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

Christopher E Pearson

Showing results (71-80 of 98) with videos related to

Pageof 10
Sort By:
Biorxiv : the Preprint Server for Biology|December 19, 2025
Striatal pathology in Spinocerebellar Ataxia Type 1 mice: A comparative study with Huntington's diseasePragya Goel, Praseuth Yang, Lisa Duvick, et al.
Human Molecular Genetics|December 20, 2002
Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic miceRandell T Libby, Darren G Monckton, Ying-Hui Fu, et al.
Brain Communications|October 8, 2021
Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox-Gastaut syndromeFarah Qaiser, Tara Sadoway, Yue Yin, et al.
Science Advances|July 31, 2021
FAN1-MLH1 interaction affects repair of DNA interstrand cross-links and slipped-CAG/CTG repeatsAntonio Porro, Mohiuddin Mohiuddin, Christina Zurfluh, et al.
Cell Reports|December 8, 2021
FAN1 exo- not endo-nuclease pausing on disease-associated slipped-DNA repeats: A mechanism of repeat instabilityAmit Laxmikant Deshmukh, Marie-Christine Caron, Mohiuddin Mohiuddin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 15, 2024
Stability of Mosaic Divergent Repeat Interruptions in X-Linked Dystonia-ParkinsonismJoshua Laß, Theresa Lüth, Kathleen Schlüter, et al.
Genes, Chromosomes & Cancer|November 7, 2015
An infant with MLH3 variants, FOXG1-duplication and multiple, benign cranial and spinal tumors: A clinical exome sequencing studyRina Kansal, Xinmin Li, Joseph Shen, et al.
Disease Models & Mechanisms|November 9, 2012
Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxiaAurore Hick, Marie Wattenhofer-Donzé, Satyan Chintawar, et al.
Plos Genetics|November 9, 2013
Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approachesRicardo Mouro Pinto, Ella Dragileva, Andrew Kirby, et al.
Neuron|March 28, 2017
Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31Taro Ishiguro, Nozomu Sato, Morio Ueyama, et al.
Pageof 10

Showing results (71-80 of 98) with videos related to

Sort By:
Pageof 10
Biorxiv : the Preprint Server for Biology|December 19, 2025
Striatal pathology in Spinocerebellar Ataxia Type 1 mice: A comparative study with Huntington's diseasePragya Goel, Praseuth Yang, Lisa Duvick, et al.
Human Molecular Genetics|December 20, 2002
Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic miceRandell T Libby, Darren G Monckton, Ying-Hui Fu, et al.
Brain Communications|October 8, 2021
Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox-Gastaut syndromeFarah Qaiser, Tara Sadoway, Yue Yin, et al.
Science Advances|July 31, 2021
FAN1-MLH1 interaction affects repair of DNA interstrand cross-links and slipped-CAG/CTG repeatsAntonio Porro, Mohiuddin Mohiuddin, Christina Zurfluh, et al.
Cell Reports|December 8, 2021
FAN1 exo- not endo-nuclease pausing on disease-associated slipped-DNA repeats: A mechanism of repeat instabilityAmit Laxmikant Deshmukh, Marie-Christine Caron, Mohiuddin Mohiuddin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 15, 2024
Stability of Mosaic Divergent Repeat Interruptions in X-Linked Dystonia-ParkinsonismJoshua Laß, Theresa Lüth, Kathleen Schlüter, et al.
Genes, Chromosomes & Cancer|November 7, 2015
An infant with MLH3 variants, FOXG1-duplication and multiple, benign cranial and spinal tumors: A clinical exome sequencing studyRina Kansal, Xinmin Li, Joseph Shen, et al.
Disease Models & Mechanisms|November 9, 2012
Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxiaAurore Hick, Marie Wattenhofer-Donzé, Satyan Chintawar, et al.
Plos Genetics|November 9, 2013
Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approachesRicardo Mouro Pinto, Ella Dragileva, Andrew Kirby, et al.
Neuron|March 28, 2017
Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31Taro Ishiguro, Nozomu Sato, Morio Ueyama, et al.
Pageof 10