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Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida.
Agopian AJ, Bhalla AD, Boerwinkle E, Finnell RH, Grove ML, Hixson JE, Shimmin LC, Sewda A, Stuart C, Zhong Y, Zhu H, Mitchell LE. Agopian AJ, et al. Among authors: stuart c. Birth Defects Res A Clin Mol Teratol. 2013 Sep;97(9):597-601. doi: 10.1002/bdra.23163. Epub 2013 Aug 2. Birth Defects Res A Clin Mol Teratol. 2013. PMID: 23913553 Free PMC article.
Genome-wide linkage and positional candidate gene study of blood pressure response to dietary potassium intervention: the genetic epidemiology network of salt sensitivity study.
Kelly TN, Hixson JE, Rao DC, Mei H, Rice TK, Jaquish CE, Shimmin LC, Schwander K, Chen CS, Liu D, Chen J, Bormans C, Shukla P, Farhana N, Stuart C, Whelton PK, He J, Gu D. Kelly TN, et al. Among authors: stuart c. Circ Cardiovasc Genet. 2010 Dec;3(6):539-47. doi: 10.1161/CIRCGENETICS.110.940635. Epub 2010 Sep 22. Circ Cardiovasc Genet. 2010. PMID: 20861505 Free PMC article. Clinical Trial.
Ex vivo gene editing and cell therapy for hereditary tyrosinemia type 1.
Ates I, Stuart C, Rathbone T, Barzi M, He G, Major AM, Shankar V, Lyman RA, Angner SS, Mackay TFC, Srinivasan S, Farris AB, Bissig KD, Cottle RN. Ates I, et al. Among authors: stuart c. Hepatol Commun. 2024 Apr 26;8(5):e0424. doi: 10.1097/HC9.0000000000000424. eCollection 2024 May 1. Hepatol Commun. 2024. PMID: 38668730 Free article.
443 results