UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 39

Sortiert nach

Methotrexate pharmacogenetics in the treatment of rheumatoid arthritis

Pharmacogenomics, 2019-11, Vol.20 (17), p.1235-1245

2019

Volltextzugriff (PDF)

Genetic variant rs16944 in IL1B gene is a risk factor for early-onset sepsis susceptibility and outcome in preterm infants

Inflammation research, 2020-02, Vol.69 (2), p.155-157

2020

Volltextzugriff (PDF)

Association between Tumor Necrosis Factor-α Promoter -308 G/A Polymorphism and Early Onset Sepsis in Preterm Infants

The Tohoku Journal of Experimental Medicine, 2019, Vol.247(4), pp.259-264

2019

Volltextzugriff (PDF)

Analysis of association of ADORA2A and ADORA3 polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis

The pharmacogenomics journal, 2020-12, Vol.20 (6), p.784-791

2020

Volltextzugriff (PDF)

Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents

Archives of medical science, 2023-01, Vol.19 (3), p.593-599

2023

Volltextzugriff (PDF)

Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis Pigmentosa

American journal of human genetics, 2010-09, Vol.87 (3), p.376-381

2010

Volltextzugriff (PDF)

Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism

Neurological research (New York), 2021-04, Vol.43 (4), p.321-326

2021

Volltextzugriff (PDF)

High-quality draft genome sequence of Pseudomonas aeruginosa san ai, an environmental isolate resistant to heavy metals

Extremophiles : life under extreme conditions, 2019-07, Vol.23 (4), p.399-405

2019

Volltextzugriff (PDF)

Association of C35T polymorphism in dihydrofolate reductase gene with toxicity of methotrexate in rheumatoid arthritis patients

Expert opinion on drug metabolism & toxicology, 2019-03, Vol.15 (3), p.253-257

2019

Volltextzugriff (PDF)

PPARGC1A gene polymorphism and its association with obesity-related metabolic traits in Serbian adolescent population

Genetika (Beograd), 2022, Vol.54 (3), p.1375-1384

2022

Volltextzugriff (PDF)

Galectin 3 (LGALS3) Gene Polymorphisms Are Associated with Biochemical Parameters and Primary Disease in Patients with End-Stage Renal Disease in Serbian Population

Journal of clinical medicine, 2022-07, Vol.11 (13), p.3874

2022

Volltextzugriff (PDF)

Association between isolated mild symmetrical ventriculomegaly and fetal chromosomal aberrations

Genetika (Beograd), 2021, Vol.53 (3), p.1007-1015

2021

Volltextzugriff (PDF)

Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies

Vojnosanitetski pregled, 2020, Vol.77 (4), p.387-394

2020

Volltextzugriff (PDF)

Analysis of T-786C and 4a/b endothelial nitric oxide synthase gene polymorphisms in retinopathy of prematurity

Genetika (Beograd), 2016, Vol.48 (2), p.707-716

2016

Volltextzugriff (PDF)

Galectin 3 rs4644 gene polymorphism is associated with metabolic traits in Serbian adolescent population

Journal of medical biochemistry, 2024-06, Vol.43 (4), p.445-450

2024

Volltextzugriff (PDF)

Phenotypic presentation of thrombophilia in double heterozygote for factor v leiden and prothrombin 20210 G>A mutations: Case report

Genetika (Beograd), 2014, Vol.46 (2), p.621-629

2014

Volltextzugriff (PDF)

Prevalence of five pharmacologically most important CYP2C9 and CYP2C19 allelic variants in the population from the Republic of Srpska in Bosnia and Herzegovina

Arhiv za higijenu rada i toksikologiju, 2021-06, Vol.72 (2), p.129-134

2021

Volltextzugriff (PDF)

The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies

Vojnosanitetski pregled, 2023, Vol.80 (3), p.201-207

2023

Volltextzugriff (PDF)

4472 POLYMORPHISMS OF THE GENE FOR GALECTIN-3 IN PATIENTS IN THE TERMINAL PHASE OF RENAL INSUFFICIENCY

Nephrology, dialysis, transplantation, 2023-06, Vol.38 (Supplement_1)

2023

Volltextzugriff (PDF)

Distribution of apolipoprotein E gene polymorphism in students and in high-educated elderly from Serbia

Genetika (Beograd), 2013, Vol.45 (3), p.865-872

2013

Volltextzugriff (PDF)

Association of IL-6 rs1800795, but not TNF-α rs1800629, and IL-1β rs16944 polymorphisms' genotypes with recovery of ischemic stroke patients following thrombolysis

Neurological research (New York), 2024-02, Vol.46 (2), p.157-164

2024

Volltextzugriff (PDF)

Analysis of association of ADORA.sub.2A and ADORA.sub.3 polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis

The pharmacogenomics journal, 2020-12, Vol.20 (6), p.784

2020

Volltextzugriff (PDF)

TT genotype of the MMP‐9‐1562C/T polymorphism may be a risk factor for thrombolytic therapy‐induced hemorrhagic complications after acute ischemic stroke

Pharmacotherapy, 2021-07, Vol.41 (7), p.562-571

2021

Volltextzugriff (PDF)

Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients

Journal of clinical laboratory analysis, 2022-06, Vol.36 (6), p.e24441-n/a

2022

Volltextzugriff (PDF)

Genetic polymorphisms and Methotrexate response in patients with rheumatoid arthritis

Journal of Research in Pharmacy, 2024, Vol.28(4) (28(4)), p.1285-1292

2024

Volltextzugriff (PDF)

1 – 25 von 39

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(28)
Mit Volltextzugriff
(30)

Publikationsform

Artikel
(38)
Dissertationen
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Methotrexate pharmacogenetics in the treatment of rheumatoid arthritis

Genetic variant rs16944 in IL1B gene is a risk factor for early-onset sepsis susceptibility and outcome in preterm infants

Association between Tumor Necrosis Factor-α Promoter -308 G/A Polymorphism and Early Onset Sepsis in Preterm Infants

Analysis of association of ADORA2A and ADORA3 polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis

Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents

Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis Pigmentosa

Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism

High-quality draft genome sequence of Pseudomonas aeruginosa san ai, an environmental isolate resistant to heavy metals

Association of C35T polymorphism in dihydrofolate reductase gene with toxicity of methotrexate in rheumatoid arthritis patients

PPARGC1A gene polymorphism and its association with obesity-related metabolic traits in Serbian adolescent population

Galectin 3 (LGALS3) Gene Polymorphisms Are Associated with Biochemical Parameters and Primary Disease in Patients with End-Stage Renal Disease in Serbian Population

Association between isolated mild symmetrical ventriculomegaly and fetal chromosomal aberrations

Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies

Analysis of T-786C and 4a/b endothelial nitric oxide synthase gene polymorphisms in retinopathy of prematurity

Galectin 3 rs4644 gene polymorphism is associated with metabolic traits in Serbian adolescent population

Phenotypic presentation of thrombophilia in double heterozygote for factor v leiden and prothrombin 20210 G>A mutations: Case report

Prevalence of five pharmacologically most important CYP2C9 and CYP2C19 allelic variants in the population from the Republic of Srpska in Bosnia and Herzegovina

The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies

4472 POLYMORPHISMS OF THE GENE FOR GALECTIN-3 IN PATIENTS IN THE TERMINAL PHASE OF RENAL INSUFFICIENCY

Distribution of apolipoprotein E gene polymorphism in students and in high-educated elderly from Serbia

Association of IL-6 rs1800795, but not TNF-α rs1800629, and IL-1β rs16944 polymorphisms' genotypes with recovery of ischemic stroke patients following thrombolysis

Analysis of association of ADORA.sub.2A and ADORA.sub.3 polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis

TT genotype of the MMP‐9‐1562C/T polymorphism may be a risk factor for thrombolytic therapy‐induced hemorrhagic complications after acute ischemic stroke

Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients

Genetic polymorphisms and Methotrexate response in patients with rheumatoid arthritis

Suchergebnisse filtern