Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Fred van Ruissen

Showing results (11-20 of 36) with videos related to

Pageof 4
Sort By:
Neuromuscular Disorders : NMD|September 11, 2007
Congenital hypomyelinating neuropathy, a long term follow-up study in an affected familyLiesbeth S Smit, Daniella Roofthooft, Fred van Ruissen, et al.
Genomics|May 7, 2002
A partial transcriptome of human epidermisFred van Ruissen, Bastiaan J H Jansen, Gys J de Jongh, et al.
BMC Genomics|June 16, 2005
Evaluation of the similarity of gene expression data estimated with SAGE and Affymetrix GeneChipsFred van Ruissen, Jan M Ruijter, Gerben J Schaaf, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 24, 2015
A Dutch family with autosomal recessively inherited lower motor neuron predominant motor neuron disease due to optineurin mutationsEmma Beeldman, Anneke J van der Kooi, Marianne de Visser, et al.
The Journal of Investigative Dermatology|December 17, 2003
Tumor necrosis factor related apoptosis inducing ligand triggers apoptosis in dividing but not in differentiating human epidermal keratinocytesBastiaan J H Jansen, Fred van Ruissen, Stefanie Cerneus, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 5, 2002
Differential gene expression in premalignant human epidermis revealed by cluster analysis of serial analysis of gene expression (SAGE) librariesFred van Ruissen, Bastiaan J H Jansen, Gys J de Jongh, et al.
Journal of the Peripheral Nervous System : JPNS|August 25, 2017
Pseudodominant inheritance pattern in a family with CMT2 caused by GDAP1 mutationsBarbara W van Paassen, Marieke Bronk, Camiel Verhamme, et al.
European Journal of Human Genetics : EJHG|March 4, 2011
TSEN54 mutations cause pontocerebellar hypoplasia type 5Yasmin Namavar, David Chitayat, Peter G Barth, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
Copy number variation upstream of PMP22 in Charcot-Marie-Tooth diseaseMarian A J Weterman, Fred van Ruissen, Marit de Wissel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 28, 2021
Early life involvement in C9orf72 repeat expansion carriersFlora Gossink, Annemiek Dols, Max L Stek, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Neuromuscular Disorders : NMD|September 11, 2007
Congenital hypomyelinating neuropathy, a long term follow-up study in an affected familyLiesbeth S Smit, Daniella Roofthooft, Fred van Ruissen, et al.
Genomics|May 7, 2002
A partial transcriptome of human epidermisFred van Ruissen, Bastiaan J H Jansen, Gys J de Jongh, et al.
BMC Genomics|June 16, 2005
Evaluation of the similarity of gene expression data estimated with SAGE and Affymetrix GeneChipsFred van Ruissen, Jan M Ruijter, Gerben J Schaaf, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 24, 2015
A Dutch family with autosomal recessively inherited lower motor neuron predominant motor neuron disease due to optineurin mutationsEmma Beeldman, Anneke J van der Kooi, Marianne de Visser, et al.
The Journal of Investigative Dermatology|December 17, 2003
Tumor necrosis factor related apoptosis inducing ligand triggers apoptosis in dividing but not in differentiating human epidermal keratinocytesBastiaan J H Jansen, Fred van Ruissen, Stefanie Cerneus, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 5, 2002
Differential gene expression in premalignant human epidermis revealed by cluster analysis of serial analysis of gene expression (SAGE) librariesFred van Ruissen, Bastiaan J H Jansen, Gys J de Jongh, et al.
Journal of the Peripheral Nervous System : JPNS|August 25, 2017
Pseudodominant inheritance pattern in a family with CMT2 caused by GDAP1 mutationsBarbara W van Paassen, Marieke Bronk, Camiel Verhamme, et al.
European Journal of Human Genetics : EJHG|March 4, 2011
TSEN54 mutations cause pontocerebellar hypoplasia type 5Yasmin Namavar, David Chitayat, Peter G Barth, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
Copy number variation upstream of PMP22 in Charcot-Marie-Tooth diseaseMarian A J Weterman, Fred van Ruissen, Marit de Wissel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 28, 2021
Early life involvement in C9orf72 repeat expansion carriersFlora Gossink, Annemiek Dols, Max L Stek, et al.
Pageof 4