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

M B Davis

Showing results (31-40 of 106) with videos related to

Pageof 11
Sort By:
Glia|August 1, 1993
Intracellular pH regulation in single cultured astrocytes from rat forebrainG Boyarsky, B Ransom, W R Schlue, et al.
Nature Genetics|March 4, 2000
Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxiaP F Worth, H Houlden, P Giunti, et al.
Journal of Neurology|October 1, 1995
Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)M M Reilly, D Adams, M B Davis, et al.
Annals of Human Genetics|July 1, 1987
Localization of PEPD to the long arm of chromosome 19M B Davis, D Schonk, M Monteiro, et al.
Annals of Human Genetics|July 1, 1987
The gene for human alpha-lactalbumin is assigned to chromosome 12q13M S Davies, L F West, M B Davis, et al.
Lancet (London, England)|September 10, 1994
Mutation analysis in patients with possible but apparently sporadic Huntington's diseaseM B Davis, D Bateman, N P Quinn, et al.
Disease Markers|June 1, 1988
Spontaneous and induced chromosome damage in lymphocytes of medullary thyroid carcinoma patients and their family membersK Tsioupra, L F West, M B Davis, et al.
Annals of Human Genetics|March 30, 2000
Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutationsE M Valente, S Povey, T T Warner, et al.
American Journal of Human Genetics|March 1, 1992
Prenatal diagnosis of mitochondrial DNA8993 T----G diseaseA E Harding, I J Holt, M G Sweeney, et al.
Journal of Molecular Biology|January 10, 1997
Myosin rod protein: a novel thick filament component of Drosophila muscleD M Standiford, M B Davis, K Miedema, et al.
Pageof 11

Showing results (31-40 of 106) with videos related to

Sort By:
Pageof 11
Glia|August 1, 1993
Intracellular pH regulation in single cultured astrocytes from rat forebrainG Boyarsky, B Ransom, W R Schlue, et al.
Nature Genetics|March 4, 2000
Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxiaP F Worth, H Houlden, P Giunti, et al.
Journal of Neurology|October 1, 1995
Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)M M Reilly, D Adams, M B Davis, et al.
Annals of Human Genetics|July 1, 1987
Localization of PEPD to the long arm of chromosome 19M B Davis, D Schonk, M Monteiro, et al.
Annals of Human Genetics|July 1, 1987
The gene for human alpha-lactalbumin is assigned to chromosome 12q13M S Davies, L F West, M B Davis, et al.
Lancet (London, England)|September 10, 1994
Mutation analysis in patients with possible but apparently sporadic Huntington's diseaseM B Davis, D Bateman, N P Quinn, et al.
Disease Markers|June 1, 1988
Spontaneous and induced chromosome damage in lymphocytes of medullary thyroid carcinoma patients and their family membersK Tsioupra, L F West, M B Davis, et al.
Annals of Human Genetics|March 30, 2000
Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutationsE M Valente, S Povey, T T Warner, et al.
American Journal of Human Genetics|March 1, 1992
Prenatal diagnosis of mitochondrial DNA8993 T----G diseaseA E Harding, I J Holt, M G Sweeney, et al.
Journal of Molecular Biology|January 10, 1997
Myosin rod protein: a novel thick filament component of Drosophila muscleD M Standiford, M B Davis, K Miedema, et al.
Pageof 11