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Anne-Kathrin Kienzler

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Movement Disorders : Official Journal of the Movement Disorder Society|September 16, 2018
The clinical features, underlying immunology, and treatment of autoantibody-mediated movement disordersValentina Damato, Bettina Balint, Anne-Kathrin Kienzler, et al.
Current Allergy and Asthma Reports|March 18, 2014
B cell biology: an overviewHermann Eibel, Helene Kraus, Heiko Sic, et al.
The Journal of Allergy and Clinical Immunology|March 8, 2013
Inhibition of human B-cell development into plasmablasts by histone deacetylase inhibitor valproic acidAnne-Kathrin Kienzler, Marta Rizzi, Maike Reith, et al.
The Journal of Allergy and Clinical Immunology|August 21, 2016
Variable phenotype and discrete alterations of immune phenotypes in CTP synthase 1 deficiency: Report of 2 siblingsJohannes Trück, Dominic F Kelly, John M Taylor, et al.
Brain : a Journal of Neurology|February 16, 2018
Condition-dependent generation of aquaporin-4 antibodies from circulating B cells in neuromyelitis opticaRobert Wilson, Mateusz Makuch, Anne-Kathrin Kienzler, et al.
Annals of Neurology|February 7, 2018
N-methyl-D-aspartate receptor antibody production from germinal center reactions: Therapeutic implicationsMateusz Makuch, Robert Wilson, Adam Al-Diwani, et al.
The Journal of Allergy and Clinical Immunology|March 2, 2015
Key stages of bone marrow B-cell maturation are defective in patients with common variable immunodeficiency disordersConsuelo Anzilotti, Anne-Kathrin Kienzler, Eduardo Lopez-Granados, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 12, 2009
B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humansKlaus Warnatz, Ulrich Salzer, Marta Rizzi, et al.
The Journal of Allergy and Clinical Immunology|February 5, 2013
Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjectsPolina Stepensky, Baerbel Keller, Mary Buchta, et al.
Clinical Immunology (Orlando, Fla.)|December 19, 2015
Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgEAnne-Kathrin Kienzler, Pauline A van Schouwenburg, John Taylor, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Movement Disorders : Official Journal of the Movement Disorder Society|September 16, 2018
The clinical features, underlying immunology, and treatment of autoantibody-mediated movement disordersValentina Damato, Bettina Balint, Anne-Kathrin Kienzler, et al.
Current Allergy and Asthma Reports|March 18, 2014
B cell biology: an overviewHermann Eibel, Helene Kraus, Heiko Sic, et al.
The Journal of Allergy and Clinical Immunology|March 8, 2013
Inhibition of human B-cell development into plasmablasts by histone deacetylase inhibitor valproic acidAnne-Kathrin Kienzler, Marta Rizzi, Maike Reith, et al.
The Journal of Allergy and Clinical Immunology|August 21, 2016
Variable phenotype and discrete alterations of immune phenotypes in CTP synthase 1 deficiency: Report of 2 siblingsJohannes Trück, Dominic F Kelly, John M Taylor, et al.
Brain : a Journal of Neurology|February 16, 2018
Condition-dependent generation of aquaporin-4 antibodies from circulating B cells in neuromyelitis opticaRobert Wilson, Mateusz Makuch, Anne-Kathrin Kienzler, et al.
Annals of Neurology|February 7, 2018
N-methyl-D-aspartate receptor antibody production from germinal center reactions: Therapeutic implicationsMateusz Makuch, Robert Wilson, Adam Al-Diwani, et al.
The Journal of Allergy and Clinical Immunology|March 2, 2015
Key stages of bone marrow B-cell maturation are defective in patients with common variable immunodeficiency disordersConsuelo Anzilotti, Anne-Kathrin Kienzler, Eduardo Lopez-Granados, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 12, 2009
B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humansKlaus Warnatz, Ulrich Salzer, Marta Rizzi, et al.
The Journal of Allergy and Clinical Immunology|February 5, 2013
Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjectsPolina Stepensky, Baerbel Keller, Mary Buchta, et al.
Clinical Immunology (Orlando, Fla.)|December 19, 2015
Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgEAnne-Kathrin Kienzler, Pauline A van Schouwenburg, John Taylor, et al.
Pageof 3