260 results on '"Elango, Ramu"'
Search Results
2. The use of therapeutic drug monitoring for early identification of vedolizumab response in Saudi Arabian patients with inflammatory bowel disease
3. Exploring somatic mutations in BRAF , KRAS , and NRAS as therapeutic targets in Saudi colorectal cancer patients through massive parallel sequencing and variant classification.
4. Genetic association study of NOD2 and IL23R amino acid substitution polymorphisms in Saudi Inflammatory Bowel Disease patients
5. Multilevel systems biology analysis of lung transcriptomics data identifies key miRNAs and potential miRNA target genes for SARS-CoV-2 infection
6. Diagnostic Revolution Post-Human Genome Sequence Project: High-Throughput Technologies and Bioinformatics
7. Finding a Needle in a Haystack: Variant Effect Predictor (VEP) Prioritizes Disease Causative Variants from Millions of Neutral Ones
8. Driving Forces of Bioinformatics
9. Understanding the Regulatory Features of Co-regulated Genes Using Distant Regulatory Elements (DiRE) Genomic Tool in Health and Disease
10. Genetic Association from RFLPs to Millions of Variant Markers: Unravelling the Genetic Complexity of Diseases
11. Tools and Methods in Analysis of Complex Sequences
12. Introduction to Biological Databases
13. Molecular Docking
14. In Silico PCR
15. Myocardial infarction biomarker discovery with integrated gene expression, pathways and biological networks analysis
16. Whole exome sequencing of a Saudi family and systems biology analysis identifies CPED1 as a putative causative gene to Celiac Disease
17. Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients
18. Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects
19. Exploring celiac disease candidate pathways by global gene expression profiling and gene network cluster analysis
20. Protein structural insights into a rare PCSK9 gain-of-function variant (R496W) causing familial hypercholesterolemia in a Saudi family: whole exome sequencing and computational analysis
21. Rare variant burden analysis from exomes of three consanguineous families reveals LILRB1 and PRSS3 as potential key proteins in inflammatory bowel disease pathogenesis
22. Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment
23. Computational approaches for discovering significant microRNAs, microRNA-mRNA regulatory pathways, and therapeutic protein targets in endometrial cancer
24. Potential Biomarkers for Parkinson Disease from Functional Enrichment and Bioinformatic Analysis of Global Gene Expression Patterns of Blood and Substantia Nigra Tissues
25. Bioinformatics insights into the genes and pathways on severe COVID-19 pathology in patients with comorbidities
26. Structural characterization and conformational dynamics of alpha-1 antitrypsin pathogenic variants causing alpha-1-antitrypsin deficiency
27. A comparative mRNA- and miRNA transcriptomics reveals novel molecular signatures associated with metastatic prostate cancers
28. Identification of miRNA–mRNA–TFs regulatory network and crucial pathways involved in asthma through advanced systems biology approaches
29. Integrative weighted molecular network construction from transcriptomics and genome wide association data to identify shared genetic biomarkers for COPD and lung cancer
30. Distribution of CYP2C8 and CYP2C9 amino acid substitution alleles in South Indian diabetes patients: A genotypic and computational protein phenotype study
31. Replication of GWAS loci revealed the moderate effect of TNRC6B locus on susceptibility of Saudi women to develop uterine leiomyomas
32. Integrative global co-expression analysis identifies key microRNA-target gene networks as key blood biomarkers for obesity
33. Complex Inheritance of Rare Missense Variants in PAK2, TAP2, and PLCL1 Genes in a Consanguineous Arab Family With Multiple Autoimmune Diseases Including Celiac Disease
34. Exome Sequencing Identifies the Extremely Rare ITGAV and FN1 Variants in Early Onset Inflammatory Bowel Disease Patients
35. iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors
36. Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease
37. Transcriptome-Based Molecular Networks Uncovered Interplay Between Druggable Genes of CD8+ T Cells and Changes in Immune Cell Landscape in Patients With Pulmonary Tuberculosis
38. Evidence for the presence of somatic mitochondrial DNA mutations in right atrial appendage tissues of coronary artery disease patients
39. Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects
40. LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study
41. Saudi Familial Hypercholesterolemia Patients With Rare LDLR Stop Gain Variant Showed Variable Clinical Phenotype and Resistance to Multiple Drug Regimen
42. TagSNP approach for HLA risk allele genotyping of Saudi celiac disease patients: effectiveness and pitfalls
43. Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families
44. Molecular differential analysis of uterine leiomyomas and leiomyosarcomas through weighted gene network and pathway tracing approaches
45. Fine mapping of Ath6, a quantitative trait locus for atherosclerosis in mice
46. Integrative system biology and mathematical modeling of genetic networks identifies shared biomarkers for obesity and diabetes.
47. Identification of Causative Variants Contributing to Nonsyndromic Orofacial Clefts Using Whole-Exome Sequencing in a Saudi Family
48. Assessing the role of serum prolactin levels and coding region somatic mutations of the prolactin gene in Saudi uterine leiomyoma patients
49. Molecular profiling of lamellar ichthyosis pathogenic missense mutations on the structural and stability aspects of TGM1 protein
50. Myocardial Infarction Biomarker Discovery with Integrated Gene Expression, Pathways and Biological Networks analysis
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