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Frontiers in Immunology
|
August 4, 2025
Case Report: Heterozygous <i>ADAR</i> c.3019G>A pathogenic variant associated with variable neurological symptoms and incomplete penetrance in a four-generational family
Ann-Kathrin Bauer, Iris Marquardt, Benedikt Sundermann, et al.
European Journal of Immunology
|
August 29, 2025
Signal Transducer and Activator of Transcription 3 (STAT3) Variant p.K709N Causes Hyper-IgE Syndrome Likely by Impaired STAT3-Dimer Formation
Beate Hagl, Benedikt D Spielberger, Betina Neumann, et al.
Annals of the Rheumatic Diseases
|
January 22, 2014
SAMHD1 prevents autoimmunity by maintaining genome stability
Stefanie Kretschmer, Christine Wolf, Nadja König, et al.
Nature Structural & Molecular Biology
|
April 29, 2008
Mouse Eri1 interacts with the ribosome and catalyzes 5.8S rRNA processing
K Mark Ansel, William A Pastor, Nicola Rath, et al.
Nature Communications
|
April 29, 2017
Elevated levels of Bcl-3 inhibits Treg development and function resulting in spontaneous colitis
Sonja Reißig, Yilang Tang, Alexei Nikolaev, et al.
International Journal of Cancer
|
September 19, 2017
NFATC1 activation by DNA hypomethylation in chronic lymphocytic leukemia correlates with clinical staging and can be inhibited by ibrutinib
Christine Wolf, Angela Garding, Katharina Filarsky, et al.
Open Forum Infectious Diseases
|
January 5, 2024
Absence of Type I Interferon Autoantibodies or Significant Interferon Signature Alterations in Adults With Post-COVID-19 Syndrome
Martin Achleitner, Nina K Mair, Juliane Dänhardt, et al.
People and Nature (Hoboken, N.J.)
|
July 7, 2020
Action needed for the EU Common Agricultural Policy to address sustainability challenges
Guy Pe'er, Aletta Bonn, Helge Bruelheide, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
June 15, 2026
Innate immune signaling as a potential pathomechanistic biomarker for distinct subtypes in amyotrophic lateral sclerosis
Marcel Naumann, Stefanie Kretschmer, Johannes Dorst, et al.
The CRISPR Journal
|
April 20, 2021
Rescue of STAT3 Function in Hyper-IgE Syndrome Using Adenine Base Editing
Andreas C Eberherr, Andre Maaske, Christine Wolf, et al.
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of 6
Search research articles
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Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
Frontiers in Immunology
|
August 4, 2025
Case Report: Heterozygous <i>ADAR</i> c.3019G>A pathogenic variant associated with variable neurological symptoms and incomplete penetrance in a four-generational family
Ann-Kathrin Bauer, Iris Marquardt, Benedikt Sundermann, et al.
European Journal of Immunology
|
August 29, 2025
Signal Transducer and Activator of Transcription 3 (STAT3) Variant p.K709N Causes Hyper-IgE Syndrome Likely by Impaired STAT3-Dimer Formation
Beate Hagl, Benedikt D Spielberger, Betina Neumann, et al.
Annals of the Rheumatic Diseases
|
January 22, 2014
SAMHD1 prevents autoimmunity by maintaining genome stability
Stefanie Kretschmer, Christine Wolf, Nadja König, et al.
Nature Structural & Molecular Biology
|
April 29, 2008
Mouse Eri1 interacts with the ribosome and catalyzes 5.8S rRNA processing
K Mark Ansel, William A Pastor, Nicola Rath, et al.
Nature Communications
|
April 29, 2017
Elevated levels of Bcl-3 inhibits Treg development and function resulting in spontaneous colitis
Sonja Reißig, Yilang Tang, Alexei Nikolaev, et al.
International Journal of Cancer
|
September 19, 2017
NFATC1 activation by DNA hypomethylation in chronic lymphocytic leukemia correlates with clinical staging and can be inhibited by ibrutinib
Christine Wolf, Angela Garding, Katharina Filarsky, et al.
Open Forum Infectious Diseases
|
January 5, 2024
Absence of Type I Interferon Autoantibodies or Significant Interferon Signature Alterations in Adults With Post-COVID-19 Syndrome
Martin Achleitner, Nina K Mair, Juliane Dänhardt, et al.
People and Nature (Hoboken, N.J.)
|
July 7, 2020
Action needed for the EU Common Agricultural Policy to address sustainability challenges
Guy Pe'er, Aletta Bonn, Helge Bruelheide, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
June 15, 2026
Innate immune signaling as a potential pathomechanistic biomarker for distinct subtypes in amyotrophic lateral sclerosis
Marcel Naumann, Stefanie Kretschmer, Johannes Dorst, et al.
The CRISPR Journal
|
April 20, 2021
Rescue of STAT3 Function in Hyper-IgE Syndrome Using Adenine Base Editing
Andreas C Eberherr, Andre Maaske, Christine Wolf, et al.
Page
of 6