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WWP1 Gain-of-Function Inactivation of PTEN in Cancer Predisposition.
N Engl J Med. 2020 May 28;382(22):2103-2116. doi: 10.1056/NEJMoa1914919.
N Engl J Med. 2020.
PMID: 32459922
Free PMC article.
Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer.
Yehia L, Niazi F, Ni Y, Ngeow J, Sankunny M, Liu Z, Wei W, Mester JL, Keri RA, Zhang B, Eng C.
Yehia L, et al.
Am J Hum Genet. 2015 Nov 5;97(5):661-76. doi: 10.1016/j.ajhg.2015.10.001. Epub 2015 Oct 29.
Am J Hum Genet. 2015.
PMID: 26522472
Free PMC article.
Item in Clipboard
Neural transcriptome of constitutional Pten dysfunction in mice and its relevance to human idiopathic autism spectrum disorder.
Tilot AK, Bebek G, Niazi F, Altemus JB, Romigh T, Frazier TW, Eng C.
Tilot AK, et al.
Mol Psychiatry. 2016 Jan;21(1):118-25. doi: 10.1038/mp.2015.17. Epub 2015 Mar 10.
Mol Psychiatry. 2016.
PMID: 25754085
Free PMC article.
Item in Clipboard
Germline disruption of Pten localization causes enhanced sex-dependent social motivation and increased glial production.
Tilot AK, Gaugler MK, Yu Q, Romigh T, Yu W, Miller RH, Frazier TW 2nd, Eng C.
Tilot AK, et al.
Hum Mol Genet. 2014 Jun 15;23(12):3212-27. doi: 10.1093/hmg/ddu031. Epub 2014 Jan 26.
Hum Mol Genet. 2014.
PMID: 24470394
Free PMC article.
Item in Clipboard
Lifetime cancer risks in individuals with germline PTEN mutations.
Tan MH, Mester JL, Ngeow J, Rybicki LA, Orloff MS, Eng C.
Tan MH, et al.
Clin Cancer Res. 2012 Jan 15;18(2):400-7. doi: 10.1158/1078-0432.CCR-11-2283.
Clin Cancer Res. 2012.
PMID: 22252256
Free PMC article.
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A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands.
Tan MH, Mester J, Peterson C, Yang Y, Chen JL, Rybicki LA, Milas K, Pederson H, Remzi B, Orloff MS, Eng C.
Tan MH, et al.
Am J Hum Genet. 2011 Jan 7;88(1):42-56. doi: 10.1016/j.ajhg.2010.11.013. Epub 2010 Dec 30.
Am J Hum Genet. 2011.
PMID: 21194675
Free PMC article.
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