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Pharmacogenetics
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February 24, 2001
Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FM03) gene in patients with fish-odour syndrome
C T Dolphin, A Janmohamed, R L Smith, et al.
Clinical Anatomy (New York, N.Y.)
|
June 4, 2008
Palatal asymmetry during development: an anatomical study
R 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 rabbit
F 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 humans
M Al-Waiz, R Ayesh, S C Mitchell, et al.
Cytokine
|
July 6, 2000
Monocyte migration inhibitory factor synthesis and gene expression in particle-activated macrophages
M 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 family
M 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 population
D A Evans, A Mahgoub, T P Sloan, et al.
The Biochemical Journal
|
April 1, 1972
Species variations in the metabolism of phenol
I 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 family
C 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 syndrome
C T Dolphin, A Janmohamed, R L Smith, et al.
Page
of 79
Search research articles
Search
Showing results (541-550 of 789) with videos related to
Sort By:
Page
of 79
Pharmacogenetics
|
February 24, 2001
Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FM03) gene in patients with fish-odour syndrome
C T Dolphin, A Janmohamed, R L Smith, et al.
Clinical Anatomy (New York, N.Y.)
|
June 4, 2008
Palatal asymmetry during development: an anatomical study
R 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 rabbit
F 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 humans
M Al-Waiz, R Ayesh, S C Mitchell, et al.
Cytokine
|
July 6, 2000
Monocyte migration inhibitory factor synthesis and gene expression in particle-activated macrophages
M 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 family
M 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 population
D A Evans, A Mahgoub, T P Sloan, et al.
The Biochemical Journal
|
April 1, 1972
Species variations in the metabolism of phenol
I 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 family
C 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 syndrome
C T Dolphin, A Janmohamed, R L Smith, et al.
Page
of 79