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Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption.
Meyer S, Stevens A, Paredes R, Schneider M, Walker MJ, Williamson AJK, Gonzalez-Sanchez MB, Smetsers S, Dalal V, Teng HY, White DJ, Taylor S, Muter J, Pierce A, de Leonibus C, Rockx DAP, Rooimans MA, Spooncer E, Stauffer S, Biswas K, Godthelp B, Dorsman J, Clayton PE, Sharan SK, Whetton AD. Meyer S, et al. Among authors: stevens a. Cell Death Dis. 2017 Jun 15;8(6):e2875. doi: 10.1038/cddis.2017.264. Cell Death Dis. 2017. PMID: 28617445 Free PMC article.
Network analysis: a new approach to study endocrine disorders.
Stevens A, De Leonibus C, Hanson D, Dowsey AW, Whatmore A, Meyer S, Donn RP, Chatelain P, Banerjee I, Cosgrove KE, Clayton PE, Dunne MJ. Stevens A, et al. J Mol Endocrinol. 2013 Dec 19;52(1):R79-93. doi: 10.1530/JME-13-0112. Print 2014 Feb. J Mol Endocrinol. 2013. PMID: 24085748 Review.
3-M syndrome: a growth disorder associated with IGF2 silencing.
Murray PG, Hanson D, Coulson T, Stevens A, Whatmore A, Poole RL, Mackay DJ, Black GC, Clayton PE. Murray PG, et al. Among authors: stevens a. Endocr Connect. 2013 Nov 11;2(4):225-35. doi: 10.1530/EC-13-0065. Print 2013. Endocr Connect. 2013. PMID: 24148222 Free PMC article.
Pediatric perspective on pharmacogenomics.
Stevens A, De Leonibus C, Hanson D, Whatmore A, Murray P, Donn R, Meyer S, Chatelain P, Clayton P. Stevens A, et al. Pharmacogenomics. 2013 Nov;14(15):1889-905. doi: 10.2217/pgs.13.193. Pharmacogenomics. 2013. PMID: 24236488 Review.
Pharmacogenomics related to growth disorders.
Stevens A, De Leonibus C, Whatmore A, Hanson D, Murray P, Chatelain P, Westwood M, Clayton P. Stevens A, et al. Horm Res Paediatr. 2013;80(6):477-90. doi: 10.1159/000355658. Epub 2013 Nov 27. Horm Res Paediatr. 2013. PMID: 24296333 Review.
2,007 results