208 results on '"Sharma, Swarkar"'
Search Results
2. Human Y Chromosome: Genetic Markers, Implications, and Pathologies
3. SOX9 gene shows association with adolescent idiopathic scoliosis predisposition in Northwest Indians
4. A novel ZRS variant causes preaxial polydactyly type I by increased sonic hedgehog expression in the developing limb bud
5. Metabolic syndrome and underlying genetic determinants-A systematic review
6. Genotyping of T2D susceptible genes in a high risk North-East Indian population
7. Candidate gene association study of UCP3 variant rs1800849 with T2D in Mizo population of Northeast India
8. MACF1 gene variant rs2296172 is associated with T2D susceptibility in Mizo population from Northeast India
9. A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females.
10. Gastric cancer in Jammu and Kashmir, India: A review of genetic perspectives
11. Replication of MACF1 gene variant rs2296172 with type 2 diabetes susceptibility in the Bania population group of Punjab, India
12. Publisher Correction: A genetic analysis identifies a haplotype at adiponectin locus: Association with obesity and type 2 diabetes
13. Telomere Maintenance Genes are associated with Type 2 Diabetes Susceptibility in Northwest Indian Population Group
14. A genetic analysis identifies a haplotype at adiponectin locus: Association with obesity and type 2 diabetes
15. ddRAD sequencing-based identification of inter-genepool SNPs and association analysis in Brassica juncea
16. Association of Human Leukocyte Antigen Gene Variants rs13192471 and rs6457617 with Rheumatoid Arthritis Susceptibility: A Case-control Study from North-western India
17. Genetic Characterisation of Pantothenate Kinase Associated Neurodegeneration (PKAN) in a Consanguineous Family from Jammu and Kashmir India
18. First Report of Evaluation of Variant rs11190870 near LBX1 with Adolescent Idiopathic Scoliosis Susceptibility in a South-Asian Indian Population
19. First Report of Evaluation of Variant rs11190870 nearby LBX1 Gene with Adolescent Idiopathic Scoliosis Susceptibility in a South-Asian Indian Population.
20. Current Understanding of Genetic Factors in Idiopathic Scoliosis
21. LRFN2 gene variant rs2494938 provides susceptibility to esophageal cancer in the population of Jammu and Kashmir
22. Origin and spread of human mitochondrial DNA haplogroup U7
23. Missense Variation in TPP1 Gene causes Neuronal Ceroid Lipofuscinosis Type 2 in a Family from Jammu and Kashmir-India
24. Missense Variation in TPP1 Gene causes Neuronal Ceroid Lipofuscinosis Type 2 in a Family from Jammu and Kashmir-India
25. Biophysical characterization of double-stranded oligonucleotides using ETBR and isothermal fluorescence spectroscopy: Implication for SNP genotyping
26. A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups
27. Newly identified genetic variant rs2294693 in UNC5CL gene is associated with decreased risk of esophageal carcinoma in the J&K Population–India
28. Dual labeled fluorescence probe based qPCR assay to measure the telomere length
29. Association of Genetic Variants of ELMO1 Gene With Diabetic Nephropathy in the North Indian Population
30. PGC-1α Thr394Thr and Gly482Ser variants are significantly associated with T2DM in two North Indian populations: a replicate case-control study
31. The possible role of 10398A and 16189C mtDNA variants in providing susceptibility toT2DM in two North Indian populations: a replicative study
32. Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer
33. IL-10 promoter single nucleotide polymorphisms are significantly associated with resistance to leprosy
34. Human mtDNA hypervariable regions, HVR I and II, hint at deep common maternal founder and subsequent maternal gene flow in Indian population groups
35. Current Understanding of Genetic Factors in Idiopathic Scoliosis
36. Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes
37. Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India
38. ACE2 Homo-dimerization, Human Genomic variants and Interaction of Host Proteins Explain High Population Specific Differences in Outcomes of COVID19
39. Gastric cancer in Jammu and Kashmir, India: A review of genetic perspectives
40. LRFN2 gene variant rs2494938 provides susceptibility to esophageal cancer in the population of Jammu and Kashmir
41. Concomitant presence of mutations in mitochondrial genome and p53 in cancer development—A study in north Indian sporadic breast and esophageal cancer patients
42. Genetic affinity among five different population groups in India reflecting a Y-chromosome gene flow
43. TDT-HET: A new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data
44. A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcifications
45. Novel Dual Labeled Fluorescence Probe Based Assay to Measure the Telomere Length
46. A novel subgroup Q5 of human Y-chromosomal haplogroup Q in India
47. gene variant rs2494938 provides susceptibility to esophageal cancer in the population of Jammu and Kashmir.
48. Ancient Human Migrations to and through Jammu Kashmir- India were not of Males Exclusively
49. Replication of MACF1 gene variant rs2296172 with type 2 diabetes susceptibility in the Bania population group of Punjab, India
50. Geographic Isolation and Endogamous Practices Provide Higher Risk of Genetic Disorders in Jammu and Kashmir
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