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

D M Hunt

Showing results (121-130 of 185) with videos related to

Pageof 19
Sort By:
Cytogenetics and Cell Genetics|June 14, 2002
Assignment of panopsin (OPN3) to human chromosome band 1q43 by in situ hybridization and somatic cell hybridsS Halford, J Bellingham, L Ocaka, et al.
Chemistry & Biology|January 4, 2001
Cloning, sequencing and analysis of the enterocin biosynthesis gene cluster from the marine isolate 'Streptomyces maritimus': evidence for the derailment of an aromatic polyketide synthaseJ Piel, C Hertweck, P R Shipley, et al.
The British Journal of Ophthalmology|March 20, 2004
Oligocone trichromacy: a rare and unusual cone dysfunction syndromeM Michaelides, G E Holder, K Bradshaw, et al.
Journal of Medical Genetics|August 27, 1998
Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1)A Gehrig, U Felbor, R E Kelsell, et al.
Genomics|June 10, 1995
Sequence and evolution of the blue cone pigment gene in Old and New World primatesD M Hunt, J A Cowing, R Patel, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 1999
Biochemical analysis of a dimerization domain mutation in RetGC-1 associated with dominant cone-rod dystrophyC L Tucker, S C Woodcock, R E Kelsell, et al.
British Journal of Haematology|November 1, 1980
The genetic basis of Hb Q-H diseaseD R Higgs, D M Hunt, H C Drysdale, et al.
Human Molecular Genetics|April 1, 1997
Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17pR E Kelsell, K Evans, C Y Gregory, et al.
Biochemistry|July 13, 2000
Spectral tuning of avian violet- and ultraviolet-sensitive visual pigmentsS E Wilkie, P R Robinson, T W Cronin, et al.
Schizophrenia Research|May 24, 1997
The number of triplet repeats in five brain-expressed loci with CAG repeats is not associated with schizophreniaE J Gaitonde, S Sivagnanasundaram, A G Morris, et al.
Pageof 19

Showing results (121-130 of 185) with videos related to

Sort By:
Pageof 19
Cytogenetics and Cell Genetics|June 14, 2002
Assignment of panopsin (OPN3) to human chromosome band 1q43 by in situ hybridization and somatic cell hybridsS Halford, J Bellingham, L Ocaka, et al.
Chemistry & Biology|January 4, 2001
Cloning, sequencing and analysis of the enterocin biosynthesis gene cluster from the marine isolate 'Streptomyces maritimus': evidence for the derailment of an aromatic polyketide synthaseJ Piel, C Hertweck, P R Shipley, et al.
The British Journal of Ophthalmology|March 20, 2004
Oligocone trichromacy: a rare and unusual cone dysfunction syndromeM Michaelides, G E Holder, K Bradshaw, et al.
Journal of Medical Genetics|August 27, 1998
Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1)A Gehrig, U Felbor, R E Kelsell, et al.
Genomics|June 10, 1995
Sequence and evolution of the blue cone pigment gene in Old and New World primatesD M Hunt, J A Cowing, R Patel, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 1999
Biochemical analysis of a dimerization domain mutation in RetGC-1 associated with dominant cone-rod dystrophyC L Tucker, S C Woodcock, R E Kelsell, et al.
British Journal of Haematology|November 1, 1980
The genetic basis of Hb Q-H diseaseD R Higgs, D M Hunt, H C Drysdale, et al.
Human Molecular Genetics|April 1, 1997
Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17pR E Kelsell, K Evans, C Y Gregory, et al.
Biochemistry|July 13, 2000
Spectral tuning of avian violet- and ultraviolet-sensitive visual pigmentsS E Wilkie, P R Robinson, T W Cronin, et al.
Schizophrenia Research|May 24, 1997
The number of triplet repeats in five brain-expressed loci with CAG repeats is not associated with schizophreniaE J Gaitonde, S Sivagnanasundaram, A G Morris, et al.
Pageof 19