119 results on '"Iourov I"'
Search Results
2. Causes and Consequences of Genome Instability in Psychiatric and Neurodegenerative Diseases
3. Serologic Markers of Autism Spectrum Disorder
4. Identification of candidate genes of autism on the basis of molecular cytogenetic and in silico studies of the genome organization of chromosomal regions involved in unbalanced rearrangements
5. Chromosomal mosaicism in spontaneous abortions: Analysis of 650 cases
6. Fluorescence intensity profiles of in situ hybridization signals depict genome architecture within human interphase nuclei
7. Analysis of germ cell populations in ejaculate of men infected with herpes simplex virus
8. Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB)
9. Instability of chromosomes in human nerve cells (Normal and with Neuromental Diseases)
10. Methods of molecular cytogenetics for studying interphase chromosomes in human brain cells
11. Unexplained autism is frequently associated with low-level mosaic aneuploidy
12. Algorithm of diagnostics of cognitive functions development violation in children born extremally premature
13. Candidate processes for autism spectrum disorders revealed by copy number variation analysis
14. Chromosomal abnormalities and copy number variations in children with idiopathic mental illness
15. Epigenomic variations manifesting as a loss of heterozygosity affecting imprinted genes represent a molecular mechanism of autism spectrum disorders and intellectual disability in children
16. Combination of atomic force microscopy and mass spectrometry for the target protein in the serum samples of children with autism spectrum disorders
17. Combination of atomic force microscopy and mass spectrometry for the detection of target protein in the serum samples of children with autism spectrum disorders
18. Комбинация атомно-силовой микроскопии и масс-спектрометрии для регистрации целевых белков в образцах сыворотки крови детей с расстройствами аутистического спектра
19. Alzheimer’s insight
20. Structural variations of the genome in autistic spectrum disorders with intellectual disability
21. Genomic instability in the brain: chromosomal mosaicism in schizophrenia
22. Brain tissue preparations for chromosomal PRINS labeling
23. Clinical and genetic characteristics of the X chromosome distal long arm microduplications encompassing the MECP2 gene
24. Trisomy 21 Mosaicism: We May All Have a Touch of Down Syndrome
25. Molecular Cytogenetic Diagnosis and Somatic Genome Variations
26. Somatic Genome Variations in Health and Disease
27. Ontogenetic Variation of the Human Genome
28. Molecular Cytogenetics and Cytogenomics of Brain Diseases
29. Small Supernumerary Marker Chromosomes (sSMC) in Patients with a 45,X/46,X,+mar Karyotype – 17 New Cases and a Review of the Literature
30. Intercellular Genomic (Chromosomal) Variations Resulting in Somatic Mosaicism: Mechanisms and Consequences
31. Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia.
32. Small Supernumerary Marker Chromosomes (sSMC) in Patients with a 45,X/46,X,+mar Karyotype - 17 New Cases and a Review of the Literature.
33. P31.9 Genotype-phenotype correlation in Rett syndrome (EEG investigation)
34. Pericentric inversion inv(7)(p11q21.1): Report on two cases and genotype-phenotype correlations
35. In vitro cultivation of fetal human brain cells induces aneuploidy: A caution for neural stem cell therapy?
36. FISH analysis of interphase cells at Rett syndrome: The search of the targeting loci in the chromosome X
37. Cytogenetic, molecular cytogenetic, clinical and genealogical study of mothers of children with autism: a search for family genetic markers of autistic disorders
38. Evidence for large scale chromosomal variations in neuronal cells of the fetal human brain
39. Genomic abnormalities in children with mental retardation and autism: The use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)
40. Chimerism and multiple numerical chromosome imbalances in a spontaneously aborted fetus
41. Chromosome abnormalities in spontaneous abortions: Application of multicolor fluorescent in situ hybridization and original DNA probes for chromosomes 1, 9, 13, 14, 16, 18, 22, X and Y
42. Alphoid DNA variations and non-disjunction in down's syndrome: Fluorescence in situ hybridization and cytogenetic studies
43. Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations
44. The study of X chromosome inactivation in mental retardation: Comparative analysis of molecular-cytogenetic and polymerase chain reaction-based techniques in Rett syndrome
45. The applicability of interphase chromosome-specific multicolor banding (ICS-MCB) for studying neurodevelopmental and neurodegenerative disorders
46. Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies
47. Human interphase chromosomes: a review of available molecular cytogenetic technologies
48. GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny
49. Chromosomal mosaicism goes global
50. Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature
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