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R L Smith

Showing results (541-550 of 789) with videos related to

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Pharmacogenetics|February 24, 2001
Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FM03) gene in patients with fish-odour syndromeC T Dolphin, A Janmohamed, R L Smith, et al.
Clinical Anatomy (New York, N.Y.)|June 4, 2008
Palatal asymmetry during development: an anatomical studyR S Moreira, E A Sgrott, H Stuker, et al.
The Biochemical Journal|November 1, 1971
The biliary excretion of anions of molecular weight 300-800 in the rat, guinea pig and rabbitF T Aziz, P C Hirom, P Millburn, et al.
Clinical Pharmacology and Therapeutics|November 1, 1987
A genetic polymorphism of the N-oxidation of trimethylamine in humansM Al-Waiz, R Ayesh, S C Mitchell, et al.
Cytokine|July 6, 2000
Monocyte migration inhibitory factor synthesis and gene expression in particle-activated macrophagesM Lind, M C Trindade, D J Schurman, et al.
Clinical Science (London, England : 1979)|March 1, 1988
Trimethylaminuria ('fish-odour syndrome'): a study of an affected familyM Al-Waiz, R Ayesh, S C Mitchell, et al.
Journal of Medical Genetics|April 1, 1980
A family and population study of the genetic polymorphism of debrisoquine oxidation in a white British populationD A Evans, A Mahgoub, T P Sloan, et al.
The Biochemical Journal|April 1, 1972
Species variations in the metabolism of phenolI D Capel, M R French, P Millburn, et al.
The Biochemical Journal|October 1, 1992
Cloning, primary sequence and chromosomal localization of human FMO2, a new member of the flavin-containing mono-oxygenase familyC T Dolphin, E A Shephard, S Povey, et al.
Nature Genetics|December 17, 1997
Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndromeC T Dolphin, A Janmohamed, R L Smith, et al.
Pageof 79

Showing results (541-550 of 789) with videos related to

Sort By:
Pageof 79
Pharmacogenetics|February 24, 2001
Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FM03) gene in patients with fish-odour syndromeC T Dolphin, A Janmohamed, R L Smith, et al.
Clinical Anatomy (New York, N.Y.)|June 4, 2008
Palatal asymmetry during development: an anatomical studyR S Moreira, E A Sgrott, H Stuker, et al.
The Biochemical Journal|November 1, 1971
The biliary excretion of anions of molecular weight 300-800 in the rat, guinea pig and rabbitF T Aziz, P C Hirom, P Millburn, et al.
Clinical Pharmacology and Therapeutics|November 1, 1987
A genetic polymorphism of the N-oxidation of trimethylamine in humansM Al-Waiz, R Ayesh, S C Mitchell, et al.
Cytokine|July 6, 2000
Monocyte migration inhibitory factor synthesis and gene expression in particle-activated macrophagesM Lind, M C Trindade, D J Schurman, et al.
Clinical Science (London, England : 1979)|March 1, 1988
Trimethylaminuria ('fish-odour syndrome'): a study of an affected familyM Al-Waiz, R Ayesh, S C Mitchell, et al.
Journal of Medical Genetics|April 1, 1980
A family and population study of the genetic polymorphism of debrisoquine oxidation in a white British populationD A Evans, A Mahgoub, T P Sloan, et al.
The Biochemical Journal|April 1, 1972
Species variations in the metabolism of phenolI D Capel, M R French, P Millburn, et al.
The Biochemical Journal|October 1, 1992
Cloning, primary sequence and chromosomal localization of human FMO2, a new member of the flavin-containing mono-oxygenase familyC T Dolphin, E A Shephard, S Povey, et al.
Nature Genetics|December 17, 1997
Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndromeC T Dolphin, A Janmohamed, R L Smith, et al.
Pageof 79