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Jay Shendure

Showing results (311-320 of 437) with videos related to

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Science Advances|October 12, 2023
A single-cell multi-omic atlas spanning the adult rhesus macaque brainKenneth L Chiou, Xingfan Huang, Martin O Bohlen, et al.
Cell|August 7, 2018
A Single-Cell Atlas of In Vivo Mammalian Chromatin AccessibilityDarren A Cusanovich, Andrew J Hill, Delasa Aghamirzaie, et al.
Biorxiv : the Preprint Server for Biology|October 17, 2024
Linking candidate causal autoimmune variants to T cell networks using genetic and epigenetic screens in primary human T cellsChing-Huang Ho, Maxwell A Dippel, Meghan S McQuade, et al.
Plos One|September 6, 2014
Genome sequencing of idiopathic pulmonary fibrosis in conjunction with a medical school human anatomy courseAkash Kumar, Max Dougherty, Gregory M Findlay, et al.
Brain : a Journal of Neurology|February 28, 2015
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasiaLaura A Jansen, Ghayda M Mirzaa, Gisele E Ishak, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 28, 2011
Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancersAkash Kumar, Thomas A White, Alexandra P MacKenzie, et al.
Science (New York, N.Y.)|November 13, 2020
A human cell atlas of fetal chromatin accessibilitySilvia Domcke, Andrew J Hill, Riza M Daza, et al.
Biorxiv : the Preprint Server for Biology|May 7, 2026
Designed Minibinders Rewire Receptor Signaling to Enable Functional Human Myogenic ReprogrammingRiya Keshri, Zachary Foreman, Phillip Barrett, et al.
Nature Genetics|September 18, 2025
Genetic and epigenetic screens in primary human T cells link candidate causal autoimmune variants to T cell networksChing-Huang Ho, Maxwell A Dippel, Meghan S McQuade, et al.
Genome Biology|January 23, 2015
Deep sequencing of multiple regions of glial tumors reveals spatial heterogeneity for mutations in clinically relevant genesAkash Kumar, Evan A Boyle, Mari Tokita, et al.
Pageof 44

Showing results (311-320 of 437) with videos related to

Sort By:
Pageof 44
Science Advances|October 12, 2023
A single-cell multi-omic atlas spanning the adult rhesus macaque brainKenneth L Chiou, Xingfan Huang, Martin O Bohlen, et al.
Cell|August 7, 2018
A Single-Cell Atlas of In Vivo Mammalian Chromatin AccessibilityDarren A Cusanovich, Andrew J Hill, Delasa Aghamirzaie, et al.
Biorxiv : the Preprint Server for Biology|October 17, 2024
Linking candidate causal autoimmune variants to T cell networks using genetic and epigenetic screens in primary human T cellsChing-Huang Ho, Maxwell A Dippel, Meghan S McQuade, et al.
Plos One|September 6, 2014
Genome sequencing of idiopathic pulmonary fibrosis in conjunction with a medical school human anatomy courseAkash Kumar, Max Dougherty, Gregory M Findlay, et al.
Brain : a Journal of Neurology|February 28, 2015
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasiaLaura A Jansen, Ghayda M Mirzaa, Gisele E Ishak, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 28, 2011
Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancersAkash Kumar, Thomas A White, Alexandra P MacKenzie, et al.
Science (New York, N.Y.)|November 13, 2020
A human cell atlas of fetal chromatin accessibilitySilvia Domcke, Andrew J Hill, Riza M Daza, et al.
Biorxiv : the Preprint Server for Biology|May 7, 2026
Designed Minibinders Rewire Receptor Signaling to Enable Functional Human Myogenic ReprogrammingRiya Keshri, Zachary Foreman, Phillip Barrett, et al.
Nature Genetics|September 18, 2025
Genetic and epigenetic screens in primary human T cells link candidate causal autoimmune variants to T cell networksChing-Huang Ho, Maxwell A Dippel, Meghan S McQuade, et al.
Genome Biology|January 23, 2015
Deep sequencing of multiple regions of glial tumors reveals spatial heterogeneity for mutations in clinically relevant genesAkash Kumar, Evan A Boyle, Mari Tokita, et al.
Pageof 44