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Year | Number of Results |
---|---|
2007 | 1 |
2008 | 2 |
2009 | 2 |
2014 | 3 |
2024 | 0 |
PubMed (OMIM) for id: 282809
6 results
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Mutation of POC1B in a severe syndromic retinal ciliopathy.
Hum Mutat. 2014 Oct;35(10):1153-62. doi: 10.1002/humu.22618. Epub 2014 Aug 11.
Hum Mutat. 2014.
PMID: 25044745
Free PMC article.
Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy.
Roosing S, Lamers IJ, de Vrieze E, van den Born LI, Lambertus S, Arts HH; POC1B Study Group; Peters TA, Hoyng CB, Kremer H, Hetterschijt L, Letteboer SJ, van Wijk E, Roepman R, den Hollander AI, Cremers FP.
Roosing S, et al.
Am J Hum Genet. 2014 Aug 7;95(2):131-42. doi: 10.1016/j.ajhg.2014.06.012. Epub 2014 Jul 10.
Am J Hum Genet. 2014.
PMID: 25018096
Free PMC article.
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Novel recessive cone-rod dystrophy caused by POC1B mutation.
Durlu YK, Köroğlu Ç, Tolun A.
Durlu YK, et al.
JAMA Ophthalmol. 2014 Oct;132(10):1185-91. doi: 10.1001/jamaophthalmol.2014.1658.
JAMA Ophthalmol. 2014.
PMID: 24945461
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Basal body stability and ciliogenesis requires the conserved component Poc1.
Pearson CG, Osborn DP, Giddings TH Jr, Beales PL, Winey M.
Pearson CG, et al.
J Cell Biol. 2009 Dec 14;187(6):905-20. doi: 10.1083/jcb.200908019.
J Cell Biol. 2009.
PMID: 20008567
Free PMC article.
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Molecular architecture of the centriole proteome: the conserved WD40 domain protein POC1 is required for centriole duplication and length control.
Keller LC, Geimer S, Romijn E, Yates J 3rd, Zamora I, Marshall WF.
Keller LC, et al.
Mol Biol Cell. 2009 Feb;20(4):1150-66. doi: 10.1091/mbc.e08-06-0619. Epub 2008 Dec 24.
Mol Biol Cell. 2009.
PMID: 19109428
Free PMC article.
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Pix1 and Pix2 are novel WD40 microtubule-associated proteins that colocalize with mitochondria in Xenopus germ plasm and centrosomes in human cells.
Hames RS, Hames R, Prosser SL, Euteneuer U, Lopes CA, Moore W, Woodland HR, Fry AM.
Hames RS, et al.
Exp Cell Res. 2008 Feb 1;314(3):574-89. doi: 10.1016/j.yexcr.2007.10.019. Epub 2007 Nov 6.
Exp Cell Res. 2008.
PMID: 18068700
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