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Deborah Nickerson

Showing results (11-20 of 24) with videos related to

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Ebiomedicine|November 26, 2020
Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasiaMaya Barad, Fabiana Csukasi, Michaela Bosakova, et al.
Scientific Reports|February 17, 2017
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosisJennifer Zieba, Wenjuan Zhang, Jessica X Chong, et al.
Journal of Lipid Research|February 14, 2006
TagSNP analyses of the PON gene cluster: effects on PON1 activity, LDL oxidative susceptibility, and vascular diseaseChristopher S Carlson, Patrick J Heagerty, Thomas S Hatsukami, et al.
American Journal of Respiratory and Critical Care Medicine|December 17, 2015
Desmoplakin Variants Are Associated with Idiopathic Pulmonary FibrosisSusan K Mathai, Brent S Pedersen, Keith Smith, et al.
Pharmacogenetics and Genomics|May 7, 2015
Variation in genes controlling warfarin disposition and response in American Indian and Alaska Native people: CYP2C9, VKORC1, CYP4F2, CYP4F11, GGCXAlison E Fohner, Renee Robinson, Joseph Yracheta, et al.
Clinical and Translational Science|February 14, 2018
Cytochrome P450 Genetic Variation Associated with Tamoxifen Biotransformation in American Indian and Alaska Native PeopleBurhan A Khan, Renee Robinson, Alison E Fohner, et al.
Human Molecular Genetics|July 29, 2016
An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndromeS Paige Taylor, Michaela Kunova Bosakova, Miroslav Varecha, et al.
Journal of the American College of Cardiology|February 25, 2014
Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndromePeter Weeke, Jonathan D Mosley, David Hanna, et al.
Genome Medicine|March 29, 2022
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research ProgramEric Venner, Donna Muzny, Joshua D Smith, et al.
American Journal of Human Genetics|May 5, 2018
A Mixed-Effects Model for Powerful Association Tests in Integrative Functional GenomicsYu-Ru Su, Chongzhi Di, Stephanie Bien, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Ebiomedicine|November 26, 2020
Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasiaMaya Barad, Fabiana Csukasi, Michaela Bosakova, et al.
Scientific Reports|February 17, 2017
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosisJennifer Zieba, Wenjuan Zhang, Jessica X Chong, et al.
Journal of Lipid Research|February 14, 2006
TagSNP analyses of the PON gene cluster: effects on PON1 activity, LDL oxidative susceptibility, and vascular diseaseChristopher S Carlson, Patrick J Heagerty, Thomas S Hatsukami, et al.
American Journal of Respiratory and Critical Care Medicine|December 17, 2015
Desmoplakin Variants Are Associated with Idiopathic Pulmonary FibrosisSusan K Mathai, Brent S Pedersen, Keith Smith, et al.
Pharmacogenetics and Genomics|May 7, 2015
Variation in genes controlling warfarin disposition and response in American Indian and Alaska Native people: CYP2C9, VKORC1, CYP4F2, CYP4F11, GGCXAlison E Fohner, Renee Robinson, Joseph Yracheta, et al.
Clinical and Translational Science|February 14, 2018
Cytochrome P450 Genetic Variation Associated with Tamoxifen Biotransformation in American Indian and Alaska Native PeopleBurhan A Khan, Renee Robinson, Alison E Fohner, et al.
Human Molecular Genetics|July 29, 2016
An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndromeS Paige Taylor, Michaela Kunova Bosakova, Miroslav Varecha, et al.
Journal of the American College of Cardiology|February 25, 2014
Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndromePeter Weeke, Jonathan D Mosley, David Hanna, et al.
Genome Medicine|March 29, 2022
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research ProgramEric Venner, Donna Muzny, Joshua D Smith, et al.
American Journal of Human Genetics|May 5, 2018
A Mixed-Effects Model for Powerful Association Tests in Integrative Functional GenomicsYu-Ru Su, Chongzhi Di, Stephanie Bien, et al.
Pageof 3