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Journal of Clinical Immunology
|
August 23, 2024
Immunophenotyping and Therapeutic Insights from Chronic Mucocutaneous Candidiasis Cases with STAT1 Gain-of-Function Mutations
Wei-Te Lei, Yu-Fang Lo, Miyuki Tsumura, et al.
The Journal of Allergy and Clinical Immunology
|
March 13, 2026
Discovering patterns in the pathologic significance of non-missense deleterious variants in RELA
Hiroko Hayakawa, Miyuki Tsumura, Takanori Utsumi, et al.
Nature Communications
|
November 25, 2021
Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency
Nobuo Kanazawa, Hiroaki Hemmi, Noriko Kinjo, et al.
Surgery Today
|
July 17, 2019
Changes in the rate of and trends in colectomy for ulcerative colitis during the era of biologics and calcineurin inhibitors based on a Japanese nationwide cohort study
Motoi Uchino, Hiroki Ikeuchi, Keisuke Hata, et al.
Blood
|
August 22, 2013
Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation
Marcela Moncada-Vélez, Rubén Martinez-Barricarte, Dusan Bogunovic, et al.
Annals of the Rheumatic Diseases
|
July 11, 2020
Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the <i>NOD2</i> mutation
Tomoko Matsuda, Naotomo Kambe, Yoko Ueki, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
February 14, 2024
Clinical, immunological, and genetic description of a Mexican cohort of patients with DOCK8 deficiency
Eduardo Liquidano-Perez, Gibert Maza-Ramos, Bethy Alexandra Perez Arias, et al.
The Journal of Allergy and Clinical Immunology
|
July 19, 2016
Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency
Yuki Tsujita, Kanako Mitsui-Sekinaka, Kohsuke Imai, et al.
Nature
|
January 1, 2025
Monoallelic expression can govern penetrance of inborn errors of immunity
O'Jay Stewart, Conor Gruber, Haley E Randolph, et al.
The Journal of Experimental Medicine
|
October 19, 2011
DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice
Katrina L Randall, Stephanie S-Y Chan, Cindy S Ma, et al.
Page
of 41
Search research articles
Search
Showing results (361-370 of 408) with videos related to
Sort By:
Page
of 41
Journal of Clinical Immunology
|
August 23, 2024
Immunophenotyping and Therapeutic Insights from Chronic Mucocutaneous Candidiasis Cases with STAT1 Gain-of-Function Mutations
Wei-Te Lei, Yu-Fang Lo, Miyuki Tsumura, et al.
The Journal of Allergy and Clinical Immunology
|
March 13, 2026
Discovering patterns in the pathologic significance of non-missense deleterious variants in RELA
Hiroko Hayakawa, Miyuki Tsumura, Takanori Utsumi, et al.
Nature Communications
|
November 25, 2021
Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency
Nobuo Kanazawa, Hiroaki Hemmi, Noriko Kinjo, et al.
Surgery Today
|
July 17, 2019
Changes in the rate of and trends in colectomy for ulcerative colitis during the era of biologics and calcineurin inhibitors based on a Japanese nationwide cohort study
Motoi Uchino, Hiroki Ikeuchi, Keisuke Hata, et al.
Blood
|
August 22, 2013
Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation
Marcela Moncada-Vélez, Rubén Martinez-Barricarte, Dusan Bogunovic, et al.
Annals of the Rheumatic Diseases
|
July 11, 2020
Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the <i>NOD2</i> mutation
Tomoko Matsuda, Naotomo Kambe, Yoko Ueki, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
February 14, 2024
Clinical, immunological, and genetic description of a Mexican cohort of patients with DOCK8 deficiency
Eduardo Liquidano-Perez, Gibert Maza-Ramos, Bethy Alexandra Perez Arias, et al.
The Journal of Allergy and Clinical Immunology
|
July 19, 2016
Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency
Yuki Tsujita, Kanako Mitsui-Sekinaka, Kohsuke Imai, et al.
Nature
|
January 1, 2025
Monoallelic expression can govern penetrance of inborn errors of immunity
O'Jay Stewart, Conor Gruber, Haley E Randolph, et al.
The Journal of Experimental Medicine
|
October 19, 2011
DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice
Katrina L Randall, Stephanie S-Y Chan, Cindy S Ma, et al.
Page
of 41