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

Stephan Züchner

Showing results (71-80 of 198) with videos related to

Pageof 20
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2021
TSG101 negatively regulates mitochondrial biogenesis in axonsTzu-Huai Lin, Dana M Bis-Brewer, Amy E Sheehan, et al.
Methods in Enzymology|March 29, 2018
Zebrafish: A Pharmacogenetic Model for AnesthesiaVictoria Bedell, Elena Buglo, Daniel Marcato, et al.
Psychosomatic Medicine|June 23, 2007
Associations of a regulatory polymorphism of monoamine oxidase-A gene promoter (MAOA-uVNTR) with symptoms of depression and sleep qualityBeverly H Brummett, Andrew D Krystal, Ilene C Siegler, et al.
Behavior Genetics|October 24, 2007
Effects of environmental stress and gender on associations among symptoms of depression and the serotonin transporter gene linked polymorphic region (5-HTTLPR)Beverly H Brummett, Stephen H Boyle, Ilene C Siegler, et al.
Brain : a Journal of Neurology|February 5, 2003
Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathyJan Senderek, Carsten Bergmann, Vincent T Ramaekers, et al.
Cell Metabolism|November 27, 2010
The mtDNA mutation spectrum of the progeroid Polg mutator mouse includes abundant control region multimersSiôn L Williams, Jia Huang, Yvonne J K Edwards, et al.
Orphanet Journal of Rare Diseases|April 19, 2014
Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohortsMatthis Synofzik, Rebecca Schüle, Martin Schulze, et al.
Investigative Ophthalmology & Visual Science|December 23, 2008
Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficienciesRavikanth Metlapally, Michel Michaelides, Anuradha Bulusu, et al.
Journal of Medical Genetics|December 4, 2009
Functional evidence implicating a novel TOR1A mutation in idiopathic, late-onset focal dystoniaNicole Calakos, Viren D Patel, Melissa Gottron, et al.
Neurology|September 16, 2016
SIGMAR1 mutation associated with autosomal recessive Silver-like syndromeAlejandro Horga, Pedro J Tomaselli, Michael A Gonzalez, et al.
Pageof 20

Showing results (71-80 of 198) with videos related to

Sort By:
Pageof 20
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2021
TSG101 negatively regulates mitochondrial biogenesis in axonsTzu-Huai Lin, Dana M Bis-Brewer, Amy E Sheehan, et al.
Methods in Enzymology|March 29, 2018
Zebrafish: A Pharmacogenetic Model for AnesthesiaVictoria Bedell, Elena Buglo, Daniel Marcato, et al.
Psychosomatic Medicine|June 23, 2007
Associations of a regulatory polymorphism of monoamine oxidase-A gene promoter (MAOA-uVNTR) with symptoms of depression and sleep qualityBeverly H Brummett, Andrew D Krystal, Ilene C Siegler, et al.
Behavior Genetics|October 24, 2007
Effects of environmental stress and gender on associations among symptoms of depression and the serotonin transporter gene linked polymorphic region (5-HTTLPR)Beverly H Brummett, Stephen H Boyle, Ilene C Siegler, et al.
Brain : a Journal of Neurology|February 5, 2003
Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathyJan Senderek, Carsten Bergmann, Vincent T Ramaekers, et al.
Cell Metabolism|November 27, 2010
The mtDNA mutation spectrum of the progeroid Polg mutator mouse includes abundant control region multimersSiôn L Williams, Jia Huang, Yvonne J K Edwards, et al.
Orphanet Journal of Rare Diseases|April 19, 2014
Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohortsMatthis Synofzik, Rebecca Schüle, Martin Schulze, et al.
Investigative Ophthalmology & Visual Science|December 23, 2008
Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficienciesRavikanth Metlapally, Michel Michaelides, Anuradha Bulusu, et al.
Journal of Medical Genetics|December 4, 2009
Functional evidence implicating a novel TOR1A mutation in idiopathic, late-onset focal dystoniaNicole Calakos, Viren D Patel, Melissa Gottron, et al.
Neurology|September 16, 2016
SIGMAR1 mutation associated with autosomal recessive Silver-like syndromeAlejandro Horga, Pedro J Tomaselli, Michael A Gonzalez, et al.
Pageof 20