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A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group.
Brody LC, Conley M, Cox C, Kirke PN, McKeever MP, Mills JL, Molloy AM, O'Leary VB, Parle-McDermott A, Scott JM, Swanson DA. Brody LC, et al. Am J Hum Genet. 2002 Nov;71(5):1207-15. doi: 10.1086/344213. Epub 2002 Oct 16. Am J Hum Genet. 2002. PMID: 12384833 Free PMC article.
Expression and processing of human ornithine-delta-aminotransferase in Saccharomyces cerevisiae.
Dougherty KM, Swanson DA, Brody LC, Valle D. Dougherty KM, et al. Among authors: brody lc. Hum Mol Genet. 1993 Nov;2(11):1835-40. doi: 10.1093/hmg/2.11.1835. Hum Mol Genet. 1993. PMID: 8281144
Targeted disruption of the methionine synthase gene in mice.
Swanson DA, Liu ML, Baker PJ, Garrett L, Stitzel M, Wu J, Harris M, Banerjee R, Shane B, Brody LC. Swanson DA, et al. Among authors: brody lc. Mol Cell Biol. 2001 Feb;21(4):1058-65. doi: 10.1128/MCB.21.4.1058-1065.2001. Mol Cell Biol. 2001. PMID: 11158293 Free PMC article.
Methionine synthase: high-resolution mapping of the human gene and evaluation as a candidate locus for neural tube defects.
Brody LC, Baker PJ, Chines PS, Musick A, Molloy AM, Swanson DA, Kirke PN, Ghosh S, Scott JM, Mills JL. Brody LC, et al. Mol Genet Metab. 1999 Aug;67(4):324-33. doi: 10.1006/mgme.1999.2881. Mol Genet Metab. 1999. PMID: 10444343
BRCA1 regulates the G2/M checkpoint by activating Chk1 kinase upon DNA damage.
Yarden RI, Pardo-Reoyo S, Sgagias M, Cowan KH, Brody LC. Yarden RI, et al. Among authors: brody lc. Nat Genet. 2002 Mar;30(3):285-9. doi: 10.1038/ng837. Epub 2002 Feb 11. Nat Genet. 2002. PMID: 11836499
BRCA1 Circos: a visualisation resource for functional analysis of missense variants.
Jhuraney A, Velkova A, Johnson RC, Kessing B, Carvalho RS, Whiley P, Spurdle AB, Vreeswijk MP, Caputo SM, Millot GA, Vega A, Coquelle N, Galli A, Eccles D, Blok MJ, Pal T, van der Luijt RB, Santamariña Pena M, Neuhausen SL, Donenberg T, Machackova E, Thomas S, Vallée M, Couch FJ, Tavtigian SV, Glover JN, Carvalho MA, Brody LC, Sharan SK, Monteiro AN; Evidence-based Network for the Interpretation of Germline Mutant Alleles Consortium. Jhuraney A, et al. Among authors: brody lc. J Med Genet. 2015 Apr;52(4):224-30. doi: 10.1136/jmedgenet-2014-102766. Epub 2015 Feb 2. J Med Genet. 2015. PMID: 25643705 Free PMC article.
Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.
Alter BP, Rosenberg PS, Brody LC. Alter BP, et al. Among authors: brody lc. J Med Genet. 2007 Jan;44(1):1-9. doi: 10.1136/jmg.2006.043257. Epub 2006 Jul 6. J Med Genet. 2007. PMID: 16825431 Free PMC article.
The murine homolog of the human breast and ovarian cancer susceptibility gene Brca1 maps to mouse chromosome 11D.
Schröck E, Badger P, Larson D, Erdos M, Wynshaw-Boris A, Ried T, Brody L. Schröck E, et al. Hum Genet. 1996 Feb;97(2):256-9. doi: 10.1007/BF02265277. Hum Genet. 1996. PMID: 8566965
BRCA1 mutations in African Americans.
Panguluri RC, Brody LC, Modali R, Utley K, Adams-Campbell L, Day AA, Whitfield-Broome C, Dunston GM. Panguluri RC, et al. Among authors: brody lc. Hum Genet. 1999 Jul-Aug;105(1-2):28-31. doi: 10.1007/s004399900085. Hum Genet. 1999. PMID: 10480351
Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays.
Hacia JG, Fan JB, Ryder O, Jin L, Edgemon K, Ghandour G, Mayer RA, Sun B, Hsie L, Robbins CM, Brody LC, Wang D, Lander ES, Lipshutz R, Fodor SP, Collins FS. Hacia JG, et al. Among authors: brody lc. Nat Genet. 1999 Jun;22(2):164-7. doi: 10.1038/9674. Nat Genet. 1999. PMID: 10369258
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