L C Brody|B B Biesecker - JoVE Visualize

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Oncogene|July 14, 1998

BRCA1 as a potential human prostate tumor suppressor: modulation of proliferation, damage responses and expression of cell regulatory proteinsS Fan, J A Wang, R Q Yuan, et al.

Journal of Medical Genetics|December 19, 2001

Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1C Eng, L C Brody, T M Wagner, et al.

Somatic Cell and Molecular Genetics|September 1, 1995

Localization of the human homolog of the yeast cell division control 27 gene (CDC27) proximal to ITGB3 on human chromosome 17q21.3P P Ho, F J Couch, L C Brody, et al.

Genomics|January 1, 1995

A YAC-, P1-, and cosmid-based physical map of the BRCA1 region on chromosome 17q21F J Couch, L H Castilla, J Xu, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in FinnsG A Mitchell, L C Brody, I Sipila, et al.

Genomics|January 1, 1995

Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17L C Brody, K J Abel, L H Castilla, et al.

Nature Genetics|December 1, 1994

Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancerL H Castilla, F J Couch, M R Erdos, et al.

Molecular Genetics and Metabolism|August 13, 1999

Methionine synthase: high-resolution mapping of the human gene and evaluation as a candidate locus for neural tube defectsL C Brody, P J Baker, P S Chines, et al.

Nature Genetics|October 1, 1996

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%C Oddoux, J P Struewing, C M Clayton, et al.

Journal of Thrombosis and Haemostasis : JTH|July 1, 2016

Genome-wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearanceA B Ozel, B McGee, D Siemieniak, et al.

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Showing results (71-80 of 83) with videos related to

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Pageof 9

Oncogene|July 14, 1998

BRCA1 as a potential human prostate tumor suppressor: modulation of proliferation, damage responses and expression of cell regulatory proteinsS Fan, J A Wang, R Q Yuan, et al.

Journal of Medical Genetics|December 19, 2001

Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1C Eng, L C Brody, T M Wagner, et al.

Somatic Cell and Molecular Genetics|September 1, 1995

Localization of the human homolog of the yeast cell division control 27 gene (CDC27) proximal to ITGB3 on human chromosome 17q21.3P P Ho, F J Couch, L C Brody, et al.

Genomics|January 1, 1995

A YAC-, P1-, and cosmid-based physical map of the BRCA1 region on chromosome 17q21F J Couch, L H Castilla, J Xu, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in FinnsG A Mitchell, L C Brody, I Sipila, et al.

Genomics|January 1, 1995

Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17L C Brody, K J Abel, L H Castilla, et al.

Nature Genetics|December 1, 1994

Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancerL H Castilla, F J Couch, M R Erdos, et al.

Molecular Genetics and Metabolism|August 13, 1999

Methionine synthase: high-resolution mapping of the human gene and evaluation as a candidate locus for neural tube defectsL C Brody, P J Baker, P S Chines, et al.

Nature Genetics|October 1, 1996

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%C Oddoux, J P Struewing, C M Clayton, et al.

Journal of Thrombosis and Haemostasis : JTH|July 1, 2016

Genome-wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearanceA B Ozel, B McGee, D Siemieniak, et al.

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