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N D Carter

Showing results (31-40 of 140) with videos related to

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Biochemical Genetics|April 1, 1972
Genetic variation of phosphoglucose isomerase in some hystricomorph rodentsN D Carter, M R Hill, B J Weir
Journal of Gastroenterology and Hepatology|January 1, 1989
IgM abnormalities in the families of patients with primary biliary cirrhosisD R Triger, R J Muggleton, N D Carter
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|April 1, 1991
Immunocytochemical localization of mitochondrial carbonic anhydrase in rat tissuesH K Väänänen, N D Carter, S J Dodgson
Journal of Chromatography|May 30, 1989
Purification of human muscle phosphoglycerate mutase by fast protein liquid chromatography based on hydrophobic interactionsR J Edwards, N D Carter, S Jeffery, et al.
Journal of Medical Genetics|January 14, 2000
A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)K Heathcote, P Syrris, N D Carter, et al.
The British Journal of Nutrition|March 1, 1986
Physiological zinc-binding proteins of medium molecular weight in the rat gutM J Jackson, D Holt, M Webb, et al.
EXS|March 28, 2001
Use of carbonic anhydrase II-deficient mice in uncovering the cellular location of membrane-associated isoformsY Ridderstråle, P J Wistrand, L Holm, et al.
Human Heredity|January 1, 1980
Association of glyoxalase I allotypes with Graves' disease and diabetes mellitusH Moens, R Payne, N D Carter, et al.
Journal of Human Hypertension|August 1, 1994
Molecular approach to assessing the genetic risk of cerebral infarction: deletion polymorphism in the gene encoding angiotensin 1-converting enzymeP Sharma, N D Carter, J Barley, et al.
Archives of Disease in Childhood|September 1, 1987
Human milk and preterm formula compared for effects on growth and metabolismO G Brooke, O Onubogu, R Heath, et al.
Pageof 14

Showing results (31-40 of 140) with videos related to

Sort By:
Pageof 14
Biochemical Genetics|April 1, 1972
Genetic variation of phosphoglucose isomerase in some hystricomorph rodentsN D Carter, M R Hill, B J Weir
Journal of Gastroenterology and Hepatology|January 1, 1989
IgM abnormalities in the families of patients with primary biliary cirrhosisD R Triger, R J Muggleton, N D Carter
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|April 1, 1991
Immunocytochemical localization of mitochondrial carbonic anhydrase in rat tissuesH K Väänänen, N D Carter, S J Dodgson
Journal of Chromatography|May 30, 1989
Purification of human muscle phosphoglycerate mutase by fast protein liquid chromatography based on hydrophobic interactionsR J Edwards, N D Carter, S Jeffery, et al.
Journal of Medical Genetics|January 14, 2000
A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)K Heathcote, P Syrris, N D Carter, et al.
The British Journal of Nutrition|March 1, 1986
Physiological zinc-binding proteins of medium molecular weight in the rat gutM J Jackson, D Holt, M Webb, et al.
EXS|March 28, 2001
Use of carbonic anhydrase II-deficient mice in uncovering the cellular location of membrane-associated isoformsY Ridderstråle, P J Wistrand, L Holm, et al.
Human Heredity|January 1, 1980
Association of glyoxalase I allotypes with Graves' disease and diabetes mellitusH Moens, R Payne, N D Carter, et al.
Journal of Human Hypertension|August 1, 1994
Molecular approach to assessing the genetic risk of cerebral infarction: deletion polymorphism in the gene encoding angiotensin 1-converting enzymeP Sharma, N D Carter, J Barley, et al.
Archives of Disease in Childhood|September 1, 1987
Human milk and preterm formula compared for effects on growth and metabolismO G Brooke, O Onubogu, R Heath, et al.
Pageof 14