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Ulrich Salzer

Showing results (101-110 of 121) with videos related to

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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 cellsMirzokhid Rakhmanov, Baerbel Keller, Sylvia Gutenberger, et al.
Nature Communications|September 26, 2022
Circulating multimeric immune complexes contribute to immunopathology in COVID-19Jakob Ankerhold, Sebastian Giese, Philipp Kolb, et al.
Blood|March 12, 2020
Nonpermissive bone marrow environment impairs early B-cell development in common variable immunodeficiencyArianna 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 immunodeficiencyKathrin 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 differentiationMirzokhid Rakhmanov, Heiko Sic, Anne-Kathrin Kienzler, et al.
The Journal of Allergy and Clinical Immunology|November 1, 2011
Genetic CD21 deficiency is associated with hypogammaglobulinemiaJens 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 sclerosisHeiko Sic, Helene Kraus, Josef Madl, et al.
The New England Journal of Medicine|January 2, 2009
A syndrome with congenital neutropenia and mutations in G6PC3Kaan 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 deficiencyTimo Volk, Ulrich Pannicke, Ismail Reisli, et al.
Pageof 13

Showing results (101-110 of 121) with videos related to

Sort By:
Pageof 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 cellsMirzokhid Rakhmanov, Baerbel Keller, Sylvia Gutenberger, et al.
Nature Communications|September 26, 2022
Circulating multimeric immune complexes contribute to immunopathology in COVID-19Jakob Ankerhold, Sebastian Giese, Philipp Kolb, et al.
Blood|March 12, 2020
Nonpermissive bone marrow environment impairs early B-cell development in common variable immunodeficiencyArianna 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 immunodeficiencyKathrin 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 differentiationMirzokhid Rakhmanov, Heiko Sic, Anne-Kathrin Kienzler, et al.
The Journal of Allergy and Clinical Immunology|November 1, 2011
Genetic CD21 deficiency is associated with hypogammaglobulinemiaJens 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 sclerosisHeiko Sic, Helene Kraus, Josef Madl, et al.
The New England Journal of Medicine|January 2, 2009
A syndrome with congenital neutropenia and mutations in G6PC3Kaan 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 deficiencyTimo Volk, Ulrich Pannicke, Ismail Reisli, et al.
Pageof 13