158 results on '"Baranov, Vladislav S."'
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2. Differential effect of estrogen and progesterone on in vitro growth of uterine leiomyoma cells with chromosome 7 deletions
3. Nuclear stability in early embryo. Chromosomal aberrations
4. Contributors
5. Concise History of Prenatal Diagnostic Service in Russia
6. Immunofluorescence Staining for Cytosine Modifications Like 5-Methylcytosine and Its Oxidative Derivatives and FISH
7. Current Trends in the Diagnosis, Screening and Treatment of Spinal Muscular Atrophy
8. Molecular Genetics and Pathogenesis of the Floating Harbor Syndrome: Case Report of Long-Term Growth Hormone Treatment and a Literature Review
9. Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative for MED12 exon 2 mutations
10. Identification of Genetic Risk Factors of Severe COVID-19 Using Extensive Phenotypic Data: A Proof-of-Concept Study in a Cohort of Russian Patients
11. Cytogenomic Profile of Uterine Leiomyoma: In Vivo vs. In Vitro Comparison
12. A comparative cytogenetic study of miscarriages after IVF and natural conception in women aged under and over 35 years
13. Role of WNT4, HOXA10 and TWIST1 genes in the pathogenesis of external genital endometriosis and uterine leiomyoma
14. Telomere Length in Chromosomally Normal and Abnormal Miscarriages and Ongoing Pregnancies and Its Association with 5-hydroxymethylcytosine Patterns
15. Telomere Length in Metaphase Chromosomes of Human Triploid Zygotes
16. The role of genetic markers of thrombophilia in the structure of the causes of placenta-associated complications in pregnant women with thrombocytopenia
17. Uterine Leiomyomas with an Apparently Normal Karyotype Comprise Minor Heteroploid Subpopulations Differently Represented in vivo and in vitro
18. Recent Advances in Gene Therapy of Endometriosis
19. Analysis of the Spectrum of ACE2 Variation Suggests a Possible Influence of Rare and Common Variants on Susceptibility to COVID-19 and Severity of Outcome
20. Mosaicism in preimplantation human embryos
21. Pathogenomics of Uterine Fibroids Development
22. Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities
23. Case of chromothripsis in a large solitary non-recurrent uterine leiomyoma
24. Study of acetylated histone h3k9 – an active chromatin mark – in chromosomes from adult and fetal human lymphocytes
25. Synergistic Anti-Angiogenic Effects Using Peptide-Based Combinatorial Delivery of siRNAs Targeting VEGFA, VEGFR1, and Endoglin Genes
26. Aromatase CYP19A1, progesterone receptor PGR and estrogen receptor ESR1 gene expression in biopsy specimens of endometrioid heterotopia and endometrial tissue by reverse transcription PCR
27. On the Complexity of Mechanisms and Consequences of Chromothripsis: An Update
28. Genetic and expression studies of SMN2 gene in Russian patients with spinal muscular atrophy type II and III
29. Genomic distribution of 5‐formylcytosine and 5‐carboxylcytosine in human preimplantation embryos
30. Two new mutations detected by single-strand conformation polymorphism analysis in cystic fibrosis from Russia
31. Genetic pass as a background of predictive, preventive, personalized medicine options and limitations
32. Molecular Factors Involved in Spinal Muscular Atrophy Pathways as Possible Disease-modifying Candidates
33. Fertility recovery in patients with non-classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency
34. Targeted sequencing analysis of ACVR2A gene identifies novel risk variants associated with preeclampsia
35. Inter-Cell and Inter-Chromosome Variability of 5-Hydroxymethylcytosine Patterns in Noncultured Human Embryonic and Extraembryonic Cells
36. Mutations in the ghrelin receptor gene GHSR in congenital hypopituitarism
37. Peculiarities of placental microRNA expression in pregnancies complicated by gestational diabetes mellitus and preeclampsia
38. Genome-wide 5-hydroxymethylcytosine patterns in human spermatogenesis are associated with semen quality
39. New technologies and trends of prenatal diagnostics
40. The evolution of ideas on the biological role of 5-methylcytosine oxidative derivatives in the mammalian genome
41. Frequency and Spectrum of MED12 Exon 2 Mutations in Multiple Versus Solitary Uterine Leiomyomas From Russian Patients
42. Targeted sequencing analysis of gene identifies novel risk variants associated with preeclampsia.
43. Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative forMED12exon 2 mutations
44. Placental microRNA expression in pregnancies complicated by superimposed pre-eclampsia on chronic hypertension
45. Achievements, sensations and problemsof molecular prenatal diagnostics
46. Comparative systems genetics view of endometriosis and uterine leiomyoma: Two sides of the same coin?
47. Comparative system genetics view of endometriosis and uterine leiomyoma
48. Targeted next-generation sequencing (NGS) of nine candidate genes with custom AmpliSeq in patients and a cardiomyopathy risk group
49. Molecular association of pathogenetic contributors to pre-eclampsia (pre-eclampsia associome)
50. Methylation Levels of SLC23A2 and NCOR2 Genes Correlate with Spinal Muscular Atrophy Severity
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