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Frank Baas

Showing results (131-140 of 231) with videos related to

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Human Molecular Genetics|April 2, 2003
Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patientsAnnemieke Aartsma-Rus, Anneke A M Janson, Wendy E Kaman, et al.
Clocks & Sleep|September 22, 2025
The Acute Effects of Morning Bright Light on the Human White Adipose Tissue Transcriptome: Exploratory Post Hoc AnalysisAnhui Wang, Jeroen Vreijling, Aldo Jongejan, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 3, 2008
Molecular risk stratification of medulloblastoma patients based on immunohistochemical analysis of MYC, LDHB, and CCNB1 expressionTalitha de Haas, Nancy Hasselt, Dirk Troost, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 20, 2007
The membrane attack complex of the complement system is essential for rapid Wallerian degenerationValeria Ramaglia, Rosalind Helen Mary King, Michelle Nourallah, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 5, 2005
Full transcriptome analysis of rhabdomyosarcoma, normal, and fetal skeletal muscle: statistical comparison of multiple SAGE librariesGerben J Schaaf, Jan M Ruijter, Fred van Ruissen, et al.
Nature Communications|September 29, 2021
Assembly defects of human tRNA splicing endonuclease contribute to impaired pre-tRNA processing in pontocerebellar hypoplasiaSamoil Sekulovski, Pascal Devant, Silvia Panizza, et al.
Neurology. Genetics|November 24, 2025
Search for Additional Pathogenic Variants to Explain Variation in <i>PMP22</i>-Related NeuropathiesBarbara W van Paassen, Camiel Verhamme, Fred van Ruissen, et al.
Journal of Neuroinflammation|January 15, 2017
Mannose-binding lectin-associated serine protease 2 (MASP-2) contributes to poor disease outcome in humans and mice with pneumococcal meningitisE Soemirien Kasanmoentalib, Mercedes Valls Seron, Bart Ferwerda, et al.
Stroke|July 21, 2022
Effect of <i>NOTCH3</i> EGFr Group, Sex, and Cardiovascular Risk Factors on CADASIL Clinical and Neuroimaging OutcomesRemco J Hack, Minne N Cerfontaine, Gido Gravesteijn, et al.
Acta Neuropathologica|March 4, 2010
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literatureCasper Jansen, Willem Voet, Mark W Head, et al.
Pageof 24

Showing results (131-140 of 231) with videos related to

Sort By:
Pageof 24
Human Molecular Genetics|April 2, 2003
Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patientsAnnemieke Aartsma-Rus, Anneke A M Janson, Wendy E Kaman, et al.
Clocks & Sleep|September 22, 2025
The Acute Effects of Morning Bright Light on the Human White Adipose Tissue Transcriptome: Exploratory Post Hoc AnalysisAnhui Wang, Jeroen Vreijling, Aldo Jongejan, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 3, 2008
Molecular risk stratification of medulloblastoma patients based on immunohistochemical analysis of MYC, LDHB, and CCNB1 expressionTalitha de Haas, Nancy Hasselt, Dirk Troost, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 20, 2007
The membrane attack complex of the complement system is essential for rapid Wallerian degenerationValeria Ramaglia, Rosalind Helen Mary King, Michelle Nourallah, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 5, 2005
Full transcriptome analysis of rhabdomyosarcoma, normal, and fetal skeletal muscle: statistical comparison of multiple SAGE librariesGerben J Schaaf, Jan M Ruijter, Fred van Ruissen, et al.
Nature Communications|September 29, 2021
Assembly defects of human tRNA splicing endonuclease contribute to impaired pre-tRNA processing in pontocerebellar hypoplasiaSamoil Sekulovski, Pascal Devant, Silvia Panizza, et al.
Neurology. Genetics|November 24, 2025
Search for Additional Pathogenic Variants to Explain Variation in <i>PMP22</i>-Related NeuropathiesBarbara W van Paassen, Camiel Verhamme, Fred van Ruissen, et al.
Journal of Neuroinflammation|January 15, 2017
Mannose-binding lectin-associated serine protease 2 (MASP-2) contributes to poor disease outcome in humans and mice with pneumococcal meningitisE Soemirien Kasanmoentalib, Mercedes Valls Seron, Bart Ferwerda, et al.
Stroke|July 21, 2022
Effect of <i>NOTCH3</i> EGFr Group, Sex, and Cardiovascular Risk Factors on CADASIL Clinical and Neuroimaging OutcomesRemco J Hack, Minne N Cerfontaine, Gido Gravesteijn, et al.
Acta Neuropathologica|March 4, 2010
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literatureCasper Jansen, Willem Voet, Mark W Head, et al.
Pageof 24