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Year | Number of Results |
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2000 | 1 |
2007 | 2 |
2008 | 1 |
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2015 | 1 |
2024 | 0 |
PubMed (cited) for id: 614610
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Page 1
KANK deficiency leads to podocyte dysfunction and nephrotic syndrome.
J Clin Invest. 2015 Jun;125(6):2375-84. doi: 10.1172/JCI79504. Epub 2015 May 11.
J Clin Invest. 2015.
PMID: 25961457
Free PMC article.
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair.
Ramot Y, Molho-Pessach V, Meir T, Alper-Pinus R, Siam I, Tams S, Babay S, Zlotogorski A.
Ramot Y, et al.
J Med Genet. 2014 Jun;51(6):388-94. doi: 10.1136/jmedgenet-2014-102346. Epub 2014 Mar 26.
J Med Genet. 2014.
PMID: 24671081
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Kank proteins: a new family of ankyrin-repeat domain-containing proteins.
Zhu Y, Kakinuma N, Wang Y, Kiyama R.
Zhu Y, et al.
Biochim Biophys Acta. 2008 Feb;1780(2):128-33. doi: 10.1016/j.bbagen.2007.09.017. Epub 2007 Oct 4.
Biochim Biophys Acta. 2008.
PMID: 17996375
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SIP, a novel ankyrin repeat containing protein, sequesters steroid receptor coactivators in the cytoplasm.
Zhang Y, Zhang H, Liang J, Yu W, Shang Y.
Zhang Y, et al.
EMBO J. 2007 Jun 6;26(11):2645-57. doi: 10.1038/sj.emboj.7601710. Epub 2007 May 3.
EMBO J. 2007.
PMID: 17476305
Free PMC article.
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Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
Nagase T, Kikuno R, Ishikawa K, Hirosawa M, Ohara O.
Nagase T, et al.
DNA Res. 2000 Apr 28;7(2):143-50. doi: 10.1093/dnares/7.2.143.
DNA Res. 2000.
PMID: 10819331
Free article.
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