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C Brody

Showing results (121-130 of 234) with videos related to

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Nature Genetics|September 10, 1998
The APCI1307K allele and cancer risk in a community-based study of Ashkenazi JewsT Woodage, S M King, S Wacholder, et al.
The Journal of Biological Chemistry|February 15, 1992
Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequencesL C Brody, G A Mitchell, C Obie, et al.
American Journal of Human Genetics|July 1, 1995
Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancerJ P Struewing, L C Brody, M R Erdos, et al.
Human Genetics|January 9, 2009
Analysis of the MTHFD1 promoter and risk of neural tube defectsNicola Carroll, Faith Pangilinan, Anne M Molloy, et al.
Cancer|August 1, 1994
Familial breast cancer. Approaching the isolation of a susceptibility geneB L Weber, K J Abel, L C Brody, et al.
Biodata Mining|February 4, 2016
r2VIM: A new variable selection method for random forests in genome-wide association studiesSilke Szymczak, Emily Holzinger, Abhijit Dasgupta, et al.
PNAS Nexus|April 1, 2024
Vitamin B12 status and folic acid supplementation influence mitochondrial heteroplasmy levels in miceDarren J Walsh, David J Bernard, Joanna L Fiddler, et al.
Molecular and Cellular Biology|February 7, 2001
Targeted disruption of the methionine synthase gene in miceD A Swanson, M L Liu, P J Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1991
Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutationG A Mitchell, D Labuda, G Fontaine, et al.
BMC Developmental Biology|April 7, 2012
Disruption of the folate pathway in zebrafish causes developmental defectsMarina S Lee, Jenna R Bonner, David J Bernard, et al.
Pageof 24

Showing results (121-130 of 234) with videos related to

Sort By:
Pageof 24
Nature Genetics|September 10, 1998
The APCI1307K allele and cancer risk in a community-based study of Ashkenazi JewsT Woodage, S M King, S Wacholder, et al.
The Journal of Biological Chemistry|February 15, 1992
Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequencesL C Brody, G A Mitchell, C Obie, et al.
American Journal of Human Genetics|July 1, 1995
Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancerJ P Struewing, L C Brody, M R Erdos, et al.
Human Genetics|January 9, 2009
Analysis of the MTHFD1 promoter and risk of neural tube defectsNicola Carroll, Faith Pangilinan, Anne M Molloy, et al.
Cancer|August 1, 1994
Familial breast cancer. Approaching the isolation of a susceptibility geneB L Weber, K J Abel, L C Brody, et al.
Biodata Mining|February 4, 2016
r2VIM: A new variable selection method for random forests in genome-wide association studiesSilke Szymczak, Emily Holzinger, Abhijit Dasgupta, et al.
PNAS Nexus|April 1, 2024
Vitamin B12 status and folic acid supplementation influence mitochondrial heteroplasmy levels in miceDarren J Walsh, David J Bernard, Joanna L Fiddler, et al.
Molecular and Cellular Biology|February 7, 2001
Targeted disruption of the methionine synthase gene in miceD A Swanson, M L Liu, P J Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1991
Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutationG A Mitchell, D Labuda, G Fontaine, et al.
BMC Developmental Biology|April 7, 2012
Disruption of the folate pathway in zebrafish causes developmental defectsMarina S Lee, Jenna R Bonner, David J Bernard, et al.
Pageof 24