MEGF10: Difference between revisions
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'''MEGF10''' ( multiple [[EGF-like domain|EGF-like-domains]] 10 ) is a a regulator of [[satellite cell]] [[myogenesis]]. It has been shown to be the cause of onset myopathy, [[areflexia]], [[respiratory distress]] and [[dysphagia]].<ref>{{cite journal |
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'''Multiple EGF-like-domains 10''' is a [[protein]] that in humans is encoded by the ''MEGF10'' [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: Multiple EGF-like-domains 10| url = http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=retrieve&list_uids=84466| accessdate = 2011-11-26T12:01:36.734-08:00}}</ref> |
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| quotes = yes |
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|last=Logan |
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|first=Clare V |
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|authorlink= |
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|coauthors=& al. |
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|year=2011|month=Nov. |
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|title=Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD) |
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|journal=Nature genetics |
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|volume= |
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|issue= |
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|pages= |
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|publisher= |location = | issn = | pmid = 22101682 |
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| bibcode = | oclc =| id = | url = | doi = 10.1038/ng.995 | language = ENG| format = | accessdate = | laysummary = | laysource = | laydate = | quote = |
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}}</ref> |
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MEGF10 is a a regulator of [[satellite cell]] [[myogenesis]]. It has been shown to be the cause of onset myopathy, [[areflexia]], [[respiratory distress]] and [[dysphagia]].<ref name="pmid22101682">{{cite journal | author = Logan CV, Lucke B, Pottinger C, Abdelhamed ZA, Parry DA, Szymanska K, Diggle CP, Riesen AV, Morgan JE, Markham G, Ellis I, Manzur AY, Markham AF, Shires M, Helliwell T, Scoto M, Hübner C, Bonthron DT, Taylor GR, Sheridan E, Muntoni F, Carr IM, Schuelke M, Johnson CA | title = Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD) | journal = Nat Genet | volume = | issue = | pages = | year = 2011 | month = November | pmid = 22101682 | doi = 10.1038/ng.995 }}</ref> |
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==Reference== |
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<references/> |
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==References== |
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{{reflist}} |
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==Further reading == |
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{{refbegin | 2}} |
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*{{Cite pmid|17205124}} |
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*{{Cite pmid|17498693}} |
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*{{Cite pmid|17643423}} |
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*{{Cite pmid|18179784}} |
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*{{Cite pmid|19197986}} |
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*{{Cite pmid|19721717}} |
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*{{Cite pmid|20813413}} |
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*{{Cite pmid|20828568}} |
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{{refend}} |
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{{gene-5-stub}} |
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==External links== |
==External links== |
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* [http://www.ncbi.nlm.nih.gov/gene/84466 NCBI gene] |
* [http://www.ncbi.nlm.nih.gov/gene/84466 NCBI gene] |
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{{Uncategorized stub|date=November 2011}} |
{{Uncategorized stub|date=November 2011}} |
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{{gene-5-stub}} |
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Revision as of 20:05, 26 November 2011
Template:PBB Multiple EGF-like-domains 10 is a protein that in humans is encoded by the MEGF10 gene.[1]
MEGF10 is a a regulator of satellite cell myogenesis. It has been shown to be the cause of onset myopathy, areflexia, respiratory distress and dysphagia.[2]
References
- ^ "Entrez Gene: Multiple EGF-like-domains 10". Retrieved 2011-11-26T12:01:36.734-08:00.
{{cite web}}: Check date values in:|accessdate=(help) - ^ Logan CV, Lucke B, Pottinger C, Abdelhamed ZA, Parry DA, Szymanska K, Diggle CP, Riesen AV, Morgan JE, Markham G, Ellis I, Manzur AY, Markham AF, Shires M, Helliwell T, Scoto M, Hübner C, Bonthron DT, Taylor GR, Sheridan E, Muntoni F, Carr IM, Schuelke M, Johnson CA (2011). "Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)". Nat Genet. doi:10.1038/ng.995. PMID 22101682.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link)
Further reading
- Attention: This template ({{cite pmid}}) is deprecated. To cite the publication identified by PMID 17205124, please use {{cite journal}} with
|pmid=17205124instead. - Attention: This template ({{cite pmid}}) is deprecated. To cite the publication identified by PMID 17498693, please use {{cite journal}} with
|pmid=17498693instead. - Attention: This template ({{cite pmid}}) is deprecated. To cite the publication identified by PMID 17643423, please use {{cite journal}} with
|pmid=17643423instead. - Attention: This template ({{cite pmid}}) is deprecated. To cite the publication identified by PMID 18179784, please use {{cite journal}} with
|pmid=18179784instead. - Attention: This template ({{cite pmid}}) is deprecated. To cite the publication identified by PMID 19197986, please use {{cite journal}} with
|pmid=19197986instead. - Attention: This template ({{cite pmid}}) is deprecated. To cite the publication identified by PMID 19721717, please use {{cite journal}} with
|pmid=19721717instead. - Attention: This template ({{cite pmid}}) is deprecated. To cite the publication identified by PMID 20813413, please use {{cite journal}} with
|pmid=20813413instead. - Attention: This template ({{cite pmid}}) is deprecated. To cite the publication identified by PMID 20828568, please use {{cite journal}} with
|pmid=20828568instead.
 | This article on a gene on human chromosome 5 is a stub. You can help Wikipedia by expanding it. |
External links
 | This article has not been added to any content categories. Please help out by adding categories to it so that it can be listed with similar articles, in addition to a stub category. (November 2011) |
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