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

Marina P Hommersom

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Trends in Pharmacological Sciences|July 6, 2025
Shining light on parvalbumin interneuron plasticityMarina P Hommersom, Dirk Schubert, Nael Nadif Kasri
Stem Cell Research|March 14, 2022
Generation of induced pluripotent stem cell lines carrying monoallelic (UCSFi001-A-60) or biallelic (UCSFi001-A-61; UCSFi001-A-62) frameshift variants in CACNA1A using CRISPR/Cas9Marina P Hommersom, Chantal Bijnagte-Schoenmaker, Silvia Albert, et al.
Stem Cell Reviews and Reports|May 25, 2021
Human Induced Pluripotent Stem Cell-Based Modelling of Spinocerebellar AtaxiasMarina P Hommersom, Ronald A M Buijsen, Willeke M C van Roon-Mom, et al.
Journal of Neurology|November 22, 2021
The complexities of CACNA1A in clinical neurogeneticsMarina P Hommersom, Teije H van Prooije, Maartje Pennings, et al.
Stem Cell Research|August 4, 2024
Generation of induced pluripotent stem cell line (UCSFi001-A-77) carrying a biallelic frameshift variant in exon 4 of SGIP1 through CRISPR/Cas9Neelam Fatima, Lieke Dillen, Marina P Hommersom, et al.
Stem Cell Reports|January 23, 2026
Human neuronal networks on micro-electrode arrays as a tool to assess genotype-phenotype correlation in CACNA1A-related disordersMarina P Hommersom, Sofía Puvogel, Nicky Scheefhals, et al.
Stem Cell Research|May 13, 2024
Generation of induced pluripotent stem cell lines from two unrelated patients affected by intellectual disability carrying homozygous variants in SGIP1Lieke Dillen, Neelam Fatima, Marina P Hommersom, et al.
Brain : a Journal of Neurology|October 26, 2024
CACNA1A haploinsufficiency leads to reduced synaptic function and increased intrinsic excitabilityMarina P Hommersom, Nina Doorn, Sofía Puvogel, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant ClassificationTobias Brünger, Ilona Krey, Suyeon Kim, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Trends in Pharmacological Sciences|July 6, 2025
Shining light on parvalbumin interneuron plasticityMarina P Hommersom, Dirk Schubert, Nael Nadif Kasri
Stem Cell Research|March 14, 2022
Generation of induced pluripotent stem cell lines carrying monoallelic (UCSFi001-A-60) or biallelic (UCSFi001-A-61; UCSFi001-A-62) frameshift variants in CACNA1A using CRISPR/Cas9Marina P Hommersom, Chantal Bijnagte-Schoenmaker, Silvia Albert, et al.
Stem Cell Reviews and Reports|May 25, 2021
Human Induced Pluripotent Stem Cell-Based Modelling of Spinocerebellar AtaxiasMarina P Hommersom, Ronald A M Buijsen, Willeke M C van Roon-Mom, et al.
Journal of Neurology|November 22, 2021
The complexities of CACNA1A in clinical neurogeneticsMarina P Hommersom, Teije H van Prooije, Maartje Pennings, et al.
Stem Cell Research|August 4, 2024
Generation of induced pluripotent stem cell line (UCSFi001-A-77) carrying a biallelic frameshift variant in exon 4 of SGIP1 through CRISPR/Cas9Neelam Fatima, Lieke Dillen, Marina P Hommersom, et al.
Stem Cell Reports|January 23, 2026
Human neuronal networks on micro-electrode arrays as a tool to assess genotype-phenotype correlation in CACNA1A-related disordersMarina P Hommersom, Sofía Puvogel, Nicky Scheefhals, et al.
Stem Cell Research|May 13, 2024
Generation of induced pluripotent stem cell lines from two unrelated patients affected by intellectual disability carrying homozygous variants in SGIP1Lieke Dillen, Neelam Fatima, Marina P Hommersom, et al.
Brain : a Journal of Neurology|October 26, 2024
CACNA1A haploinsufficiency leads to reduced synaptic function and increased intrinsic excitabilityMarina P Hommersom, Nina Doorn, Sofía Puvogel, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant ClassificationTobias Brünger, Ilona Krey, Suyeon Kim, et al.
Pageof 1