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Showing results (141-150 of 159) with videos related to

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International Journal of Molecular Sciences|May 27, 2023
Biallelic Loss-of-Function Variants in <i>BICD1</i> Are Associated with Peripheral Neuropathy and Hearing LossYoel Hirsch, Wendy K Chung, Sergey Novoselov, et al.
Cell Metabolism|February 20, 2024
IgG is an aging factor that drives adipose tissue fibrosis and metabolic declineLexiang Yu, Qianfen Wan, Qiongming Liu, et al.
Blood|August 3, 2013
Genetic loss of SH2B3 in acute lymphoblastic leukemiaArianne Perez-Garcia, Alberto Ambesi-Impiombato, Michael Hadler, et al.
Fetal Diagnosis and Therapy|May 23, 2015
New Insights into the Genetics of Fetal Megacystis: ACTG2 Mutations, Encoding γ-2 Smooth Muscle Actin in Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome)Lea Tuzovic, Sha Tang, Russell S Miller, et al.
The Journal of Clinical Investigation|January 3, 2015
Differentiation of hypothalamic-like neurons from human pluripotent stem cellsLiheng Wang, Kana Meece, Damian J Williams, et al.
Cancer|January 5, 1999
American Cancer Society Lymphedema Workshop. Workgroup III: Diagnosis and management of lymphedemaS G Rockson, L T Miller, R Senie, et al.
Journal of Medical Genetics|October 12, 2012
De novo copy number variants are associated with congenital diaphragmatic herniaLan Yu, Julia Wynn, Lijiang Ma, et al.
The Journal of Clinical Investigation|March 12, 2011
A mutation in the leptin receptor is associated with Entamoeba histolytica infection in childrenPriya Duggal, Xiaoti Guo, Rashidul Haque, et al.
The Journal of Clinical Investigation|February 25, 2021
Bardet-Biedl syndrome proteins regulate intracellular signaling and neuronal function in patient-specific iPSC-derived neuronsLiheng Wang, Yang Liu, George Stratigopoulos, et al.
Communications Biology|August 2, 2022
Reduced calcium levels and accumulation of abnormal insulin granules in stem cell models of HNF1A deficiencyBryan J González, Haoquan Zhao, Jacqueline Niu, et al.
Pageof 16

Showing results (141-150 of 159) with videos related to

Sort By:
Pageof 16
International Journal of Molecular Sciences|May 27, 2023
Biallelic Loss-of-Function Variants in <i>BICD1</i> Are Associated with Peripheral Neuropathy and Hearing LossYoel Hirsch, Wendy K Chung, Sergey Novoselov, et al.
Cell Metabolism|February 20, 2024
IgG is an aging factor that drives adipose tissue fibrosis and metabolic declineLexiang Yu, Qianfen Wan, Qiongming Liu, et al.
Blood|August 3, 2013
Genetic loss of SH2B3 in acute lymphoblastic leukemiaArianne Perez-Garcia, Alberto Ambesi-Impiombato, Michael Hadler, et al.
Fetal Diagnosis and Therapy|May 23, 2015
New Insights into the Genetics of Fetal Megacystis: ACTG2 Mutations, Encoding γ-2 Smooth Muscle Actin in Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome)Lea Tuzovic, Sha Tang, Russell S Miller, et al.
The Journal of Clinical Investigation|January 3, 2015
Differentiation of hypothalamic-like neurons from human pluripotent stem cellsLiheng Wang, Kana Meece, Damian J Williams, et al.
Cancer|January 5, 1999
American Cancer Society Lymphedema Workshop. Workgroup III: Diagnosis and management of lymphedemaS G Rockson, L T Miller, R Senie, et al.
Journal of Medical Genetics|October 12, 2012
De novo copy number variants are associated with congenital diaphragmatic herniaLan Yu, Julia Wynn, Lijiang Ma, et al.
The Journal of Clinical Investigation|March 12, 2011
A mutation in the leptin receptor is associated with Entamoeba histolytica infection in childrenPriya Duggal, Xiaoti Guo, Rashidul Haque, et al.
The Journal of Clinical Investigation|February 25, 2021
Bardet-Biedl syndrome proteins regulate intracellular signaling and neuronal function in patient-specific iPSC-derived neuronsLiheng Wang, Yang Liu, George Stratigopoulos, et al.
Communications Biology|August 2, 2022
Reduced calcium levels and accumulation of abnormal insulin granules in stem cell models of HNF1A deficiencyBryan J González, Haoquan Zhao, Jacqueline Niu, et al.
Pageof 16