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Weimin He

Showing results (81-90 of 97) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|December 9, 2003
Adipose-specific peroxisome proliferator-activated receptor gamma knockout causes insulin resistance in fat and liver but not in muscleWeimin He, Yaacov Barak, Andrea Hevener, et al.
Birth Defects Research. Part B, Developmental and Reproductive Toxicology|February 8, 2012
Cannabinoid receptor 1 signaling in embryo neurodevelopmentDelphine Psychoyos, K Yaragudri Vinod, Jin Cao, et al.
Cell Metabolism|July 10, 2007
ERRgamma directs and maintains the transition to oxidative metabolism in the postnatal heartWilliam A Alaynick, Richard P Kondo, Wen Xie, et al.
Annals of Neurology|July 28, 2016
KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunctionJessica Duis, Shannon Dean, Carolyn Applegate, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|September 24, 2011
Immunomodulatory action of dietary fish oil and targeted deletion of intestinal epithelial cell PPARδ in inflammation-induced colon carcinogenesisJennifer M Monk, Wooki Kim, Evelyn Callaway, et al.
American Journal of Medical Genetics. Part A|November 19, 2016
Homozygous variants in pyrroline-5-carboxylate reductase 2 (PYCR2) in patients with progressive microcephaly and hypomyelinating leukodystrophyLinyan Meng, Taraka Donti, Fan Xia, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
Clinical and molecular characterization of de novo loss of function variants in HNRNPUMagalie S Leduc, Hsiao-Tuan Chao, Chunjing Qu, et al.
Genome Medicine|September 30, 2018
Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorderElizabeth A Normand, Alicia Braxton, Salma Nassef, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 25, 2020
CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indelsBo Yuan, Lei Wang, Pengfei Liu, et al.
Nature Communications|February 19, 2016
Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasisNatalia Gomez-Ospina, Carol J Potter, Rui Xiao, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
Proceedings of the National Academy of Sciences of the United States of America|December 9, 2003
Adipose-specific peroxisome proliferator-activated receptor gamma knockout causes insulin resistance in fat and liver but not in muscleWeimin He, Yaacov Barak, Andrea Hevener, et al.
Birth Defects Research. Part B, Developmental and Reproductive Toxicology|February 8, 2012
Cannabinoid receptor 1 signaling in embryo neurodevelopmentDelphine Psychoyos, K Yaragudri Vinod, Jin Cao, et al.
Cell Metabolism|July 10, 2007
ERRgamma directs and maintains the transition to oxidative metabolism in the postnatal heartWilliam A Alaynick, Richard P Kondo, Wen Xie, et al.
Annals of Neurology|July 28, 2016
KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunctionJessica Duis, Shannon Dean, Carolyn Applegate, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|September 24, 2011
Immunomodulatory action of dietary fish oil and targeted deletion of intestinal epithelial cell PPARδ in inflammation-induced colon carcinogenesisJennifer M Monk, Wooki Kim, Evelyn Callaway, et al.
American Journal of Medical Genetics. Part A|November 19, 2016
Homozygous variants in pyrroline-5-carboxylate reductase 2 (PYCR2) in patients with progressive microcephaly and hypomyelinating leukodystrophyLinyan Meng, Taraka Donti, Fan Xia, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
Clinical and molecular characterization of de novo loss of function variants in HNRNPUMagalie S Leduc, Hsiao-Tuan Chao, Chunjing Qu, et al.
Genome Medicine|September 30, 2018
Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorderElizabeth A Normand, Alicia Braxton, Salma Nassef, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 25, 2020
CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indelsBo Yuan, Lei Wang, Pengfei Liu, et al.
Nature Communications|February 19, 2016
Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasisNatalia Gomez-Ospina, Carol J Potter, Rui Xiao, et al.
Pageof 10