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Immunology and Cell Biology
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April 30, 2016
B-cell signaling in persistent polyclonal B lymphocytosis (PPBL)
Nadine Voelxen, Claudia Wehr, Sylvia Gutenberger, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 12, 2009
Circulating CD21low B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells
Mirzokhid Rakhmanov, Baerbel Keller, Sylvia Gutenberger, et al.
Nature Communications
|
September 26, 2022
Circulating multimeric immune complexes contribute to immunopathology in COVID-19
Jakob Ankerhold, Sebastian Giese, Philipp Kolb, et al.
Blood
|
March 12, 2020
Nonpermissive bone marrow environment impairs early B-cell development in common variable immunodeficiency
Arianna Troilo, Claudia Wehr, Iga Janowska, et al.
The Journal of Allergy and Clinical Immunology
|
January 11, 2014
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency
Kathrin Pieper, Marta Rizzi, Matthaios Speletas, et al.
Plos One
|
June 20, 2014
High levels of SOX5 decrease proliferative capacity of human B cells, but permit plasmablast differentiation
Mirzokhid Rakhmanov, Heiko Sic, Anne-Kathrin Kienzler, et al.
The Journal of Allergy and Clinical Immunology
|
November 1, 2011
Genetic CD21 deficiency is associated with hypogammaglobulinemia
Jens Thiel, Lucas Kimmig, Ulrich Salzer, et al.
The Journal of Allergy and Clinical Immunology
|
April 1, 2014
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis
Heiko Sic, Helene Kraus, Josef Madl, et al.
The New England Journal of Medicine
|
January 2, 2009
A syndrome with congenital neutropenia and mutations in G6PC3
Kaan Boztug, Giridharan Appaswamy, Angel Ashikov, et al.
Human Molecular Genetics
|
October 18, 2015
DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency
Timo Volk, Ulrich Pannicke, Ismail Reisli, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 121) with videos related to
Sort By:
Page
of 13
Immunology and Cell Biology
|
April 30, 2016
B-cell signaling in persistent polyclonal B lymphocytosis (PPBL)
Nadine Voelxen, Claudia Wehr, Sylvia Gutenberger, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 12, 2009
Circulating CD21low B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells
Mirzokhid Rakhmanov, Baerbel Keller, Sylvia Gutenberger, et al.
Nature Communications
|
September 26, 2022
Circulating multimeric immune complexes contribute to immunopathology in COVID-19
Jakob Ankerhold, Sebastian Giese, Philipp Kolb, et al.
Blood
|
March 12, 2020
Nonpermissive bone marrow environment impairs early B-cell development in common variable immunodeficiency
Arianna Troilo, Claudia Wehr, Iga Janowska, et al.
The Journal of Allergy and Clinical Immunology
|
January 11, 2014
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency
Kathrin Pieper, Marta Rizzi, Matthaios Speletas, et al.
Plos One
|
June 20, 2014
High levels of SOX5 decrease proliferative capacity of human B cells, but permit plasmablast differentiation
Mirzokhid Rakhmanov, Heiko Sic, Anne-Kathrin Kienzler, et al.
The Journal of Allergy and Clinical Immunology
|
November 1, 2011
Genetic CD21 deficiency is associated with hypogammaglobulinemia
Jens Thiel, Lucas Kimmig, Ulrich Salzer, et al.
The Journal of Allergy and Clinical Immunology
|
April 1, 2014
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis
Heiko Sic, Helene Kraus, Josef Madl, et al.
The New England Journal of Medicine
|
January 2, 2009
A syndrome with congenital neutropenia and mutations in G6PC3
Kaan Boztug, Giridharan Appaswamy, Angel Ashikov, et al.
Human Molecular Genetics
|
October 18, 2015
DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency
Timo Volk, Ulrich Pannicke, Ismail Reisli, et al.
Page
of 13