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Manfred Fliegauf

Showing results (21-30 of 64) with videos related to

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Human Mutation|April 27, 2011
U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutationFabian Schmid, Esther Glaus, Daniel Barthelmes, et al.
Human Molecular Genetics|July 23, 2004
Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formationInés Ibañez-Tallon, Axel Pagenstecher, Manfred Fliegauf, et al.
Biochemical and Biophysical Research Communications|April 14, 2016
The atypical cadherin Dachsous1 localizes to the base of the ciliary apparatus in airway epitheliaCécile Dau, Manfred Fliegauf, Heymut Omran, et al.
Advanced Biology|July 29, 2025
Activation of NF-κB Signaling by Optogenetic Clustering of IKKα and βAlexandra Anna Maria Fischer, Markus Michael Kramer, Miguel Baños, et al.
Haematologica|September 16, 2008
Transcriptional upregulation of p21/WAF/Cip1 in myeloid leukemic blasts expressing AML1-ETOTobias Berg, Manfred Fliegauf, Jan Burger, et al.
Frontiers in Immunology|January 3, 2022
Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric StudyJessica Rojas-Restrepo, Andrés Caballero-Oteyza, Katrin Huebscher, et al.
The Journal of Allergy and Clinical Immunology|July 28, 2016
Disturbed canonical nuclear factor of κ light chain signaling in B cells of patients with common variable immunodeficiencyBaerbel Keller, Zoltan Cseresnyes, Ina Stumpf, et al.
Science Advances|August 29, 2025
STAT3 haploinsufficiency is associated with autosomal dominant hyper-IgE syndromeVirginia Andreani, Aaron James Forde, Manfred Fliegauf, et al.
Frontiers in Immunology|December 6, 2019
Late-Onset Antibody Deficiency Due to Monoallelic Alterations in <i>NFKB1</i>Claudia Schröder, Georgios Sogkas, Manfred Fliegauf, et al.
Journal of Clinical Immunology|July 10, 2026
A Detrimental NFKB2 Missense Variant is Associated with HypogammaglobulinemiaManfred Fliegauf, Laura Gamez-Diaz, Pavla Mrovecova, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
Human Mutation|April 27, 2011
U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutationFabian Schmid, Esther Glaus, Daniel Barthelmes, et al.
Human Molecular Genetics|July 23, 2004
Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formationInés Ibañez-Tallon, Axel Pagenstecher, Manfred Fliegauf, et al.
Biochemical and Biophysical Research Communications|April 14, 2016
The atypical cadherin Dachsous1 localizes to the base of the ciliary apparatus in airway epitheliaCécile Dau, Manfred Fliegauf, Heymut Omran, et al.
Advanced Biology|July 29, 2025
Activation of NF-κB Signaling by Optogenetic Clustering of IKKα and βAlexandra Anna Maria Fischer, Markus Michael Kramer, Miguel Baños, et al.
Haematologica|September 16, 2008
Transcriptional upregulation of p21/WAF/Cip1 in myeloid leukemic blasts expressing AML1-ETOTobias Berg, Manfred Fliegauf, Jan Burger, et al.
Frontiers in Immunology|January 3, 2022
Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric StudyJessica Rojas-Restrepo, Andrés Caballero-Oteyza, Katrin Huebscher, et al.
The Journal of Allergy and Clinical Immunology|July 28, 2016
Disturbed canonical nuclear factor of κ light chain signaling in B cells of patients with common variable immunodeficiencyBaerbel Keller, Zoltan Cseresnyes, Ina Stumpf, et al.
Science Advances|August 29, 2025
STAT3 haploinsufficiency is associated with autosomal dominant hyper-IgE syndromeVirginia Andreani, Aaron James Forde, Manfred Fliegauf, et al.
Frontiers in Immunology|December 6, 2019
Late-Onset Antibody Deficiency Due to Monoallelic Alterations in <i>NFKB1</i>Claudia Schröder, Georgios Sogkas, Manfred Fliegauf, et al.
Journal of Clinical Immunology|July 10, 2026
A Detrimental NFKB2 Missense Variant is Associated with HypogammaglobulinemiaManfred Fliegauf, Laura Gamez-Diaz, Pavla Mrovecova, et al.
Pageof 7