-
[文献書誌] Ariyama,T. (Abe,T.): "High-resolution cytogenetic map of the short arm of chromosome 1 with newly isolated 411 cosmid markers by flouresence in situ hybridization ; precise ordering 18 markers on 1p36.1 on prophase chromosomes and “stretched" DNAs" Genomics. 25. 114-123 (1995)
-
[文献書誌] Morishima,Y. (Abe,T.): "Chromosomal loci of 50 human keratinocyte cDNAs assigned by fluorescence in situ hybridization" Genomics. 28. 273-279 (1995)
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[文献書誌] Ichikawa,D. (Abe,T.): "Multiple primary cancers with microsatellite instability : Report of a case" Jpn.J.Cancer Res.87. 105-108 (1995)
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[文献書誌] Harada,H. (Abe,T.): "Bipolar affective disorder associated with ア-Thalassemia minor" Biol.Psychiatry. 37. 477-480 (1995)
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[文献書誌] Shiojima,I. (Abe,T.): "Assignment of Cardiac homeobox gene CSX to human chromosome 5q34" Genomics. 27. 204-206 (1995)
-
[文献書誌] Taketani,S. (Abe,T.): "The human protoporphybinogen oxidase gene : Organization and location to chromosone 1" Genomics. 29. 698-703 (1995)
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[文献書誌] Marukawa,O. (Abe,T.): "Molecular cloning of the breakpoint of t (11;22) (q23;q11) chromosome translocation in an adult acute myelomonocytic leukemia" Brit.J.Haematol.,. (in press). (1995)
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[文献書誌] Inazawa,J. (Abe,T.): "PTPN13,a Fas-associated protein tyrosine phosphatase,located on the long arm of chromosome 4 at band q21.3" Genomics,. (in press). (1995)
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[文献書誌] Ichikawa,D. (Abe,T.): "Analysis of numerical aberrations of specific chromosomes by fluorescemce in situ hybridization (FISH) as a diagnostic tool in breast cancer" Cancer,. (in press).
-
[文献書誌] Gardiner,K. (Ohki,M.): "Localization of cDNAs to a region poorly represented in the CEPH chromosome 21 YAC contig : candidate genes for genetic diseases mapped to 21q22.3" Genomics. 30. 376-379 (1995)
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[文献書誌] Goto,M. (Ohki,M.): "Assignment of the E4TF1-60 gene to human chromosome 21q21.2-21.3" Gene. 166. 337-338 (1995)
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[文献書誌] Ohira,M. (Ohki,M.): "A 1.6 Mb P1-based physical map of the Down syndrome region on chromosome 21" Genomics,. (in press). (1996)
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[文献書誌] Ohira,M. (Ohki,M.): "Identification of a novel gene containing the tetratricopeptide repeat domain from the Down syndrome region of chromosome 21" DNA Res.,. (in press). (1996)
-
[文献書誌] Okubo,K.Matsubara,K.: "Monitoring cell physiology by expression profiles and discovering cell type-specific genes by compiled expression profiles" Genomics. 30. 178-186 (1995)
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[文献書誌] Sakamoto,Y. (Ogasawara,N.,Yoshikawa,H): "The Bacillus subtilis dnaC gene encodes a protein homologous to the DnaB helicase of Escherichia coli" Microbiol.141. 641-644 (1995)
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[文献書誌] Akagawa,E. (Ogasawara,N.): "Determination of 17,484 bp nucleotide sequence around 39o region of the Bacillus subtilis chromosome andsimilarity analysis of the products of putative ORFs" Microbiol.141. 3241-3245 (1995)
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[文献書誌] Aroya,S. (Ogasawara,N.): "The Mfd protein of Bacillus subtilis 168 is involved in both transcription-coupled DNA repair and DNA recombination" J.Mol.Biol.,. (in press). (1996)
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[文献書誌] Yoshida,K. (Ogasawara,N.): "Cloning and sequencing of a 40.5 kb region of the Bacillus subtilis genome containing the bglS and cel loci ; creation of a 177 kb contig covering from the gnt to sacXY loci" DNA Res.,. (in preparation).
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[文献書誌] Barnes,T. (Kohara,Y.): "Meiotic recombination,non-coding DNA and genomic organization in Caenorhabditis elegans" Genetics. 141. 159-179 (1995)
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[文献書誌] Tabara,H. (Kohara,Y.): "A multi-well version of in situ hybridization on whole mount embryos of C.elegans" Nucl.Acids Res.,. (submitted).
-
[文献書誌] Zhao,N. (Sakaki,Y.): "High-destiny cDNA filter analysis : a novel approach for large-scale,quantitative analysis of gene expression" Gene. 156. 207-213 (1995)
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[文献書誌] Adachi,N. (Sakaki,Y.): "Differential display analysis of gene expression in developing embryos of Xenopus laevis" Biochimica et Biophysica Acta. 1262. 43-51 (1995)
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[文献書誌] Araki,E (Sakaki,Y.): "Transgenic mice expressing the amyloid protein-contaning carboxyl-terminal fragment of the Alzheimer amyloid precursor protein" Amyloid. 2. 100-106 (1995)
-
[文献書誌] Alemeida,M.R. (Sakaki,Y.): "Haplotype analysis of common transthyretin mutations" Hum.Genet.96. 350-354 (1995)
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[文献書誌] Kurose,K. (Sakaki,Y.): "RNA polymerase III dependence of the human L1 promoter and possible participation of the RNA polymerase II factor YY1 in the RNA polymerase III transcription system" Nucleic Acids Res.23. 3704-3709 (1995)
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[文献書誌] Kato,M. (Sakaki,Y.): "Altered actin binding with myosin mutation in hypertrophic cardiomyopathy and sudden death" Lancet. 345(8959). 1247 (1995)
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[文献書誌] Takahashi,N. (Sakaki,Y.): "High-density cDNA filter analysis of the expresion profiles of the genes preferentially expressed in human brain" Gene. 164. 219-227 (1995)
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[文献書誌] Toyoda,A. (Sakaki,Y.): "Mode of activation of the GC box/Spl-dependent promoter of the human NADH-cytochrome b5 reductase-encoding gene" Gene. 164. 351-355 (1995)
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[文献書誌] Cher,M.L. (Sakaki,Y.): "Mapping of Regions of Physical Deletion on Chromosome 16q in Prostate Cancer Cells by Fluorescence in situ Hybridization (FISH)" J.Urol. 153. 249-254 (1995)
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[文献書誌] Ito,T. (Sakaki,Y.): "Fluorescent differential display method for high-speed scanning of cell-specific transcripts methods" Mol.Genet.8. 229-245 (1995)
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[文献書誌] Ito.T. (Sakaki,Y.): "Fluorescent Differential Display (FDD) : A Fast and Safe Way for Reliable DD Analysis in Springer Lab Manual : Fingerprinting Methods Using PCR" Springer-Verlag, (Eds.Micheli,M.R.and Bova,R.). (in press). (1996)
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[文献書誌] Shibata,A. (Sakaki,Y.): "Identification of cis-acting elements involved in an alternative splicing of the amylod precursor protein (APP) gene" Gene,. (in press). (1996)
-
[文献書誌] Hattori,M. (Sakaki,Y.): "Mutation detection by orphan peak analysis in CRC Press book : The Detection of DNA sequence polymorphisms and mutations" Methods and Applications,. (in press). (1996)
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[文献書誌] Suzuki,T. (Sakaki,Y.): "Regional and cellular presenilin 1 gene expression in human and rat tissues" Biochem.Biophys.Res.Commun.,. (in press). (1996)
-
[文献書誌] Naruse,K. (Sakaki,Y.): "A YAC contig of the human CC chemokine genes clustered on chromosome 17q11.2" Genomics,. (in press). (1996)
-
[文献書誌] Hattori,M. (Sakaki,Y.): "Novel method for making nested deletions and its application for sequencing of a 300 kb APP gene locus" (submitted). (1996)
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[文献書誌] Tsukahara,F. (Sakaki,Y.): "Cloning of a novel cDNA encoding tetratricopeptide repeat (TPR) motif from Down syndrome critical region 21q22.2" (submitted). (1996)
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[文献書誌] Ito,T. (Sakaki,Y.): "Fluorescent Differential Display Reveals a Male-Specific Band in Mouse Liver That Encodes a Member of Cytochrome P450 4A Family" (submitted). (1996)
-
[文献書誌] Kito,K. (Sakaki,Y.): "Fluorescent Differential Display Analysis of Gene Expression of Differentiating Neuroblastoma" (submitted). (1996)
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[文献書誌] Satou,K. (Takagi,T.): "Development of a deductive database system for computing closures of similarity relationships among protein structures" Journal of Japanese Society for Artificial Intelligence. 11(3). (1996)
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[文献書誌] Shibayama,G. (Takagi,T.): "Mining association rules from signals found in mammalian promoter sequence" Genome Informatics Workshop 1995. 108-109 (1995)
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[文献書誌] Uchiyama,I. (Takagi,T.): "Protein sequence grouping by peptide word motifs" Genome Informatics Workshop 1995. 116-117 (1995)
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[文献書誌] Murakami,K. (Takagi,T.): "Evaluation of exon prediction tools using a long DNA sequence data" Genome Informatics Workshop 1995. 98-99 (1995)
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[文献書誌] Ogiwara,A. (Takagi,T.): "A WWW Database of Bacillus Subtilis ORFs determined by the International Project of Sequencing B.Subtilis Genome" Genome Informatics Workshop 1995. 162-163 (1995)
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[文献書誌] Ogiwara,A. (Takagi,T.): "Sequence Analysis using Databases and Networks (Part 1),in Japanese" Cell Technology. 14(5). 577-588 (1995)
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[文献書誌] Ogiwara,A. (Takagi,T.): "Sequence Analysis using Databases and Networks (Part 2),in Japanese" Cell Technology. 14(6). 709-721 (1995)
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[文献書誌] 高木 利久: "ゲノム情報" ゲノム情報,情報処理学会編 新版 情報処理ハンドブック. 862-867 (1996)
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[文献書誌] Ikeuchi,T. (Tsuji,S.): "Dentatorubral-Pallidoluysian Atrophy (DRPLA) : Clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat" Ann.Neurol.37. 769-775 (1995)
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[文献書誌] Onodera,O. (Tsuji,S.): "Molecular cloning of cDNA for dentatorubral-pallidoluysian atrophy (DRPLA) and regional expressions of the expanded alleles in the central nervous system" Am.J.Hum.Genet.57. 1050-1060 (1995)
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[文献書誌] Ichinose,H. (Tsuji,S.): "Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene" Nature Genet.8. 236-242 (1995)
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[文献書誌] Burke,J.R. (Tsuji,S.): "Dentatorubral-pallidoluysian atrophy and Haw River syndrome" Lancet. 344. 1711-1712 (1995)
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[文献書誌] Tanaka,H. (Tsuji,S.): "The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14q" Ann.Neurol.37(3). 769-775 (1995)
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[文献書誌] Ikeuchi,T. (Tsuji,S.): "Dentatorubral-pallidoluysian atrophy (DRPLA) : close correlationof CAG repeat expansions with the wide spectrum of clinical presentations and prominent anticipaiton" Seminars in Cell Biology. 6(1). 37-44 (1995)
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[文献書誌] Ikeuchi,T. (Tsuji,S.): "Dentatorbral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLA" Clin.Neurosci.3(1). 23-27 (1995)
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[文献書誌] Sanpei,K. (Tsuji,S.): "Direct detection of expanded (CAG/CTG) repeats in the myotonin-protein kinase genes of myotonic dystrophy patients using a high-stringency hybridization method" Biochem.Biophys.Res.Commun.212(2). 341-346 (1995)
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[文献書誌] Okuizumi,K. (Tsuji,S.): "Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease" Nature Genet.11. 207-209 (1995)
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[文献書誌] Onodera,O. (Tsuji,S.): "Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expression of the expanded alleles in the CNS" Am.J.Hum.Genet.57(5). 1050-1060 (1995)
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[文献書誌] Takiyama,Y. (Tsuji,S.): "Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease" Hum.Mol.Genet.4(7). 1137-1146 (1995)
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[文献書誌] Koike,R. (Tsuji,S.): "Partial deletions of putative adrenoleukodystrophy (ALD) gene in Japanese ALD patietns" Hum.Mutation. 6. 263-267 (1995)
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[文献書誌] Yoneda,M. (Tsuji,S.): "Detection and quantification of point mutations in mtDNA by PCR" Methods in Enzymology,. (in press).
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[文献書誌] Nakatsuru,S. (Nakamura,Y.): "Isolation and mapping of a novel human gene encoding a product homologous to yeast proteins involving in DNA replication" Cytogenet.Cell Genet.68. 226-230 (1995)
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[文献書誌] Fujiwara,Y. (Nakamura,Y.): "Isolation of a candidate tumor suppressor gene on chromosome 8p21.3-p22 that is homologous to an extracellular domain of the PDGF receptor deta gene" Oncogene. 10. 891-895 (1995)
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[文献書誌] Katagiri,T. (Nakamura,Y.): "Human metalloprotease/disintegrin-like (MDC) Gene : Exon-intron organization and alternative splicing" Cytogenet.Cell Genet.68. 39-44 (1995)
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[文献書誌] Arakawa,H. (Nakamura,Y.): "Molecular cloning,characterization,and chromosomal mapping of a novel human gene that is highly homologous to Xenopus transcription factor III" Cytogenet.Cell Genet.70. 235-238 (1995)
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[文献書誌] Chinen,K. (Nakamura,Y.): "Isolation and mapping of human beta-signal sequence receptor gene" Cytogenet.Cell Genet.70. 215-217 (1995)
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[文献書誌] Kawakami,T. (Nakamura,Y.): "Isolation and mapping of a human gene that is highly homologous to PR-8,a rat gene associated with programmed cell death" Cytogenet.Cell Genet.71. 41-43 (1995)
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[文献書誌] Ariyama,T. (Nakamura,Y.,Abe,T.): "Precise ordering of 26 cosmid markers on chromosome region 3p23-p21.3 by two-color FISH on human prophase chromosomes and stretched DNAs" Cytogenet.Cell Genet.70. 129-133 (1995)
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[文献書誌] Ariyama,T. (Nakamura,Y.,Abe,T.): "High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization : The precise order of 18 markers on 1p36.1 on prophase chromosomes and “stretched" DNAs" Genomics. 25. 114-123 (1995)
-
[文献書誌] Koyama,K. (Nakamura,Y.): "Isolation of 115 human chromosome 8-specific expressed-sequence tags by exon amplification" Genomics. 26. 245-253 (1995)
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[文献書誌] Ikegawa,S. (Nakamura,Y.): "Isolation,characterization and chromosomal assignment of human colligin2" Cytogenet.Cell Genet.71. 182-186 (1995)
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[文献書誌] Ikegawa,S. (Nakamura,Y.): "Mutations of the fibroblast growth factor-3 gene in one familial and six sporadic cases of Japanese patients with achondroplasia" Human Genet.96. 309-311 (1995)
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[文献書誌] Spurr,N.K. (Nakamura,Y.): "Report of the second international workshop on human chromosome 8 mapping 1994" Cytogenet.Cell Genet.68. 147-164 (1995)
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[文献書誌] Miura,K. (Nakamura,Y.): "Deletion mapping in squamous cell carcinomas of the esophagus defines a region containing a Tumor Suppressor Gene Within a 4-cM Interval of the distal long arm of chromosome 9" Cancer Res.55. 1828-1830 (1995)
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[文献書誌] Inoue,S. (Nakamura,Y.): "Chromosomal mapping of human (ZNF147) and mouse gene for estrogen-responsive finger protein (efp),a member of the RING finger family" Genomics. 25. 581-583 (1995)
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[文献書誌] Sudo,K. (Nakamura,Y.): "Isolation,and mapping of human cDNA homologous to murine protein synthesis initiation factor 4A-II (eIF4A-II)" Cytogenet.Cell Genet.71. 385-388 (1995)
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[文献書誌] Saito,H. (Nakamura,Y.): "Isolation,and mapping of a novel human gene encoding a protein contaiing Zinc-finger structures" Genomics,in press.
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[文献書誌] Koyama,K. (Nakamura,Y.): "The human homologue of the murine mgl-I gene maps within the Smith-Magenis-Syndrome region in 17p11.2" Cytogenet.Cell Genet.,. (in press).
-
[文献書誌] Saito,H. (Nakamura,Y.): "Cloning and mapping of a human novel cDNA that encodes a protein highly homologous to yeast nuclear protein NHP2" Cytogenet.Cell Genet.,. (in press).
-
[文献書誌] Fujiwara,T. (Nakamura,Y.): "Cloning,sequencing and expression of a novel cDNA encoding human vacuolar ATPase (14-kDa subunit)" DNA Research. 2. 107-111 (1995)
-
[文献書誌] Toda,T. (Nakamura,Y.): "Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome" Ann.Neurol.37. 99-101 (1995)
-
[文献書誌] Soejima,H. (Nakamura,Y.): "Fifty novel sequences-tagged sites (STSs) on human chromosome 11q13.4-q25 identified from microclones generated by microdissection" Cytogenet.Cell Genet.70. 108-111 (1995)
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[文献書誌] Takiguchi-Shirahama,S. (Nakamura,Y.): "Germline mutations of the RET proto oncogene in eight Japanese patients with multiple endocrine neoplasia (MEN2A)" Hum.Genet.95. 187-190 (1995)
-
[文献書誌] Hofstra,R.M.W. (Nakamura,Y.): "Ordering of markers in the pericentromeric region of chromosome 10" Hum.Genet.96. 116-118 (1995)
-
[文献書誌] Nahmias,J. (Nakamura,Y.): "Cosmid contigs spanning 9q34 including the candidate region for TSC1" Eur.J.Hum.Genet.3. 65-77 (1995)
-
[文献書誌] Inoue,M. (Nakamura,Y.): "Isotation and characterization of a novel human cDNA clone homologous to a yeast transcription activator,GCN5" Cytogenet.Cell Genet.,. (in press).
-
[文献書誌] Furukawa,Y. (Nakamura,Y.): "Isolation and mapping of a novel human gene that is homologous to RPD3,a transcription factor in Saccharomyces cerevisiae" Cytogenet.Cell Genet.,. (in press).
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[文献書誌] Watanabe,T. (Nakamura,Y.): "Molecular cloning of a novel human cDNA,RT14,containing a putative ORF highly conserved between human,fruit fly,and nematode" DNA Research. 2. 235-237 (1995)
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[文献書誌] Toda,T. (Nakamura,Y.): "Dinucleotide repeat polymorphism on chromosome 9q32" Jpn.J.Hum.Genet.40. 333-334 (1995)
-
[文献書誌] Isomura,M. (Nakamura,Y.): "Cloning and mapping of a novel human cDNA homologous to DR OER,the enhancer of the Drosophila melanogaster rudimentary gene" Genomics,. (in press).
-
[文献書誌] Tanaka,T. (Nakamura,Y.): "Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase" Cytogenet.Cell Genet.,. (in press).
-
[文献書誌] Ninomiya,S. (Nakamura,Y.): "Isolation of a testis-specific cDNA on chromosome 17q from a region adjacent to the breakpoint of t (12;17) observed in a patient with acampomelic campomelic dysplasia and sex reversal" Hum.Mol.Genet.5. 69-72 (1995)
-
[文献書誌] Watanabe,T. (Nakamura,Y.): "Cloning,expression,and mapping of h-UBC9,a gene encoding a human homologue of ubiquitin-conjugating enzymes that are critical for regulating the cell cycle in teas" Cytogenet.Cell Genet.,. (in press).
-
[文献書誌] Ikegawa,S. (Nakamura,Y.): "Mutations in the N-terminal globular domain of the type X collagen gene (COL10A1) In patients with Schmid metaphyseal chondrodysplasia" Human Mutation,. (in press).
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[文献書誌] Tokino,T. (Nakamura,Y.): "Characterization of the human p57 KIP2 gene ; Alternative splicing,Insertion/deletion polymorphisms in VNTR sequences in the coding region,and mutational analysis" Hum.Genet.,. (in press).
-
[文献書誌] Tanaka,T. (Nakamura,Y.): "Molecular cloning of a novel human cDNA encoding putative cysteine protease and its chromosomal assignment to 14q32.1" Cytogenet.Cell Genet.,. (in press).
-
[文献書誌] Mori,T. (Nakamura,Y.): "Isolation and mapping of a novel human gene homologous to yeast CDCs 3,10,11,and 12,and mouse DIFF" Cytogenet.Cell Genet.,. (in press).
-
[文献書誌] Okita,K. (Nakamura,Y.): "Definition of the locus responsible for systemic carnitine deficiency within a 1.6-cM region of mouse chromosome 11 by detailed linkage analysis" Genomics,. (in press).
-
[文献書誌] Chinen,K. (Nakamura,Y.): "Isolation and mapping of a novel gene,partially homologous to yeast SEC14,that contains variable number of tandem repeat (VNTR) in the 3′ untranslated region" Cytogenet.Cell Genet.,. (in press).
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[文献書誌] Ohta,T. (Nakamura,Y.): "Isolation of a cosmid clone corresponding to an inv (21) breakpoint of a patient with transient abnormal myelopoiesis" Am.J.Hum.Genet.,. (in press).
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[文献書誌] 高木 利久: "ゲノムネットのデータベース利用法" 共立出版, (1996)
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[文献書誌] 藤山 秋佐夫: "染色体操作技術、組織培養" 5-6 (1996)
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[文献書誌] 藤山 秋佐夫: "ヒト染色体のソーティング、組織培養" 47-51 (1996)
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[文献書誌] Honjo,T.and Matsuda,F.: "Immunoglobulin heavy chain loci of mouse and man Immunoglobulin Genes (T.Honjo and FW.Alt,eds.)" Academic Press,London,U.K., 145-171 (1995)
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[文献書誌] Matsuda,F.and Honjo,T.: "Organization of the human immunoglobulin heavy-chain locus Advances in Immunology (F.Dixon,ed.)" Academic Press,San Diego,in press,
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[文献書誌] 小原 雄治: "線虫C.エレガンスの細胞死の遺伝子カスケード 「アポトーシスの分子医学」(橋本嘉幸、山田武 編)" 羊土社, 26-36 (1995)
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[文献書誌] 小原 雄治: "線虫C.elegansゲノムの発現マップ、細胞工学 14" 秀潤社, 661-666 (1995)
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[文献書誌] 小原 雄治: "座談会、情報生物学の現状と将来、蛋白質核酸酵素 40" 羊土社, 1784-1802 (1995)
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[文献書誌] 林崎 良英: "ゲノム解析研究と医学分野における将来への展望" Pharma Medica, 51-56 (1995)
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[文献書誌] 林崎 良英: "DNA多型検出の戦略 DNA多型 3" 東洋書店, 10-15 (1995)
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[文献書誌] Hayashizaki,Y.: "Restriction landmark genomic scanning (RLGS), Molecular Biology and Biotechnology" VCH publishers, 813-817 (1995)
