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David T Humphreys

Showing results (41-50 of 51) with videos related to

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Journal of Crohn'S & Colitis|December 9, 2023
Epigenetic and Metabolic Reprogramming of Fibroblasts in Crohn's Disease Strictures Reveals Histone Deacetylases as Therapeutic TargetsAmy Lewis, David T Humphreys, Belen Pan-Castillo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Identification of clinically actionable variants from genome sequencing of families with congenital heart diseaseDimuthu Alankarage, Eddie Ip, Justin O Szot, et al.
HGG Advances|July 7, 2025
Haploinsufficient variants in SMAD5 are associated with isolated congenital heart diseaseDimuthu Alankarage, Iryna Leshchynska, Stephanie Portelli, et al.
Nature|December 5, 2024
Ageing limits stemness and tumorigenesis by reprogramming iron homeostasisXueqian Zhuang, Qing Wang, Simon Joost, et al.
Nature|May 22, 2025
Publisher Correction: Ageing limits stemness and tumorigenesis by reprogramming iron homeostasisXueqian Zhuang, Qing Wang, Simon Joost, et al.
Scientific Reports|September 11, 2023
Fibulin-3 is necessary to prevent cardiac rupture following myocardial infarctionLucy A Murtha, Sean A Hardy, Nishani S Mabotuwana, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2024
Aging limits stemness and tumorigenesis in the lung by reprogramming iron homeostasisXueqian Zhuang, Qing Wang, Simon Joost, et al.
Circulation. Genomic and Precision Medicine|May 18, 2022
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome SequencingIngrid Tarr, Stephanie Hesselson, Siiri E Iismaa, et al.
Nature Genetics|December 24, 2025
Designing synthetic regulatory elements using the generative AI framework DNA-DiffusionLucas Ferreira DaSilva, Simon Senan, Judith F Kribelbauer-Swietek, et al.
Human Molecular Genetics|December 4, 2020
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and miceElla M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Journal of Crohn'S & Colitis|December 9, 2023
Epigenetic and Metabolic Reprogramming of Fibroblasts in Crohn's Disease Strictures Reveals Histone Deacetylases as Therapeutic TargetsAmy Lewis, David T Humphreys, Belen Pan-Castillo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Identification of clinically actionable variants from genome sequencing of families with congenital heart diseaseDimuthu Alankarage, Eddie Ip, Justin O Szot, et al.
HGG Advances|July 7, 2025
Haploinsufficient variants in SMAD5 are associated with isolated congenital heart diseaseDimuthu Alankarage, Iryna Leshchynska, Stephanie Portelli, et al.
Nature|December 5, 2024
Ageing limits stemness and tumorigenesis by reprogramming iron homeostasisXueqian Zhuang, Qing Wang, Simon Joost, et al.
Nature|May 22, 2025
Publisher Correction: Ageing limits stemness and tumorigenesis by reprogramming iron homeostasisXueqian Zhuang, Qing Wang, Simon Joost, et al.
Scientific Reports|September 11, 2023
Fibulin-3 is necessary to prevent cardiac rupture following myocardial infarctionLucy A Murtha, Sean A Hardy, Nishani S Mabotuwana, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2024
Aging limits stemness and tumorigenesis in the lung by reprogramming iron homeostasisXueqian Zhuang, Qing Wang, Simon Joost, et al.
Circulation. Genomic and Precision Medicine|May 18, 2022
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome SequencingIngrid Tarr, Stephanie Hesselson, Siiri E Iismaa, et al.
Nature Genetics|December 24, 2025
Designing synthetic regulatory elements using the generative AI framework DNA-DiffusionLucas Ferreira DaSilva, Simon Senan, Judith F Kribelbauer-Swietek, et al.
Human Molecular Genetics|December 4, 2020
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and miceElla M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.
Pageof 6