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A Corfield

Showing results (11-20 of 64) with videos related to

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Human Molecular Genetics|October 1, 1993
Identification of a new missense mutation at Arg403, a CpG mutation hotspot, in exon 13 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathyJ C Moolman, P A Brink, V A Corfield
Gene|September 15, 1991
Synthesis of a wild-type and three mutant Cucurbita maxima trypsin inhibitor-encoding genes by a single-strand approachD P Botes, M D Qobose, V A Corfield
Biochemical Society Transactions|May 1, 1994
Secreted and cellular mucins show structural changes in adeno- and mucinous carcinoma cells in cultureN Myerscough, M Gough, P Durdey, et al.
Cardiovascular Journal of Africa|March 17, 2009
Mendelian-inherited heart disease: a gateway to understanding mechanisms in heart disease Update on work done at the University of StellenboschP A Brink, J C Moolman-Smook, V A Corfield
Transfusion|February 1, 1993
Polymerase chain reaction-based detection of MN blood group-specific sequences in the human genomeV A Corfield, J C Moolman, R Martell, et al.
Gene|October 1, 1984
A modified protoplast-regeneration protocol facilitating the detection of cloned exoenzyme genes in Bacillus subtilisV A Corfield, S J Reid, J Bodmer, et al.
Journal of Medical Genetics|April 16, 1998
Identification of a new missense mutation in MyBP-C associated with hypertrophic cardiomyopathyJ C Moolman-Smook, B Mayosi, P Brink, et al.
Biochemical Society Transactions|May 1, 1994
Evidence of hyaluronan in human tears and secretions of conjunctival culturesM Frescura, M Berry, A Corfield, et al.
Nucleic Acids Research|July 25, 1993
Nucleotide sequence of cytochrome oxidase (subunit III) from the mitochondrion of the tunicate Pyura stolonifera: evidence that AGR encodes glycineG A Durrheim, V A Corfield, E H Harley, et al.
British Heart Journal|July 1, 1995
Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutationsB M Posen, J C Moolman, V A Corfield, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|October 1, 1993
Identification of a new missense mutation at Arg403, a CpG mutation hotspot, in exon 13 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathyJ C Moolman, P A Brink, V A Corfield
Gene|September 15, 1991
Synthesis of a wild-type and three mutant Cucurbita maxima trypsin inhibitor-encoding genes by a single-strand approachD P Botes, M D Qobose, V A Corfield
Biochemical Society Transactions|May 1, 1994
Secreted and cellular mucins show structural changes in adeno- and mucinous carcinoma cells in cultureN Myerscough, M Gough, P Durdey, et al.
Cardiovascular Journal of Africa|March 17, 2009
Mendelian-inherited heart disease: a gateway to understanding mechanisms in heart disease Update on work done at the University of StellenboschP A Brink, J C Moolman-Smook, V A Corfield
Transfusion|February 1, 1993
Polymerase chain reaction-based detection of MN blood group-specific sequences in the human genomeV A Corfield, J C Moolman, R Martell, et al.
Gene|October 1, 1984
A modified protoplast-regeneration protocol facilitating the detection of cloned exoenzyme genes in Bacillus subtilisV A Corfield, S J Reid, J Bodmer, et al.
Journal of Medical Genetics|April 16, 1998
Identification of a new missense mutation in MyBP-C associated with hypertrophic cardiomyopathyJ C Moolman-Smook, B Mayosi, P Brink, et al.
Biochemical Society Transactions|May 1, 1994
Evidence of hyaluronan in human tears and secretions of conjunctival culturesM Frescura, M Berry, A Corfield, et al.
Nucleic Acids Research|July 25, 1993
Nucleotide sequence of cytochrome oxidase (subunit III) from the mitochondrion of the tunicate Pyura stolonifera: evidence that AGR encodes glycineG A Durrheim, V A Corfield, E H Harley, et al.
British Heart Journal|July 1, 1995
Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutationsB M Posen, J C Moolman, V A Corfield, et al.
Pageof 7