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G Biesecker

Showing results (351-360 of 475) with videos related to

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Human Molecular Genetics|May 23, 2007
Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determinationEmma N Hilton, Forbes D C Manson, Jill E Urquhart, et al.
American Journal of Human Genetics|December 29, 2005
Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome geneDarryl Y Nishimura, Ruth E Swiderski, Charles C Searby, et al.
Atherosclerosis|July 13, 2010
FOS expression in blood as a LDL-independent marker of statin treatmentJu-Gyeong Kang, Ho Joong Sung, Sarah I Jawed, et al.
American Journal of Human Genetics|March 21, 2000
Detection of chromosomal aberrations by a whole-genome microsatellite screenM J Rosenberg, D Vaske, C E Killoran, et al.
Pediatric Obesity|June 19, 2013
Hyperphagia among patients with Bardet-Biedl syndromeR Sherafat-Kazemzadeh, L Ivey, S R Kahn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 2, 2018
Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq<sup>®</sup> cohortKatie L Lewis, Alexis R Heidlebaugh, Sandra Epps, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2015
High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data setsChristopher A Wassif, Joanna L Cross, James Iben, et al.
Circulation. Cardiovascular Genetics|July 18, 2013
Interpreting secondary cardiac disease variants in an exome cohortDavid Ng, Jennifer J Johnston, Jamie K Teer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 26, 2021
Variant curation expert panel recommendations for RYR1 pathogenicity classifications in malignant hyperthermia susceptibilityJennifer J Johnston, Robert T Dirksen, Thierry Girard, et al.
American Journal of Human Genetics|February 5, 2013
Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorderSanthosh Girirajan, Megan Y Dennis, Carl Baker, et al.
Pageof 48

Showing results (351-360 of 475) with videos related to

Sort By:
Pageof 48
Human Molecular Genetics|May 23, 2007
Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determinationEmma N Hilton, Forbes D C Manson, Jill E Urquhart, et al.
American Journal of Human Genetics|December 29, 2005
Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome geneDarryl Y Nishimura, Ruth E Swiderski, Charles C Searby, et al.
Atherosclerosis|July 13, 2010
FOS expression in blood as a LDL-independent marker of statin treatmentJu-Gyeong Kang, Ho Joong Sung, Sarah I Jawed, et al.
American Journal of Human Genetics|March 21, 2000
Detection of chromosomal aberrations by a whole-genome microsatellite screenM J Rosenberg, D Vaske, C E Killoran, et al.
Pediatric Obesity|June 19, 2013
Hyperphagia among patients with Bardet-Biedl syndromeR Sherafat-Kazemzadeh, L Ivey, S R Kahn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 2, 2018
Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq<sup>®</sup> cohortKatie L Lewis, Alexis R Heidlebaugh, Sandra Epps, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2015
High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data setsChristopher A Wassif, Joanna L Cross, James Iben, et al.
Circulation. Cardiovascular Genetics|July 18, 2013
Interpreting secondary cardiac disease variants in an exome cohortDavid Ng, Jennifer J Johnston, Jamie K Teer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 26, 2021
Variant curation expert panel recommendations for RYR1 pathogenicity classifications in malignant hyperthermia susceptibilityJennifer J Johnston, Robert T Dirksen, Thierry Girard, et al.
American Journal of Human Genetics|February 5, 2013
Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorderSanthosh Girirajan, Megan Y Dennis, Carl Baker, et al.
Pageof 48