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T M Cox

Showing results (21-30 of 146) with videos related to

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Journal of the Royal Society of Medicine|March 18, 2008
William Bateson, the rediscoverer of MendelMilo Keynes, T M Cox
American Journal of Human Genetics|April 1, 1995
Diverse mutations in the aldolase B gene that underlie the prevalence of hereditary fructose intoleranceM Ali, T M Cox
Journal of the Royal College of Physicians of London|April 1, 1993
The MB PhD programme. Training to be a clinician-scientist in the UKT M Cox, R Wakeford
Journal of Medical Genetics|November 1, 1993
The glucocerebrosidase locus in Gaucher's disease: molecular analysis of a lysosomal enzymeP K Mistry, T M Cox
The Journal of Biological Chemistry|January 14, 1994
Purple acid phosphatase of the human macrophage and osteoclast. Characterization, molecular properties, and crystallization of the recombinant di-iron-oxo protein secreted by baculovirus-infected insect cellsA R Hayman, T M Cox
American Journal of Human Genetics|July 1, 1990
Partial aldolase B gene deletions in hereditary fructose intoleranceN C Cross, T M Cox
European Journal of Haematology|February 1, 1989
Hereditary haemochromatosisT M Cox, D K Lord
Bailliere'S Clinical Haematology|March 14, 1998
Gaucher's disease: clinical features and natural historyT M Cox, J P Schofield
British Journal of Haematology|January 1, 1980
Cellular mechanisms in the regulation of iron absorption by the human intestine: studies in patients with iron deficiency before and after treatmentT M Cox, T J Peters
The Journal of Biological Chemistry|May 15, 1988
Biosynthesis of heme in immature erythroid cells. The regulatory step for heme formation in the human erythronL C Gardner, T M Cox
Pageof 15

Showing results (21-30 of 146) with videos related to

Sort By:
Pageof 15
Journal of the Royal Society of Medicine|March 18, 2008
William Bateson, the rediscoverer of MendelMilo Keynes, T M Cox
American Journal of Human Genetics|April 1, 1995
Diverse mutations in the aldolase B gene that underlie the prevalence of hereditary fructose intoleranceM Ali, T M Cox
Journal of the Royal College of Physicians of London|April 1, 1993
The MB PhD programme. Training to be a clinician-scientist in the UKT M Cox, R Wakeford
Journal of Medical Genetics|November 1, 1993
The glucocerebrosidase locus in Gaucher's disease: molecular analysis of a lysosomal enzymeP K Mistry, T M Cox
The Journal of Biological Chemistry|January 14, 1994
Purple acid phosphatase of the human macrophage and osteoclast. Characterization, molecular properties, and crystallization of the recombinant di-iron-oxo protein secreted by baculovirus-infected insect cellsA R Hayman, T M Cox
American Journal of Human Genetics|July 1, 1990
Partial aldolase B gene deletions in hereditary fructose intoleranceN C Cross, T M Cox
European Journal of Haematology|February 1, 1989
Hereditary haemochromatosisT M Cox, D K Lord
Bailliere'S Clinical Haematology|March 14, 1998
Gaucher's disease: clinical features and natural historyT M Cox, J P Schofield
British Journal of Haematology|January 1, 1980
Cellular mechanisms in the regulation of iron absorption by the human intestine: studies in patients with iron deficiency before and after treatmentT M Cox, T J Peters
The Journal of Biological Chemistry|May 15, 1988
Biosynthesis of heme in immature erythroid cells. The regulatory step for heme formation in the human erythronL C Gardner, T M Cox
Pageof 15