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Showing results (1051-1060 of 1,079) with videos related to
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Blood
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July 1, 2020
Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency
Sujal Ghosh, Sevgi Köstel Bal, Emily S J Edwards, et al.
The Journal of Clinical Investigation
|
October 1, 2024
IL-7-dependent and -independent lineages of IL-7R-dependent human T cells
Carlos A Arango-Franco, Masato Ogishi, Susanne Unger, et al.
Nature
|
August 28, 2024
Tuberculosis in otherwise healthy adults with inherited TNF deficiency
Andrés A Arias, Anna-Lena Neehus, Masato Ogishi, et al.
The New England Journal of Medicine
|
October 25, 2013
HLA-B*13:01 and the dapsone hypersensitivity syndrome
F-R Zhang, H Liu, A Irwanto, et al.
Nature Immunology
|
January 16, 2026
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function
Taja Vatovec, Anna-Lena Neehus, Katherine J L Jackson, et al.
Cell
|
February 3, 2023
Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria
Jérémie Rosain, Anna-Lena Neehus, Jérémy Manry, et al.
The Journal of Experimental Medicine
|
July 9, 2026
Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis
Diana Olguín Calderón, Laura E Kilpatrick, Clément Conil, et al.
Biorxiv : the Preprint Server for Biology
|
April 3, 2026
Homozygosity for rare or common hypomorphic <i>IL23R</i> variants confers a predisposition to tuberculosis in humans
Diana Olguín Calderón, Laura E Kilpatrick, Clément Conil, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 22, 2024
<i>De novo</i> variants in the non-coding spliceosomal snRNA gene <i>RNU4-2</i> are a frequent cause of syndromic neurodevelopmental disorders
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Nature
|
July 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
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Showing results (1051-1060 of 1,079) with videos related to
Sort By:
Page
of 108
Blood
|
July 1, 2020
Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency
Sujal Ghosh, Sevgi Köstel Bal, Emily S J Edwards, et al.
The Journal of Clinical Investigation
|
October 1, 2024
IL-7-dependent and -independent lineages of IL-7R-dependent human T cells
Carlos A Arango-Franco, Masato Ogishi, Susanne Unger, et al.
Nature
|
August 28, 2024
Tuberculosis in otherwise healthy adults with inherited TNF deficiency
Andrés A Arias, Anna-Lena Neehus, Masato Ogishi, et al.
The New England Journal of Medicine
|
October 25, 2013
HLA-B*13:01 and the dapsone hypersensitivity syndrome
F-R Zhang, H Liu, A Irwanto, et al.
Nature Immunology
|
January 16, 2026
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function
Taja Vatovec, Anna-Lena Neehus, Katherine J L Jackson, et al.
Cell
|
February 3, 2023
Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria
Jérémie Rosain, Anna-Lena Neehus, Jérémy Manry, et al.
The Journal of Experimental Medicine
|
July 9, 2026
Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis
Diana Olguín Calderón, Laura E Kilpatrick, Clément Conil, et al.
Biorxiv : the Preprint Server for Biology
|
April 3, 2026
Homozygosity for rare or common hypomorphic <i>IL23R</i> variants confers a predisposition to tuberculosis in humans
Diana Olguín Calderón, Laura E Kilpatrick, Clément Conil, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 22, 2024
<i>De novo</i> variants in the non-coding spliceosomal snRNA gene <i>RNU4-2</i> are a frequent cause of syndromic neurodevelopmental disorders
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Nature
|
July 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Page
of 108