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

H Watkins

Showing results (181-190 of 212) with videos related to

Pageof 22
Sort By:
Journal of Thrombosis and Haemostasis : JTH|January 3, 2013
Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from SpainG Athanasiadis, M Sabater-Lleal, A Buil, et al.
The American Journal of Physiology|February 1, 1994
Human kidney proximal tubules are the main source of plasma glutathione peroxidaseN Avissar, D B Ornt, Y Yagil, et al.
Nature Genetics|December 1, 1995
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathyH Watkins, D Conner, L Thierfelder, et al.
Journal of Bacteriology|May 29, 2012
Characterization of a Vibrio fischeri aminopeptidase and evidence for its influence on an early stage of squid colonizationPat M Fidopiastis, Bethany A Rader, David G Gerling, et al.
Brain : a Journal of Neurology|July 29, 1998
The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's diseaseA D Lawrence, R A Weeks, D J Brooks, et al.
Translational Psychiatry|February 6, 2019
Longitudinal investigation of DNA methylation changes preceding adolescent psychotic experiencesSusanna Roberts, Matthew Suderman, Stanley Zammit, et al.
Journal of Neuroscience Methods|July 27, 2017
An intra-neural microstimulation system for ultra-high field magnetic resonance imaging and magnetoencephalographyPaul M Glover, Roger H Watkins, George C O'Neill, et al.
Nature Genetics|June 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1N G Laing, S D Wilton, P A Akkari, et al.
Nature Genetics|January 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyN G Laing, S D Wilton, P A Akkari, et al.
The New England Journal of Medicine|April 20, 1995
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathyH Watkins, W J McKenna, L Thierfelder, et al.
Pageof 22

Showing results (181-190 of 212) with videos related to

Sort By:
Pageof 22
Journal of Thrombosis and Haemostasis : JTH|January 3, 2013
Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from SpainG Athanasiadis, M Sabater-Lleal, A Buil, et al.
The American Journal of Physiology|February 1, 1994
Human kidney proximal tubules are the main source of plasma glutathione peroxidaseN Avissar, D B Ornt, Y Yagil, et al.
Nature Genetics|December 1, 1995
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathyH Watkins, D Conner, L Thierfelder, et al.
Journal of Bacteriology|May 29, 2012
Characterization of a Vibrio fischeri aminopeptidase and evidence for its influence on an early stage of squid colonizationPat M Fidopiastis, Bethany A Rader, David G Gerling, et al.
Brain : a Journal of Neurology|July 29, 1998
The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's diseaseA D Lawrence, R A Weeks, D J Brooks, et al.
Translational Psychiatry|February 6, 2019
Longitudinal investigation of DNA methylation changes preceding adolescent psychotic experiencesSusanna Roberts, Matthew Suderman, Stanley Zammit, et al.
Journal of Neuroscience Methods|July 27, 2017
An intra-neural microstimulation system for ultra-high field magnetic resonance imaging and magnetoencephalographyPaul M Glover, Roger H Watkins, George C O'Neill, et al.
Nature Genetics|June 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1N G Laing, S D Wilton, P A Akkari, et al.
Nature Genetics|January 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyN G Laing, S D Wilton, P A Akkari, et al.
The New England Journal of Medicine|April 20, 1995
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathyH Watkins, W J McKenna, L Thierfelder, et al.
Pageof 22