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Nature Communications
|
February 27, 2020
Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, et al.
Nature Communications
|
April 22, 2020
Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, et al.
The Journal of Experimental Medicine
|
November 24, 2020
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects
Atar Lev, Yu Nee Lee, Guangping Sun, et al.
The Journal of Experimental Medicine
|
July 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects
Amos J Simon, Atar Lev, Yong Zhang, et al.
The New England Journal of Medicine
|
June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45
Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Gastroenterology
|
September 30, 2018
Intestinal Inflammation and Dysregulated Immunity in Patients With Inherited Caspase-8 Deficiency
Anna S Lehle, Henner F Farin, Benjamin Marquardt, et al.
Blood
|
September 11, 2019
CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis
Ido Somekh, Marini Thian, David Medgyesi, et al.
American Journal of Human Genetics
|
March 19, 2024
Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndrome
Caspar I van der Made, Simone Kersten, Odelia Chorin, et al.
The Journal of Experimental Medicine
|
April 1, 2024
Helper T cell immunity in humans with inherited CD4 deficiency
Antoine Guérin, Marcela Moncada-Vélez, Katherine Jackson, et al.
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Search research articles
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Showing results (81-90 of 89) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 89 results.
Nature Communications
|
February 27, 2020
Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, et al.
Nature Communications
|
April 22, 2020
Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, et al.
The Journal of Experimental Medicine
|
November 24, 2020
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects
Atar Lev, Yu Nee Lee, Guangping Sun, et al.
The Journal of Experimental Medicine
|
July 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects
Amos J Simon, Atar Lev, Yong Zhang, et al.
The New England Journal of Medicine
|
June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45
Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Gastroenterology
|
September 30, 2018
Intestinal Inflammation and Dysregulated Immunity in Patients With Inherited Caspase-8 Deficiency
Anna S Lehle, Henner F Farin, Benjamin Marquardt, et al.
Blood
|
September 11, 2019
CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis
Ido Somekh, Marini Thian, David Medgyesi, et al.
American Journal of Human Genetics
|
March 19, 2024
Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndrome
Caspar I van der Made, Simone Kersten, Odelia Chorin, et al.
The Journal of Experimental Medicine
|
April 1, 2024
Helper T cell immunity in humans with inherited CD4 deficiency
Antoine Guérin, Marcela Moncada-Vélez, Katherine Jackson, et al.
Page
of 9