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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2001 | 1 |
2006 | 1 |
2011 | 1 |
2012 | 3 |
2013 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 29887
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Page 1
Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia.
Eur J Med Genet. 2013 Jan;56(1):32-5. doi: 10.1016/j.ejmg.2012.10.010. Epub 2012 Oct 31.
Eur J Med Genet. 2013.
PMID: 23123320
An SNX10 mutation causes malignant osteopetrosis of infancy.
Aker M, Rouvinski A, Hashavia S, Ta-Shma A, Shaag A, Zenvirt S, Israel S, Weintraub M, Taraboulos A, Bar-Shavit Z, Elpeleg O.
Aker M, et al.
J Med Genet. 2012 Apr;49(4):221-6. doi: 10.1136/jmedgenet-2011-100520.
J Med Genet. 2012.
PMID: 22499339
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A SNX10/V-ATPase pathway regulates ciliogenesis in vitro and in vivo.
Chen Y, Wu B, Xu L, Li H, Xia J, Yin W, Li Z, Shi D, Li S, Lin S, Shu X, Pei D.
Chen Y, et al.
Cell Res. 2012 Feb;22(2):333-45. doi: 10.1038/cr.2011.134. Epub 2011 Aug 16.
Cell Res. 2012.
PMID: 21844891
Free PMC article.
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Sorting nexin 10 induces giant vacuoles in mammalian cells.
Qin B, He M, Chen X, Pei D.
Qin B, et al.
J Biol Chem. 2006 Dec 1;281(48):36891-6. doi: 10.1074/jbc.M608884200. Epub 2006 Sep 29.
J Biol Chem. 2006.
PMID: 17012226
Free article.
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A large family of endosome-localized proteins related to sorting nexin 1.
Teasdale RD, Loci D, Houghton F, Karlsson L, Gleeson PA.
Teasdale RD, et al.
Biochem J. 2001 Aug 15;358(Pt 1):7-16. doi: 10.1042/0264-6021:3580007.
Biochem J. 2001.
PMID: 11485546
Free PMC article.
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