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Bruce Beutler

Showing results (121-130 of 271) with videos related to

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Human Molecular Genetics|February 12, 2008
A model for familial exudative vitreoretinopathy caused by LPR5 mutationsChun-Hong Xia, Haiquan Liu, Debra Cheung, et al.
Investigative Ophthalmology & Visual Science|September 11, 2009
Severe retinal degeneration caused by a novel rhodopsin mutationHaiquan Liu, Meng Wang, Chun-Hong Xia, et al.
Biorxiv : the Preprint Server for Biology|December 18, 2023
Lrp10 suppresses IL7R limiting CD8 T cell homeostatic expansion and anti-tumor immunityJamie Russell, Luming Chen, Aijie Liu, et al.
The Journal of Biological Chemistry|April 3, 2007
Recognition of hyaluronan released in sterile injury involves a unique receptor complex dependent on Toll-like receptor 4, CD44, and MD-2Kristen R Taylor, Kenshi Yamasaki, Katherine A Radek, et al.
Scientific Reports|July 14, 2021
Quantification of early learning and movement sub-structure predictive of motor performanceVikram Jakkamsetti, William Scudder, Gauri Kathote, et al.
Frontiers in Immunology|November 7, 2022
IκBNS expression in B cells is dispensable for IgG responses to T cell-dependent antigensSharesta Khoenkhoen, Monika Ádori, Darío Solís-Sayago, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2010
JNK1 controls mast cell degranulation and IL-1{beta} production in inflammatory arthritisMonica Guma, Jun-ichi Kashiwakura, Brian Crain, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2013
Essential requirement for IRF8 and SLC15A4 implicates plasmacytoid dendritic cells in the pathogenesis of lupusRoberto Baccala, Rosana Gonzalez-Quintial, Amanda L Blasius, et al.
Genetics|March 17, 2004
Velvet, a dominant Egfr mutation that causes wavy hair and defective eyelid development in miceXin Du, Koichi Tabeta, Kasper Hoebe, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 10, 2015
Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencingMichelle M Simon, Eva Marie Y Moresco, Katherine R Bull, et al.
Pageof 28

Showing results (121-130 of 271) with videos related to

Sort By:
Pageof 28
Human Molecular Genetics|February 12, 2008
A model for familial exudative vitreoretinopathy caused by LPR5 mutationsChun-Hong Xia, Haiquan Liu, Debra Cheung, et al.
Investigative Ophthalmology & Visual Science|September 11, 2009
Severe retinal degeneration caused by a novel rhodopsin mutationHaiquan Liu, Meng Wang, Chun-Hong Xia, et al.
Biorxiv : the Preprint Server for Biology|December 18, 2023
Lrp10 suppresses IL7R limiting CD8 T cell homeostatic expansion and anti-tumor immunityJamie Russell, Luming Chen, Aijie Liu, et al.
The Journal of Biological Chemistry|April 3, 2007
Recognition of hyaluronan released in sterile injury involves a unique receptor complex dependent on Toll-like receptor 4, CD44, and MD-2Kristen R Taylor, Kenshi Yamasaki, Katherine A Radek, et al.
Scientific Reports|July 14, 2021
Quantification of early learning and movement sub-structure predictive of motor performanceVikram Jakkamsetti, William Scudder, Gauri Kathote, et al.
Frontiers in Immunology|November 7, 2022
IκBNS expression in B cells is dispensable for IgG responses to T cell-dependent antigensSharesta Khoenkhoen, Monika Ádori, Darío Solís-Sayago, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2010
JNK1 controls mast cell degranulation and IL-1{beta} production in inflammatory arthritisMonica Guma, Jun-ichi Kashiwakura, Brian Crain, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2013
Essential requirement for IRF8 and SLC15A4 implicates plasmacytoid dendritic cells in the pathogenesis of lupusRoberto Baccala, Rosana Gonzalez-Quintial, Amanda L Blasius, et al.
Genetics|March 17, 2004
Velvet, a dominant Egfr mutation that causes wavy hair and defective eyelid development in miceXin Du, Koichi Tabeta, Kasper Hoebe, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 10, 2015
Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencingMichelle M Simon, Eva Marie Y Moresco, Katherine R Bull, et al.
Pageof 28