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Annals of the Rheumatic Diseases
|
January 22, 2014
SAMHD1 prevents autoimmunity by maintaining genome stability
Stefanie Kretschmer, Christine Wolf, Nadja König, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 28, 2016
A product of immunoreactive trypsinogen and pancreatitis-associated protein as second-tier strategy in cystic fibrosis newborn screening
Sophia Weidler, Konrad H Stopsack, Jutta Hammermann, et al.
Science Advances
|
March 1, 2024
Aberrant RNA sensing in regulatory T cells causes systemic autoimmunity
Domnica Luca, Sumin Lee, Keiji Hirota, et al.
Biology of Reproduction
|
August 28, 2009
Rat hd mutation reveals an essential role of centrobin in spermatid head shaping and assembly of the head-tail coupling apparatus
Frantisek Liska, Claudia Gosele, Eugene Rivkin, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 13, 2021
The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literature
Walid Fazeli, Daniel Bamborschke, Abubakar Moawia, 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.
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.
Plos Genetics
|
March 11, 2015
Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance
Jorge Esparza-Gordillo, Anja Matanovic, Ingo Marenholz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 10, 2013
Epilepsy in Aicardi-Goutières syndrome
Georgia Ramantani, Louis G Maillard, Thomas Bast, et al.
Studies in Health Technology and Informatics
|
June 25, 2020
The Status Quo of Rare Diseases Centres for the Development of a Clinical Decision Support System - A Cross-Sectional Study
Jannik Schaaf, Martin Sedlmayr, Hans-Ulrich Prokosch, et al.
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of 9
Search research articles
Search
Showing results (51-60 of 86) with videos related to
Sort By:
Page
of 9
Annals of the Rheumatic Diseases
|
January 22, 2014
SAMHD1 prevents autoimmunity by maintaining genome stability
Stefanie Kretschmer, Christine Wolf, Nadja König, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 28, 2016
A product of immunoreactive trypsinogen and pancreatitis-associated protein as second-tier strategy in cystic fibrosis newborn screening
Sophia Weidler, Konrad H Stopsack, Jutta Hammermann, et al.
Science Advances
|
March 1, 2024
Aberrant RNA sensing in regulatory T cells causes systemic autoimmunity
Domnica Luca, Sumin Lee, Keiji Hirota, et al.
Biology of Reproduction
|
August 28, 2009
Rat hd mutation reveals an essential role of centrobin in spermatid head shaping and assembly of the head-tail coupling apparatus
Frantisek Liska, Claudia Gosele, Eugene Rivkin, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 13, 2021
The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literature
Walid Fazeli, Daniel Bamborschke, Abubakar Moawia, 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.
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.
Plos Genetics
|
March 11, 2015
Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance
Jorge Esparza-Gordillo, Anja Matanovic, Ingo Marenholz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 10, 2013
Epilepsy in Aicardi-Goutières syndrome
Georgia Ramantani, Louis G Maillard, Thomas Bast, et al.
Studies in Health Technology and Informatics
|
June 25, 2020
The Status Quo of Rare Diseases Centres for the Development of a Clinical Decision Support System - A Cross-Sectional Study
Jannik Schaaf, Martin Sedlmayr, Hans-Ulrich Prokosch, et al.
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of 9