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Immunology and Cell Biology
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May 24, 2018
CD57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated PI3 kinase delta syndrome
Paola Cura Daball, Monica Sofia Ventura Ferreira, Sandra Ammann, et al.
The Journal of Allergy and Clinical Immunology
|
January 9, 2023
Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutations
Maria Elena Maccari, Pascal Schneider, Cristian Roberto Smulski, et al.
Clinical Immunology (Orlando, Fla.)
|
November 27, 2019
Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunity
Sabine Jägle, Maximilian Heeg, Sarah Grün, et al.
Blood
|
June 5, 2014
Abnormally differentiated CD4+ or CD8+ T cells with phenotypic and genetic features of double negative T cells in human Fas deficiency
Anne Rensing-Ehl, Simon Völkl, Carsten Speckmann, et al.
Blood
|
April 22, 2016
Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndrome
Simon Völkl, Anne Rensing-Ehl, Andrea Allgäuer, et al.
The Journal of Allergy and Clinical Immunology
|
August 2, 2016
Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells
Hannah H Chen, Norman Händel, Joanne Ngeow, et al.
The Lancet. Haematology
|
February 1, 2024
Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study
Pauline Hägele, Paulina Staus, Raphael Scheible, et al.
Blood
|
June 11, 2020
Germline TET2 loss of function causes childhood immunodeficiency and lymphoma
Jarmila Stremenova Spegarova, Dylan Lawless, Siti Mardhiana Binti Mohamad, et al.
Cell
|
September 19, 2017
Mitochondrial Priming by CD28
Ramon I Klein Geltink, David O'Sullivan, Mauro Corrado, et al.
Frontiers in Immunology
|
October 10, 2017
Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency
Carsten Speckmann, Sushree Sangita Sahoo, Marta Rizzi, et al.
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of 5
Search research articles
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Showing results (21-30 of 43) with videos related to
Sort By:
Page
of 5
Immunology and Cell Biology
|
May 24, 2018
CD57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated PI3 kinase delta syndrome
Paola Cura Daball, Monica Sofia Ventura Ferreira, Sandra Ammann, et al.
The Journal of Allergy and Clinical Immunology
|
January 9, 2023
Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutations
Maria Elena Maccari, Pascal Schneider, Cristian Roberto Smulski, et al.
Clinical Immunology (Orlando, Fla.)
|
November 27, 2019
Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunity
Sabine Jägle, Maximilian Heeg, Sarah Grün, et al.
Blood
|
June 5, 2014
Abnormally differentiated CD4+ or CD8+ T cells with phenotypic and genetic features of double negative T cells in human Fas deficiency
Anne Rensing-Ehl, Simon Völkl, Carsten Speckmann, et al.
Blood
|
April 22, 2016
Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndrome
Simon Völkl, Anne Rensing-Ehl, Andrea Allgäuer, et al.
The Journal of Allergy and Clinical Immunology
|
August 2, 2016
Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells
Hannah H Chen, Norman Händel, Joanne Ngeow, et al.
The Lancet. Haematology
|
February 1, 2024
Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study
Pauline Hägele, Paulina Staus, Raphael Scheible, et al.
Blood
|
June 11, 2020
Germline TET2 loss of function causes childhood immunodeficiency and lymphoma
Jarmila Stremenova Spegarova, Dylan Lawless, Siti Mardhiana Binti Mohamad, et al.
Cell
|
September 19, 2017
Mitochondrial Priming by CD28
Ramon I Klein Geltink, David O'Sullivan, Mauro Corrado, et al.
Frontiers in Immunology
|
October 10, 2017
Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency
Carsten Speckmann, Sushree Sangita Sahoo, Marta Rizzi, et al.
Page
of 5