Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Brody

Showing results (141-150 of 234) with videos related to

Pageof 24
Sort By:
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.
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.
The Journal of Nutrition|February 11, 2023
Investigating Genetic Determinants of Plasma Inositol Status in Adult HumansEleanor Weston, Faith Pangilinan, Simon Eaton, et al.
Molecular Genetics and Metabolism|July 24, 2024
SLC25A48 influences plasma levels of choline and localizes to the inner mitochondrial membraneDavid J Bernard, Faith Pangilinan, Caitlin Mendina, 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.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 13, 2009
Uncoupling protein 2 polymorphisms as risk factors for NTDsAdam Mitchell, Faith Pangilinan, Julie Van der Meer, 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.
American Journal of Medical Genetics. Part A|September 12, 2012
Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficienciesMarilyn L Browne, Tonia C Carter, Denise M Kay, et al.
JCO Oncology Practice|December 2, 2021
Systemic Therapy Decision Making in Advanced Cancer: A Qualitative Analysis of Patient-Oncologist EncountersGarrett T Wasp, Kristin E Knutzen, Genevra F Murray, et al.
Molecular Genetics and Metabolism|December 14, 2005
Reduced folate carrier polymorphisms and neural tube defect riskValerie B O'leary, Faith Pangilinan, Christopher Cox, et al.
Pageof 24

Showing results (141-150 of 234) with videos related to

Sort By:
Pageof 24
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.
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.
The Journal of Nutrition|February 11, 2023
Investigating Genetic Determinants of Plasma Inositol Status in Adult HumansEleanor Weston, Faith Pangilinan, Simon Eaton, et al.
Molecular Genetics and Metabolism|July 24, 2024
SLC25A48 influences plasma levels of choline and localizes to the inner mitochondrial membraneDavid J Bernard, Faith Pangilinan, Caitlin Mendina, 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.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 13, 2009
Uncoupling protein 2 polymorphisms as risk factors for NTDsAdam Mitchell, Faith Pangilinan, Julie Van der Meer, 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.
American Journal of Medical Genetics. Part A|September 12, 2012
Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficienciesMarilyn L Browne, Tonia C Carter, Denise M Kay, et al.
JCO Oncology Practice|December 2, 2021
Systemic Therapy Decision Making in Advanced Cancer: A Qualitative Analysis of Patient-Oncologist EncountersGarrett T Wasp, Kristin E Knutzen, Genevra F Murray, et al.
Molecular Genetics and Metabolism|December 14, 2005
Reduced folate carrier polymorphisms and neural tube defect riskValerie B O'leary, Faith Pangilinan, Christopher Cox, et al.
Pageof 24