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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2003 | 1 |
2005 | 1 |
2008 | 1 |
2014 | 1 |
2015 | 1 |
2018 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 55275
6 results
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Progressive cerebello-cerebral atrophy and progressive encephalopathy with edema, hypsarrhythmia and optic atrophy may be allelic syndromes.
Eur J Paediatr Neurol. 2018 Nov;22(6):1133-1138. doi: 10.1016/j.ejpn.2018.07.003. Epub 2018 Jul 26.
Eur J Paediatr Neurol. 2018.
PMID: 30100179
EARP is a multisubunit tethering complex involved in endocytic recycling.
Schindler C, Chen Y, Pu J, Guo X, Bonifacino JS.
Schindler C, et al.
Nat Cell Biol. 2015 May;17(5):639-50. doi: 10.1038/ncb3129. Epub 2015 Mar 23.
Nat Cell Biol. 2015.
PMID: 25799061
Free PMC article.
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VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2).
Feinstein M, Flusser H, Lerman-Sagie T, Ben-Zeev B, Lev D, Agamy O, Cohen I, Kadir R, Sivan S, Leshinsky-Silver E, Markus B, Birk OS.
Feinstein M, et al.
J Med Genet. 2014 May;51(5):303-8. doi: 10.1136/jmedgenet-2013-101823. Epub 2014 Feb 27.
J Med Genet. 2014.
PMID: 24577744
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Identification of host proteins required for HIV infection through a functional genomic screen.
Brass AL, Dykxhoorn DM, Benita Y, Yan N, Engelman A, Xavier RJ, Lieberman J, Elledge SJ.
Brass AL, et al.
Science. 2008 Feb 15;319(5865):921-6. doi: 10.1126/science.1152725. Epub 2008 Jan 10.
Science. 2008.
PMID: 18187620
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Characterization of the human GARP (Golgi associated retrograde protein) complex.
Liewen H, Meinhold-Heerlein I, Oliveira V, Schwarzenbacher R, Luo G, Wadle A, Jung M, Pfreundschuh M, Stenner-Liewen F.
Liewen H, et al.
Exp Cell Res. 2005 May 15;306(1):24-34. doi: 10.1016/j.yexcr.2005.01.022.
Exp Cell Res. 2005.
PMID: 15878329
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Progressive cerebellocerebral atrophy: a new syndrome with microcephaly, mental retardation, and spastic quadriplegia.
Ben-Zeev B, Hoffman C, Lev D, Watemberg N, Malinger G, Brand N, Lerman-Sagie T.
Ben-Zeev B, et al.
J Med Genet. 2003 Aug;40(8):e96. doi: 10.1136/jmg.40.8.e96.
J Med Genet. 2003.
PMID: 12920088
Free PMC article.
No abstract available.
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