UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 53

Sortiert nach

Effect of CYP2C19 and ABCB1 single nucleotide polymorphisms on outcomes of treatment with ticagrelor versus clopidogrel for acute coronary syndromes: a genetic substudy of the PLATO trial

The Lancet (British edition), 2010-10, Vol.376 (9749), p.1320-1328

2010

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide association studies: theoretical and practical concerns

Nature reviews. Genetics, 2005-02, Vol.6 (2), p.109-118

2005

Link zum Volltext

Verfügbarkeit prüfen

Lack of association between SLCO1B1 polymorphisms and clinical myalgia following rosuvastatin therapy

The American heart journal, 2013-06, Vol.165 (6), p.1008-1014

2013

Link zum Volltext

Verfügbarkeit prüfen

Effect of genetic variations on ticagrelor plasma levels and clinical outcomes

European heart journal, 2015-08, Vol.36 (29), p.1901-1912

2015

Link zum Volltext

Verfügbarkeit prüfen

Remapping the Insulin Gene/IDDM2 Locus in Type 1 Diabetes

Diabetes (New York, N.Y.), 2004-07, Vol.53 (7), p.1884-1889

2004

Link zum Volltext

Verfügbarkeit prüfen

Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet inhibition and patient Outcomes study

The American heart journal, 2014-07, Vol.168 (1), p.96-102.e2

2014

Link zum Volltext

Verfügbarkeit prüfen

Pharmacogenetic determinants of statin-induced reductions in C-reactive protein

Circulation. Cardiovascular genetics, 2012-02, Vol.5 (1), p.58

2012

Link zum Volltext

Verfügbarkeit prüfen

Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial

Circulation. Cardiovascular genetics, 2012-04, Vol.5 (2), p.257

2012

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome

Human molecular genetics, 2016-04, Vol.25 (7), p.1447-1456

2016

Link zum Volltext

Verfügbarkeit prüfen

Molecular and genetic association of interleukin-6 in tacrine-induced hepatotoxicity

Pharmacogenetics and genomics, 2007-11, Vol.17 (11), p.961-972

2007

Link zum Volltext

Verfügbarkeit prüfen

Maternal-Fetal Interactions and Birth Order Influence Insulin Variable Number of Tandem Repeats Allele Class Associations with Head Size at Birth and Childhood Weight Gain

Diabetes (New York, N.Y.), 2004-04, Vol.53 (4), p.1128-1133

2004

Link zum Volltext

Verfügbarkeit prüfen

Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects

Genetic epidemiology, 2004-04, Vol.26 (3), p.167-185

2004

Link zum Volltext

Verfügbarkeit prüfen

SNP allele frequency estimation in DNA pools and variance components analysis

BioTechniques, 2004-05, Vol.36 (5), p.840-845

2004

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy

Circulation. Cardiovascular genetics, 2012-12, Vol.5 (6), p.676

2012

Link zum Volltext

Verfügbarkeit prüfen

NLRC4 Inflammasome Is an Important Regulator of Interleukin-18 Levels in Patients With Acute Coronary Syndromes: Genome-Wide Association Study in the PLATelet inhibition and patient Outcomes Trial (PLATO)

Circulation. Cardiovascular genetics, 2015-06, Vol.8 (3), p.498

2015

Link zum Volltext

Verfügbarkeit prüfen

Haplotype Tag Single Nucleotide Polymorphism Analysis of the Human Orthologues of the Rat Type 1 Diabetes Genes Ian4 (Lyp/Iddm1) and Cblb

Diabetes (New York, N.Y.), 2004-02, Vol.53 (2), p.505-509

2004

Link zum Volltext

Verfügbarkeit prüfen

Differential Genetic Effects on Statin-Induced Changes Across Low-Density Lipoprotein-Related Measures

Circulation. Cardiovascular genetics, 2015-10, Vol.8 (5), p.688

2015

Link zum Volltext

Verfügbarkeit prüfen

Investigating the utility of combining Φ29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray™ genotyping

BMC biotechnology, 2004-07, Vol.4 (1), p.15-15

2004

Link zum Volltext

Verfügbarkeit prüfen

Tacrine-induced liver damage: an analysis of 19 candidate genes

Pharmacogenetics and genomics, 2007-12, Vol.17 (12), p.1091-1100

2007

Link zum Volltext

Verfügbarkeit prüfen

Association Analysis of the Lymphocyte-Specific Protein Tyrosine Kinase (LCK) Gene in Type 1 Diabetes

Diabetes (New York, N.Y.), 2004-09, Vol.53 (9), p.2479-2482

2004

Link zum Volltext

Verfügbarkeit prüfen

Serious carbamazepine-induced hypersensitivity reactions associated with the HSP70 gene cluster

Pharmacogenetics and genomics, 2006-04, Vol.16 (4), p.287-296

2006

Link zum Volltext

Verfügbarkeit prüfen

Optimizing the power of genome-wide association studies by using publicly available reference samples to expand the control group

Genetic epidemiology, 2010-05, Vol.34 (4), p.319-326

2010

Link zum Volltext

Verfügbarkeit prüfen

Interstitial lung disease in gefitinib-treated Japanese patients with non-small-cell lung cancer: genome-wide analysis of genetic data

Pharmacogenomics, 2011-07, Vol.12 (7), p.965-975

2011

Link zum Volltext

Verfügbarkeit prüfen

Lack of Association of the Ala45Thr Polymorphism and Other Common Variants of the NeuroD Gene With Type 1 Diabetes

Diabetes (New York, N.Y.), 2004-04, Vol.53 (4), p.1158-1161

2004

Link zum Volltext

Verfügbarkeit prüfen

Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics

Human genomics, 2004-01, Vol.1 (2), p.98-109

2004

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 53

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(50)
Mit Volltextzugriff
(45)

Publikationsform

Artikel
(52)
Buchkapitel
(1)

Sprache

Englisch
(53)
Japanisch
(8)

Erscheinungsjahr

n.n

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Effect of CYP2C19 and ABCB1 single nucleotide polymorphisms on outcomes of treatment with ticagrelor versus clopidogrel for acute coronary syndromes: a genetic substudy of the PLATO trial

Genome-wide association studies: theoretical and practical concerns

Lack of association between SLCO1B1 polymorphisms and clinical myalgia following rosuvastatin therapy

Effect of genetic variations on ticagrelor plasma levels and clinical outcomes

Remapping the Insulin Gene/IDDM2 Locus in Type 1 Diabetes

Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet inhibition and patient Outcomes study

Pharmacogenetic determinants of statin-induced reductions in C-reactive protein

Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial

Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome

Molecular and genetic association of interleukin-6 in tacrine-induced hepatotoxicity

Maternal-Fetal Interactions and Birth Order Influence Insulin Variable Number of Tandem Repeats Allele Class Associations with Head Size at Birth and Childhood Weight Gain

Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects

SNP allele frequency estimation in DNA pools and variance components analysis

Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy

NLRC4 Inflammasome Is an Important Regulator of Interleukin-18 Levels in Patients With Acute Coronary Syndromes: Genome-Wide Association Study in the PLATelet inhibition and patient Outcomes Trial (PLATO)

Haplotype Tag Single Nucleotide Polymorphism Analysis of the Human Orthologues of the Rat Type 1 Diabetes Genes Ian4 (Lyp/Iddm1) and Cblb

Differential Genetic Effects on Statin-Induced Changes Across Low-Density Lipoprotein-Related Measures

Investigating the utility of combining Φ29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray™ genotyping

Tacrine-induced liver damage: an analysis of 19 candidate genes

Association Analysis of the Lymphocyte-Specific Protein Tyrosine Kinase (LCK) Gene in Type 1 Diabetes

Serious carbamazepine-induced hypersensitivity reactions associated with the HSP70 gene cluster

Optimizing the power of genome-wide association studies by using publicly available reference samples to expand the control group

Interstitial lung disease in gefitinib-treated Japanese patients with non-small-cell lung cancer: genome-wide analysis of genetic data

Lack of Association of the Ala45Thr Polymorphism and Other Common Variants of the NeuroD Gene With Type 1 Diabetes

Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics

Suchergebnisse filtern