148 results on '"Lebedev, Igor N."'
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2. iPSC Models of Ring Chromosomes, Genome Editing, and Chromosome Therapy
3. Molecular Mechanisms of Ring Chromosome Formation and Instability
4. Ring Chromosome 8
5. Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss
6. Design of iPSC-based cell model to study the functions of the UBE2A gene
7. Identification of differentially methylated genes in first-trimester placentas with trisomy 16
8. NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss
9. From contemplation to classification of chromosomal mosaicism in human preimplantation embryos
10. LINE-1 retrotransposon methylation in chorionic villi of first trimester miscarriages with aneuploidy
11. A cookbook for DNase Hi-C
12. Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells
13. Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortium
14. ADAMTS1 Is Differentially Expressed in Human Lymphocytes with Various Frequencies of Endogenous γH2AX Foci and Radiation-Induced Micronuclei
15. Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 Gene
16. The Precise Breakpoint Mapping in Paracentric Inversion 10q22.2q23.3 by Comprehensive Cytogenomic Analysis, Multicolor Banding, and Single-Copy Chromosome Sequencing
17. Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22
18. Stem Cell-Based Trophoblast Models to Unravel the Genetic Causes of Human Miscarriages
19. Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss
20. Relationship between morphological and cytogenetic heterogeneity in invasive micropapillary carcinoma of the breast: a report of one case
21. BiasCorrector : Fast and accurate correction of all types of experimental biases in quantitative DNA methylation data derived by different technologies
22. Additional file 1 of A cookbook for DNase Hi-C
23. Method of targeted bisulfite massive parallel sequencing of the human LINE-1 retrotransposon promoter
24. Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay
25. 46,XY,r(8)/45,XY,−8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study
26. LINE-1 retrotransposon methylation in chorionic villi of first trimester miscarriages with aneuploidy
27. Aneuploidy and DNA Methylation as Mirrored Features of Early Human Embryo Development
28. Delineation of Clinical Manifestations of the Inherited Xq24 Microdeletion Segregating with sXCI in Mothers: Two Novel Cases with Distinct Phenotypes Ranging from UBE2A Deficiency Syndrome to Recurrent Pregnancy Loss
29. A mathematical model for evaluation of maternal cell contamination in cultured cells from spontaneous abortions: Significance for cytogenetic analysis of prenatal selection factors
30. Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells.
31. Generation and characterization of iPSCs from human embryonic dermal fibroblasts of a healthy donor from Siberian population
32. A mosaic intragenic microduplication of LAMA1 and a constitutional 18p11.32 microduplication in a patient with keratosis pilaris and intellectual disability
33. Karyotype of the blastocoel fluid demonstrates low concordance with both trophectoderm and inner cell mass
34. A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss
35. Clinically relevant morphological structures in breast cancer represent transcriptionally distinct tumor cell populations with varied degrees of epithelial-mesenchymal transition and CD44+CD24- stemness
36. Genomic structural variations for cardiovascular and metabolic comorbidity
37. Methylation status of LINE-1 retrotransposon in chromosomal mosaicism during early stages of human embryonic development
38. A de novo microtriplication at 4q21.21‐q21.22 in a patient with a vascular malignant hemangioma, elongated sigmoid colon, developmental delay, and absence of speech
39. Comparative Cytogenetic Analysis of Spontaneous Abortions in Recurrent and Sporadic Pregnancy Losses
40. A Comparison of Genome-Wide DNA Methylation Patterns between Different Vascular Tissues from Patients with Coronary Heart Disease
41. Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability
42. EPIGENETIC ASPECTS OF ABNORMALITIES OF HUMAN EMBRYO DEVELOPMENT
43. Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis
44. Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing.
45. Array-CGH analysis of cells dissected from atherosclerotic plaque
46. Increased methylation of genes responsible for fetal-maternal interaction in chorionic villi of miscarriages with trisomy 16
47. Patterns of gene expression in neurons derived from induced pluripotent stem cells of patients with reciprocal 3p26.3 microdeletion and microduplication
48. Identification of regions with loss of heterozygosity in miscarriages from families with recurrent pregnancy loss
49. DNA methylation in inherited copy number variations with incomplete penetrance
50. Deciphering the genetic cause of recurrent and sporadic pregnancy loss
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