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

Jill M Weimer

Showing results (51-60 of 84) with videos related to

Pageof 9
Sort By:
Scientific Reports|November 3, 2018
Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1Tyler B Johnson, Keegan Mechels, Ruthellen H Anderson, et al.
Scientific Reports|April 17, 2020
Author Correction: Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1Tyler B Johnson, Keegan Mechels, Ruthellen H Anderson, et al.
Frontiers in Neuroscience|March 17, 2025
Mutation in <i>Wdr45</i> leads to early motor dysfunction and widespread aberrant axon terminals in a beta-propeller protein associated neurodegeneration (BPAN) patient-inspired mouse modelBrandon L Meyerink, Krishna S Karia, Mitchell J Rechtzigel, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
Nonsense pathogenic variants in exon 1 of PHOX2B lead to translational reinitiation in congenital central hypoventilation syndromeJacob T Cain, Dae I Kim, Megan Quast, et al.
Brain Research|July 10, 2007
Alterations in striatal dopamine catabolism precede loss of substantia nigra neurons in a mouse model of juvenile neuronal ceroid lipofuscinosisJill M Weimer, Jared W Benedict, Yasser M Elshatory, et al.
Communications Medicine|March 3, 2026
Longitudinal deep multi-omics profiling in a CLN3<sup>Δex7/8</sup> minipig model identifies biomarker signatures of diseaseMitchell J Rechtzigel, Brittany Lee, Christine Neville, et al.
Disease Models & Mechanisms|June 12, 2023
A novel porcine model of CLN3 Batten disease recapitulates clinical phenotypesVicki J Swier, Katherine A White, Tyler B Johnson, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|September 13, 2022
A Novel Porcine Model of CLN2 Batten Disease that Recapitulates Patient PhenotypesVicki J Swier, Katherine A White, Tyler B Johnson, et al.
Plos One|May 29, 2015
Abbreviated exposure to hypoxia is sufficient to induce CNS dysmyelination, modulate spinal motor neuron composition, and impair motor development in neonatal miceJens O Watzlawik, Robert J Kahoud, Ryan J O'Toole, et al.
Frontiers in Immunology|April 10, 2023
Immune transgene-dependent myocarditis in macaques after systemic administration of adeno-associated virus expressing human acid alpha-glucosidaseJuliette Hordeaux, Ali Ramezani, Steve Tuske, et al.
Pageof 9

Showing results (51-60 of 84) with videos related to

Sort By:
Pageof 9
Scientific Reports|November 3, 2018
Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1Tyler B Johnson, Keegan Mechels, Ruthellen H Anderson, et al.
Scientific Reports|April 17, 2020
Author Correction: Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1Tyler B Johnson, Keegan Mechels, Ruthellen H Anderson, et al.
Frontiers in Neuroscience|March 17, 2025
Mutation in <i>Wdr45</i> leads to early motor dysfunction and widespread aberrant axon terminals in a beta-propeller protein associated neurodegeneration (BPAN) patient-inspired mouse modelBrandon L Meyerink, Krishna S Karia, Mitchell J Rechtzigel, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
Nonsense pathogenic variants in exon 1 of PHOX2B lead to translational reinitiation in congenital central hypoventilation syndromeJacob T Cain, Dae I Kim, Megan Quast, et al.
Brain Research|July 10, 2007
Alterations in striatal dopamine catabolism precede loss of substantia nigra neurons in a mouse model of juvenile neuronal ceroid lipofuscinosisJill M Weimer, Jared W Benedict, Yasser M Elshatory, et al.
Communications Medicine|March 3, 2026
Longitudinal deep multi-omics profiling in a CLN3<sup>Δex7/8</sup> minipig model identifies biomarker signatures of diseaseMitchell J Rechtzigel, Brittany Lee, Christine Neville, et al.
Disease Models & Mechanisms|June 12, 2023
A novel porcine model of CLN3 Batten disease recapitulates clinical phenotypesVicki J Swier, Katherine A White, Tyler B Johnson, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|September 13, 2022
A Novel Porcine Model of CLN2 Batten Disease that Recapitulates Patient PhenotypesVicki J Swier, Katherine A White, Tyler B Johnson, et al.
Plos One|May 29, 2015
Abbreviated exposure to hypoxia is sufficient to induce CNS dysmyelination, modulate spinal motor neuron composition, and impair motor development in neonatal miceJens O Watzlawik, Robert J Kahoud, Ryan J O'Toole, et al.
Frontiers in Immunology|April 10, 2023
Immune transgene-dependent myocarditis in macaques after systemic administration of adeno-associated virus expressing human acid alpha-glucosidaseJuliette Hordeaux, Ali Ramezani, Steve Tuske, et al.
Pageof 9