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Joshua D Milner

Showing results (131-140 of 183) with videos related to

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The Journal of Experimental Medicine|February 27, 2013
Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndromeDaniel Kotlarz, Natalia Ziętara, Gulbu Uzel, et al.
The Journal of Allergy and Clinical Immunology|May 19, 2019
GATA-2-deficient mast cells limit IgE-mediated immediate hypersensitivity reactions in human subjectsAvanti Desai, Kathryn Sowerwine, Yihui Liu, et al.
The Journal of Allergy and Clinical Immunology|March 29, 2013
Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndromeGulbu Uzel, Elizabeth P Sampaio, Monica G Lawrence, et al.
The Journal of Allergy and Clinical Immunology|March 5, 2014
Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairmentYu Zhang, Xiaomin Yu, Mie Ichikawa, et al.
Biorxiv : the Preprint Server for Biology|June 26, 2025
Th9-endothelial cell crosstalk promotes inflammatory atherosclerotic cardiovascular diseaseIshita Baral, Yvonne Baumer, Aarohan Burma, et al.
The Journal of Allergy and Clinical Immunology|April 18, 2021
Small intestinal immunopathology and GI-associated antibody formation in hereditary alpha-tryptasemiaLiza Konnikova, Tanya O Robinson, Anna H Owings, et al.
The Journal of Experimental Medicine|July 28, 2017
A biallelic mutation in <i>IL6ST</i> encoding the GP130 co-receptor causes immunodeficiency and craniosynostosisTobias Schwerd, Stephen R F Twigg, Dominik Aschenbrenner, et al.
Annals of the Rheumatic Diseases|December 13, 2025
Th9-arterial endothelial cell crosstalk promotes psoriatic atherosclerosisIshita Baral, Yvonne Baumer, Aarohan Mukerjhee Burma, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 2016
Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory diseaseQing Zhou, Xiaomin Yu, Erkan Demirkaya, et al.
The Journal of Clinical Investigation|February 6, 2018
Clonally expanded γδ T cells protect against Staphylococcus aureus skin reinfectionCarly A Dillen, Bret L Pinsker, Alina I Marusina, et al.
Pageof 19

Showing results (131-140 of 183) with videos related to

Sort By:
Pageof 19
The Journal of Experimental Medicine|February 27, 2013
Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndromeDaniel Kotlarz, Natalia Ziętara, Gulbu Uzel, et al.
The Journal of Allergy and Clinical Immunology|May 19, 2019
GATA-2-deficient mast cells limit IgE-mediated immediate hypersensitivity reactions in human subjectsAvanti Desai, Kathryn Sowerwine, Yihui Liu, et al.
The Journal of Allergy and Clinical Immunology|March 29, 2013
Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndromeGulbu Uzel, Elizabeth P Sampaio, Monica G Lawrence, et al.
The Journal of Allergy and Clinical Immunology|March 5, 2014
Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairmentYu Zhang, Xiaomin Yu, Mie Ichikawa, et al.
Biorxiv : the Preprint Server for Biology|June 26, 2025
Th9-endothelial cell crosstalk promotes inflammatory atherosclerotic cardiovascular diseaseIshita Baral, Yvonne Baumer, Aarohan Burma, et al.
The Journal of Allergy and Clinical Immunology|April 18, 2021
Small intestinal immunopathology and GI-associated antibody formation in hereditary alpha-tryptasemiaLiza Konnikova, Tanya O Robinson, Anna H Owings, et al.
The Journal of Experimental Medicine|July 28, 2017
A biallelic mutation in <i>IL6ST</i> encoding the GP130 co-receptor causes immunodeficiency and craniosynostosisTobias Schwerd, Stephen R F Twigg, Dominik Aschenbrenner, et al.
Annals of the Rheumatic Diseases|December 13, 2025
Th9-arterial endothelial cell crosstalk promotes psoriatic atherosclerosisIshita Baral, Yvonne Baumer, Aarohan Mukerjhee Burma, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 2016
Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory diseaseQing Zhou, Xiaomin Yu, Erkan Demirkaya, et al.
The Journal of Clinical Investigation|February 6, 2018
Clonally expanded γδ T cells protect against Staphylococcus aureus skin reinfectionCarly A Dillen, Bret L Pinsker, Alina I Marusina, et al.
Pageof 19