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D M Swallow

Showing results (21-30 of 88) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1990
Pyrimidine 5'-nucleotidase activity in normal and deficient human lymphoblastoid cellsD A Hopkinson, D M Swallow, A Marinaki, et al.
Disease Markers|December 1, 1986
Detection of the urinary 'PUM' polymorphism by the tumour-binding monoclonal antibodies Ca1, Ca2, Ca3, HMFG1, and HMFG2D M Swallow, B Griffiths, M Bramwell, et al.
Annals of Human Genetics|May 1, 1981
Complementation analysis of human sialidase deficiency using natural substratesD M Swallow, A T Hoogeveen, F W Verheijen, et al.
Experimental and Clinical Immunogenetics|January 1, 1993
A monoclonal antibody to alcohol dehydrogenase cross-reacts with human complement component C3N A Leone, D B Whitehouse, D M Swallow, et al.
Hybridoma and Hybridomics|December 18, 2003
New monoclonal antibodies to non-glycosylated domains of the secreted mucins MUC5B and MUC7K Rousseau, C Wickstrom, D B Whitehouse, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
Common polymorphism in a highly variable region upstream of the human lactase gene affects DNA-protein interactionsE J Hollox, M Poulter, Y Wang, et al.
Annals of Human Genetics|February 1, 1981
Electrophoretic analysis of glycoprotein enzymes in the sialidoses and mucolipidosesD M Swallow, J S O'Brien, A T Hoogeveen, et al.
Journal of Medical Genetics|December 1, 1984
Glycoproteins in cystic fibrosis: a lectin binding studyS Karlsson, B Griffiths, D M Swallow, et al.
Annals of Human Genetics|July 1, 1979
Sialidosis type 1: cherry red spot-myoclonus syndrome with sialidase deficiency and altered electrophoretic mobility of some enzymes known to be glycoproteins. II. Enzymes studiesD M Swallow, L Evans, G Stewart, et al.
Annals of Human Genetics|July 1, 1977
The deficiency of a lysosomal acid hydrolase in two clones derived from the human lymphoblastoid line F137 after mutagen treatmentS E Gardiner, D M Swallow, H Harris, et al.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
Journal of Inherited Metabolic Disease|January 1, 1990
Pyrimidine 5'-nucleotidase activity in normal and deficient human lymphoblastoid cellsD A Hopkinson, D M Swallow, A Marinaki, et al.
Disease Markers|December 1, 1986
Detection of the urinary 'PUM' polymorphism by the tumour-binding monoclonal antibodies Ca1, Ca2, Ca3, HMFG1, and HMFG2D M Swallow, B Griffiths, M Bramwell, et al.
Annals of Human Genetics|May 1, 1981
Complementation analysis of human sialidase deficiency using natural substratesD M Swallow, A T Hoogeveen, F W Verheijen, et al.
Experimental and Clinical Immunogenetics|January 1, 1993
A monoclonal antibody to alcohol dehydrogenase cross-reacts with human complement component C3N A Leone, D B Whitehouse, D M Swallow, et al.
Hybridoma and Hybridomics|December 18, 2003
New monoclonal antibodies to non-glycosylated domains of the secreted mucins MUC5B and MUC7K Rousseau, C Wickstrom, D B Whitehouse, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
Common polymorphism in a highly variable region upstream of the human lactase gene affects DNA-protein interactionsE J Hollox, M Poulter, Y Wang, et al.
Annals of Human Genetics|February 1, 1981
Electrophoretic analysis of glycoprotein enzymes in the sialidoses and mucolipidosesD M Swallow, J S O'Brien, A T Hoogeveen, et al.
Journal of Medical Genetics|December 1, 1984
Glycoproteins in cystic fibrosis: a lectin binding studyS Karlsson, B Griffiths, D M Swallow, et al.
Annals of Human Genetics|July 1, 1979
Sialidosis type 1: cherry red spot-myoclonus syndrome with sialidase deficiency and altered electrophoretic mobility of some enzymes known to be glycoproteins. II. Enzymes studiesD M Swallow, L Evans, G Stewart, et al.
Annals of Human Genetics|July 1, 1977
The deficiency of a lysosomal acid hydrolase in two clones derived from the human lymphoblastoid line F137 after mutagen treatmentS E Gardiner, D M Swallow, H Harris, et al.
Pageof 9