Suchergebnisse - "Fliegauf, Manfred"

PubPharm (119)

1

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

enthalten in: Small (Weinheim an der Bergstrasse, Germany) | 2024

von Fischer, A. | Robertson, H. | Kong, D. | +10

2

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

enthalten in: bioRxiv.org | 2024

von Fischer, A. | Robertson, H. | Kong, D. | +10

3

Integrated Multi-omics Analyses of NFKB1 patients B cells points towards an up regulation of NF-κB network inhibitors

enthalten in: bioRxiv.org | 2022

von Camacho-Ordonez, N. | Ramirez, N. | Posadas-Cantera, S. | +12

4

Allele-Specific Disruption of a Common STAT3 Autosomal Dominant Allele Is Not Sufficient to Restore Downstream Signaling in Patient-Derived T Cells

enthalten in: Genes | 2022

von König, S. | Fliegauf, M. | Rhiel, M. | +4

5

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

enthalten in: Frontiers in immunology | 2022

von Fliegauf, M. | Kinnunen, M. | Posadas-Cantera, S. | +24

6

Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency

enthalten in: The Journal of experimental medicine | 2021

von Li, J. | Lei, W. | Zhang, P. | +38

7

The expansion of human T-bethighCD21low B cells is T cell dependent

enthalten in: Science immunology | 2021

von Keller, B. | Strohmeier, V. | Harder, I. | +59

8

Recurrent necrotizing cellulitis, multi-organ autoimmune disease and humoral immunodeficiency due to a novel NFKB1 frameshift mutation

enthalten in: European journal of medical genetics | 2021

von Bergbreiter, A. | Jaeger, T. | Karle, A. | +15

9

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

sonderdruck aus: Frontiers in immunology | 2021

von Fliegauf, M. | Krüger, R. | Steiner, S. | +5

10

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

sonderdruck aus: Frontiers in immunology | 2021

von Rojas Restrepo, J. | Caballero Oteyza, A. | Hübscher, K. | +8

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