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

J R Yates

Showing results (211-220 of 227) with videos related to

Pageof 23
Sort By:
Human Molecular Genetics|December 1, 1995
Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinismM V Schiaffino, M T Bassi, L Galli, et al.
The Journal of Biological Chemistry|June 25, 1990
Metabolism-based covalent bonding of the heme prosthetic group to its apoprotein during the reductive debromination of BrCCl3 by myoglobinY Osawa, B M Martin, P R Griffin, et al.
Archives of Disease in Childhood|April 1, 1993
Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural historyM R Green, L T Weaver, A F Heeley, et al.
Biochemical and Biophysical Research Communications|May 14, 1987
Sequence homology in the metalloproteins; purple acid phosphatase from beef spleen and uteroferrin from porcine uterusD F Hunt, J R Yates, J Shabanowitz, et al.
Journal of Medical Genetics|February 1, 1993
Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28J R Yates, J P Warner, J A Smith, et al.
Analytical Chemistry|September 20, 2000
MS for identification of single nucleotide polymorphisms and MS/MS for discrimination of isomeric PCR productsM T Krahmer, J J Walters, K F Fox, et al.
American Journal of Human Genetics|May 1, 1996
A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United KingdomS J Knight, R J Ritchie, L Chakrabarti, et al.
Journal of Medical Genetics|June 27, 1998
Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significanceJ C Barber, C A Joyce, M N Collinson, et al.
The Journal of Experimental Biology|September 25, 2003
Utilization of genomic sequence information to develop malaria vaccinesD L Doolan, J C Aguiar, W R Weiss, et al.
Human Mutation|January 1, 1997
Nine novel L1 CAM mutations in families with X-linked hydrocephalusJ R MacFarlane, J S Du, M E Pepys, et al.
Pageof 23

Showing results (211-220 of 227) with videos related to

Sort By:
Pageof 23
Human Molecular Genetics|December 1, 1995
Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinismM V Schiaffino, M T Bassi, L Galli, et al.
The Journal of Biological Chemistry|June 25, 1990
Metabolism-based covalent bonding of the heme prosthetic group to its apoprotein during the reductive debromination of BrCCl3 by myoglobinY Osawa, B M Martin, P R Griffin, et al.
Archives of Disease in Childhood|April 1, 1993
Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural historyM R Green, L T Weaver, A F Heeley, et al.
Biochemical and Biophysical Research Communications|May 14, 1987
Sequence homology in the metalloproteins; purple acid phosphatase from beef spleen and uteroferrin from porcine uterusD F Hunt, J R Yates, J Shabanowitz, et al.
Journal of Medical Genetics|February 1, 1993
Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28J R Yates, J P Warner, J A Smith, et al.
Analytical Chemistry|September 20, 2000
MS for identification of single nucleotide polymorphisms and MS/MS for discrimination of isomeric PCR productsM T Krahmer, J J Walters, K F Fox, et al.
American Journal of Human Genetics|May 1, 1996
A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United KingdomS J Knight, R J Ritchie, L Chakrabarti, et al.
Journal of Medical Genetics|June 27, 1998
Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significanceJ C Barber, C A Joyce, M N Collinson, et al.
The Journal of Experimental Biology|September 25, 2003
Utilization of genomic sequence information to develop malaria vaccinesD L Doolan, J C Aguiar, W R Weiss, et al.
Human Mutation|January 1, 1997
Nine novel L1 CAM mutations in families with X-linked hydrocephalusJ R MacFarlane, J S Du, M E Pepys, et al.
Pageof 23