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T Daniel Andrews

Showing results (31-40 of 40) with videos related to

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Elife|December 17, 2013
Rasgrp1 mutation increases naive T-cell CD44 expression and drives mTOR-dependent accumulation of Helios⁺ T cells and autoantibodiesStephen R Daley, Kristen M Coakley, Daniel Y Hu, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Nature|January 20, 2021
NINJ1 mediates plasma membrane rupture during lytic cell deathNobuhiko Kayagaki, Opher S Kornfeld, Bettina L Lee, et al.
Nature Immunology|July 26, 2024
A TNIP1-driven systemic autoimmune disorder with elevated IgG4Arti Medhavy, Vicki Athanasopoulos, Katharine Bassett, et al.
Cell Reports|February 10, 2021
Atypical B cells are part of an alternative lineage of B cells that participates in responses to vaccination and infection in humansHenry J Sutton, Racheal Aye, Azza H Idris, et al.
Genome Research|April 14, 2004
An overview of EnsemblEwan Birney, T Daniel Andrews, Paul Bevan, et al.
Nature|November 24, 2006
Global variation in copy number in the human genomeRichard Redon, Shumpei Ishikawa, Karen R Fitch, et al.
Nature|April 28, 2022
TLR7 gain-of-function genetic variation causes human lupusGrant J Brown, Pablo F Cañete, Hao Wang, et al.
Nature|April 3, 2010
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls, Nick Craddock, Matthew E Hurles, et al.
Nature|March 18, 2005
The DNA sequence of the human X chromosomeMark T Ross, Darren V Grafham, Alison J Coffey, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Elife|December 17, 2013
Rasgrp1 mutation increases naive T-cell CD44 expression and drives mTOR-dependent accumulation of Helios⁺ T cells and autoantibodiesStephen R Daley, Kristen M Coakley, Daniel Y Hu, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Nature|January 20, 2021
NINJ1 mediates plasma membrane rupture during lytic cell deathNobuhiko Kayagaki, Opher S Kornfeld, Bettina L Lee, et al.
Nature Immunology|July 26, 2024
A TNIP1-driven systemic autoimmune disorder with elevated IgG4Arti Medhavy, Vicki Athanasopoulos, Katharine Bassett, et al.
Cell Reports|February 10, 2021
Atypical B cells are part of an alternative lineage of B cells that participates in responses to vaccination and infection in humansHenry J Sutton, Racheal Aye, Azza H Idris, et al.
Genome Research|April 14, 2004
An overview of EnsemblEwan Birney, T Daniel Andrews, Paul Bevan, et al.
Nature|November 24, 2006
Global variation in copy number in the human genomeRichard Redon, Shumpei Ishikawa, Karen R Fitch, et al.
Nature|April 28, 2022
TLR7 gain-of-function genetic variation causes human lupusGrant J Brown, Pablo F Cañete, Hao Wang, et al.
Nature|April 3, 2010
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls, Nick Craddock, Matthew E Hurles, et al.
Nature|March 18, 2005
The DNA sequence of the human X chromosomeMark T Ross, Darren V Grafham, Alison J Coffey, et al.
Pageof 4