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

R A Lewis

Showing results (301-310 of 381) with videos related to

Pageof 39
Sort By:
Neurology|January 30, 2008
Neuropathy progression in Charcot-Marie-Tooth disease type 1AM E Shy, L Chen, E R Swan, et al.
Advances in Biophysics|January 1, 1991
Two-dimensional time resolved X-ray diffraction of muscle: recent resultsJ Bordas, G P Diakun, J E Harries, et al.
American Journal of Human Genetics|December 1, 1999
Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigreesN Katsanis, R A Lewis, D W Stockton, et al.
Annals of the New York Academy of Sciences|February 24, 2001
Conjugation of camptothecins to poly-(L-glutamic acid)J W Singer, P De Vries, R Bhatt, et al.
Physical Review Letters|January 15, 2011
Spontaneous periodic deformations in nonchiral planar-aligned bimesogens with a nematic-nematic transition and a negative elastic constantV P Panov, M Nagaraj, J K Vij, et al.
Neurology|April 13, 2005
Reliability and validity of the CMT neuropathy score as a measure of disabilityM E Shy, J Blake, K Krajewski, et al.
European Journal of Radiology|November 11, 2008
Towards the clinical application of X-ray phase contrast imagingI M Williams, K K W Siu, R Gan, et al.
Brain : a Journal of Neurology|January 29, 2000
Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapyJ Kamholz, D Menichella, A Jani, et al.
Nature|July 16, 1992
The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphataseO Attree, I M Olivos, I Okabe, et al.
Human Molecular Genetics|February 3, 2000
Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locusB A Bejjani, D W Stockton, R A Lewis, et al.
Pageof 39

Showing results (301-310 of 381) with videos related to

Sort By:
Pageof 39
Neurology|January 30, 2008
Neuropathy progression in Charcot-Marie-Tooth disease type 1AM E Shy, L Chen, E R Swan, et al.
Advances in Biophysics|January 1, 1991
Two-dimensional time resolved X-ray diffraction of muscle: recent resultsJ Bordas, G P Diakun, J E Harries, et al.
American Journal of Human Genetics|December 1, 1999
Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigreesN Katsanis, R A Lewis, D W Stockton, et al.
Annals of the New York Academy of Sciences|February 24, 2001
Conjugation of camptothecins to poly-(L-glutamic acid)J W Singer, P De Vries, R Bhatt, et al.
Physical Review Letters|January 15, 2011
Spontaneous periodic deformations in nonchiral planar-aligned bimesogens with a nematic-nematic transition and a negative elastic constantV P Panov, M Nagaraj, J K Vij, et al.
Neurology|April 13, 2005
Reliability and validity of the CMT neuropathy score as a measure of disabilityM E Shy, J Blake, K Krajewski, et al.
European Journal of Radiology|November 11, 2008
Towards the clinical application of X-ray phase contrast imagingI M Williams, K K W Siu, R Gan, et al.
Brain : a Journal of Neurology|January 29, 2000
Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapyJ Kamholz, D Menichella, A Jani, et al.
Nature|July 16, 1992
The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphataseO Attree, I M Olivos, I Okabe, et al.
Human Molecular Genetics|February 3, 2000
Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locusB A Bejjani, D W Stockton, R A Lewis, et al.
Pageof 39