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Wyeth W Wasserman

Showing results (161-170 of 172) with videos related to

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Cell|May 15, 2018
Interfaces of Malignant and Immunologic Clonal Dynamics in Ovarian CancerAllen W Zhang, Andrew McPherson, Katy Milne, et al.
The New England Journal of Medicine|April 11, 2019
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in <i>GLS</i>André B P van Kuilenburg, Maja Tarailo-Graovac, Phillip A Richmond, et al.
Journal of Human Immunity|June 1, 2026
Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic diseaseSimran Samra, Mehul Sharma, Julia Körholz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2024
CIAO1 and MMS19 deficiency: A lethal neurodegenerative phenotype caused by cytosolic Fe-S cluster protein assembly disordersClara D M van Karnebeek, Maja Tarailo-Graovac, René Leen, et al.
Nature|April 13, 2012
The clonal and mutational evolution spectrum of primary triple-negative breast cancersSohrab P Shah, Andrew Roth, Rodrigo Goya, et al.
The New England Journal of Medicine|June 9, 2016
Exome Sequencing and the Management of Neurometabolic DisordersMaja Tarailo-Graovac, Casper Shyr, Colin J Ross, et al.
Brain : a Journal of Neurology|January 23, 2019
PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insightsDevon L Johnstone, Hilal H Al-Shekaili, Maja Tarailo-Graovac, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 3, 2010
A regulatory toolbox of MiniPromoters to drive selective expression in the brainElodie Portales-Casamar, Douglas J Swanson, Li Liu, et al.
The Journal of Experimental Medicine|March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic diseaseMehul Sharma, Daniel Leung, Mana Momenilandi, et al.
Science Immunology|January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency, Oriol Fornes, Alicia Jia, et al.
Pageof 18

Showing results (161-170 of 172) with videos related to

Sort By:
Pageof 18
Cell|May 15, 2018
Interfaces of Malignant and Immunologic Clonal Dynamics in Ovarian CancerAllen W Zhang, Andrew McPherson, Katy Milne, et al.
The New England Journal of Medicine|April 11, 2019
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in <i>GLS</i>André B P van Kuilenburg, Maja Tarailo-Graovac, Phillip A Richmond, et al.
Journal of Human Immunity|June 1, 2026
Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic diseaseSimran Samra, Mehul Sharma, Julia Körholz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2024
CIAO1 and MMS19 deficiency: A lethal neurodegenerative phenotype caused by cytosolic Fe-S cluster protein assembly disordersClara D M van Karnebeek, Maja Tarailo-Graovac, René Leen, et al.
Nature|April 13, 2012
The clonal and mutational evolution spectrum of primary triple-negative breast cancersSohrab P Shah, Andrew Roth, Rodrigo Goya, et al.
The New England Journal of Medicine|June 9, 2016
Exome Sequencing and the Management of Neurometabolic DisordersMaja Tarailo-Graovac, Casper Shyr, Colin J Ross, et al.
Brain : a Journal of Neurology|January 23, 2019
PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insightsDevon L Johnstone, Hilal H Al-Shekaili, Maja Tarailo-Graovac, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 3, 2010
A regulatory toolbox of MiniPromoters to drive selective expression in the brainElodie Portales-Casamar, Douglas J Swanson, Li Liu, et al.
The Journal of Experimental Medicine|March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic diseaseMehul Sharma, Daniel Leung, Mana Momenilandi, et al.
Science Immunology|January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency, Oriol Fornes, Alicia Jia, et al.
Pageof 18