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N D Carter

Showing results (71-80 of 140) with videos related to

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Human Heredity|January 1, 1976
Superoxide dismutase variants in Newfoundland--a gene from Scandinavia?N D Carter, J A Auton, S G Welch, et al.
Nucleic Acids Research|September 11, 1993
Tsp45I, a new thermostable site-specific endonuclease that cleaves the recognition sequence 5'-decreases GTSAC-3'N D Raven, R A Williams, K E Smith, et al.
Diabetologia|January 13, 2006
Common polymorphisms in SOCS3 are not associated with body weight, insulin sensitivity or lipid profile in normal female twinsY Jamshidi, H Snieder, X Wang, et al.
Journal of the Neurological Sciences|August 1, 1984
Plasma phosphoglycerate mutase as a marker of muscular dystrophyP J Chown, E A Barnard, P J Barnard, et al.
The American Journal of Physiology|July 1, 1993
Differentiation-dependent expression of carbonic anhydrase II and III in 3T3 adipocytesC J Lynch, S A Hazen, R L Horetsky, et al.
Cardiovascular Research|July 11, 1998
'Comments on circulating transforming growth factor beta 1 and coronary artery disease'S Fredericks, P Syrris, J C Kaski, et al.
Shock (Augusta, Ga.)|September 1, 1994
Altered expression of skeletal muscle proteins during sepsisE L Owens, C J Lynch, K M McCall, et al.
The American Journal of Clinical Nutrition|June 1, 1981
Is preterm milk nutritionally advantageous?C M Hibberd, O G Brooke, I R Brown, et al.
Lancet (London, England)|December 25, 1976
Rapid diagnosis of thyroid disease using carbonic-anhydrase immunoassayJ A Auton, J M Barragry, N D Carter, et al.
Brain : a Journal of Neurology|September 1, 1983
Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophyM Swash, M S Schwartz, N D Carter, et al.
Pageof 14

Showing results (71-80 of 140) with videos related to

Sort By:
Pageof 14
Human Heredity|January 1, 1976
Superoxide dismutase variants in Newfoundland--a gene from Scandinavia?N D Carter, J A Auton, S G Welch, et al.
Nucleic Acids Research|September 11, 1993
Tsp45I, a new thermostable site-specific endonuclease that cleaves the recognition sequence 5'-decreases GTSAC-3'N D Raven, R A Williams, K E Smith, et al.
Diabetologia|January 13, 2006
Common polymorphisms in SOCS3 are not associated with body weight, insulin sensitivity or lipid profile in normal female twinsY Jamshidi, H Snieder, X Wang, et al.
Journal of the Neurological Sciences|August 1, 1984
Plasma phosphoglycerate mutase as a marker of muscular dystrophyP J Chown, E A Barnard, P J Barnard, et al.
The American Journal of Physiology|July 1, 1993
Differentiation-dependent expression of carbonic anhydrase II and III in 3T3 adipocytesC J Lynch, S A Hazen, R L Horetsky, et al.
Cardiovascular Research|July 11, 1998
'Comments on circulating transforming growth factor beta 1 and coronary artery disease'S Fredericks, P Syrris, J C Kaski, et al.
Shock (Augusta, Ga.)|September 1, 1994
Altered expression of skeletal muscle proteins during sepsisE L Owens, C J Lynch, K M McCall, et al.
The American Journal of Clinical Nutrition|June 1, 1981
Is preterm milk nutritionally advantageous?C M Hibberd, O G Brooke, I R Brown, et al.
Lancet (London, England)|December 25, 1976
Rapid diagnosis of thyroid disease using carbonic-anhydrase immunoassayJ A Auton, J M Barragry, N D Carter, et al.
Brain : a Journal of Neurology|September 1, 1983
Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophyM Swash, M S Schwartz, N D Carter, et al.
Pageof 14