UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Pharmacogenetics and adverse drug reactions

The Lancet (British edition), 2000-11, Vol.356 (9242), p.1667-1671

Meyer, Urs A

2000

Volltextzugriff (PDF)

The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans

The Journal of biological chemistry, 1994-06, Vol.269 (22), p.15419-15422

1994

Volltextzugriff (PDF)

Personalized Medicine: A Personal View

Clinical pharmacology and therapeutics, 2012-03, Vol.91 (3), p.373-375

Meyer, U A

2012

Volltextzugriff (PDF)

Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese

Molecular pharmacology, 1994-10, Vol.46 (4), p.594-598

1994

Volltextzugriff (PDF)

Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification

The Lancet (British edition), 1990-09, Vol.336 (8714), p.529-532

1990

Volltextzugriff (PDF)

Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4

Molecular pharmacology, 1989-07, Vol.36 (1), p.89-96

1989

Volltextzugriff (PDF)

Molecular Mechanism of Slow Acetylation of Drugs and Carcinogens in Humans

Proceedings of the National Academy of Sciences - PNAS, 1991-06, Vol.88 (12), p.5237-5241

1991

Volltextzugriff (PDF)

Multiple mutations of the human cytochrome P450IID6 gene (CYP2D6) in poor metabolizers of debrisoquine. Study of the functional significance of individual mutations by expression of chimeric genes

The Journal of biological chemistry, 1990-10, Vol.265 (28), p.17209-17214

1990

Volltextzugriff (PDF)

Metabolic interactions of the proton-pump inhibitors lansoprazole, omeprazole and pantoprazole with other drugs

European journal of gastroenterology & hepatology, 1996-10, Vol.8 Suppl 1 (Supplement 1), p.S21-S25

Meyer, U A

1996

Volltextzugriff (PDF)

The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene

American journal of human genetics, 1989-12, Vol.45 (6), p.889-904

1989

Volltextzugriff (PDF)

Pharmacogenetics: The Slow, The Rapid, and the Ultrarapid

Proceedings of the National Academy of Sciences - PNAS, 1994-03, Vol.91 (6), p.1983-1984

Meyer, Urs A.

1994

Volltextzugriff (PDF)

Cytochrome P-450 hPCN3, a novel cytochrome P-450 IIIA gene product that is differentially expressed in adult human liver. cDNA and deduced amino acid sequence and distinct specificities of cDNA-expressed hPCN1 and hPCN3 for the metabolism of steroid hormones and cyclosporine

The Journal of biological chemistry, 1989-06, Vol.264 (18), p.10388-10395

1989

Volltextzugriff (PDF)

Monomorphic and polymorphic human arylamine N-acetyltransferases: a comparison of liver isozymes and expressed products of two cloned genes

Molecular pharmacology, 1991-02, Vol.39 (2), p.184-191

1991

Volltextzugriff (PDF)

Site-directed mutation studies of human liver cytochrome P-450 isoenzymes in the CYP2C subfamily

Biochemical journal, 1993-01, Vol.289 (2), p.533-538

1993

Volltextzugriff (PDF)

Debrisoquine/sparteine hydroxylation genotype and phenotype: analysis of common mutations and alleles of CYP2D6 in a European population

DNA and cell biology, 1991-10, Vol.10 (8), p.545-558

1991

Volltextzugriff (PDF)

Cyclosporine metabolism in human liver: Identification of a cytochrome P-450III gene family as the major cyclosporine-metabolizing enzyme explains interactions of cyclosporine with other drugs

Clinical pharmacology and therapeutics, 1988-06, Vol.43 (6), p.630-635

1988

Volltextzugriff (PDF)

Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyria

Nature genetics, 1996-02, Vol.12 (2), p.195-199

1996

Volltextzugriff (PDF)

Lidocaine metabolism in human liver microsomes by cytochrome P450IIIA4

Clinical pharmacology and therapeutics, 1989-11, Vol.46 (5), p.521-527

1989

Volltextzugriff (PDF)

Antibodies against Human Cytochrome P-450db1 in Autoimmune Hepatitis Type II

Proceedings of the National Academy of Sciences - PNAS, 1988-11, Vol.85 (21), p.8256-8260

1988

Volltextzugriff (PDF)

Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism

American journal of human genetics, 1991-05, Vol.48 (5), p.943-950

1991

Volltextzugriff (PDF)

The molecular basis of genetic polymorphisms of drug metabolism

Journal of pharmacy and pharmacology, 1994-05, Vol.46 Suppl 1, p.409-415

Meyer, U A

1994

Volltextzugriff (PDF)

Tolbutamide and mephenytoin hydroxylation by human cytochrome P450s in the CYP2C subfamily

The Journal of pharmacology and experimental therapeutics, 1990-01, Vol.252 (1), p.442

1990

Volltextzugriff (PDF)

Identification of human liver cytochrome P450 isoforms mediating omeprazole metabolism

British journal of clinical pharmacology, 1993-12, Vol.36 (6), p.521-530

1993

Volltextzugriff (PDF)

Regulatory network of lipid-sensing nuclear receptors: roles for CAR, PXR, LXR, and FXR

Archives of biochemistry and biophysics, 2005-01, Vol.433 (2), p.387-396

2005

Volltextzugriff (PDF)

Cytokines, Oxidative Stress and Cellular Markers of Inflammation in Schizophrenia

Current topics in behavioral neurosciences, 2020, Vol.44, p.49-66

2020

Volltextzugriff (PDF)

1 – 25 von 7.742

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(6.286)
Mit Volltextzugriff
(6.154)

Publikationsform

5 weitere anzeigen...

Weniger anzeigen...

Sprache

7 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(4.173)
Life Sciences & Biomedicine
(2.594)
Humans
(2.144)
Physical Sciences
(1.386)
Biological And Medical Sciences
(1.352)
Male
(1.269)
Female
(1.247)
Physics
(1.184)
Medical Sciences
(944)
Adult
(845)
Middle Aged
(825)
Animals
(821)
Technology
(664)
Aged
(542)
Exact Sciences And Technology
(536)
Fundamental And Applied Biological Sciences. Psychology
(460)
Physics, Particles & Fields
(404)
High Energy Physics - Experiment
(327)
Adolescent
(297)
Chemistry
(290)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

IngentaConnect Journals
(3.470)
MEDLINE
(2.889)
Free E-Journal (出版社公開部分のみ）
(2.578)
Elsevier ScienceDirect Journals Complete
(1.722)
Journals@Ovid Ovid Full Text
(1.610)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(1.496)
SpringerLink Journals - AutoHoldings
(1.252)
NUS Single-Journal Subscriptions
(1.113)
IngentaConnect Journals
(1.040)
Wiley-Blackwell Journals
(939)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(757)
Wiley Online Library Full Collection 2018
(639)
Thieme_化学药学期刊
(414)
American Physical Society
(288)
PROLA - Physical Review Online Archive
(271)
IEEE Xplore
(245)
Oxford Journals
(222)
JSTOR
(205)
Ebook Central Perpetual and DDA
(203)
eBooks on EBSCOhost
(202)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Pharmacogenetics and adverse drug reactions

The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans

Personalized Medicine: A Personal View

Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese

Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification

Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4

Molecular Mechanism of Slow Acetylation of Drugs and Carcinogens in Humans

Multiple mutations of the human cytochrome P450IID6 gene (CYP2D6) in poor metabolizers of debrisoquine. Study of the functional significance of individual mutations by expression of chimeric genes

Metabolic interactions of the proton-pump inhibitors lansoprazole, omeprazole and pantoprazole with other drugs

The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene

Pharmacogenetics: The Slow, The Rapid, and the Ultrarapid

Cytochrome P-450 hPCN3, a novel cytochrome P-450 IIIA gene product that is differentially expressed in adult human liver. cDNA and deduced amino acid sequence and distinct specificities of cDNA-expressed hPCN1 and hPCN3 for the metabolism of steroid hormones and cyclosporine

Monomorphic and polymorphic human arylamine N-acetyltransferases: a comparison of liver isozymes and expressed products of two cloned genes

Site-directed mutation studies of human liver cytochrome P-450 isoenzymes in the CYP2C subfamily

Debrisoquine/sparteine hydroxylation genotype and phenotype: analysis of common mutations and alleles of CYP2D6 in a European population

Cyclosporine metabolism in human liver: Identification of a cytochrome P-450III gene family as the major cyclosporine-metabolizing enzyme explains interactions of cyclosporine with other drugs

Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyria

Lidocaine metabolism in human liver microsomes by cytochrome P450IIIA4

Antibodies against Human Cytochrome P-450db1 in Autoimmune Hepatitis Type II

Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism

The molecular basis of genetic polymorphisms of drug metabolism

Tolbutamide and mephenytoin hydroxylation by human cytochrome P450s in the CYP2C subfamily

Identification of human liver cytochrome P450 isoforms mediating omeprazole metabolism

Regulatory network of lipid-sensing nuclear receptors: roles for CAR, PXR, LXR, and FXR

Cytokines, Oxidative Stress and Cellular Markers of Inflammation in Schizophrenia

Suchergebnisse filtern