-weight: bold; text-decoration: none;">)</ins>[https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false])</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td></tr>
</table>
Sebastian
https://cellbio.subwiki.org/w/index.php?title=Organelle&diff=164&oldid=prev
Sebastian at 20:21, 25 November 2017
2017-11-25T20:21:47Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<col class="diff-content" />
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:21, 25 November 2017</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l8">Line 8:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian [[w:<del style="font-weight: bold; text-decoration: none;">Camilo </del>Golgi|<del style="font-weight: bold; text-decoration: none;">Camilo </del>Golgi]][https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false])</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian [[w:<ins style="font-weight: bold; text-decoration: none;">Camillo </ins>Golgi|<ins style="font-weight: bold; text-decoration: none;">Camillo </ins>Golgi]][https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false])</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td></tr>
</table>
Sebastian
https://cellbio.subwiki.org/w/index.php?title=Organelle&diff=163&oldid=prev
Sebastian at 20:21, 25 November 2017
2017-11-25T20:21:23Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<tr class="diff-title" lang="en">
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:21, 25 November 2017</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l8">Line 8:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian [[w:Camilo Golgi]][https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false])</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || 1898 (by Italian [[w:<ins style="font-weight: bold; text-decoration: none;">Camilo Golgi|</ins>Camilo Golgi]][https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false])</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td></tr>
</table>
Sebastian
https://cellbio.subwiki.org/w/index.php?title=Organelle&diff=162&oldid=prev
Sebastian at 20:21, 25 November 2017
2017-11-25T20:21:07Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:21, 25 November 2017</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l8">Line 8:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] ||</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/] || <ins style="font-weight: bold; text-decoration: none;">1898 (by Italian [[w:Camilo Golgi]][https://books.google.com.ar/books?id=3DQQggoHy6YC&pg=PA21&lpg=PA21&dq=%22golgi+apparatus+was+discovered+in%22&source=bl&ots=1_yGf-DgFQ&sig=EnnimRK0LNYXnGK-kcD0U40ctMo&hl=en&sa=X&ved=0ahUKEwibhfGcxtrXAhWJh5AKHSYcB6wQ6AEIQTAG#v=onepage&q=%22golgi%20apparatus%20was%20discovered%20in%22&f=false])</ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td></tr>
</table>
Sebastian
https://cellbio.subwiki.org/w/index.php?title=Organelle&diff=161&oldid=prev
Sebastian at 20:17, 25 November 2017
2017-11-25T20:17:13Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:17, 25 November 2017</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l8">Line 8:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Rough endoplasmic reticulum || || || || || || || || ||</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome<del style="font-weight: bold; text-decoration: none;"><ref>{{cite journal|last1=Bexiga|first1=Mariana G.|last2=Simpson|first2=Jeremy C.|title=Human Diseases Associated with Form and Function of the Golgi Complex|doi=10.3390/ijms140918670|url=</del>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/<del style="font-weight: bold; text-decoration: none;">|accessdate=25 November 2017|pmc=3794802}}</ref> </del>||</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome<ins style="font-weight: bold; text-decoration: none;">[</ins>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/<ins style="font-weight: bold; text-decoration: none;">] </ins>||</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td></tr>
</table>
Sebastian
https://cellbio.subwiki.org/w/index.php?title=Organelle&diff=160&oldid=prev
Sebastian at 20:10, 25 November 2017
2017-11-25T20:10:06Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:10, 25 November 2017</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l8">Line 8:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome ||</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| Golgi aparatus || || || || || || || || Dyschromatosis universalis hereditaria, Cutis laxa, Menkes disease, occipital horn syndrome, Wilson disease, Congenital disorders of glycosylation, Duchenne muscular dystrophy, Aarskog-Scott syndrome/faciogenital dysplasia, “North Sea” progressive myoclonus epilepsy, Pelizaeus-Merzbacher disease, Parkinson’s disease, Dyggve-Melchior-Clausen disease, Smith-McCort Dysplasia, X-linked mental retardation associated with autism, epilepsy and macrocephaly, Macrocephaly, alopecia, cutis laxa and scoliosis (MACS) syndrome, RIN2 syndrome, Gerodermia osteodysplastica, Proximal spinal muscular atrophy, Congenital disorder of glycosylation type II (CGD-II), Angelman syndrome<ins style="font-weight: bold; text-decoration: none;"><ref>{{cite journal|last1=Bexiga|first1=Mariana G.|last2=Simpson|first2=Jeremy C.|title=Human Diseases Associated with Form and Function of the Golgi Complex|doi=10.3390/ijms140918670|url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794802/|accessdate=25 November 2017|pmc=3794802}}</ref> </ins>||</div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| Smooth endoplasmic reticulum || || || || || || || || ||</div></td></tr>
</table>
Sebastian