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

Neurogenetics

Showing results (911-920 of 949) with videos related to

Pageof 95
Sort By:
Neurogenetics|August 28, 2014
Clinical and molecular genetic findings in autosomal dominant OPA3-related optic neuropathyPanagiotis I Sergouniotis, Rahat Perveen, Dawn L Thiselton, et al.
Neurogenetics|October 23, 2014
Hindbrain malformation and myoclonic seizures associated with a deleterious mutation in the INPP4A geneRuth Sheffer, Odeya Bennett-Back, Barak Yaacov, et al.
Neurogenetics|October 25, 2014
Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptomP Laššuthová, D Šafka Brožková, M Krůtová, et al.
Neurogenetics|November 6, 2014
Transcriptome analysis of grey and white matter cortical tissue in multiple system atrophyJames D Mills, Woojin S Kim, Glenda M Halliday, et al.
Neurogenetics|March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotypeT Smol, F Petit, A Piton, et al.
Neurogenetics|December 24, 2013
Genetic determinants of neuroglobin transcriptionR Wang, E Halper-Stromberg, M Szymanski-Pierce, et al.
Neurogenetics|May 7, 2018
Toward deciphering the mechanistic role of variations in the Rep1 repeat site in the transcription regulation of SNCA geneA Afek, L Tagliafierro, O C Glenn, et al.
Neurogenetics|July 25, 2018
The polynucleotide kinase 3'-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25Alejandro Leal, Sixto Bogantes-Ledezma, Arif B Ekici, et al.
Neurogenetics|December 22, 2005
The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's diseaseSilke Metzger, Peter Bauer, Juergen Tomiuk, et al.
Neurogenetics|December 14, 2005
Whole genome expression profiling of the medial and lateral substantia nigra in Parkinson's diseaseL B Moran, D C Duke, M Deprez, et al.
Pageof 95

Showing results (911-920 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|August 28, 2014
Clinical and molecular genetic findings in autosomal dominant OPA3-related optic neuropathyPanagiotis I Sergouniotis, Rahat Perveen, Dawn L Thiselton, et al.
Neurogenetics|October 23, 2014
Hindbrain malformation and myoclonic seizures associated with a deleterious mutation in the INPP4A geneRuth Sheffer, Odeya Bennett-Back, Barak Yaacov, et al.
Neurogenetics|October 25, 2014
Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptomP Laššuthová, D Šafka Brožková, M Krůtová, et al.
Neurogenetics|November 6, 2014
Transcriptome analysis of grey and white matter cortical tissue in multiple system atrophyJames D Mills, Woojin S Kim, Glenda M Halliday, et al.
Neurogenetics|March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotypeT Smol, F Petit, A Piton, et al.
Neurogenetics|December 24, 2013
Genetic determinants of neuroglobin transcriptionR Wang, E Halper-Stromberg, M Szymanski-Pierce, et al.
Neurogenetics|May 7, 2018
Toward deciphering the mechanistic role of variations in the Rep1 repeat site in the transcription regulation of SNCA geneA Afek, L Tagliafierro, O C Glenn, et al.
Neurogenetics|July 25, 2018
The polynucleotide kinase 3'-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25Alejandro Leal, Sixto Bogantes-Ledezma, Arif B Ekici, et al.
Neurogenetics|December 22, 2005
The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's diseaseSilke Metzger, Peter Bauer, Juergen Tomiuk, et al.
Neurogenetics|December 14, 2005
Whole genome expression profiling of the medial and lateral substantia nigra in Parkinson's diseaseL B Moran, D C Duke, M Deprez, et al.
Pageof 95