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Year | Number of Results |
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2005 | 1 |
2016 | 1 |
2020 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 51729
3 results
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Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.
Hum Mol Genet. 2020 Dec 4;29(22):3662-3678. doi: 10.1093/hmg/ddaa258.
Hum Mol Genet. 2020.
PMID: 33276377
Free PMC article.
Changes in the folding landscape of the WW domain provide a molecular mechanism for an inherited genetic syndrome.
Pucheta-Martinez E, D'Amelio N, Lelli M, Martinez-Torrecuadrada JL, Sudol M, Saladino G, Gervasio FL.
Pucheta-Martinez E, et al.
Sci Rep. 2016 Jul 26;6:30293. doi: 10.1038/srep30293.
Sci Rep. 2016.
PMID: 27456546
Free PMC article.
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Nucleocytoplasmic shuttling of the splicing factor SIPP1.
Llorian M, Beullens M, Lesage B, Nicolaescu E, Beke L, Landuyt W, Ortiz JM, Bollen M.
Llorian M, et al.
J Biol Chem. 2005 Nov 18;280(46):38862-9. doi: 10.1074/jbc.M509185200. Epub 2005 Sep 14.
J Biol Chem. 2005.
PMID: 16162498
Free article.
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