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Year | Number of Results |
---|---|
2006 | 1 |
2013 | 1 |
2023 | 2 |
2024 | 0 |
PubMed (GeneRIF) for id: 22832
4 results
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The association of five polymorphisms with diabetic retinopathy in a Chinese population.
Ophthalmic Genet. 2023 Aug;44(4):346-351. doi: 10.1080/13816810.2023.2194494. Epub 2023 Apr 17.
Ophthalmic Genet. 2023.
PMID: 37066695
CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis.
Nuzhat N, Van Schil K, Liakopoulos S, Bauwens M, Rey AD, Käseberg S, Jäger M, Willer JR, Winter J, Truong HM, Gruartmoner N, Van Heetvelde M, Wolf J, Merget R, Grasshoff-Derr S, Van Dorpe J, Hoorens A, Stöhr H, Mansard L, Roux AF, Langmann T, Dannhausen K, Rosenkranz D, Wissing KM, Van Lint M, Rossmann H, Häuser F, Nürnberg P, Thiele H, Zechner U, Pearring JN, De Baere E, Bolz HJ.
Nuzhat N, et al.
J Clin Invest. 2023 Apr 17;133(8):e161156. doi: 10.1172/JCI161156.
J Clin Invest. 2023.
PMID: 36862503
Free PMC article.
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CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base.
Wang WJ, Tay HG, Soni R, Perumal GS, Goll MG, Macaluso FP, Asara JM, Amack JD, Tsou MF.
Wang WJ, et al.
Nat Cell Biol. 2013 Jun;15(6):591-601. doi: 10.1038/ncb2739. Epub 2013 May 5.
Nat Cell Biol. 2013.
PMID: 23644468
Free PMC article.
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QN1/KIAA1009: a new essential protein for chromosome segregation and mitotic spindle assembly.
Leon A, Omri B, Gely A, Klein C, Crisanti P.
Leon A, et al.
Oncogene. 2006 Mar 23;25(13):1887-95. doi: 10.1038/sj.onc.1209215.
Oncogene. 2006.
PMID: 16302001
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