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Year | Number of Results |
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2005 | 1 |
2014 | 1 |
2015 | 1 |
2020 | 3 |
2024 | 0 |
PubMed (OMIM) for id: 146845
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Page 1
CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module.
Nat Commun. 2020 Nov 2;11(1):5520. doi: 10.1038/s41467-020-19113-0.
Nat Commun. 2020.
PMID: 33139725
Free PMC article.
The WD40-protein CFAP52/WDR16 is a centrosome/basal body protein and localizes to the manchette and the flagellum in male germ cells.
Tapia Contreras C, Hoyer-Fender S.
Tapia Contreras C, et al.
Sci Rep. 2020 Aug 28;10(1):14240. doi: 10.1038/s41598-020-71120-9.
Sci Rep. 2020.
PMID: 32859975
Free PMC article.
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The genetics of situs inversus without primary ciliary dyskinesia.
Postema MC, Carrion-Castillo A, Fisher SE, Vingerhoets G, Francks C.
Postema MC, et al.
Sci Rep. 2020 Feb 28;10(1):3677. doi: 10.1038/s41598-020-60589-z.
Sci Rep. 2020.
PMID: 32111882
Free PMC article.
Clinical Trial.
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A human laterality disorder associated with a homozygous WDR16 deletion.
Ta-Shma A, Perles Z, Yaacov B, Werner M, Frumkin A, Rein AJ, Elpeleg O.
Ta-Shma A, et al.
Eur J Hum Genet. 2015 Sep;23(9):1262-5. doi: 10.1038/ejhg.2014.265. Epub 2014 Dec 3.
Eur J Hum Genet. 2015.
PMID: 25469542
Free PMC article.
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WDRPUH, a novel WD-repeat-containing protein, is highly expressed in human hepatocellular carcinoma and involved in cell proliferation.
Silva FP, Hamamoto R, Nakamura Y, Furukawa Y.
Silva FP, et al.
Neoplasia. 2005 Apr;7(4):348-55. doi: 10.1593/neo.04544.
Neoplasia. 2005.
PMID: 15967112
Free PMC article.
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