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

Jamil Ahmad

Showing results (251-260 of 260) with videos related to

Pageof 26
Sort By:
You have reached the last page of results.This site can display upto 260 results.
Biorxiv : the Preprint Server for Biology|November 28, 2023
The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neuronsJace Jones-Tabah, Kathy He, Konstantin Senkevich, et al.
Molecular Neurodegeneration|November 26, 2024
The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neuronsJace Jones-Tabah, Kathy He, Nathan Karpilovsky, et al.
American Journal of Human Genetics|January 25, 2011
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42Guntram Borck, Atteeq Ur Rehman, Kwanghyuk Lee, et al.
Neurobiology of Aging|April 9, 2023
NPC1 variants are not associated with Parkinson's disease, REM-sleep behavior disorder or dementia with Lewy bodies in European cohortsEmma N Somerville, Lynne Krohn, Eric Yu, et al.
Nature Genetics|November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric DisordersZhao Zhang, Emma N Somerville, Zih-Hua Fang, et al.
NPJ Parkinson'S Disease|May 21, 2026
Genetic associations between post-traumatic stress disorder and REM-sleep behavior disorderMorvarid Ghamgosar Shahkhali, Lang Liu, Mohammad H Ghamgosar Shahkhali, et al.
Medrxiv : the Preprint Server for Health Sciences|September 18, 2025
Post-traumatic stress disorder and REM-sleep behavior disorder: exploring genetic associations and causal linksMorvarid Ghamgosar Shahkhali, Lang Liu, Mohammad H Ghamgosar Shahkhali, et al.
Journal of Medical Genetics|February 28, 2016
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testingDouglas F Easton, Fabienne Lesueur, Brennan Decker, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|November 5, 2022
The International Natural Product Sciences Taskforce (INPST) and the power of Twitter networking exemplified through #INPST hashtag analysisRajeev K Singla, Ronita De, Thomas Efferth, et al.
Pageof 26

Showing results (251-260 of 260) with videos related to

Sort By:
Pageof 26
You have reached the last page of results.This site can display upto 260 results.
Biorxiv : the Preprint Server for Biology|November 28, 2023
The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neuronsJace Jones-Tabah, Kathy He, Konstantin Senkevich, et al.
Molecular Neurodegeneration|November 26, 2024
The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neuronsJace Jones-Tabah, Kathy He, Nathan Karpilovsky, et al.
American Journal of Human Genetics|January 25, 2011
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42Guntram Borck, Atteeq Ur Rehman, Kwanghyuk Lee, et al.
Neurobiology of Aging|April 9, 2023
NPC1 variants are not associated with Parkinson's disease, REM-sleep behavior disorder or dementia with Lewy bodies in European cohortsEmma N Somerville, Lynne Krohn, Eric Yu, et al.
Nature Genetics|November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric DisordersZhao Zhang, Emma N Somerville, Zih-Hua Fang, et al.
NPJ Parkinson'S Disease|May 21, 2026
Genetic associations between post-traumatic stress disorder and REM-sleep behavior disorderMorvarid Ghamgosar Shahkhali, Lang Liu, Mohammad H Ghamgosar Shahkhali, et al.
Medrxiv : the Preprint Server for Health Sciences|September 18, 2025
Post-traumatic stress disorder and REM-sleep behavior disorder: exploring genetic associations and causal linksMorvarid Ghamgosar Shahkhali, Lang Liu, Mohammad H Ghamgosar Shahkhali, et al.
Journal of Medical Genetics|February 28, 2016
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testingDouglas F Easton, Fabienne Lesueur, Brennan Decker, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|November 5, 2022
The International Natural Product Sciences Taskforce (INPST) and the power of Twitter networking exemplified through #INPST hashtag analysisRajeev K Singla, Ronita De, Thomas Efferth, et al.
Pageof 26