Pages that link to "Q33358619"

The following pages link to Highly multiplexed genotyping of thiopurine s-methyltransferase variants using MALD-TOF mass spectrometry: reliable genotyping in different ethnic groups (Q33358619):

Displaying 49 items.

• Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies (Q30244222) (← links)
• Interleukin-6 receptor rs7529229 T/C polymorphism is associated with left main coronary artery disease phenotype in a Chinese population (Q31155261) (← links)
• Expression of organic cation transporters OCT1 (SLC22A1) and OCT3 (SLC22A3) is affected by genetic factors and cholestasis in human liver (Q33480591) (← links)
• A multiplex MALDI-TOF MS approach facilitates genotyping of DNA from formalin-fixed paraffin-embedded tumour specimens (Q33677062) (← links)
• Polymorphisms in genes of interleukin 12 and its receptors and their association with protection against severe malarial anaemia in children in western Kenya (Q33806859) (← links)
• Application of the iPLEX™ Gold SNP genotyping method for the analysis of Amerindian ancient DNA samples: benefits for ancient population studies (Q33813793) (← links)
• Variant allele of CHEK2 is associated with a decreased risk of esophageal cancer lymph node metastasis in a Chinese population (Q34112490) (← links)
• A Polymorphism in Hepatocyte Nuclear Factor 1 Alpha, rs7310409, Is Associated with Left Main Coronary Artery Disease (Q34118788) (← links)
• Influence of MIF, CD40, and CD226 polymorphisms on risk of rheumatoid arthritis (Q34149621) (← links)
• Influence of BLK polymorphisms on the risk of rheumatoid arthritis (Q34319443) (← links)
• A variant allele of ADH1B and ALDH2, is associated with the risk of esophageal cancer (Q34444267) (← links)
• Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population (Q34660639) (← links)
• Evaluation of nanofluidics technology for high-throughput SNP genotyping in a clinical setting (Q34801132) (← links)
• The genetic contribution of CIDEA polymorphisms, haplotypes and loci interaction to obesity in a Han Chinese population (Q34993945) (← links)
• TOMM40 rs2075650 polymorphism shows no association with neovascular age-related macular degeneration or polypoidal choroidal vasculopathy in a Chinese population (Q35022261) (← links)
• Pharmacogenetics in Ghana: reviewing the evidence (Q35172002) (← links)
• Uracil-DNA glycosylase (UNG) rs246079 G/A polymorphism is associated with decreased risk of esophageal cancer in a Chinese population (Q35318470) (← links)
• Gene-gene interaction of CFH, ARMS2, and ARMS2/HTRA1 on the risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in Chinese population (Q35577431) (← links)
• COL8A1 rs13095226 polymorphism shows no association with neovascular age-related macular degeneration or polypoidal choroidal vasculopathy in Chinese subjects (Q35855286) (← links)
• Effect of High-Density Lipoprotein Metabolic Pathway Gene Variations and Risk Factors on Neovascular Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy in China (Q35857083) (← links)
• Thiopurine S-methyltransferase testing for averting drug toxicity in patients receiving thiopurines: a systematic review (Q35971977) (← links)
• Association between Polymorphisms in Interleukins 4 and 13 Genes and Chronic Periodontitis in a Han Chinese Population (Q36022021) (← links)
• MiR-196a2 rs11614913 T>C Polymorphism is Associated with an Increased Risk of Tetralogy of Fallot in a Chinese Population. (Q36721564) (← links)
• Genetics is a major determinant of expression of the human hepatic uptake transporter OATP1B1, but not of OATP1B3 and OATP2B1 (Q36998199) (← links)
• Nomenclature for alleles of the thiopurine methyltransferase gene (Q37056505) (← links)
• TPMT genetic variants are associated with increased rejection with azathioprine use in heart transplantation (Q37490046) (← links)
• Common Variant in Glycoprotein Ia Increases Long-Term Adverse Events Risk After Coronary Artery Bypass Graft Surgery (Q37556281) (← links)
• A Variant in COX-2 Gene Is Associated with Left Main Coronary Artery Disease and Clinical Outcomes of Coronary Artery Bypass Grafting. (Q37618237) (← links)
• Inosine triphosphate pyrophosphatase 94C>A polymorphism: clinical implications for patients with systemic lupus erythematosus treated with azathioprine (Q37724360) (← links)
• Part 3: Pharmacogenetic variability in phase II anticancer drug metabolism (Q37887337) (← links)
• Pharmacogenetics and immunosuppressive drugs in solid organ transplantation (Q38253383) (← links)
• Association of Single-Nucleotide Polymorphisms in DC-SIGN with Nasopharyngeal Carcinoma Susceptibility. (Q38685289) (← links)
• Long noncoding RNAs POLR2E rs3787016 C/T and HULC rs7763881 A/C polymorphisms are associated with decreased risk of esophageal cancer (Q39018064) (← links)
• Genetic polymorphisms of NQO1, CYP1A1 and TPMT and susceptibility to acute lymphoblastic leukemia in a Tunisian population (Q39330661) (← links)
• Thiopurine S-Methyltransferase as a Pharmacogenetic Biomarker: Significance of Testing and Review of Major Methods. (Q39334739) (← links)
• Genetic susceptibility to salt-sensitive hypertension in a Han Chinese population: a validation study of candidate genes (Q40226150) (← links)
• Validation of new allele-specific real-time PCR system for thiopurine methyltransferase genotyping in Korean population (Q41790387) (← links)
• TNNT2 gene polymorphisms are associated with susceptibility to idiopathic dilated cardiomyopathy in the Han Chinese population (Q41808802) (← links)
• Heterozygote of PLCE1 rs2274223 increases susceptibility to human papillomavirus infection in patients with esophageal carcinoma among the Kazakh populations (Q42262374) (← links)
• Relationships between thiopurine S-methyltransferase polymorphism and azathioprine-related adverse drug reactions in Chinese renal transplant recipients (Q46219966) (← links)
• Genetic Polymorphism of Thiopurine S-methyltransferase in Children with Acute Lymphoblastic Leukemia in Jordan (Q49648488) (← links)
• Mucosal improvement in patients with moderate to severe postoperative endoscopic recurrence of Crohn's disease and azathioprine metabolite levels (Q50495588) (← links)
• A pragmatic randomized controlled trial of thiopurine methyltransferase genotyping prior to azathioprine treatment: the TARGET study (Q50518269) (← links)
• Pharmacogenetics of Adverse Drug Reactions (Q57302675) (← links)
• Germline oncopharmacogenetics, a promising field in cancer therapy (Q59504056) (← links)
• Epistatic interactions between thiopurine methyltransferase (TPMT) and inosine triphosphate pyrophosphatase (ITPA) variations determine 6-mercaptopurine toxicity in Indian children with acute lymphoblastic leukemia (Q82082980) (← links)
• Pretreatment determination of TPMT--state of the art in clinical practice (Q83308517) (← links)
• Replication study of PLCE1 and C20orf54 polymorphism and risk of esophageal cancer in a Chinese population (Q84490516) (← links)
• A functional polymorphism in the promoter of αA-crystallin increases the risk of nAMD (Q92618125) (← links)