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Rainer Seidl

Showing results (71-80 of 77) with videos related to

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Immunity|June 25, 2013
RORγt⁺ innate lymphoid cells acquire a proinflammatory program upon engagement of the activating receptor NKp44Timor Glatzer, Monica Killig, Johannes Meisig, et al.
Human Mutation|September 8, 2016
Chondroitin Sulfate N-acetylgalactosaminyltransferase-1 (CSGalNAcT-1) Deficiency Results in a Mild Skeletal Dysplasia and Joint LaxityJulia Vodopiutz, Shuji Mizumoto, Ekkehart Lausch, et al.
JAMA Neurology|February 20, 2013
Natalizumab therapy for highly active pediatric multiple sclerosisBarbara Kornek, Fahmy Aboul-Enein, Kevin Rostasy, et al.
Cell Stem Cell|May 8, 2024
ARID1B controls transcriptional programs of axon projection in an organoid model of the human corpus callosumCatarina Martins-Costa, Andrea Wiegers, Vincent A Pham, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|June 4, 2020
Antibodies to nodal/paranodal proteins in paediatric immune-mediated neuropathyDesiree De Simoni, Gerda Ricken, Michael Winklehner, et al.
Human Mutation|July 1, 2015
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney DiseaseJulia Vodopiutz, Rainer Seidl, Daniela Prayer, et al.
Journal of Clinical Immunology|January 7, 2021
Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I InterferonopathiesLorenzo Lodi, Isabelle Melki, Vincent Bondet, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
Immunity|June 25, 2013
RORγt⁺ innate lymphoid cells acquire a proinflammatory program upon engagement of the activating receptor NKp44Timor Glatzer, Monica Killig, Johannes Meisig, et al.
Human Mutation|September 8, 2016
Chondroitin Sulfate N-acetylgalactosaminyltransferase-1 (CSGalNAcT-1) Deficiency Results in a Mild Skeletal Dysplasia and Joint LaxityJulia Vodopiutz, Shuji Mizumoto, Ekkehart Lausch, et al.
JAMA Neurology|February 20, 2013
Natalizumab therapy for highly active pediatric multiple sclerosisBarbara Kornek, Fahmy Aboul-Enein, Kevin Rostasy, et al.
Cell Stem Cell|May 8, 2024
ARID1B controls transcriptional programs of axon projection in an organoid model of the human corpus callosumCatarina Martins-Costa, Andrea Wiegers, Vincent A Pham, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|June 4, 2020
Antibodies to nodal/paranodal proteins in paediatric immune-mediated neuropathyDesiree De Simoni, Gerda Ricken, Michael Winklehner, et al.
Human Mutation|July 1, 2015
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney DiseaseJulia Vodopiutz, Rainer Seidl, Daniela Prayer, et al.
Journal of Clinical Immunology|January 7, 2021
Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I InterferonopathiesLorenzo Lodi, Isabelle Melki, Vincent Bondet, et al.
Pageof 8