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Alla Bulashevska

Showing results (11-20 of 29) with videos related to

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Journal of Clinical Immunology|February 29, 2016
Deficiency of Adenosine Deaminase 2 Causes Antibody DeficiencyJohanna Schepp, Alla Bulashevska, Wilma Mannhardt-Laakmann, et al.
Frontiers in Immunology|May 7, 2019
Assessing the Functional Relevance of Variants in the <i>IKAROS Family Zinc Finger Protein 1</i> (<i>IKZF1</i>) in a Cohort of Patients With Primary ImmunodeficiencyZoya Eskandarian, Manfred Fliegauf, Alla Bulashevska, et al.
Clinical Immunology (Orlando, Fla.)|April 21, 2019
Evaluating laboratory criteria for combined immunodeficiency in adult patients diagnosed with common variable immunodeficiencyCaroline von Spee-Mayer, Verena Koemm, Claudia Wehr, et al.
The Journal of Allergy and Clinical Immunology|July 28, 2016
Disturbed canonical nuclear factor of κ light chain signaling in B cells of patients with common variable immunodeficiencyBaerbel Keller, Zoltan Cseresnyes, Ina Stumpf, et al.
Frontiers in Immunology|August 28, 2020
Altered Microbiota, Impaired Quality of Life, Malabsorption, Infection, and Inflammation in CVID Patients With DiarrhoeaCornelia M van Schewick, Christina Nöltner, Svenja Abel, et al.
The Journal of Allergy and Clinical Immunology|May 31, 2017
The T<sub>H</sub>1 phenotype of follicular helper T cells indicates an IFN-γ-associated immune dysregulation in patients with CD21low common variable immunodeficiencySusanne Unger, Maximilian Seidl, Pauline van Schouwenburg, et al.
Haematologica|July 18, 2020
Bile acids regulate intestinal antigen presentation and reduce graft-versus-host disease without impairing the graft-versus-leukemia effectEileen Haring, Franziska M Uhl, Geoffroy Andrieux, et al.
Frontiers in Immunology|April 4, 2019
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in <i>NFKB2</i>Christian Klemann, Nadezhda Camacho-Ordonez, Linlin Yang, et al.
American Journal of Human Genetics|August 18, 2015
Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable ImmunodeficiencyManfred Fliegauf, Vanessa L Bryant, Natalie Frede, 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 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Journal of Clinical Immunology|February 29, 2016
Deficiency of Adenosine Deaminase 2 Causes Antibody DeficiencyJohanna Schepp, Alla Bulashevska, Wilma Mannhardt-Laakmann, et al.
Frontiers in Immunology|May 7, 2019
Assessing the Functional Relevance of Variants in the <i>IKAROS Family Zinc Finger Protein 1</i> (<i>IKZF1</i>) in a Cohort of Patients With Primary ImmunodeficiencyZoya Eskandarian, Manfred Fliegauf, Alla Bulashevska, et al.
Clinical Immunology (Orlando, Fla.)|April 21, 2019
Evaluating laboratory criteria for combined immunodeficiency in adult patients diagnosed with common variable immunodeficiencyCaroline von Spee-Mayer, Verena Koemm, Claudia Wehr, et al.
The Journal of Allergy and Clinical Immunology|July 28, 2016
Disturbed canonical nuclear factor of κ light chain signaling in B cells of patients with common variable immunodeficiencyBaerbel Keller, Zoltan Cseresnyes, Ina Stumpf, et al.
Frontiers in Immunology|August 28, 2020
Altered Microbiota, Impaired Quality of Life, Malabsorption, Infection, and Inflammation in CVID Patients With DiarrhoeaCornelia M van Schewick, Christina Nöltner, Svenja Abel, et al.
The Journal of Allergy and Clinical Immunology|May 31, 2017
The T<sub>H</sub>1 phenotype of follicular helper T cells indicates an IFN-γ-associated immune dysregulation in patients with CD21low common variable immunodeficiencySusanne Unger, Maximilian Seidl, Pauline van Schouwenburg, et al.
Haematologica|July 18, 2020
Bile acids regulate intestinal antigen presentation and reduce graft-versus-host disease without impairing the graft-versus-leukemia effectEileen Haring, Franziska M Uhl, Geoffroy Andrieux, et al.
Frontiers in Immunology|April 4, 2019
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in <i>NFKB2</i>Christian Klemann, Nadezhda Camacho-Ordonez, Linlin Yang, et al.
American Journal of Human Genetics|August 18, 2015
Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable ImmunodeficiencyManfred Fliegauf, Vanessa L Bryant, Natalie Frede, 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 3