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

S W Scherer

Showing results (11-20 of 164) with videos related to

Pageof 17
Sort By:
Journal of Neuroimmunology|May 18, 2000
Localization of the human SP3 gene to chromosome 7p14-p15.2. The lack of expression in multiple sclerosis does not reflect abnormal gene organizationM C Grekova, S W Scherer, J Trabb, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Localization of the human dihydrolipoamide dehydrogenase gene (DLD) to 7q31----q32S W Scherer, G Otulakowski, B H Robinson, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A gene (HTR5A) to human chromosome band 7q36.1N C Schanen, S W Scherer, L C Tsui, et al.
Genomics|November 26, 1998
Human GBF1 is a ubiquitously expressed gene of the sec7 domain family mapping to 10q24S J Mansour, J A Herbrick, S W Scherer, et al.
Journal of Medical Genetics|June 1, 1996
Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3J Ignatius, S Knuutila, S W Scherer, et al.
Cytogenetic and Genome Research|November 25, 2006
Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genomeJ Zhang, L Feuk, G E Duggan, et al.
Scientific Reports|May 6, 2020
Genome-wide association study of emotional empathy in childrenM R Woodbury-Smith, A D Paterson, P Szatmari, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 13, 2016
Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human Chromosome band 5ql4M A Crackower, S W Scherer, H H Heng, et al.
Neurology|February 11, 2000
Identification of new and common mutations in the EPM2A gene in Lafora diseaseB A Minassian, L Ianzano, A V Delgado-Escueta, et al.
Brain Research. Molecular Brain Research|February 27, 2001
Localization of the human mGluR4 gene within an epilepsy susceptibility locus(1)C G Wong, S W Scherer, O C Snead, et al.
Pageof 17

Showing results (11-20 of 164) with videos related to

Sort By:
Pageof 17
Journal of Neuroimmunology|May 18, 2000
Localization of the human SP3 gene to chromosome 7p14-p15.2. The lack of expression in multiple sclerosis does not reflect abnormal gene organizationM C Grekova, S W Scherer, J Trabb, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Localization of the human dihydrolipoamide dehydrogenase gene (DLD) to 7q31----q32S W Scherer, G Otulakowski, B H Robinson, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A gene (HTR5A) to human chromosome band 7q36.1N C Schanen, S W Scherer, L C Tsui, et al.
Genomics|November 26, 1998
Human GBF1 is a ubiquitously expressed gene of the sec7 domain family mapping to 10q24S J Mansour, J A Herbrick, S W Scherer, et al.
Journal of Medical Genetics|June 1, 1996
Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3J Ignatius, S Knuutila, S W Scherer, et al.
Cytogenetic and Genome Research|November 25, 2006
Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genomeJ Zhang, L Feuk, G E Duggan, et al.
Scientific Reports|May 6, 2020
Genome-wide association study of emotional empathy in childrenM R Woodbury-Smith, A D Paterson, P Szatmari, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 13, 2016
Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human Chromosome band 5ql4M A Crackower, S W Scherer, H H Heng, et al.
Neurology|February 11, 2000
Identification of new and common mutations in the EPM2A gene in Lafora diseaseB A Minassian, L Ianzano, A V Delgado-Escueta, et al.
Brain Research. Molecular Brain Research|February 27, 2001
Localization of the human mGluR4 gene within an epilepsy susceptibility locus(1)C G Wong, S W Scherer, O C Snead, et al.
Pageof 17