59 results on '"Genetic polymorphisms -- Health aspects"'
Search Results
2. NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses
3. Use of regularly scheduled albuterol treatment in asthma: genotype-stratified, randomised, placebo-controlled cross-over trial
4. Juvenile chronic arthritis
5. Familial Mediterranean fever
6. Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease
7. Association between beta(sub)2-adrenoceptor polymorphism and susceptibility to bronchodilator desensitisation in moderately severe stable asthmatics
8. Association between polymorphism in gene for microsomal epoxide hydrolase and susceptibility to emphysema
9. Pl(super)A1/A2 polymorphism of platelet glycoprotein IIIa and risks of myocardial infarction, stroke, and venous thrombosis
10. Synergistic effects of angiotensin-converting enzyme and angiotensin-II type 1 receptor gene polymorphisms on risk of myocardial infarction
11. Association of apolipoprotein E polymorphism with outcome after head injury
12. Distribution of codon 129 genotype in human growth hormone-treated CJD patients in France and the UK. (Research Letters)
13. Association between tuberculosis and a polymorphic NFkB binding site in the interferon g gene. (Research letters)
14. Polymorphism in the P2X7 receptor gene and survival in chronic lymphocytic leukaemia. (Mechanism of disease)
15. The P2X7 receptor of CLL lymphocytes--a molecule with a split personality. (Commentary)
16. Prohibitin 39 untranslated region polymorphism and breast cancer risk in Australian women. (Research letters)
17. Association between functional polymorphism in EGF gene and malignant melanoma
18. Autosomal dominant polycystic kidney disease: modification of disease progression
19. CCR5-D32 polymorphism in asthma
20. Cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism confers susceptibility to thyroid associated orbitopathy
21. 4G/5G promoter polymorphism in the plasminogen-activator-inhibitor-1 gene and outcome of meningococcal disease
22. Variation in plasminogen-activator-inhibitor-1 gene and risk of meningococcal septic shock
23. Codon 72 polymorphism of p53 and its association with cervical cancer
24. b2-adrenoceptor gene polymorphism and obesity
25. Warfarin dose requirement and CYP2C9 polymorphisms
26. International consortium SN(i)Ps away at individuality
27. MTHFR gene polymorphism and diabetic nephropathy in type 1 diabetes
28. 5-HT2A promoter polymorphism -1438G/A, anorexia nervosa, and obsessive-compulsive disorder
29. Association at LRP gene locus with sporadic late-onset Alzheimer's disease
30. Heterozygote advantage of the MTHFR gene in patients with neural-tube defect and their relatives
31. Deafness due to Pro250Arg mutation of FGFR3
32. Polymorphism in promoter region of inducible nitric oxide synthase gene and protection against malaria
33. Mitochondrial genotype associated with longevity
34. Chemokine-receptor polymorphisms: clarity or confusion for HIV-1 prognosis?
35. Molecular basis of resistance and susceptibility to malaria
36. Association of Glu 27 beta2-adrenoceptor polymorphism with lower airway reactivity in asthmatic subjects
37. Blood pressure, coronary artery disease, and glycaemic control in type 2 diabetes mellitus: relation to apolipoprotein-CIII gene polymorphism
38. Deletion polymorphism in angiotensin-converting enzyme gene associated with parental history of myocardial infarction
39. Polymorphisms, proteins, and phenotypes
40. Mitochondrial 16189 variant, thinness at birth, and type-2 diabetes
41. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling
42. 5-HT2A gene promoter polymorphism and anorexia nervosa
43. Genetic variation of CYP2A6, smoking, and risk of cancer
44. Beta 2-adrenoceptor gene polymorphism, body weight, and physical activity
45. Assessment of genetic markers for coronary thrombosis: promise and precaution
46. A1/A2 polymorphism of glycoprotein IIIa and association with excess procedural risk for coronary catheter interventions: a case-controlled study
47. Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis
48. Association of two silent polymorphisms of platelet glycoprotein Ia/IIa receptor with risk of myocardial infarction: a case-control study
49. Prevalence of internalisation-associated gene, prtF1, among persisting group-A streptococcus strains isolated from asymptomatic carriers
50. New susceptibility gene for Alzheimer's disease on chromosome 12?
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