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Jamie Russell

Showing results (21-30 of 38) with videos related to

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Disease Models & Mechanisms|December 20, 2018
A viable hypomorphic <i>Arnt2</i> mutation causes hyperphagic obesity, diabetes and hepatic steatosisEmre E Turer, Miguel San Miguel, Kuan-Wen Wang, et al.
Science Advances|March 1, 2024
Genetic determinants of blood pressure and heart rate identified through ENU-induced mutagenesis with automated meiotic mappingSamantha K Teixeira, Roberto Pontes, Luiz Fernando G Zuleta, et al.
JCI Insight|July 22, 2025
A hypomorphic Mpi mutation unlocks an in vivo tool for studying global N-glycosylation deficiencyElisa B Lin, Steve Meregini, Zhao Zhang, et al.
The Journal of Experimental Medicine|January 28, 2020
Essential cell-extrinsic requirement for PDIA6 in lymphoid and myeloid developmentJin Huk Choi, Xue Zhong, Zhao Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 28, 2020
Forward genetic analysis using OCT screening identifies <i>Sfxn3</i> mutations leading to progressive outer retinal degeneration in miceBo Chen, Bogale Aredo, Yi Ding, et al.
Disease Models & Mechanisms|October 4, 2018
The class I myosin MYO1D binds to lipid and protects against colitisWilliam McAlpine, Kuan-Wen Wang, Jin Huk Choi, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 18, 2019
Enhanced susceptibility to chemically induced colitis caused by excessive endosomal TLR signaling in LRBA-deficient miceKuan-Wen Wang, Xiaoming Zhan, William McAlpine, et al.
Allergy|August 19, 2020
Dominant atopy risk mutations identified by mouse forward genetic analysisJeffrey A SoRelle, Zhe Chen, Jianhui Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 17, 2018
Excessive endosomal TLR signaling causes inflammatory disease in mice with defective SMCR8-WDR41-C9ORF72 complex functionWilliam McAlpine, Lei Sun, Kuan-Wen Wang, et al.
Cell Metabolism|October 13, 2022
Obesity caused by an OVOL2 mutation reveals dual roles of OVOL2 in promoting thermogenesis and limiting white adipogenesisZhao Zhang, Yiao Jiang, Lijing Su, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Disease Models & Mechanisms|December 20, 2018
A viable hypomorphic <i>Arnt2</i> mutation causes hyperphagic obesity, diabetes and hepatic steatosisEmre E Turer, Miguel San Miguel, Kuan-Wen Wang, et al.
Science Advances|March 1, 2024
Genetic determinants of blood pressure and heart rate identified through ENU-induced mutagenesis with automated meiotic mappingSamantha K Teixeira, Roberto Pontes, Luiz Fernando G Zuleta, et al.
JCI Insight|July 22, 2025
A hypomorphic Mpi mutation unlocks an in vivo tool for studying global N-glycosylation deficiencyElisa B Lin, Steve Meregini, Zhao Zhang, et al.
The Journal of Experimental Medicine|January 28, 2020
Essential cell-extrinsic requirement for PDIA6 in lymphoid and myeloid developmentJin Huk Choi, Xue Zhong, Zhao Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 28, 2020
Forward genetic analysis using OCT screening identifies <i>Sfxn3</i> mutations leading to progressive outer retinal degeneration in miceBo Chen, Bogale Aredo, Yi Ding, et al.
Disease Models & Mechanisms|October 4, 2018
The class I myosin MYO1D binds to lipid and protects against colitisWilliam McAlpine, Kuan-Wen Wang, Jin Huk Choi, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 18, 2019
Enhanced susceptibility to chemically induced colitis caused by excessive endosomal TLR signaling in LRBA-deficient miceKuan-Wen Wang, Xiaoming Zhan, William McAlpine, et al.
Allergy|August 19, 2020
Dominant atopy risk mutations identified by mouse forward genetic analysisJeffrey A SoRelle, Zhe Chen, Jianhui Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 17, 2018
Excessive endosomal TLR signaling causes inflammatory disease in mice with defective SMCR8-WDR41-C9ORF72 complex functionWilliam McAlpine, Lei Sun, Kuan-Wen Wang, et al.
Cell Metabolism|October 13, 2022
Obesity caused by an OVOL2 mutation reveals dual roles of OVOL2 in promoting thermogenesis and limiting white adipogenesisZhao Zhang, Yiao Jiang, Lijing Su, et al.
Pageof 4