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Matthias Rath

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Molecular Genetics & Genomic Medicine|January 25, 2017
Constitutional de novo and postzygotic mutations in isolated cases of cerebral cavernous malformationsMatthias Rath, Stefanie Spiegler, Neetika Nath, et al.
Critical Care Medicine|July 27, 2010
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) improves the innate immune response and enhances survival in murine polymicrobial sepsisKatharina Cziupka, Alexandra Busemann, Lars Ivo Partecke, et al.
Journal of Thrombosis and Haemostasis : JTH|December 16, 2023
Aggregates of nonmuscular myosin IIA in erythrocytes associate with GATA1- and GFI1B-related thrombocytopeniaCarlo Zaninetti, Jose' Rivera, Leonard Vater, et al.
Angiogenesis|June 6, 2025
High-throughput differentiation of human blood vessel organoids reveals overlapping and distinct functions of the cerebral cavernous malformation proteinsDariush Skowronek, Robin A Pilz, Valeriia V Saenko, et al.
Veterinaria Italiana|April 15, 2010
Standardisation of a new model of H9N2/Escherichia coli challenge in broilers in the LebanonElie K Barbour, Fouad A Mastori, Afif M Abdel Nour, et al.
European Journal of Cancer (Oxford, England : 1990)|June 24, 2026
Spectrum of double heterozygosity in individuals diagnosed with hereditary breast and ovarian cancerNatalie Herold, Christoph Engel, Dorothee Speiser, et al.
Science Translational Medicine|March 2, 2022
Pathogenic variants in <i>MDFIC</i> cause recessive central conducting lymphatic anomaly with lymphedemaAlicia B Byrne, Pascal Brouillard, Drew L Sutton, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 18, 2018
A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 geneLars R Jensen, Lillian Garrett, Sabine M Hölter, et al.
European Journal of Human Genetics : EJHG|May 22, 2024
Comparison of the ABC and ACMG systems for variant classificationGunnar Houge, Eirik Bratland, Ingvild Aukrust, et al.
Neurology|July 10, 2025
Lifetime Risk of First Symptomatic ICH or Seizure in Familial Cerebral Cavernous Malformations: A Multicenter Patient Data AnalysisPhilipp Dammann, Alejandro N Santos, Laven Mavarani, et al.
Pageof 13

Showing results (121-130 of 130) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 130 results.
Molecular Genetics & Genomic Medicine|January 25, 2017
Constitutional de novo and postzygotic mutations in isolated cases of cerebral cavernous malformationsMatthias Rath, Stefanie Spiegler, Neetika Nath, et al.
Critical Care Medicine|July 27, 2010
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) improves the innate immune response and enhances survival in murine polymicrobial sepsisKatharina Cziupka, Alexandra Busemann, Lars Ivo Partecke, et al.
Journal of Thrombosis and Haemostasis : JTH|December 16, 2023
Aggregates of nonmuscular myosin IIA in erythrocytes associate with GATA1- and GFI1B-related thrombocytopeniaCarlo Zaninetti, Jose' Rivera, Leonard Vater, et al.
Angiogenesis|June 6, 2025
High-throughput differentiation of human blood vessel organoids reveals overlapping and distinct functions of the cerebral cavernous malformation proteinsDariush Skowronek, Robin A Pilz, Valeriia V Saenko, et al.
Veterinaria Italiana|April 15, 2010
Standardisation of a new model of H9N2/Escherichia coli challenge in broilers in the LebanonElie K Barbour, Fouad A Mastori, Afif M Abdel Nour, et al.
European Journal of Cancer (Oxford, England : 1990)|June 24, 2026
Spectrum of double heterozygosity in individuals diagnosed with hereditary breast and ovarian cancerNatalie Herold, Christoph Engel, Dorothee Speiser, et al.
Science Translational Medicine|March 2, 2022
Pathogenic variants in <i>MDFIC</i> cause recessive central conducting lymphatic anomaly with lymphedemaAlicia B Byrne, Pascal Brouillard, Drew L Sutton, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 18, 2018
A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 geneLars R Jensen, Lillian Garrett, Sabine M Hölter, et al.
European Journal of Human Genetics : EJHG|May 22, 2024
Comparison of the ABC and ACMG systems for variant classificationGunnar Houge, Eirik Bratland, Ingvild Aukrust, et al.
Neurology|July 10, 2025
Lifetime Risk of First Symptomatic ICH or Seizure in Familial Cerebral Cavernous Malformations: A Multicenter Patient Data AnalysisPhilipp Dammann, Alejandro N Santos, Laven Mavarani, et al.
Pageof 13