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Pharmacogenetics
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October 1, 1995
A novel CYP2D6 allele with an abolished splice recognition site associated with the poor metabolizer phenotype
D Marez, N Sabbagh, M Legrand, et al.
Pharmacogenetics
|
April 1, 1997
NAT2 genotyping and efficacy of sulfasalazine in patients with chronic discoid lupus erythematosus
N Sabbagh, E Delaporte, D Marez, et al.
Carcinogenesis
|
October 1, 1996
Influence of a mutation reducing the catalytic activity of the cytochrome P450 CYP2D6 on lung cancer susceptibility
M Legrand, I Stucker, D Marez, et al.
Human Genetics
|
May 1, 1996
An additional allelic variant of the CYP2D6 gene causing impaired metabolism of sparteine
D Marez, M Legrand, N Sabbagh, et al.
Pharmacogenetics
|
September 2, 1999
A rare G2061 insertion affecting the open reading frame of CYP2D6 and responsible for the poor metabolizer phenotype
D Marez-Allorge, S W Ellis, J M Lo Guidice, et al.
Human Genetics
|
November 1, 1995
A nonsense mutation in the cytochrome P450 CYP2D6 gene identified in a Caucasian with an enzyme deficiency
F Broly, D Marez, J M Lo Guidice, et al.
Biochemical and Biophysical Research Communications
|
February 12, 1998
Evidence for CYP2D6 expression in human lung
J M Guidice, D Marez, N Sabbagh, et al.
Pharmacogenetics
|
December 1, 1995
An efficient strategy for detection of known and new mutations of the CYP2D6 gene using single strand conformation polymorphism analysis
F Broly, D Marez, N Sabbagh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 26, 1999
CYP2D6 polymorphism and Parkinson's disease susceptibility
N Sabbagh, A Brice, D Marez, et al.
Pharmacogenetics
|
June 1, 1997
Polymorphism of the cytochrome P450 CYP2D6 gene in a European population: characterization of 48 mutations and 53 alleles, their frequencies and evolution
D Marez, M Legrand, N Sabbagh, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Pharmacogenetics
|
October 1, 1995
A novel CYP2D6 allele with an abolished splice recognition site associated with the poor metabolizer phenotype
D Marez, N Sabbagh, M Legrand, et al.
Pharmacogenetics
|
April 1, 1997
NAT2 genotyping and efficacy of sulfasalazine in patients with chronic discoid lupus erythematosus
N Sabbagh, E Delaporte, D Marez, et al.
Carcinogenesis
|
October 1, 1996
Influence of a mutation reducing the catalytic activity of the cytochrome P450 CYP2D6 on lung cancer susceptibility
M Legrand, I Stucker, D Marez, et al.
Human Genetics
|
May 1, 1996
An additional allelic variant of the CYP2D6 gene causing impaired metabolism of sparteine
D Marez, M Legrand, N Sabbagh, et al.
Pharmacogenetics
|
September 2, 1999
A rare G2061 insertion affecting the open reading frame of CYP2D6 and responsible for the poor metabolizer phenotype
D Marez-Allorge, S W Ellis, J M Lo Guidice, et al.
Human Genetics
|
November 1, 1995
A nonsense mutation in the cytochrome P450 CYP2D6 gene identified in a Caucasian with an enzyme deficiency
F Broly, D Marez, J M Lo Guidice, et al.
Biochemical and Biophysical Research Communications
|
February 12, 1998
Evidence for CYP2D6 expression in human lung
J M Guidice, D Marez, N Sabbagh, et al.
Pharmacogenetics
|
December 1, 1995
An efficient strategy for detection of known and new mutations of the CYP2D6 gene using single strand conformation polymorphism analysis
F Broly, D Marez, N Sabbagh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 26, 1999
CYP2D6 polymorphism and Parkinson's disease susceptibility
N Sabbagh, A Brice, D Marez, et al.
Pharmacogenetics
|
June 1, 1997
Polymorphism of the cytochrome P450 CYP2D6 gene in a European population: characterization of 48 mutations and 53 alleles, their frequencies and evolution
D Marez, M Legrand, N Sabbagh, et al.
Page
of 2