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Manfred Fliegauf

*born* 1968

*BiographicalDetails*
Diss. Fakultät für Biologie

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Gemeinsame Normdatei (GND) im Katalog der Deutschen Nationalbibliothek

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1

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

Meissner, Jan (Verfasser)

Freiburg : Universität, 2024

*eBook*

2

STAT3 haploinsufficiency is associated with autosomal dominant hyper-IgE syndrome

Andreani, Virginia (Verfasser)

Freiburg : Universität, 2025

*eBook*

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

*eBook*

4

Compound heterozygous NFKB1 missense variants in cis associated with immunodeficiency

Fliegauf, Manfred (Verfasser)

Freiburg : Universität, 2025

*eBook*

5

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

Yang, Linlin (Verfasser)

Freiburg : Universität, 2025

*eBook*

6

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

*eBook*

7

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

Klammer, Nils (Verfasser)

Freiburg : Universität, 2022

*eBook*

8

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

Fischer, Alexandra A. M. (Verfasser)

Freiburg : Universität, 2025

*eBook*

9

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

Fliegauf, Manfred (Verfasser)

Freiburg : Universität, 2021

*eBook*

10

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

Fliegauf, Manfred (Verfasser)

Freiburg : Universität, 2022

*eBook*

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

*eBook*

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

*eBook*

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

*eBook*

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

*eBook*

15

Late-onset antibody deficiency due to monoallelic alterations in NFKB1

Schroeder, Claudia (Verfasser)

Freiburg : Universität, 2020

*eBook*

16

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

Klemann, Christian (Verfasser)

Freiburg : Universität, 2019

*eBook*