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Normdaten (Quelle GND / Entity Facts )

Manfred Fliegauf

geboren 1968

Biografische Angaben
Diss. Fakultät für Biologie

Weiterführende Links

Gemeinsame Normdatei (GND) im Katalog der Deutschen Nationalbibliothek

Open Researcher and Contributor ID (ORCID)

Deutsche Digitale Bibliothek

Virtual International Authority File (VIAF)

International Standard Name Identifier (ISNI)

1

Type-specific impacts of protein defects in pathogenic NFKB2 variants: novel clinical findings from 138 patients

Meissner, Jan (Verfasser)

Freiburg : Universität, 2024

E-Book

2

STAT3 haploinsufficiency is associated with autosomal dominant hyper-IgE syndrome

Andreani, Virginia (Verfasser)

Freiburg : Universität, 2025

E-Book

3

Activation of NF-κB signaling by optogenetic clustering of IKKα and β

Fischer, Alexandra A. M. (Verfasser)

Saarbrücken : Leibniz-Institut für Neue Materialien, 2024

E-Book

4

Compound heterozygous NFKB1 missense variants in cis associated with immunodeficiency

Fliegauf, Manfred (Verfasser)

Freiburg : Universität, 2025

E-Book

5

PGM3 insufficiency: a glycosylation disorder causing a notable T cell defect

Yang, Linlin (Verfasser)

Freiburg : Universität, 2025

E-Book

6

Clinical phenotype, functional assessment, and impact prediction of NF-κB1 missense variants

Klammer, Nils (Verfasser)

Freiburg : Universität, 2022

E-Book

7

A pathogenic missense variant in NFKB1 causes common variable immunodeficiency due to detrimental protein damage

Fliegauf, Manfred (Verfasser)

Freiburg : Universität, 2021

E-Book

8

Activation of NF‐κB signaling by optogenetic clustering of IKKα and β = Activation of NF‐[kappa]B signaling by optogenetic clustering of IKK[alpha] and [beta]

Fischer, Alexandra A. M. (Verfasser)

Online first

Freiburg : Universität, 2025

E-Book

9

Engineering material properties of transcription factor condensates to control gene expression in mammalian cells and mice

Fischer, Alexandra A. M. (Verfasser)

Freiburg : Universität, 2025

E-Book

10

Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50

Fliegauf, Manfred (Verfasser)

Freiburg : Universität, 2022

E-Book

11

Allele-specific disruption of a common STAT3 autosomal dominant allele is not sufficient to restore downstream signaling in patient-derived T cells

König, Saskia (Verfasser)

Freiburg : Universität, 2022

E-Book

12

Assessing the functional relevance of variants in the IKAROS family zinc finger protein 1 (IKZF1) in a cohort of patients with primary immunodeficiency

Eskandarian, Zoya (Verfasser)

Freiburg : Universität, 2019

E-Book

13

Corrigendum: Assessing the functional relevance of variants in the IKAROS family zinc finger protein 1 (IKZF1) in a cohort of patients with primary immunodeficiency

Eskandarian, Zoya (Verfasser)

Freiburg : Universität, 2025

E-Book

14

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

Rojas Restrepo, Jessica L. (Verfasser)

Freiburg : Universität, 2022

E-Book

15

Late-onset antibody deficiency due to monoallelic alterations in NFKB1

Schroeder, Claudia (Verfasser)

Freiburg : Universität, 2020

E-Book

16

Clinical and immunological phenotype of patients with primary immunodeficiency due to damaging mutations in NFKB2

Klemann, Christian (Verfasser)

Freiburg : Universität, 2019

E-Book