{"id":4576,"date":"2020-06-22T18:06:15","date_gmt":"2020-06-22T09:06:15","guid":{"rendered":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/?page_id=4576"},"modified":"2020-06-22T18:31:43","modified_gmt":"2020-06-22T09:31:43","slug":"publications_-1999","status":"publish","type":"page","link":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/publications\/publications_-1999\/","title":{"rendered":"Publications (-1999)"},"content":{"rendered":"<p><\/p>\n<ul>\n<li>Ishida, T., Hippo, Y., Nakahori, Y., Matsushita, I., Kodama, T., Nishimura, S., and Aburatani, H. Structure and chromosomal localization of human MMH\/OGG1 gene. <strong>Cytogenetics and Cell Genetics<\/strong>, 85(3-4):232-6. 1999<\/li>\n<li>Monden, Y., Arai, T., Asano, M., Ohtsuka, E., Aburatani, H., and Nishimura, S. Human MMH (OGG1) type 1a protein is a major enzyme for repair of 8- hydroxyguanine lesions in human cells. <strong>Biochem Biophys Res Commun<\/strong>258, 605-10. 1999<\/li>\n<li>Ishida, T., Takashima, R., Fukayama, M., Hamada, C., Hippo, Y., Fujii, T., Moriyama, S., Matsuba, C., Nakahori, Y., Morita, H., Yazaki, Y., Kodama, T., Nishimura, S., and <strong>Aburatani H<\/strong>. New DNA polymorphisms of human MMH\/OGG1 gene: prevalence of one polymorphism among lung-adenocarcinoma patients in Japanese.<strong> Int J Cancer<\/strong> 80, 18-21. 1999<\/li>\n<li>Ejeskar, K., <strong>Aburatani, H<\/strong>., Abrahamsson, J., Kogner, P., and Martinsson, T. Loss of heterozygosity of 3p markers in neuroblastoma tumours implicate a tumour-suppressor locus distal to the FHIT gene. <strong>Br J Cancer<\/strong> 77, 1787-91. 1998<\/li>\n<li>Takao, M., <strong>Aburatani, H<\/strong>., Kobayashi, K., and Yasui, A. Mitochondrial targeting of human DNA glycosylases for repair of oxidative DNA damage. <strong>Nucleic Acids Res<\/strong> 26, 2917-22. 1998<\/li>\n<li>Hiroi, Y., Komuro, I., Matsushita, I., Aburatani, H., Hosoda, T., Nakahori, Y., Medof, M. E., and Yazaki, Y. Assignment of the human GPAA1 gene, which encodes a product required for the attachment of glycosylphosphatidylinositols to proteins, at 8q24. <strong>Genomics <\/strong>54, 354-5. 1998<\/li>\n<li>Hallstensson, K., Thulin, S., Aburatani, H., Hippo, Y., and Martinsson, T. Representational difference analysis and loss of heterozygosity studies detect 3p deletions in neuroblastoma. <strong>Eur J Cancer<\/strong> 33, 1966-70. 1997<\/li>\n<li>Aburatani, H., Hippo, Y., Ishida, T., Takashima, R., Matsuba, C., Kodama, T., Takao, M., Yasui, A., Yamamoto, K., and Asano, M. Cloning and characterization of mammalian 8-hydroxyguanine-specific DNA glycosylase\/apurinic, apyrimidinic lyase, a functional mutM homologue. <strong>Cancer Res<\/strong> 57, 2151-6. 1997<\/li>\n<li>Doi, T., Minami, T., Itoh, M., Aburatani, H., Kawabe, Y., Kodama, T., Kondo, N., Satoh, Y., Asayama, T., and Imanishi, T. An alternative form of nucleolysin binds to a T-cluster DNA in the silencer element of platelet factor 4 gene. <strong>Biochem Biophys Res Commun<\/strong> 235, 625-30. 1997<\/li>\n<li>Suzuki, H., Kurihara, Y., Takeya, M., Kamada, N., Kataoka, M., Jishage, K., Ueda, O., Sakaguchi, H., Higashi, T., Suzuki, T., Takashima, Y., Kawabe, Y., Cynshi, O., Wada, Y., Honda, M., Kurihara, H., Aburatani, H., Doi, T., Matsumoto, A., Azuma, S., Noda, T., Toyoda, Y., Itakura, H., Yazaki, Y., Kodama, T., and et al. A role for macrophage scavenger receptors in atherosclerosis and susceptibility to infection. <strong>Nature<\/strong> 386, 292-6. 1997.<\/li>\n<li>Corless, C. L., Aburatani, H., Fletcher, J. A., Housman, D. E., Amin, M. B., and Weinberg, D. S. (1996). Papillary renal cell carcinoma: quantitation of chromosomes 7 and 17 by FISH, analysis of chromosome 3p for LOH, and DNA ploidy. <strong>Diagn Mol Pathol<\/strong> 5, 53-64.<\/li>\n<li>Aburatani H, Stanton VP Jr., and Housman DE. High-resolution physical mapping by combined Alu-hybridization\/PCR screening: construction of a yeast artificial chromosome map covering 31 centimorgans in 3p21-p14. <strong>Proc Natl Acad Sci U S A<\/strong> 93, 4474-9. 1996.<\/li>\n<li>Cai, W., Aburatani, H., Stanton, V. P., Jr., Housman, D. E., Wang, Y. K., and Schwartz, D. C. Ordered restriction endonuclease maps of yeast artificial chromosomes created by optical mapping on surfaces. <strong>Proc Natl Acad Sci U S A<\/strong> 92: 5164-8, 1995<\/li>\n<li>Hunter KW, Ontiveros SD, Watson ML, Stanton VP Jr, Gutierrez P, Bhat D, Rochelle J, Graw S, Ton C, Schalling M,<strong>Aburatani H<\/strong>, Brown SDM, Seldin MF, Housman DE. Rapid and efficient construction of yeast artificial chromosome contigs in the mouse genome with interspersed repetitive sequence PCR (IRS-PCR): generation of a 5-cM, &gt; 5 megabase contig on mouse chromosome 1. <strong>Mamm Genome<\/strong>. 1994 Oct;5(10):597-607.<\/li>\n<li>Munroe DJ, Haas M, <strong>Aburatani H<\/strong>, et al. (1994) IRE-bubble PCR: a rapid method for efficient and representative amplification of human genomic DNA sequences from complex sources.<strong> <em>Genomics<\/em><\/strong> 19: 506-14<\/li>\n<li>Haas M, <strong>Aburatani H<\/strong>, Stanton VP Jr, et al. (1993) Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3.<strong> <em>Genomics<\/em><\/strong> 16: 90-6<\/li>\n<li>Li FP, Decker HJ, <strong>Aburatani H<\/strong>, et al. (1993) Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation. Genetics of familial renal carcinoma. <strong><em>Ann Intern Med<\/em><\/strong> 118: 106-11<\/li>\n<li>Brook JD, McCurrach ME, Harley HG, Buckler AJ, Church D, <strong>Aburatani H<\/strong>, Hunter K, Stanton VP, Thirion JP, Hudson T, et al. (1992) Molecular basis of myotonic distrophy: expansion of a trinucleotide (CTG) repeat at the 3&#8242; end of a transcript encoding a protein kinase family member. <strong><em>Cell<\/em><\/strong> 69: 385<\/li>\n<li>Hubert R, Stanton VP Jr, <strong>Aburatani H<\/strong>, et al. Sperm typing allows accurate measurement of the recombination fraction between D3S2 and D3S3 on the short arm of human chromosome 3. <strong><em>Genomics<\/em><\/strong> 12: 683-7. 1992<\/li>\n<li>Naganawa S, kodama T, <strong>Aburatani H<\/strong>, et al. Genetic analysis of a Japanese family with normotriglyceridemic abetalipoproteinemia indicates a lack of linkage to the apolipoprotein B gene. <strong><em>Biochem Biophys Res Commun<\/em><\/strong> 182: 99-104. 1992<\/li>\n<li>Goradia TM, Stanton VP Jr, Cui XF,<strong> Aburatani H<\/strong>, et al. Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. <strong><em>Genomics<\/em> <\/strong>10: 748-55, 1991<\/li>\n<li>Gogos JA, <strong>Aburatani H<\/strong>, et al. Detection of single base mismatches of thymine and cytosine residues by potassium permanganate and hydroxylamine in the presence of tetralkylammonium salts. <strong><em>Nucleic Acids Res<\/em>.<\/strong> 18(23): 6807-6814. 1990<\/li>\n<li>Matsumoto A, Naito M, Itakura H, Ikemoto S, Asaoka H, Hayakawa I, Kanamori H, Aburatani H, Takaku F, Suzuki H, et al. Human macrophage scavenger receptors: primary structure, expression, and localization in atherosclerotic lesions.<strong> <em>Proc Natl Acad Sci U S A<\/em>.<\/strong> 87(23): 9133-9137. 1990<\/li>\n<li>Ishikawa T, <strong>Aburatani H<\/strong>, et al. A functional retinoic acid receptor encoded by the gene on human chromosome 12.<strong><em>Mol Endocrinol<\/em>.<\/strong> 4(6): 837-844. 1990<\/li>\n<li><strong>Aburatani H<\/strong>, et al. Single base substitution between human intestinal and hepatic apolipoprotein B mRNA detected by ribonuclease cleavage analysis. <strong><em>J Biochem (Tokyo).<\/em><\/strong>105(6): 911-915. 1989<\/li>\n<li>Ohno M, <strong>Aburatani H<\/strong>, et al. A neonatal case of apolipoprotein C-II deficiency.<strong> <em>Eur J Pediatr.<\/em><\/strong> 148(6): 550-552. 1989<\/li>\n<li>Shimano H, <strong>Aburatani H,<\/strong> et al. Down-regulation of hepatic LDL receptor protein and messenger RNA in fasted rabbits.<em> <strong>J Biochem (Tokyo)<\/strong><\/em>. 104(5): 712-716. 1988<\/li>\n<li><strong>Aburatani H<\/strong>, et al. Increased levels of messenger ribonucleic acid for apolipoprotein E in the spleen of probucol-treated rabbits.<strong> <em>Am J Cardiol.<\/em><\/strong> 62(3): 60B-65B. 1988<\/li>\n<li><strong>Aburatani H<\/strong>, et al. A study of DNA polymorphism in the apolipoprotein B gene in a Japanese population. <strong><em>Atherosclerosis<\/em><\/strong> 72: 71-76. 1988<\/li>\n<li><strong>Aburatani H<\/strong>, et al. Deoxyribonucleic Acid (DNA) Polymorphism in the Apolipoprotein AI Gene:A Study in a Japanese Population. <strong><em>Japanese Journal of Medicine<\/em><\/strong>, 27: 26-59. 1988<\/li>\n<li><strong>Aburatani H<\/strong>, et al. Apolipoprotein B-gene polymorphism and myocardial infarction.<strong> <em>New England J Med<\/em><\/strong>, 317: 52-53. 1987<\/li>\n<li>Matsumoto A, <strong>Aburatani H<\/strong>, et al. Cloning and regulation of rat apolipoprotein B mRNA. <strong><em>Biochem Biophys Res Comm<\/em><\/strong> 142: 92-99. 1987<\/li>\n<li>Ishikawa T, <strong>Aburatani H<\/strong><u>,<\/u> et al. Primary intrahepatic sclerosing cholangitis with inflamatory bowel disease. <strong><em>Acta Patol.Jpn<\/em><\/strong>. 37: 1637-1643. 1987<\/li>\n<li>Takashima Y, Kodama T, <strong>Aburatani H<\/strong>, et al. Normotriglycedemic Abetalipoproteinemia in Infancy: An isolated Apolipoproteinemia B-100 Deficiency. <strong><em>Pediartrics<\/em><\/strong>, 75, 541-546. 1985<\/li>\n<li><strong>Aburatani H<\/strong>, et al. Analysis of Apolipoproteins B100 and B48 by Sodium Dodesyl Sulfate Polyacrylamide Gradient Gel Electrophoresis. <strong><em>Biochem<\/em>.<\/strong> 94: 1241-1245. 1983<\/li>\n<li>Kodama T, Akanuma Y, Okazaki M and <strong>Aburatani H<\/strong>, et al. Abnormalities in plasma lipoprotein in familial partial lecithin:cholesterol acyltransferase deficiency. <strong><em>Biochim Biophys Acta<\/em><\/strong>, 752:407-415. 1983<\/li>\n<\/ul>\n<p><\/p>","protected":false},"excerpt":{"rendered":"<p>Ishida, T., Hippo, Y., Nakahori, Y., Matsushita, I., Kodama, T., Nishimura, S., and Aburatani, H. Structure an &hellip; <a href=\"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/publications\/publications_-1999\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":54,"featured_media":0,"parent":43,"menu_order":-1999,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-4576","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/wp-json\/wp\/v2\/pages\/4576","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/wp-json\/wp\/v2\/users\/54"}],"replies":[{"embeddable":true,"href":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/wp-json\/wp\/v2\/comments?post=4576"}],"version-history":[{"count":1,"href":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/wp-json\/wp\/v2\/pages\/4576\/revisions"}],"predecessor-version":[{"id":4608,"href":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/wp-json\/wp\/v2\/pages\/4576\/revisions\/4608"}],"up":[{"embeddable":true,"href":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/wp-json\/wp\/v2\/pages\/43"}],"wp:attachment":[{"href":"https:\/\/www.genome.rcast.u-tokyo.ac.jp\/en\/wp-json\/wp\/v2\/media?parent=4576"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}