49 results on '"Abid, Aiysha"'
Search Results
2. The prevalence of pharmacogenetic variants of vitamin K epoxide reductase complex subunit 1 gene (rs9923231), cytochrome P450 family 2 subfamily C member 9 gene (rs1799853) and cytochrome P450 family 3 subfamily-A member-5 gene (rs776746) among 13 ethnic groups of Pakistan
3. Primary hyperoxaluria and genetic linkages: an insight into the disease burden from Pakistan
4. Association of specific single nucleotide variants (SNVs) in the promoter and 3′-Untranslated region of Vascular Endothelial growth factor (VEGF) gene with risk and higher tumour grade of head and neck cancers
5. Possible ethnic associations in primary hyperoxaluria type-III-associated HOGA1 sequence variants
6. Association of vitamin D receptor gene polymorphisms and risk of urolithiasis: results of a genetic epidemiology study and comprehensive meta-analysis
7. CYP3A5 gene polymorphisms and their impact on dosage and trough concentration of tacrolimus among kidney transplant patients: a systematic review and meta-analysis
8. Osteopontin promoter polymorphisms and risk of urolithiasis: a candidate gene association and meta-analysis study
9. HOGA1 gene pathogenic variants in primary hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic association
10. The association of urinary interferon-gamma inducible protein-10 (IP10/CXCL10) levels with kidney allograft rejection
11. Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease‐associated pathogenic variants
12. Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease
13. sj-pdf-2-evb-10.1177_11769343221095834 – Supplemental material for The Prevalence of Pharmacogenomics Variants and Their Clinical Relevance Among the Pakistani Population
14. sj-docx-3-evb-10.1177_11769343221095834 – Supplemental material for The Prevalence of Pharmacogenomics Variants and Their Clinical Relevance Among the Pakistani Population
15. sj-docx-4-evb-10.1177_11769343221095834 – Supplemental material for The Prevalence of Pharmacogenomics Variants and Their Clinical Relevance Among the Pakistani Population
16. The Prevalence of Pharmacogenomics Variants and Their Clinical Relevance Among the Pakistani Population
17. Absence of Glutathione S-Transferase Theta 1 Gene Is Significantly Associated With Breast Cancer Susceptibility in Pakistani Population and Poor Overall Survival in Breast Cancer Patients: A Case-Control and Case Series Analysis
18. Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease‐associated pathogenic variants.
19. Independent and Combined Associations of 677C/T and 1298A/C Polymorphisms in the MTHFR gene with Breast Cancers in a South-Asian Population
20. Strong and Significant Associations of Single Nucleotide Variants (SNVs) in the Promoter and 3’-Untranslated Region (3’-UTR) ofVascular Endothelial Growth Factor(VEGF) Gene with Head and Neck Cancers
21. Role of Ecologic ACE I/D Polymorphism Data Towards Prediction of COVID-19 Epidemiology
22. Refinement of the locus for autosomal recessive cone–rod dystrophy (CORD8) linked to chromosome 1q23–q24 in a Pakistani family and exclusion of candidate genes
23. ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous
24. Osteopontin promoter polymorphisms and risk of urolithiasis: a candidate gene association and meta-analysis study
25. Novel Genetic Variations in Acute Myeloid Leukemia in Pakistani Population
26. Locus heterogeneity and Knobloch syndrome
27. Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2
28. Mutation screening of Pakistani families with congenital eye disorders
29. Association of vitamin D receptor gene polymorphisms and risk of urolithiasis: results of a genetic epidemiology study and comprehensive meta-analysis
30. Association analysis of the VEGF gene variants with breast cancer susceptibility and tumor characteristics in an indigenous population: A pilot study
31. A Novel Nonsense Mutation in FERMT3 Causes LAD-III in a Pakistani Family
32. Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome
33. Monocyte Chemoattractant Protein-1 (MCP-1/CCL2) Levels and Its Association with Renal Allograft Rejection
34. Analysis of the glutathione S-transferase genes polymorphisms in the risk and prognosis of renal cell carcinomas. Case-control and meta-analysis
35. Monocyte Chemoattractant Protein-1 (MCP-1/CCL2) Levels and Its Association with Renal Allograft Rejection.
36. Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan
37. RE: Steroid-resistant nephrotic syndrome: impact of genetic testing
38. HLA class I and II polymorphisms in the Gujjar population from Pakistan
39. The effect of chemokine receptor gene polymorphisms (CCR2V64I, CCR5-59029G>A and CCR5Δ32) on renal allograft survival in Pakistani transplant patients
40. A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan
41. Erratum to “Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children” [Gene 493 (2012) 165–168]
42. Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children
43. Association of a Single-Nucleotide Polymorphism in the Promoter Region of the VEGF Gene with the Risk of Renal Cell Carcinoma
44. Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotype.
45. Unique molecular alteration patterns in von Hippel-Lindau(VHL)gene in a cohort of sporadic renal cell carcinoma patients from Pakistan
46. Re: NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in south-west Iranian children.
47. Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotype.
48. Genetic heterogeneity for autosomal dominant familial hypertrophic cardiomyopathy in a Pakistani family.
49. Gene symbol: AIPL1. Disease: LCA4.
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