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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 syndrome
Daniel 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 subjects
Avanti 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 syndrome
Gulbu 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 impairment
Yu Zhang, Xiaomin Yu, Mie Ichikawa, et al.
Biorxiv : the Preprint Server for Biology
|
June 26, 2025
Th9-endothelial cell crosstalk promotes inflammatory atherosclerotic cardiovascular disease
Ishita 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-tryptasemia
Liza 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 craniosynostosis
Tobias Schwerd, Stephen R F Twigg, Dominik Aschenbrenner, et al.
Annals of the Rheumatic Diseases
|
December 13, 2025
Th9-arterial endothelial cell crosstalk promotes psoriatic atherosclerosis
Ishita 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 disease
Qing 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 reinfection
Carly A Dillen, Bret L Pinsker, Alina I Marusina, et al.
Page
of 19
Search research articles
Search
Showing results (131-140 of 183) with videos related to
Sort By:
Page
of 19
The Journal of Experimental Medicine
|
February 27, 2013
Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome
Daniel 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 subjects
Avanti 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 syndrome
Gulbu 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 impairment
Yu Zhang, Xiaomin Yu, Mie Ichikawa, et al.
Biorxiv : the Preprint Server for Biology
|
June 26, 2025
Th9-endothelial cell crosstalk promotes inflammatory atherosclerotic cardiovascular disease
Ishita 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-tryptasemia
Liza 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 craniosynostosis
Tobias Schwerd, Stephen R F Twigg, Dominik Aschenbrenner, et al.
Annals of the Rheumatic Diseases
|
December 13, 2025
Th9-arterial endothelial cell crosstalk promotes psoriatic atherosclerosis
Ishita 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 disease
Qing 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 reinfection
Carly A Dillen, Bret L Pinsker, Alina I Marusina, et al.
Page
of 19