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

J Raphael

Showing results (341-350 of 488) with videos related to

Pageof 49
Sort By:
Plos One|March 9, 2010
Genetic variability in CLU and its association with Alzheimer's diseaseRita J Guerreiro, John Beck, J Raphael Gibbs, et al.
Aging Cell|December 23, 2025
Mitochondrial DNA Variation in the Aging Human Cerebral Cortex and CerebellumAudrey A Omidsalar, David R Tyrpak, J Andrew MacKay, et al.
The Lancet. Neurology|August 31, 2010
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyHannu Laaksovirta, Terhi Peuralinna, Jennifer C Schymick, et al.
JNCI Cancer Spectrum|June 27, 2022
Real-World Cost-Effectiveness of First-Line Gemcitabine Plus Nab-Paclitaxel vs FOLFIRINOX in Patients With Advanced Pancreatic CancerVanessa Arciero, Jin Luo, Ambica Parmar, et al.
Neurology|June 8, 2012
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesAnna Sailer, Sonja W Scholz, J Raphael Gibbs, et al.
Biorxiv : the Preprint Server for Biology|December 23, 2024
Characterization of DNA methylation in PBMCs and donor-matched iPSCs shows methylation is reset during stem cell reprogrammingXylena Reed, Cory A Weller, Sara Saez-Atienzar, et al.
The Lancet. Neurology|February 5, 2008
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRASarah Camargos, Sonja Scholz, Javier Simón-Sánchez, et al.
Brain : a Journal of Neurology|June 29, 2012
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron diseaseJanel O Johnson, J Raphael Gibbs, Andre Megarbane, et al.
Acta Neuropathologica Communications|June 1, 2022
Convergent evolution and multi-wave clonal invasion in H3 K27-altered diffuse midline gliomas treated with a PDGFR inhibitorSasi Arunachalam, Karol Szlachta, Samuel W Brady, et al.
Nature|October 15, 2025
Spatial metabolic gradients in the liver and small intestineLaith Z Samarah, Clover Zheng, Xi Xing, et al.
Pageof 49

Showing results (341-350 of 488) with videos related to

Sort By:
Pageof 49
Plos One|March 9, 2010
Genetic variability in CLU and its association with Alzheimer's diseaseRita J Guerreiro, John Beck, J Raphael Gibbs, et al.
Aging Cell|December 23, 2025
Mitochondrial DNA Variation in the Aging Human Cerebral Cortex and CerebellumAudrey A Omidsalar, David R Tyrpak, J Andrew MacKay, et al.
The Lancet. Neurology|August 31, 2010
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyHannu Laaksovirta, Terhi Peuralinna, Jennifer C Schymick, et al.
JNCI Cancer Spectrum|June 27, 2022
Real-World Cost-Effectiveness of First-Line Gemcitabine Plus Nab-Paclitaxel vs FOLFIRINOX in Patients With Advanced Pancreatic CancerVanessa Arciero, Jin Luo, Ambica Parmar, et al.
Neurology|June 8, 2012
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesAnna Sailer, Sonja W Scholz, J Raphael Gibbs, et al.
Biorxiv : the Preprint Server for Biology|December 23, 2024
Characterization of DNA methylation in PBMCs and donor-matched iPSCs shows methylation is reset during stem cell reprogrammingXylena Reed, Cory A Weller, Sara Saez-Atienzar, et al.
The Lancet. Neurology|February 5, 2008
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRASarah Camargos, Sonja Scholz, Javier Simón-Sánchez, et al.
Brain : a Journal of Neurology|June 29, 2012
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron diseaseJanel O Johnson, J Raphael Gibbs, Andre Megarbane, et al.
Acta Neuropathologica Communications|June 1, 2022
Convergent evolution and multi-wave clonal invasion in H3 K27-altered diffuse midline gliomas treated with a PDGFR inhibitorSasi Arunachalam, Karol Szlachta, Samuel W Brady, et al.
Nature|October 15, 2025
Spatial metabolic gradients in the liver and small intestineLaith Z Samarah, Clover Zheng, Xi Xing, et al.
Pageof 49