BRCA1 regulates the G2/M checkpoint by activating Chk1 kinase upon DNA damage von Brody, Lawrence C, Yarden, Ronit I, Pardo-Reoyo, Sherly, Sgagias, Magda, Cowan, Kenneth H

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Treating Cancer by Targeting a Weakness von Brody, Lawrence C

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The Risk of Cancer Associated with Specific Mutations of BRCA1 and BRCA2 among Ashkenazi Jews von Struewing, Jeffery P, Hartge, Patricia, Wacholder, Sholom, Baker, Sonya M, Berlin, Martha, McAdams, Mary, Timmerman, Michelle M, Brody, Lawrence C, Tucker, Margaret A

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BRCA1 Interacts with Components of the Histone Deacetylase Complex von Yarden, Ronit I., Brody, Lawrence C.

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A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal G... von Brody, Lawrence C., Conley, Mary, Cox, Christopher, Kirke, Peadar N., McKeever, Mary P., Mills, James L., Molloy, Anne M., O’Leary, Valerie B., Parle-McDermott, Anne, Scott, John M., Swanson, Deborah A.

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Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays von Collins, Francis S, Hacia, Joseph G, Fan, Jian-Bing, Ryder, Oliver, Jin, Li, Edgemon, Keith, Ghandour, Ghassan, Mayer, R. Aeryn, Sun, Bryan, Hsie, Linda, Robbins, Christiane M, Brody, Lawrence C, Wang, David, Lander, Eric S, Lipshutz, Robert, Fodor, Stephen P.A

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Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis von Hacia, Joseph G, Brody, Lawrence C, Chee, Mark S, Fodor, Stephen P.A, Collins, Francis S

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Choline and homocysteine interrelations in umbilical cord and maternal plasma at delivery von Molloy, Anne M, Mills, James L, Cox, Christopher, Daly, Sean F, Conley, Mary, Brody, Lawrence C, Kirke, Peadar N, Scott, John M, Ueland, Per M

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The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals von Struewing, Jeffery P, Abeliovich, Dvorah, Peretz, Tamar, Avishai, Naaman, Kaback, Michael M, Collins, Francis S, Brody, Lawrence C

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The Breast Cancer Information Core: Database design, structure, and scope von Szabo, Csilla, Masiello, Anthony, Ryan, Joseph F., Brody, Lawrence C.

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Targeted Disruption of the Methionine Synthase Gene in Mice von Swanson, Deborah A., Liu, Mei-Lan, Baker, Priscilla J., Garrett, Lisa, Stitzel, Michael, Wu, Jianmin, Harris, Michelle, Banerjee, Ruma, Shane, Barry, Brody, Lawrence C.

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The Prevalence of Common BRCA1 and BRCA2 Mutations among Ashkenazi Jews von Hartge, Patricia, Struewing, Jeffery P., Wacholder, Sholom, Brody, Lawrence C., Tucker, Margaret A.

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Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1 von ENG, Charis, BRODY, Lawrence C, WAGNER, Teresa M. U, DEVILEE, Peter, VIJG, Jan, SZABO, Csilla, TAVTIGIAN, Sean V, NATHANSON, Katharine L, OSTRANDER, Elaine, FRANK, Thomas S

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The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1 von Oddoux, Carole, Struewing, Jeffery P, Clayton, C. Mark, Neuhausen, Susan, Brody, Lawrence C, Kaback, Michael, Haas, Bruce, Norton, Larry, Borgen, Patrick, Jhanwar, Suresh, Goldgar, David, Ostrer, Harry, Offit, Kenneth

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Breast cancer susceptibility genes. BRCA1 and BRCA2 von Brody, L C, Biesecker, B B

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Rapid detection of deletion, insertion, and substitution mutations via heteroduplex analysis using capillary- and microchip-based electrophoresis von Tian, H, Brody, L C, Landers, J P

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Single-Strand Conformation Polymorphism Analysis by Capillary and Microchip Electrophoresis: A Fast, Simple Method for Detection of Common Mutations in BRCA1 and BRCA2 von Tian, Huijun, Jaquins-Gerstl, Andrea, Munro, Nicole, Trucco, Massimo, Brody, Lawrence C, Landers, James P

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Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association von O’Leary, Valerie B., Mills, James L., Pangilinan, Faith, Kirke, Peadar N., Cox, Christopher, Conley, Mary, Weiler, Andrea, Peng, Kun, Shane, Barry, Scott, John M., Parle-McDermott, Anne, Molloy, Anne M., Brody, Lawrence C.

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Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer von Castilla, Lucio H, Couch, Fergus J, Erdos, Michael R, Hoskins, Kent F, Calzone, Kathy, Garber, Judy E, Boyd, Jeff, Lubin, Matthew B, Deshano, Michelle L, Brody, Lawrence C, Collins, Francis S, Weber, Barbara L

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A polymorphism in the MTHFD1 gene increases a mother’s risk of having an unexplained second trimester pregnancy loss von Parle-McDermott, Anne, Pangilinan, Faith, Mills, James L., Signore, Caroline C., Molloy, Anne M., Cotter, Amanda, Conley, Mary, Cox, Christopher, Kirke, Peadar N., Scott, John M., Brody, Lawrence C.

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