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Showing results (731-740 of 897) with videos related to

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Cellular and Molecular Gastroenterology and Hepatology|October 9, 2021
Defective Lipid Droplet-Lysosome Interaction Causes Fatty Liver Disease as Evidenced by Human Mutations in TMEM199 and CCDC115Lars E Larsen, Marjolein A W van den Boogert, Wilson A Rios-Ocampo, et al.
American Journal of Human Genetics|June 18, 2019
Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human LiverMinal Çalışkan, Elisabetta Manduchi, H Shanker Rao, et al.
Cell Stem Cell|February 2, 2021
Pathogenic LMNA variants disrupt cardiac lamina-chromatin interactions and de-repress alternative fate genesParisha P Shah, Wenjian Lv, Joshua H Rhoades, et al.
Circulation. Cardiovascular Genetics|March 26, 2016
Treatment Gaps in Adults With Heterozygous Familial Hypercholesterolemia in the United States: Data From the CASCADE-FH RegistryEmil M deGoma, Zahid S Ahmad, Emily C O'Brien, et al.
Stem Cell Research|May 23, 2020
Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen programKanika Kanchan, Kruthika Iyer, Lisa R Yanek, et al.
Journal of Clinical Lipidology|October 15, 2022
Guidance for the diagnosis and treatment of hypolipidemia disordersCindy Bredefeld, M Mahmood Hussain, Maurizio Averna, et al.
Science Translational Medicine|January 14, 2021
Kidney disease genetic risk variants alter lysosomal beta-mannosidase (<i>MANBA</i>) expression and disease severityXiangchen Gu, Hongliu Yang, Xin Sheng, et al.
Nature Genetics|January 18, 2006
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetesStruan F A Grant, Gudmar Thorleifsson, Inga Reynisdottir, et al.
Human Molecular Genetics|June 9, 2016
Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathyElizabeth E Palmer, Kelsey E Jarrett, Rani K Sachdev, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2013
Implementing genomic medicine in the clinic: the future is hereTeri A Manolio, Rex L Chisholm, Brad Ozenberger, et al.
Pageof 90

Showing results (731-740 of 897) with videos related to

Sort By:
Pageof 90
Cellular and Molecular Gastroenterology and Hepatology|October 9, 2021
Defective Lipid Droplet-Lysosome Interaction Causes Fatty Liver Disease as Evidenced by Human Mutations in TMEM199 and CCDC115Lars E Larsen, Marjolein A W van den Boogert, Wilson A Rios-Ocampo, et al.
American Journal of Human Genetics|June 18, 2019
Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human LiverMinal Çalışkan, Elisabetta Manduchi, H Shanker Rao, et al.
Cell Stem Cell|February 2, 2021
Pathogenic LMNA variants disrupt cardiac lamina-chromatin interactions and de-repress alternative fate genesParisha P Shah, Wenjian Lv, Joshua H Rhoades, et al.
Circulation. Cardiovascular Genetics|March 26, 2016
Treatment Gaps in Adults With Heterozygous Familial Hypercholesterolemia in the United States: Data From the CASCADE-FH RegistryEmil M deGoma, Zahid S Ahmad, Emily C O'Brien, et al.
Stem Cell Research|May 23, 2020
Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen programKanika Kanchan, Kruthika Iyer, Lisa R Yanek, et al.
Journal of Clinical Lipidology|October 15, 2022
Guidance for the diagnosis and treatment of hypolipidemia disordersCindy Bredefeld, M Mahmood Hussain, Maurizio Averna, et al.
Science Translational Medicine|January 14, 2021
Kidney disease genetic risk variants alter lysosomal beta-mannosidase (<i>MANBA</i>) expression and disease severityXiangchen Gu, Hongliu Yang, Xin Sheng, et al.
Nature Genetics|January 18, 2006
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetesStruan F A Grant, Gudmar Thorleifsson, Inga Reynisdottir, et al.
Human Molecular Genetics|June 9, 2016
Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathyElizabeth E Palmer, Kelsey E Jarrett, Rani K Sachdev, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2013
Implementing genomic medicine in the clinic: the future is hereTeri A Manolio, Rex L Chisholm, Brad Ozenberger, et al.
Pageof 90