Human monochromosome hybrid cell panel characterized by FISH in the JCRB/HSRRB
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M. Oshimura | K. Hashimoto | T. Sofuni | H. Tanabe | H. Mizusawa | N. Tanaka | Y. Nakagawa | D. Minegishi | Yuzuki Nakagawa
[1] M. Oshimura,et al. Double trans-chromosomic mice: maintenance of two individual human chromosome fragments containing Ig heavy and kappa loci and expression of fully human antibodies. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[2] M. Oshimura,et al. Cellular senescence of a human bladder carcinoma cell line (JTC-32) induced by a normal chromosome 11. , 2000, Cancer genetics and cytogenetics.
[3] M. Oshimura,et al. Telomerase‐independent senescence of human immortal cells induced by microcell‐mediated chromosome transfer , 1999, Molecular carcinogenesis.
[4] A. Feinberg,et al. LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids. , 1999, Human molecular genetics.
[5] M. Oshimura,et al. The XRCC2 and XRCC3 repair genes are required for chromosome stability in mammalian cells. , 1999, Mutation research.
[6] P. Bender,et al. Panel description. Regional mapping panels for chromosomes 6, 9, and 16. , 1999, Genomics.
[7] C. Cuthbert,et al. Parental origin of the isochromosome 12p in Pallister-Killian syndrome: molecular analysis of one patient and review of the reported cases. , 1999, American journal of medical genetics.
[8] Charles Lee,et al. Generation of an ∼2.4 Mb Human X Centromere-Based Minichromosome by Targeted Telomere-Associated Chromosome Fragmentation in DT40 , 1999 .
[9] A. Feinberg,et al. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[10] M. Oshimura,et al. Functional evidence for involvement of multiple putative tumor suppressor genes on the short arm of chromosome 3 in human oral squamous cell carcinogenesis. , 1998, Cancer genetics and cytogenetics.
[11] M. Oshimura,et al. Failure to complement abnormal phenotypes of simian virus 40-transformed Werner syndrome cells by introduction of a normal human chromosome 8. , 1998, Cancer research.
[12] M. Oshimura,et al. Evidence for a putative telomerase repressor gene in the 3p14.2–p21.1 region , 1998, Genes, chromosomes & cancer.
[13] P. Bender,et al. Regional mapping panels for chromosomes 8, 13, 21, and 22. , 1998, Genomics.
[14] M. Oshimura,et al. Efficient modification of a human chromosome by telomere-directed truncation in high homologous recombination-proficient chicken DT40 cells. , 1998, Nucleic acids research.
[15] M. Oshimura,et al. Repression of the telomerase catalytic subunit by a gene on human chromosome 3 that induces cellular senescence , 1998, Molecular carcinogenesis.
[16] M. Oshimura,et al. Mapping a novel cellular‐senescence gene to human chromosome 2q37 by irradiation microcell‐mediated chromosome transfer , 1998, Molecular carcinogenesis.
[17] M. Meguro,et al. Epigenetic reprogramming of the human H19 gene in mouse embryonic cells does not erase the primary parental imprint , 1998, Genes to cells : devoted to molecular & cellular mechanisms.
[18] A. Schinzel,et al. Isochromosomes 12p and 9p: parental origin and possible mechanisms of formation , 1998, European Journal of Human Genetics.
[19] P. Bender,et al. Regional mapping panels for chromosomes 3, 4, 5, 11, 15, 17, 18, and X. , 1997, Genomics.
[20] M. Meguro,et al. Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer. , 1997, Human molecular genetics.
[21] M. Oshimura,et al. Functional expression and germline atransmission of a human chromosome fragment in chimaeric mice , 1997, Nature Genetics.
[22] M. Oshimura,et al. Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24. , 1997, American journal of human genetics.
[23] M. Oshimura,et al. Gene expressions of transferred human chromosome 8 in mouse cell lines. , 1997, Biochemical and biophysical research communications.
[24] M. Oshimura,et al. Genetic regulation of telomerase in a multiple pathways model to cellular senescence. , 1996, Human cell.
[25] M. Oshimura,et al. The defect in the AT-like hamster cell mutants is complemented by mouse chromosome 9 but not by any of the human chromosomes. , 1996, Mutation research.
[26] D. Carson,et al. Identification of human tumour suppressor genes by monochromosome transfer: rapid growth-arrest response mapped to 9p21 is mediated solely by the cyclin-D-dependent kinase inhibitor gene, CDKN2A (p16INK4A). , 1996, Carcinogenesis.
[27] M. Oshimura,et al. Cosmids and transcribed sequences from chromosome 11q23 , 1995, Japanese Journal of Human Genetics.
[28] O. Pereira-smith,et al. "PCR karyotype" of monochromosomal somatic cell hybrids. , 1993, Genomics.
[29] S. Naylor,et al. Characterization of NIGMS human/rodent somatic cell hybrid mapping panel 2 by PCR. , 1993, Genomics.
[30] R. Mulivor,et al. NIGMS human/rodent somatic cell hybrid mapping panels 1 and 2. , 1993, Genomics.
[31] M. Oshimura,et al. Suppression of tumorigenicity in human colon carcinoma cells by introduction of normal chromosome 5 or 18 , 1991, Nature.
[32] D. Ledbetter,et al. "PCR-karyotype" of human chromosomes in somatic cell hybrids. , 1990, Genomics.
[33] M. Oshimura,et al. Establishment of a novel immortalized cell line from ataxia telangiectasia fibroblasts and its use for the chromosomal assignment of radiosensitivity gene. , 1990, International journal of radiation biology.
[34] M. Oshimura,et al. Suggestive evidence for functionally distinct, tumor-suppressor genes on chromosomes 1 and 11 for a human fibrosarcoma cell line, HT1080. , 1990, Oncogene.
[35] D. Kipling,et al. Hypervariable ultra-long telomeres in mice , 1990, Nature.
[36] M. Oshimura,et al. Multiple chromosomes carrying tumor suppressor activity for a uterine endometrial carcinoma cell line identified by microcell-mediated chromosome transfer. , 1990, Oncogene.
[37] C. L. Jackson,et al. Monochromosomal rodent-human hybrids from microcell fusion of human lymphoblastoid cells containing an inserted dominant selectable marker. , 1990, Genomics.
[38] P. Marynen,et al. Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome , 1989, Human Genetics.
[39] M. Oshimura,et al. Construction of Mouse A9 Clones Containing a Single Human Chromosome Tagged with Neomycin‐resistance Gene via Microcell Fusion , 1989, Japanese journal of cancer research : Gann.
[40] M. Oshimura,et al. Construction of Mouse A9 Clones Containing a Single Human Chromosome (X/Autosome Translocation) via Micro‐cell Fusion , 1989, Japanese journal of cancer research : Gann.
[41] T. Mohandas,et al. Chromosomal mosaicism in the Killian/Teschler-Nicola syndrome. , 1986, American journal of medical genetics.
[42] Yusuke Nakamura,et al. A human gene that restores the DNA-repair defect in SCID mice is located on 8p11.1→q11.1 , 2004, Human Genetics.
[43] M. Meguro,et al. Mouse A9 cells containing single human chromosomes for analysis of genomic imprinting. , 1999, DNA research : an international journal for rapid publication of reports on genes and genomes.
[44] R. Critcher,et al. Generation of an approximately 2.4 Mb human X centromere-based minichromosome by targeted telomere-associated chromosome fragmentation in DT40. , 1999, Human molecular genetics.
[45] A. Feinberg,et al. Erratum: LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids (Human Molecular Genetics (1999) 8 (1209-1217)) , 1999 .
[46] J. Barrett,et al. Construction of chicken x human microcell hybrids for human gene targeting. , 1997, Cytogenetics and cell genetics.
[47] T. Sofuni,et al. Comparative mapping of the immunoglobulin C epsilon 1 gene (IGHE) in five species of nonhuman primates by fluorescence in situ hybridization. , 1995, Cytogenetics and Cell Genetics.
[48] S. Ishikiriyama,et al. New diagnostic method for Pallister-Killian syndrome: detection of i(12p) in interphase nuclei of buccal mucosa by fluorescence in situ hybridization. , 1993, American journal of medical genetics.
[49] O. Pereira-smith,et al. Isolation of monochromosomal hybrids following fusion of human diploid fibroblast-derived microcells with mouse A9 cells. , 1992, Cytogenetics and cell genetics.