205 results on '"Ikeuchi, Tatsuro"'
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2. Induction of Nuclear Envelopes around Metaphase Chromosomes after Fusion with Interphase Cells
3. Chromosome Pulverization in Micronuclei Induced by Tritiated Thymidine
4. Assignment of the human gene for KBF2/RBP-Jk to chromosome 9p12-13 and 9q13 by fluorescencein situ hybridization
5. High-resolution chromosome R-banding in lymphoblastoid cell lines by the combined use of cell synchronization and ethidium bromide treatment
6. Monoallelic BUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome
7. Chromosome 1q terminal deletion resulting fromde novo translocation with an acrocentric chromosome
8. Direct mapping of the human TATA box-binding protein (TBP) gene to 6q27 by fluorescencein situ hybridization
9. Two modes of microsatellite instability in human cancer: differential connection of defective DNA mismatch repair to dinucleotide repeat instability
10. DNA analyses of XX and XX-hypospadiac males
11. Y/6 chromosome translocation in a male with triple primary cancers involving the breast
12. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3)
13. Induction of distamycin A-inducible rare fragile sites and increased sister chromatid exchanges at the fragile site
14. Refined determination of breakpoints of the translocation t(1;7) associated with signs of HMC syndrome
15. Common cytological and cytogenetic features of Epstein-Barr virus (EBV)-positive natural killer (NK) cells and cell lines derived from patients with nasal T/NK-cell lymphomas, chronic active EBV infection and hydroa vacciniforme-like eruptions
16. Molecular characterization of the mouse very-long-chain acyl-CoA dehydrogenase gene
17. Cloning, Characterization, and Chromosomal Mapping of Human Aquaporin of Collecting Duct
18. Identification of a Novel Promoter and Exons of the c-ERBB-2Gene
19. Chromosomal Instability Syndrome of Total Premature Chromatid Separation with Mosaic Variegated Aneuploidy Is Defective in Mitotic-Spindle Checkpoint
20. An abortus with a normal/trisomy 16 mosaicism: instability of trisomic cells in vitro
21. Chromosome banding patterns in an infant with 13q-syndrome
22. Unbalanced 13q/21q translocation: A revised study of the case previously reported as 21-monosomy
23. A case of mosaic trisomy 14 due to an isochromosome, i(14q)
24. Assignment of a polymorphic locus of OS-4(D18S5) DNA segment to human chromosome region 18q21.3→qter
25. A male infant with monosomy 21
26. Lack of association and linkage between HLA and familial polyposis coli
27. A preliminary note on the hormonal induction of NADP-linked dehydrogenases in phytohaemagglutinin-stimulated human lymphocytes
28. A chromosome survey of induced abortuses in a Japanese population
29. Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease
30. Loss of constitutional heterozygosity in colon carcinoma from patients with familial polyposis coli
31. Distal trisomy of chromosome 17q due to inverted tandem duplication
32. Cytogenetic analysis of 23 Japanese patients with amyotrophic lateral sclerosis
33. Alternative mechanisms of gene amplification in human cancers
34. Premature chromatid separation (PCS) vs. premature centromere division (PCD)
35. Induction of premature chromatid separation (PCS) in individuals with PCS trait and in normal controls
36. Cancer-prone syndrome of mosaic variegated aneuploidy and total premature chromatid separation: Report of five infants
37. Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: Possible localization of a neurofibromatosis type 2 modifier gene?
38. Functional Evidence for Involvement of Multiple Putative Tumor Suppressor Genes on the Short Arm of Chromosome 3 in Human Oral Squamous Cell Carcinogenesis
39. Human Genes for KNSL4 and MAZ Are Located Close to One Another on Chromosome 16p11.2
40. Mosaic variegated aneuploidy with multiple congenital abnormalities: Homozygosity for total premature chromatid separation trait
41. cDNA Cloning of a Short Type of Multidrug Resistance Protein Homologue,SMRP,from a Human Lung Cancer Cell Line
42. Assignment of the Genes Encoding the Human Chloride Channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32–q33 byin SituHybridization
43. A 1.6-Mb P1-Based Physical Map of the Down Syndrome Region on Chromosome 21
44. Structure and Chromosomal Localization of a Human Water Channel (AQP3) Gene
45. Translocation (9;22)(g22;ql2) A recurrent chromosome abnormality in extraskeletal myxoid chondrosarcoma
46. A Mouse Erythroleukemia Cell Line Possessing Friend Spleen Focus-forming Virus gp55 Transgene and Temperature-sensitive Mutant p53 Gene
47. In vitro growth suppression and morphological change in a human renal cell carcinoma cell line by the introduction of normal chromosome 3 via microcell fusion
48. Characterization of the translocation breakpoint on chromosome 22q12.2 in a patient with neurofibromatosis type 2 (NF2)
49. Escape from in vitro aging in SV40 large T antigen-transformed human diploid cells: A key event responsible for immortalization occurs during crisis
50. Mapping the breakpoint of a constitutional translocation on chromosome 22 in a patient with NF2
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