24 results on '"Toncheva, Draga"'
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2. Incidence of ancient variants associated with oncological diseases in modern populations
3. Molecular response in long-term monitoring of patients with chronic myelogenic leukemia (CML) on nilotinib therapy
4. Rare genetic variants prioritize molecular pathways for semaphorin interactions in Alzheimer’s disease patients
5. Genes predisposing to obesity emphasize G-protein coupled receptor associated pathways in healthy Bulgarian individuals
6. Expression profiling of muscle invasive and non-invasive bladder tumors for biomarkers identification related to drug resistance, sensitivity and tumor progression
7. Prioritization of genetic variants predisposing to coronary heart disease in the Bulgarian population using centenarian exomes
8. Preimplantation genetic testing: method and two case studies of familial three-way complex translocations
9. SCN8A p.Arg1872Gln mutation in early infantile epileptic encephalopathy type 13: Review and case report
10. Genomics of longevity: recent insights from research on centenarians
11. Long-term follow-up of a female patient with non-classical 11β-hydroxylase deficiency and two novel mutations in CYP11B1
12. Double heterozygosity of novel variants found in patients with severe clinical phenotype of cardiovascular disorders
13. Screening of pharmacogenetic variants associated with drug sensitivity in patients with papillary thyroid carcinoma using next generation sequencing
14. Whole genome microarray analysis in non-small cell lung cancer
15. Whole genome methylation analyses of schizophrenia patients before and after treatment
16. Benign and Unknown Copy Number Variations in Bulgarian Patients with Intellectual Disability and Congenital Malformations
17. Comprehensive Genomic Study in Patients with Idiopathic Azoospermia and Oligoasthenoteratozoospermia
18. Detection of Genomic Imbalances by Array-Based Comparative Genomic Hybridization in Bulgarian Patients with Autism Spectrum Disorders
19. Partial 9P Monosomy and Partial 8Q Trisomy by Adjacent 1 Segregation of Balanced Paternal Translocation Revealed by Molecular Karyotyping
20. Detection and Genotyping of Human Papillomaviruses in Bulgarian Patients for the Period of 2009–2010
21. Comparison of Two Microarray CGH Platforms for Genome-Wide Copy Number Profilings: Oligo-Based Arrays Versus Bacterial Artificial Chromosome Arrays
22. Fifty Years of Balkan Endemic Nephropathy: Challenges of Study Using Epidemiological Method
23. Diagnostic Criteria for Balkan Endemic Nephropathy: Proposal by an International Panel
24. Association of cyclinD1 copy number changes with histological type in ovarian tumors
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