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D A Hopkinson

Showing results (101-110 of 148) with videos related to

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Journal of Medical Genetics|December 1, 1984
Glycoproteins in cystic fibrosis: a lectin binding studyS Karlsson, B Griffiths, D M Swallow, et al.
Biochemical Genetics|October 1, 1979
Characterization of human carbonic anhydrase III from skeletal muscleN Carter, S Jeffery, A Shiels, et al.
Annals of Human Genetics|July 1, 1970
Genetically determined electrophoretic variants of human red cell NADH diaphoraseD A Hopkinson, G Corney, P J Cook, et al.
Oncogene|October 18, 2006
Regulation of clustered gene expression by cofactor of BRCA1 (COBRA1) in breast cancer cellsS E Aiyar, A L Blair, D A Hopkinson, et al.
Annals of Human Genetics|October 1, 1977
An interpretation of human diaphorase isozymes in terms of three gene loci DIA1, DIA2 and DIA3R A Fisher, Y H Edwards, W Putt, et al.
Annals of Human Genetics|May 1, 1985
Chromosome assignment, biochemical and immunological studies on a human aldehyde dehydrogenase, ALDH3I Santisteban, S Povey, L F West, et al.
Prenatal Diagnosis|April 1, 1992
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 casesC M Abbott, J U Lovegrove, D B Whitehouse, et al.
Birth Defects Original Article Series|January 1, 1976
Family studies on esterase D and chromosome 13 in manE B Robson, D A Hopkinson, K E Buckton, et al.
Molecular Biology and Evolution|April 29, 1998
A phylogenetic approach to the identification of phosphoglucomutase genesD B Whitehouse, J Tomkins, J U Lovegrove, et al.
Prenatal Diagnosis|June 1, 1993
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 casesC M Abbott, J U Lovegrove, D B Whitehouse, et al.
Pageof 15

Showing results (101-110 of 148) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|December 1, 1984
Glycoproteins in cystic fibrosis: a lectin binding studyS Karlsson, B Griffiths, D M Swallow, et al.
Biochemical Genetics|October 1, 1979
Characterization of human carbonic anhydrase III from skeletal muscleN Carter, S Jeffery, A Shiels, et al.
Annals of Human Genetics|July 1, 1970
Genetically determined electrophoretic variants of human red cell NADH diaphoraseD A Hopkinson, G Corney, P J Cook, et al.
Oncogene|October 18, 2006
Regulation of clustered gene expression by cofactor of BRCA1 (COBRA1) in breast cancer cellsS E Aiyar, A L Blair, D A Hopkinson, et al.
Annals of Human Genetics|October 1, 1977
An interpretation of human diaphorase isozymes in terms of three gene loci DIA1, DIA2 and DIA3R A Fisher, Y H Edwards, W Putt, et al.
Annals of Human Genetics|May 1, 1985
Chromosome assignment, biochemical and immunological studies on a human aldehyde dehydrogenase, ALDH3I Santisteban, S Povey, L F West, et al.
Prenatal Diagnosis|April 1, 1992
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 casesC M Abbott, J U Lovegrove, D B Whitehouse, et al.
Birth Defects Original Article Series|January 1, 1976
Family studies on esterase D and chromosome 13 in manE B Robson, D A Hopkinson, K E Buckton, et al.
Molecular Biology and Evolution|April 29, 1998
A phylogenetic approach to the identification of phosphoglucomutase genesD B Whitehouse, J Tomkins, J U Lovegrove, et al.
Prenatal Diagnosis|June 1, 1993
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 casesC M Abbott, J U Lovegrove, D B Whitehouse, et al.
Pageof 15