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

Peter Nürnberg

Showing results (91-100 of 517) with videos related to

Pageof 52
Sort By:
The Journal of Clinical Endocrinology and Metabolism|August 5, 2004
Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiterYvonne Bayer, Susanne Neumann, Birgit Meyer, et al.
Biology of Reproduction|January 7, 2005
Male reproductive timing in Rhesus macaques is influenced by the 5HTTLPR promoter polymorphism of the serotonin transporter geneMichael Krawczak, Andrea Trefilov, John Berard, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing lossUwe Kornak, Francesco Brancati, Martine Le Merrer, et al.
Human Immunology|August 17, 2011
Transforming growth factor-β1 variant Leu10Pro is associated with both lack of microfilariae and differential microfilarial loads in the blood of persons infected with lymphatic filariasisAlexander Yaw Debrah, Linda Batsa, Anna Albers, et al.
The Pan African Medical Journal|August 16, 2021
Homozygous nonsense mutation of <i>WNT10B</i> gene in a Moroccan family with split-hand foot malformation identified by exome sequencing: a case reportSiham Chafai Elalaoui, Nawfal Fejjal, Yun Li, et al.
Human Mutation|February 1, 2012
Assessing the enrichment performance in targeted resequencing experimentsPeter Frommolt, Ali T Abdallah, Janine Altmüller, et al.
Pflugers Archiv : European Journal of Physiology|May 2, 2013
Regulation of ClC-2 gating by intracellular ATPGabriel Stölting, Georgeta Teodorescu, Birgit Begemann, et al.
Arthritis Research & Therapy|October 7, 2005
Association of ENPP1 gene polymorphisms with hand osteoarthritis in a Chuvasha populationEun-Kyung Suk, Ida Malkin, Stefan Dahm, et al.
Cold Spring Harbor Molecular Case Studies|October 13, 2019
Novel mutations in <i>SLC6A5</i> with benign course in hyperekplexiaHormos Salimi Dafsari, Amit Kawalia, Rosanne Sprute, et al.
Journal of Medical Genetics|April 18, 2018
Mutations in plasmalemma vesicle-associated protein cause severe syndromic protein-losing enteropathyIlse Julia Broekaert, Kerstin Becker, Ingo Gottschalk, et al.
Pageof 52

Showing results (91-100 of 517) with videos related to

Sort By:
Pageof 52
The Journal of Clinical Endocrinology and Metabolism|August 5, 2004
Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiterYvonne Bayer, Susanne Neumann, Birgit Meyer, et al.
Biology of Reproduction|January 7, 2005
Male reproductive timing in Rhesus macaques is influenced by the 5HTTLPR promoter polymorphism of the serotonin transporter geneMichael Krawczak, Andrea Trefilov, John Berard, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing lossUwe Kornak, Francesco Brancati, Martine Le Merrer, et al.
Human Immunology|August 17, 2011
Transforming growth factor-β1 variant Leu10Pro is associated with both lack of microfilariae and differential microfilarial loads in the blood of persons infected with lymphatic filariasisAlexander Yaw Debrah, Linda Batsa, Anna Albers, et al.
The Pan African Medical Journal|August 16, 2021
Homozygous nonsense mutation of <i>WNT10B</i> gene in a Moroccan family with split-hand foot malformation identified by exome sequencing: a case reportSiham Chafai Elalaoui, Nawfal Fejjal, Yun Li, et al.
Human Mutation|February 1, 2012
Assessing the enrichment performance in targeted resequencing experimentsPeter Frommolt, Ali T Abdallah, Janine Altmüller, et al.
Pflugers Archiv : European Journal of Physiology|May 2, 2013
Regulation of ClC-2 gating by intracellular ATPGabriel Stölting, Georgeta Teodorescu, Birgit Begemann, et al.
Arthritis Research & Therapy|October 7, 2005
Association of ENPP1 gene polymorphisms with hand osteoarthritis in a Chuvasha populationEun-Kyung Suk, Ida Malkin, Stefan Dahm, et al.
Cold Spring Harbor Molecular Case Studies|October 13, 2019
Novel mutations in <i>SLC6A5</i> with benign course in hyperekplexiaHormos Salimi Dafsari, Amit Kawalia, Rosanne Sprute, et al.
Journal of Medical Genetics|April 18, 2018
Mutations in plasmalemma vesicle-associated protein cause severe syndromic protein-losing enteropathyIlse Julia Broekaert, Kerstin Becker, Ingo Gottschalk, et al.
Pageof 52