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Manfred Fliegauf (1968-)

Name	Manfred Fliegauf
Zeit	1968- (Lebensdaten)
Ort	Sonstiges Ausland / Unbekanntes Land
Weitere Angaben	Diss. Fakultät für Biologie
Datensatztyp	Person
GND-Nummer	123740630
Datensatz-ID	123740630
Beteiligt an alle anzeigen Compound heterozygous NFKB1 missense variants in cis associated with immunodeficiency Activation of NF‐κB Signaling by Optogenetic Clustering of IKKα and β 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] STAT3 haploinsufficiency is associated with autosomal dominant hyper-IgE syndrome Type-specific impacts of protein defects in pathogenic NFKB2 variants: novel clinical findings from 138 patients Engineering Material Properties of Transcription Factor Condensates to Control Gene Expression in Mammalian Cells and Mice Engineering Material Properties of Transcription Factor Condensates to Control Gene Expression in Mammalian Cells and Mice (Small 38/2024) Activation of NF-κB signaling by optogenetic clustering of IKKα and β Engineering material properties of transcription factor condensates to control gene expression in mammalian cells and mice Engineering Material Properties of Transcription Factor Condensates to Control Gene Expression in Mammalian Cells and Mice PGM3 insufficiency: a glycosylation disorder causing a notable T cell defect Allele-specific disruption of a common STAT3 autosomal dominant allele is not sufficient to restore downstream signaling in patient-derived T cells Clinical phenotype, functional assessment, and impact prediction of NF-κB1 missense variants Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50 A pathogenic missense variant in NFKB1 causes common variable immunodeficiency due to detrimental protein damage Establishing the molecular diagnoses in a cohort of 291 patients with predominantly antibody deficiency by targeted next-generation sequencing: Experience from a monocentric study Assessing the functional relevance of variants in the IKAROS family zinc finger protein 1 (IKZF1) in a cohort of patients with primary immunodeficiency Clinical and immunological phenotype of patients with primary immunodeficiency due to damaging mutations in NFKB2 Corrigendum: Assessing the functional relevance of variants in the IKAROS family zinc finger protein 1 (IKZF1) in a cohort of patients with primary immunodeficiency Late-onset antibody deficiency due to monoallelic alterations in NFKB1 Mycobacteria exploit nitric oxide‐induced transformation of macrophages into permissive giant cells Mycobacteria exploit nitric oxide‐induced transformation of macrophages into permissive giant cells Untersuchungen zur Funktion des leukämie-spezifischen Transkriptionsfaktors AML1-ETO durch dessen konditionelle Expression in stabil transfizierten humanen monoblastären U-937 Zellen : zelluläre Effekte und Identifizierung differentiell exprimierter Gene

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Katalog der Deutschen Nationalbibliothek

Manfred Fliegauf (1968-)

Compound heterozygous NFKB1 missense variants in cis associated with immunodeficiency

Activation of NF‐κB Signaling by Optogenetic Clustering of IKKα and β

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]

STAT3 haploinsufficiency is associated with autosomal dominant hyper-IgE syndrome

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

Engineering Material Properties of Transcription Factor Condensates to Control Gene Expression in Mammalian Cells and Mice

Engineering Material Properties of Transcription Factor Condensates to Control Gene Expression in Mammalian Cells and Mice (Small 38/2024)

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

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

Engineering Material Properties of Transcription Factor Condensates to Control Gene Expression in Mammalian Cells and Mice

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

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

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

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

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

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

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

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

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

Late-onset antibody deficiency due to monoallelic alterations in NFKB1

Mycobacteria exploit nitric oxide‐induced transformation of macrophages into permissive giant cells

Mycobacteria exploit nitric oxide‐induced transformation of macrophages into permissive giant cells

Untersuchungen zur Funktion des leukämie-spezifischen Transkriptionsfaktors AML1-ETO durch dessen konditionelle Expression in stabil transfizierten humanen monoblastären U-937 Zellen : zelluläre Effekte und Identifizierung differentiell exprimierter Gene