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Bärbel Keller

Name	Bärbel Keller
Place	Villingen-Schwenningen (Geburtsort) Deutschland
Academic degree	Dr. (Fakultät für Biologie an der Univ. Freiburg (Breisgau)) (2013)
Record type	Person
GND-Identifier	1044613939
Record ID	1044613939
Involved in show all COVID-19 progression and convalescence in common variable immunodeficiency patients show dysregulated adaptive immune responses and persistent type I interferon and inflammasome activation BCL10 deficiency presenting as severe combined immunodeficiency escaping newborn screening Combined immunodeficiency caused by a novel nonsense mutation in LCK COVID-19 progression and convalescence in common variable immunodeficiency patients show dysregulated adaptive immune responses and persistent type I interferon and inflammasome activation BCL10 Deficiency Presenting as Severe Combined Immunodeficiency Escaping Newborn Screening Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency Age-associated B cells predict impaired humoral immunity after COVID-19 vaccination in patients receiving immune checkpoint blockade Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency Interferon-driven immune dysregulation in common variable immunodeficiency-associated villous atrophy and norovirus infection Interferon-Driven Immune Dysregulation in Common Variable Immunodeficiency–Associated Villous Atrophy and Norovirus Infection Dysregulated PI3K signaling in B cells of CVID patients Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) Multi-omics analysis of naïve B cells of patients harboring the C104R mutation in TACI Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) Bronchoalveolar lavage fluid reflects a TH1-CD21low B-cell interaction in CVID-related interstitial lung disease Deep phenotyping of CD11c+ B cells in systemic autoimmunity and controls Establishing the molecular diagnoses in a cohort of 291 patients with predominantly antibody deficiency by targeted next-generation sequencing: Experience from a monocentric study Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) Targeted proteomics reveals inflammatory pathways that classify immune dysregulation in common variable immunodeficiency Targeted Proteomics Reveals Inflammatory Pathways that Classify Immune Dysregulation in Common Variable Immunodeficiency The antigen presenting potential of CD21low B cells Germline deletion of CIN85 in humans with X chromosome – linked antibody deficiency Guidelines for the use of flow cytometry and cell sorting in immunological studies * IL-21 restricts T follicular regulatory T cell proliferation through Bcl-6 mediated inhibition of responsiveness to IL-2 Early onset combined immunodeficiency and autoimmunity in patients with loss-of-function mutation in LAT Antigen receptor signalling of B-cells in common variable immunodeficiency

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Katalog der Deutschen Nationalbibliothek

Bärbel Keller

COVID-19 progression and convalescence in common variable immunodeficiency patients show dysregulated adaptive immune responses and persistent type I interferon and inflammasome activation

BCL10 deficiency presenting as severe combined immunodeficiency escaping newborn screening

Combined immunodeficiency caused by a novel nonsense mutation in LCK

COVID-19 progression and convalescence in common variable immunodeficiency patients show dysregulated adaptive immune responses and persistent type I interferon and inflammasome activation

BCL10 Deficiency Presenting as Severe Combined Immunodeficiency Escaping Newborn Screening

Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

Age-associated B cells predict impaired humoral immunity after COVID-19 vaccination in patients receiving immune checkpoint blockade

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

Interferon-driven immune dysregulation in common variable immunodeficiency-associated villous atrophy and norovirus infection

Interferon-Driven Immune Dysregulation in Common Variable Immunodeficiency–Associated Villous Atrophy and Norovirus Infection

Dysregulated PI3K signaling in B cells of CVID patients

Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition)

Multi-omics analysis of naïve B cells of patients harboring the C104R mutation in TACI

Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition)

Bronchoalveolar lavage fluid reflects a TH1-CD21low B-cell interaction in CVID-related interstitial lung disease

Deep phenotyping of CD11c+ B cells in systemic autoimmunity and controls

Establishing the molecular diagnoses in a cohort of 291 patients with predominantly antibody deficiency by targeted next-generation sequencing: Experience from a monocentric study

Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition)

Targeted proteomics reveals inflammatory pathways that classify immune dysregulation in common variable immunodeficiency

Targeted Proteomics Reveals Inflammatory Pathways that Classify Immune Dysregulation in Common Variable Immunodeficiency

The antigen presenting potential of CD21low B cells

Germline deletion of CIN85 in humans with X chromosome – linked antibody deficiency

Guidelines for the use of flow cytometry and cell sorting in immunological studies *

IL-21 restricts T follicular regulatory T cell proliferation through Bcl-6 mediated inhibition of responsiveness to IL-2

Early onset combined immunodeficiency and autoimmunity in patients with loss-of-function mutation in LAT

Antigen receptor signalling of B-cells in common variable immunodeficiency