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T M Cox

Showing results (41-50 of 146) with videos related to

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QJM : Monthly Journal of the Association of Physicians|August 1, 1995
Autosomal recessive erythropoietic protoporphyria: a syndrome of severe photosensitivity and liver failureR P Sarkany, T M Cox
The Biochemical Journal|March 15, 1981
Studies on the binding of iron by rabbit intestinal microvillus membranesT M Cox, M W O'Donnell
The International Journal of Biochemistry|January 1, 1990
Hereditary fructose intoleranceN C Cross, T M Cox
Current Opinion in Genetics & Development|August 5, 1998
Haemochromatosis: an inherited metal and toxicity syndromeT M Cox, A L Kelly
The British Journal of Nutrition|March 1, 1982
Studies on the control of iron uptake by rabbit small intestineT M Cox, M W O'Donnell
The Quarterly Journal of Medicine|January 1, 1993
DNA diagnosis of fatal fructose intolerance from archival tissueM Ali, U Rosien, T M Cox
Journal of Medical Genetics|June 4, 1998
Hereditary fructose intoleranceM Ali, P Rellos, T M Cox
Human Molecular Genetics|January 1, 1994
Identification of a novel mutation (Leu 256-->Pro) in the human aldolase B gene associated with hereditary fructose intoleranceM Ali, G Sebastio, T M Cox
Human Molecular Genetics|April 1, 1994
Identification of a novel mutation (Leu256-->Pro) in the human aldolase B gene associated with hereditary fructose intoleranceM Ali, G Sebastio, T M Cox
The Journal of Biological Chemistry|January 8, 2000
Expression, purification, and characterization of natural mutants of human aldolase B. Role of quaternary structure in catalysisP Rellos, J Sygusch, T M Cox
Pageof 15

Showing results (41-50 of 146) with videos related to

Sort By:
Pageof 15
QJM : Monthly Journal of the Association of Physicians|August 1, 1995
Autosomal recessive erythropoietic protoporphyria: a syndrome of severe photosensitivity and liver failureR P Sarkany, T M Cox
The Biochemical Journal|March 15, 1981
Studies on the binding of iron by rabbit intestinal microvillus membranesT M Cox, M W O'Donnell
The International Journal of Biochemistry|January 1, 1990
Hereditary fructose intoleranceN C Cross, T M Cox
Current Opinion in Genetics & Development|August 5, 1998
Haemochromatosis: an inherited metal and toxicity syndromeT M Cox, A L Kelly
The British Journal of Nutrition|March 1, 1982
Studies on the control of iron uptake by rabbit small intestineT M Cox, M W O'Donnell
The Quarterly Journal of Medicine|January 1, 1993
DNA diagnosis of fatal fructose intolerance from archival tissueM Ali, U Rosien, T M Cox
Journal of Medical Genetics|June 4, 1998
Hereditary fructose intoleranceM Ali, P Rellos, T M Cox
Human Molecular Genetics|January 1, 1994
Identification of a novel mutation (Leu 256-->Pro) in the human aldolase B gene associated with hereditary fructose intoleranceM Ali, G Sebastio, T M Cox
Human Molecular Genetics|April 1, 1994
Identification of a novel mutation (Leu256-->Pro) in the human aldolase B gene associated with hereditary fructose intoleranceM Ali, G Sebastio, T M Cox
The Journal of Biological Chemistry|January 8, 2000
Expression, purification, and characterization of natural mutants of human aldolase B. Role of quaternary structure in catalysisP Rellos, J Sygusch, T M Cox
Pageof 15