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

A Sahota

Showing results (51-60 of 90) with videos related to

Pageof 9
Sort By:
American Journal of Human Genetics|May 1, 1991
2,8-Dihydroxyadenine lithiasis in a Japanese patient heterozygous at the adenine phosphoribosyltransferase locusA Sahota, J Chen, M A Behzadian, et al.
Mutation Research|June 1, 1993
Analysis of germline and in vivo somatic mutations in the human adenine phosphoribosyltransferase gene: mutational hot spots at the intron 4 splice donor site and at codon 87J Chen, A Sahota, G F Martin, et al.
Klinische Wochenschrift|December 30, 1990
Identification of a splice mutation at the adenine phosphoribosyltransferase locus in a German familyB S Gathof, A Sahota, U Gresser, et al.
Annals of the New York Academy of Sciences|February 15, 2000
Effect of oxidative stress on DNA damage and beta-amyloid precursor proteins in lymphoblastoid cell lines from a Nigerian populationD K Lahiri, Y Xu, J Klaunig, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
A splice mutation at the adenine phosphoribosyltransferase locus detected in a German familyB S Gathof, A Sahota, U Gresser, et al.
Clinical and Experimental Immunology|October 1, 1978
Absence of oroticaciduria in adenosine deaminase deficiency and purine nucleoside phosphorylase deficiencyH A Simmonds, C F Potter, A Sahota, et al.
Molecular Genetics and Metabolism|March 13, 2001
2,8-Dihydroxyadenine urolithiasis in a patient with considerable residual adenine phosphoribosyltransferase activity in cell extracts but with mutations in both copies of APRTL Deng, M Yang, S Fründ, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 1999
Mitotic recombination produces the majority of recessive fibroblast variants in heterozygous miceC Shao, L Deng, O Henegariu, et al.
Neurology|January 15, 2000
Serum cholesterol, APOE genotype, and the risk of Alzheimer's disease: a population-based study of African AmericansR M Evans, C L Emsley, S Gao, et al.
American Journal of Human Genetics|December 1, 1991
Identification of a single missense mutation in the adenine phosphoribosyltransferase (APRT) gene from five Icelandic patients and a British patientJ Chen, A Sahota, T Laxdal, et al.
Pageof 9

Showing results (51-60 of 90) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|May 1, 1991
2,8-Dihydroxyadenine lithiasis in a Japanese patient heterozygous at the adenine phosphoribosyltransferase locusA Sahota, J Chen, M A Behzadian, et al.
Mutation Research|June 1, 1993
Analysis of germline and in vivo somatic mutations in the human adenine phosphoribosyltransferase gene: mutational hot spots at the intron 4 splice donor site and at codon 87J Chen, A Sahota, G F Martin, et al.
Klinische Wochenschrift|December 30, 1990
Identification of a splice mutation at the adenine phosphoribosyltransferase locus in a German familyB S Gathof, A Sahota, U Gresser, et al.
Annals of the New York Academy of Sciences|February 15, 2000
Effect of oxidative stress on DNA damage and beta-amyloid precursor proteins in lymphoblastoid cell lines from a Nigerian populationD K Lahiri, Y Xu, J Klaunig, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
A splice mutation at the adenine phosphoribosyltransferase locus detected in a German familyB S Gathof, A Sahota, U Gresser, et al.
Clinical and Experimental Immunology|October 1, 1978
Absence of oroticaciduria in adenosine deaminase deficiency and purine nucleoside phosphorylase deficiencyH A Simmonds, C F Potter, A Sahota, et al.
Molecular Genetics and Metabolism|March 13, 2001
2,8-Dihydroxyadenine urolithiasis in a patient with considerable residual adenine phosphoribosyltransferase activity in cell extracts but with mutations in both copies of APRTL Deng, M Yang, S Fründ, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 1999
Mitotic recombination produces the majority of recessive fibroblast variants in heterozygous miceC Shao, L Deng, O Henegariu, et al.
Neurology|January 15, 2000
Serum cholesterol, APOE genotype, and the risk of Alzheimer's disease: a population-based study of African AmericansR M Evans, C L Emsley, S Gao, et al.
American Journal of Human Genetics|December 1, 1991
Identification of a single missense mutation in the adenine phosphoribosyltransferase (APRT) gene from five Icelandic patients and a British patientJ Chen, A Sahota, T Laxdal, et al.
Pageof 9