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PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects.
Petit F, Longoni M, Wells J, Maser RS, Bogenschutz EL, Dysart MJ, Contreras HTM, Frénois F, Pober BR, Clark RD, Giampietro PF, Ropers HH, Hu H, Loscertales M, Wagner R, Ai X, Brand H, Jourdain AS, Delrue MA, Gilbert-Dussardier B, Devisme L, Keren B, McCulley DJ, Qiao L, Hernan R, Wynn J, Scott TM, Calame DG, Coban-Akdemir Z, Hernandez P, Hernandez-Garcia A, Yonath H, Lupski JR, Shen Y, Chung WK, Scott DA, Bult CJ, Donahoe PK, High FA. Petit F, et al. Among authors: wells j. Am J Hum Genet. 2023 Oct 5;110(10):1787-1803. doi: 10.1016/j.ajhg.2023.09.002. Epub 2023 Sep 25. Am J Hum Genet. 2023. PMID: 37751738 Free PMC article.
Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes.
Russell MK, Longoni M, Wells J, Maalouf FI, Tracy AA, Loscertales M, Ackerman KG, Pober BR, Lage K, Bult CJ, Donahoe PK. Russell MK, et al. Among authors: wells j. Proc Natl Acad Sci U S A. 2012 Feb 21;109(8):2978-83. doi: 10.1073/pnas.1121621109. Epub 2012 Feb 6. Proc Natl Acad Sci U S A. 2012. PMID: 22315423 Free PMC article.
Molecular pathogenesis of congenital diaphragmatic hernia revealed by exome sequencing, developmental data, and bioinformatics.
Longoni M, High FA, Russell MK, Kashani A, Tracy AA, Coletti CM, Hila R, Shamia A, Wells J, Ackerman KG, Wilson JM, Bult CJ, Lee C, Lage K, Pober BR, Donahoe PK. Longoni M, et al. Among authors: wells j. Proc Natl Acad Sci U S A. 2014 Aug 26;111(34):12450-5. doi: 10.1073/pnas.1412509111. Epub 2014 Aug 8. Proc Natl Acad Sci U S A. 2014. PMID: 25107291 Free PMC article.
Cancer-associated mesothelial cells are regulated by the anti-Müllerian hormone axis.
Chauvin M, Meinsohn MC, Dasari S, May P, Iyer S, Nguyen NMP, Oliva E, Lucchini Z, Nagykery N, Kashiwagi A, Mishra R, Maser R, Wells J, Bult CJ, Mitra AK, Donahoe PK, Pépin D. Chauvin M, et al. Among authors: wells j. Cell Rep. 2023 Jul 25;42(7):112730. doi: 10.1016/j.celrep.2023.112730. Epub 2023 Jul 14. Cell Rep. 2023. PMID: 37453057 Free article.
An X chromosome gene, WTX, is commonly inactivated in Wilms tumor.
Rivera MN, Kim WJ, Wells J, Driscoll DR, Brannigan BW, Han M, Kim JC, Feinberg AP, Gerald WL, Vargas SO, Chin L, Iafrate AJ, Bell DW, Haber DA. Rivera MN, et al. Among authors: wells j. Science. 2007 Feb 2;315(5812):642-5. doi: 10.1126/science.1137509. Epub 2007 Jan 4. Science. 2007. PMID: 17204608
The tumor suppressor WTX shuttles to the nucleus and modulates WT1 activity.
Rivera MN, Kim WJ, Wells J, Stone A, Burger A, Coffman EJ, Zhang J, Haber DA. Rivera MN, et al. Among authors: wells j. Proc Natl Acad Sci U S A. 2009 May 19;106(20):8338-43. doi: 10.1073/pnas.0811349106. Epub 2009 May 4. Proc Natl Acad Sci U S A. 2009. PMID: 19416806 Free PMC article.
SUMO-1 modification of the Wilms' tumor suppressor WT1.
Smolen GA, Vassileva MT, Wells J, Matunis MJ, Haber DA. Smolen GA, et al. Among authors: wells j. Cancer Res. 2004 Nov 1;64(21):7846-51. doi: 10.1158/0008-5472.CAN-04-1502. Cancer Res. 2004. PMID: 15520190
4,318 results