792 results on '"Oshimura, M."'
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2. Creation of Hybridomas from Mice Expressing Human Antibody by Introduction of a Human Chromosome
3. Creation of Mice Expressing Human Antibody by Introduction of a Human Chromosome
4. Use of Microcell Hybrids for Analysis of the 11q23 Region and Improved Localization of the A-T Group A/C Genes
5. AT-like Radiosensitive Rodent Cell Mutants: An Alternative Approach to the Isolation of the A-T Gene(s)
6. Complementation Analysis of the Murine scid Cell Line
7. Chromosomal Banding of Cultured T and B Lymphocytes
8. Correction of a genetic defect in multipotent germline stem cells using a human artificial chromosome
9. LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
10. SIRT2, a tubulin deacetylase, acts to block the entry to chromosome condensation in response to mitotic stress
11. Human artificial chromosome (HAC) vector provides long-term therapeutic transgene expression in normal human primary fibroblasts
12. PI3K-Akt pathway: Its functions and alterations in human cancer
13. Targeted regulation of imprinted genes by synthetic zinc-finger transcription factors
14. The use of chromosome-based vectors for animal transgenesis
15. Refined human artificial chromosome vectors for gene therapy and animal transgenesis
16. Development of human artificial chromosome vectors for gene therapy of hemophilia A: OC-TH-088
17. Cloneless genomic DNA analysis: an efficient and simple methods for de novo genomic sequencing projects and gap filling
18. 5-Fluorouracil (5-FU) induced apoptosis in gastric cancer cell lines: role of the p53 gene
19. A new mouse model for Down syndrome
20. LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells
21. Human chromosome 11 complements ataxia-telangiectasia cells but does not complement the defect in AT-like Chinese hamster cell mutants
22. Complementation of a DNA repair deficiency in six human tumor cell lines by chromosome 11
23. Expression of RUNX3 protein in human gastric mucosa, intestinal metaplasia and carcinoma
24. Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissues
25. Cloning of human centromeres by transformation-associated recombination in yeast and generation of functional human artificial chromosomes
26. CHROMOSOMAL ASSIGNMENT OF RADIOSENSITIVITY GENE BY THE USE OF CHROMOSOME TRANSFER INTO ATAXIA TELANGIECTASIA CELLS
27. CORRECTION OF HYPER-RADIOSENSITIVITY IN ATAXIA TELANGIECTASIA CELLS BY THE INTRODUCTION OF NORMAL HUMAN CHROMOSOME 11
28. REDUCED FREQUENCY OF CHROMOSOME ABERRATIONS INDUCED WITH X-RAYS IN ATAXIA TELANGIECTASIA CELLS BY THE INTRODUCTION OF CHROMOSOME 11
29. TUMOR SUPPRESSOR GENES, CELLULAR SENESCENCE, AND MULTISTEP CARCINOGENESIS
30. Mode of action of acidocin 8912, a bacteriocin produced by Lactobacillus acidophilus TK8912
31. Combining iPS cell-derived myogenic progenitors and human artificial chromosomes as a potential genomic integration-free cell and gene therapy for Duchenne muscular dystrophy
32. Transformation of Mammalian Cells in Culture by Asbestos and Other Mineral Dusts: A Mechanism Involving Chromosomal Mutation
33. Establishment and Characterization of Leukemic T-Cell Lines, B-Cell Lines, and Null-Cell Line: a Progress Report on Surface Antigen Study of Fresh Lymphatic Leukemias in Man
34. A novel imprinted locus on chromosome 2P12 associated with relative hand skill in humans
35. Ultrasound And Embryonic Chromosomes
36. Stunning pharmacological properties of DS-5141b, an antisense oligonucleotide consisting of 2'-O,4'-C-ethylene-bridged nucleic acids and 2'-O-methyl RNA, on dystrophin mRNA exon skipping
37. Correlation between luminescence intensity and cytotoxicity in cell-based cytotoxicity assay using luciferase
38. Human artificial chromosomes combined with iPS cells: a genomic integration-free therapy for Duchenne muscular dystrophy
39. Disruption of the imprinting center on human chromosome 15q11-q13 region using the DT40 cell shuttle system
40. Epigenetic heterogeneity at imprinted loci in normal populations
41. Identification and characterization of an antisense transcript to the MEST gene on 7q32 as a candidate imprinted locus
42. Mouse containing a human chromosome 21 models Downs syndrome
43. The human LIT1 CpG island is a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome
44. Study on the genes responsible for E2F-1-mediated neuronal death in Down syndrome brains
45. Russell-Silver Syndrome: Establishment of a possible critical region on 7p14 and characterization of putative candidate genes
46. A candidate gene responsible for transient neonatal diabetes
47. Targeted activation and repression of imprinted genes by synthetic zinc finger transcription factors.
48. Effects of duration of electric pulse on in vitro development of cloned cat embryos with human artificial chromosome vector
49. Karyotype and heterochromatin pattern of the field mouse,Apodemus argenteus Temminck
50. Chronic myelogenous leukemia with translocations (3q-;9q+) and (17q-;22q+). Possible crucial cytogenetic events in the genesis of CML
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