UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Impact of Genetic Polymorphisms of ABCB1 (MDR1, P-Glycoprotein) on Drug Disposition and Potential Clinical Implications: Update of the Literature

Clinical pharmacokinetics, 2015-07, Vol.54 (7), p.709-735

2015

Link zum Volltext

Verfügbarkeit prüfen

Clinical and Functional Relevance of the Monocarboxylate Transporter Family in Disease Pathophysiology and Drug Therapy

Clinical and translational science, 2018-07, Vol.11 (4), p.352-364

2018

Link zum Volltext

Verfügbarkeit prüfen

Hepatic solute carrier transporters and drug therapy: Regulation of expression and impact of genetic variation

Pharmacology & therapeutics (Oxford), 2022-10, Vol.238, p.108268-108268, Article 108268

2022

Link zum Volltext

Verfügbarkeit prüfen

Mechanisms and assessment of statin‐related muscular adverse effects

British journal of clinical pharmacology, 2014-09, Vol.78 (3), p.454-466

2014

Link zum Volltext

Verfügbarkeit prüfen

Impact of NUDT15 genetics on severe thiopurine-related hematotoxicity in patients with European ancestry

Genetics in medicine, 2019-09, Vol.21 (9), p.2145-2150

2019

Link zum Volltext

Verfügbarkeit prüfen

Impact of Membrane Drug Transporters on Resistance to Small-Molecule Tyrosine Kinase Inhibitors

Trends in pharmacological sciences (Regular ed.), 2016-11, Vol.37 (11), p.904-932

2016

Link zum Volltext

Verfügbarkeit prüfen

Metformin and cancer: from the old medicine cabinet to pharmacological pitfalls and prospects

Trends in pharmacological sciences (Regular ed.), 2013-02, Vol.34 (2), p.126-135

2013

Link zum Volltext

Verfügbarkeit prüfen

Expression of organic cation transporters OCT1 (SLC22A1) and OCT3 (SLC22A3) is affected by genetic factors and cholestasis in human liver

Hepatology (Baltimore, Md.), 2009-10, Vol.50 (4), p.1227-1240

2009

Link zum Volltext

Verfügbarkeit prüfen

Proton pump inhibitors inhibit metformin uptake by organic cation transporters (OCTs)

PloS one, 2011-07, Vol.6 (7), p.e22163

2011

Link zum Volltext

Verfügbarkeit prüfen

Role of Genetic and Nongenetic Factors for Fluorouracil Treatment-Related Severe Toxicity: A Prospective Clinical Trial by the German 5-FU Toxicity Study Group

Journal of clinical oncology, 2008-05, Vol.26 (13), p.2131-2138

2008

Link zum Volltext

Verfügbarkeit prüfen

Selective p38α MAP kinase/MAPK14 inhibition in enzymatically modified LDL‐stimulated human monocytes: implications for atherosclerosis

The FASEB journal, 2017-02, Vol.31 (2), p.674-686

2017

Link zum Volltext

Verfügbarkeit prüfen

Combinations of common SNPs of the transporter gene ABCB1 influence apparent bioavailability, but not renal elimination of oral digoxin

Scientific reports, 2020-07, Vol.10 (1), p.12457, Article 12457

2020

Link zum Volltext

Verfügbarkeit prüfen

Reduced Paneth Cell α-Defensins in Ileal Crohn's Disease

Proceedings of the National Academy of Sciences - PNAS, 2005-12, Vol.102 (50), p.18129-18134

2005

Link zum Volltext

Verfügbarkeit prüfen

Selective Inhibition of the Lactate Transporter MCT4 Reduces Growth of Invasive Bladder Cancer

Molecular cancer therapeutics, 2018-12, Vol.17 (12), p.2746-2755

2018

Link zum Volltext

Verfügbarkeit prüfen

Copy number variation profiling in pharmacogenes using panel-based exome resequencing and correlation to human liver expression

Human genetics, 2020-02, Vol.139 (2), p.137-149

2020

Link zum Volltext

Verfügbarkeit prüfen

Novel drug transporter substrates identification: An innovative approach based on metabolomic profiling, in silico ligand screening and biological validation

Pharmacological research, 2023-10, Vol.196, p.106941-106941, Article 106941

2023

Link zum Volltext

Verfügbarkeit prüfen

No association of genetic variants in TLR4, TNF-α, IL10, IFN-γ, and IL37 in cytomegalovirus-positive renal allograft recipients with active CMV infection-Subanalysis of the prospective randomised VIPP study

PloS one, 2021-04, Vol.16 (4), p.e0246118-e0246118

2021

Link zum Volltext

Verfügbarkeit prüfen

Platelet miRNAs: differential expression in coronary artery disease and associations with course of left ventricular systolic function

BMC cardiovascular disorders, 2023-07, Vol.23 (1), p.348-348, Article 348

2023

Link zum Volltext

Verfügbarkeit prüfen

Aberrant splicing caused by single nucleotide polymorphism c.516G>T [Q172H], a marker of CYP2B66, is responsible for decreased expression and activity of CYP2B6 in liver

The Journal of pharmacology and experimental therapeutics, 2008-04, Vol.325 (1), p.284

2008

Link zum Volltext

Verfügbarkeit prüfen

Nomenclature for alleles of the thiopurine methyltransferase gene

Pharmacogenetics and genomics, , Vol.23 (4), p.242-248

Link zum Volltext

Verfügbarkeit prüfen

CYP2C19 and nongenetic factors predict poor responsiveness to clopidogrel loading dose after coronary stent implantation

Pharmacogenomics, 2008-09, Vol.9 (9), p.1251

2008

Link zum Volltext

Verfügbarkeit prüfen

Thioredoxin 1 (Trx1) is associated with poor prognosis in clear cell renal cell carcinoma (ccRCC): an example for the crucial role of redox signaling in ccRCC

World journal of urology, 2022-03, Vol.40 (3), p.739-746

2022

Link zum Volltext

Verfügbarkeit prüfen

Improved Prediction of Endoxifen Metabolism by CYP2D6 Genotype in Breast Cancer Patients Treated with Tamoxifen

Frontiers in pharmacology, 2017-08, Vol.8, p.582

2017

Link zum Volltext

Verfügbarkeit prüfen

A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort

Frontiers in genetics, 2019, Vol.10, p.7-7

2019

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 220

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(208)
Mit Volltextzugriff
(198)

Publikationsform

Sprache

Englisch
(219)
Japanisch
(39)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Clinical Pharmacology And Therapeutics
(13)
Gastroenterology
(11)
Cancer Research
(8)
Plos One
(7)
Blood
(5)
British Journal Of Clinical Pharmacology
(5)
Genome Medicine
(5)
Pharmacogenetics
(5)
Pharmacogenetics And Genomics
(5)
Clinical Chemistry
(4)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Impact of Genetic Polymorphisms of ABCB1 (MDR1, P-Glycoprotein) on Drug Disposition and Potential Clinical Implications: Update of the Literature

Clinical and Functional Relevance of the Monocarboxylate Transporter Family in Disease Pathophysiology and Drug Therapy

Hepatic solute carrier transporters and drug therapy: Regulation of expression and impact of genetic variation

Mechanisms and assessment of statin‐related muscular adverse effects

Impact of NUDT15 genetics on severe thiopurine-related hematotoxicity in patients with European ancestry

Impact of Membrane Drug Transporters on Resistance to Small-Molecule Tyrosine Kinase Inhibitors

Metformin and cancer: from the old medicine cabinet to pharmacological pitfalls and prospects

Expression of organic cation transporters OCT1 (SLC22A1) and OCT3 (SLC22A3) is affected by genetic factors and cholestasis in human liver

Proton pump inhibitors inhibit metformin uptake by organic cation transporters (OCTs)

Role of Genetic and Nongenetic Factors for Fluorouracil Treatment-Related Severe Toxicity: A Prospective Clinical Trial by the German 5-FU Toxicity Study Group

Selective p38α MAP kinase/MAPK14 inhibition in enzymatically modified LDL‐stimulated human monocytes: implications for atherosclerosis

Combinations of common SNPs of the transporter gene ABCB1 influence apparent bioavailability, but not renal elimination of oral digoxin

Reduced Paneth Cell α-Defensins in Ileal Crohn's Disease

Selective Inhibition of the Lactate Transporter MCT4 Reduces Growth of Invasive Bladder Cancer

Copy number variation profiling in pharmacogenes using panel-based exome resequencing and correlation to human liver expression

Novel drug transporter substrates identification: An innovative approach based on metabolomic profiling, in silico ligand screening and biological validation

Hepatic sinusoidal obstruction syndrome and short-term application of 6-thioguanine in pediatric acute lymphoblastic leukemia

No association of genetic variants in TLR4, TNF-α, IL10, IFN-γ, and IL37 in cytomegalovirus-positive renal allograft recipients with active CMV infection-Subanalysis of the prospective randomised VIPP study

Platelet miRNAs: differential expression in coronary artery disease and associations with course of left ventricular systolic function

Aberrant splicing caused by single nucleotide polymorphism c.516G>T [Q172H], a marker of CYP2B66, is responsible for decreased expression and activity of CYP2B6 in liver

Nomenclature for alleles of the thiopurine methyltransferase gene

CYP2C19 and nongenetic factors predict poor responsiveness to clopidogrel loading dose after coronary stent implantation

Thioredoxin 1 (Trx1) is associated with poor prognosis in clear cell renal cell carcinoma (ccRCC): an example for the crucial role of redox signaling in ccRCC

Improved Prediction of Endoxifen Metabolism by CYP2D6 Genotype in Breast Cancer Patients Treated with Tamoxifen

A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort

Suchergebnisse filtern