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T Gibson

Showing results (601-610 of 636) with videos related to

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Human Molecular Genetics|May 2, 2023
Activation of the cGAS-STING innate immune response in cells with deficient mitochondrial topoisomerase TOP1MTIman Al Khatib, Jingti Deng, Yuanjiu Lei, et al.
American Journal of Human Genetics|December 20, 2011
Mutations in EZH2 cause Weaver syndromeWilliam T Gibson, Rebecca L Hood, Shing Hei Zhan, et al.
Clinical Epigenetics|December 21, 2022
Transient Polycomb activity represses developmental genes in growing oocytesEllen G Jarred, Zhipeng Qu, Tesha Tsai, et al.
Developmental Cell|March 10, 2023
Activation of β-catenin in mesenchymal progenitors leads to muscle mass lossNasim Kajabadi, Marcela Low, Erik Jacques, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|June 26, 2020
COVID-19 in recent heart transplant recipients: Clinicopathologic features and early outcomesBrian Lima, Gregory T Gibson, Sirish Vullaganti, et al.
Orphanet Journal of Rare Diseases|August 26, 2015
Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumoursSarah F Barclay, Casey M Rand, Lauren A Borch, et al.
Plos One|May 2, 2015
Vasoactive intestinal polypeptide promotes intestinal barrier homeostasis and protection against colitis in miceXiujuan Wu, Victoria S Conlin, Vijay Morampudi, et al.
Nature Chemistry|March 14, 2026
Spontaneous trisulfide metathesis in polar aprotic solventsHarshal D Patel, Alfrets D Tikoalu, James N Smith, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 2, 2018
The Jamaican Haemophilia Registry: Describing the burden of diseaseG Wharfe, L Buchner-Daley, T Gibson, et al.
Human Mutation|December 24, 2015
Weaver Syndrome-Associated EZH2 Protein Variants Show Impaired Histone Methyltransferase Function In VitroAna S A Cohen, Damian B Yap, M E Suzanne Lewis, et al.
Pageof 64

Showing results (601-610 of 636) with videos related to

Sort By:
Pageof 64
Human Molecular Genetics|May 2, 2023
Activation of the cGAS-STING innate immune response in cells with deficient mitochondrial topoisomerase TOP1MTIman Al Khatib, Jingti Deng, Yuanjiu Lei, et al.
American Journal of Human Genetics|December 20, 2011
Mutations in EZH2 cause Weaver syndromeWilliam T Gibson, Rebecca L Hood, Shing Hei Zhan, et al.
Clinical Epigenetics|December 21, 2022
Transient Polycomb activity represses developmental genes in growing oocytesEllen G Jarred, Zhipeng Qu, Tesha Tsai, et al.
Developmental Cell|March 10, 2023
Activation of β-catenin in mesenchymal progenitors leads to muscle mass lossNasim Kajabadi, Marcela Low, Erik Jacques, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|June 26, 2020
COVID-19 in recent heart transplant recipients: Clinicopathologic features and early outcomesBrian Lima, Gregory T Gibson, Sirish Vullaganti, et al.
Orphanet Journal of Rare Diseases|August 26, 2015
Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumoursSarah F Barclay, Casey M Rand, Lauren A Borch, et al.
Plos One|May 2, 2015
Vasoactive intestinal polypeptide promotes intestinal barrier homeostasis and protection against colitis in miceXiujuan Wu, Victoria S Conlin, Vijay Morampudi, et al.
Nature Chemistry|March 14, 2026
Spontaneous trisulfide metathesis in polar aprotic solventsHarshal D Patel, Alfrets D Tikoalu, James N Smith, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 2, 2018
The Jamaican Haemophilia Registry: Describing the burden of diseaseG Wharfe, L Buchner-Daley, T Gibson, et al.
Human Mutation|December 24, 2015
Weaver Syndrome-Associated EZH2 Protein Variants Show Impaired Histone Methyltransferase Function In VitroAna S A Cohen, Damian B Yap, M E Suzanne Lewis, et al.
Pageof 64