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T M Cox

Showing results (51-60 of 146) with videos related to

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Molecular Biology & Medicine|November 1, 1983
Allelic heterogeneity in adult hereditary fructose intolerance. Detection of structural mutations in the aldolase B moleculeT M Cox, M W O'Donnell, M Camilleri
Journal of Inherited Metabolic Disease|March 28, 2012
Lysosomal delivery of therapeutic enzymes in cell models of Fabry diseaseD Marchesan, T M Cox, P B Deegan
Human Mutation|January 1, 1996
A newly identified aldolase B splicing mutation (G-->C, 5' intron 5) in hereditary fructose intolerance from New ZealandM Ali, C L James, T M Cox
BMJ (Clinical Research Ed.)|May 12, 1990
Vitamin B-12 and folate deficiency presenting as leukaemiaI S Dokal, T M Cox, D A Galton
Cell|June 17, 1988
Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutationN C Cross, D R Tolan, T M Cox
Journal of Anatomy|June 15, 2000
Widespread expression of tartrate-resistant acid phosphatase (Acp 5) in the mouse embryoA R Hayman, A J Bune, T M Cox
Clinical Chemistry|October 1, 1987
Antibodies to porcine uteroferrin used in measurement of human tartrate-resistant acid phosphataseZ O Echetebu, T M Cox, D W Moss
Seminars in Liver Disease|March 28, 1998
ProtoporphyriaT M Cox, G J Alexander, R P Sarkany
The New England Journal of Medicine|January 16, 1986
Remission of Crohn's disease with tuberculosis chemotherapyJ B Warren, H C Rees, T M Cox
The Journal of Biological Chemistry|November 15, 1991
Biosynthesis of delta-aminolevulinic acid and the regulation of heme formation by immature erythroid cells in manL C Gardner, S J Smith, T M Cox
Pageof 15

Showing results (51-60 of 146) with videos related to

Sort By:
Pageof 15
Molecular Biology & Medicine|November 1, 1983
Allelic heterogeneity in adult hereditary fructose intolerance. Detection of structural mutations in the aldolase B moleculeT M Cox, M W O'Donnell, M Camilleri
Journal of Inherited Metabolic Disease|March 28, 2012
Lysosomal delivery of therapeutic enzymes in cell models of Fabry diseaseD Marchesan, T M Cox, P B Deegan
Human Mutation|January 1, 1996
A newly identified aldolase B splicing mutation (G-->C, 5' intron 5) in hereditary fructose intolerance from New ZealandM Ali, C L James, T M Cox
BMJ (Clinical Research Ed.)|May 12, 1990
Vitamin B-12 and folate deficiency presenting as leukaemiaI S Dokal, T M Cox, D A Galton
Cell|June 17, 1988
Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutationN C Cross, D R Tolan, T M Cox
Journal of Anatomy|June 15, 2000
Widespread expression of tartrate-resistant acid phosphatase (Acp 5) in the mouse embryoA R Hayman, A J Bune, T M Cox
Clinical Chemistry|October 1, 1987
Antibodies to porcine uteroferrin used in measurement of human tartrate-resistant acid phosphataseZ O Echetebu, T M Cox, D W Moss
Seminars in Liver Disease|March 28, 1998
ProtoporphyriaT M Cox, G J Alexander, R P Sarkany
The New England Journal of Medicine|January 16, 1986
Remission of Crohn's disease with tuberculosis chemotherapyJ B Warren, H C Rees, T M Cox
The Journal of Biological Chemistry|November 15, 1991
Biosynthesis of delta-aminolevulinic acid and the regulation of heme formation by immature erythroid cells in manL C Gardner, S J Smith, T M Cox
Pageof 15