Publications (-1999)

  • Ishida, T., Hippo, Y., Nakahori, Y., Matsushita, I., Kodama, T., Nishimura, S., and Aburatani, H. Structure and chromosomal localization of human MMH/OGG1 gene. Cytogenetics and Cell Genetics, 85(3-4):232-6. 1999
  • 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. Biochem Biophys Res Commun258, 605-10. 1999
  • 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 Aburatani H. New DNA polymorphisms of human MMH/OGG1 gene: prevalence of one polymorphism among lung-adenocarcinoma patients in Japanese. Int J Cancer 80, 18-21. 1999
  • Ejeskar, K., Aburatani, H., 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. Br J Cancer 77, 1787-91. 1998
  • Takao, M., Aburatani, H., Kobayashi, K., and Yasui, A. Mitochondrial targeting of human DNA glycosylases for repair of oxidative DNA damage. Nucleic Acids Res 26, 2917-22. 1998
  • 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. Genomics 54, 354-5. 1998
  • Hallstensson, K., Thulin, S., Aburatani, H., Hippo, Y., and Martinsson, T. Representational difference analysis and loss of heterozygosity studies detect 3p deletions in neuroblastoma. Eur J Cancer 33, 1966-70. 1997
  • 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. Cancer Res 57, 2151-6. 1997
  • 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. Biochem Biophys Res Commun 235, 625-30. 1997
  • 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. Nature 386, 292-6. 1997.
  • 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. Diagn Mol Pathol 5, 53-64.
  • 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. Proc Natl Acad Sci U S A 93, 4474-9. 1996.
  • 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. Proc Natl Acad Sci U S A 92: 5164-8, 1995
  • Hunter KW, Ontiveros SD, Watson ML, Stanton VP Jr, Gutierrez P, Bhat D, Rochelle J, Graw S, Ton C, Schalling M,Aburatani H, 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, > 5 megabase contig on mouse chromosome 1. Mamm Genome. 1994 Oct;5(10):597-607.
  • Munroe DJ, Haas M, Aburatani H, et al. (1994) IRE-bubble PCR: a rapid method for efficient and representative amplification of human genomic DNA sequences from complex sources. Genomics 19: 506-14
  • Haas M, Aburatani H, Stanton VP Jr, et al. (1993) Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3. Genomics 16: 90-6
  • Li FP, Decker HJ, Aburatani H, 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. Ann Intern Med 118: 106-11
  • Brook JD, McCurrach ME, Harley HG, Buckler AJ, Church D, Aburatani H, 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′ end of a transcript encoding a protein kinase family member. Cell 69: 385
  • Hubert R, Stanton VP Jr, Aburatani H, et al. Sperm typing allows accurate measurement of the recombination fraction between D3S2 and D3S3 on the short arm of human chromosome 3. Genomics 12: 683-7. 1992
  • Naganawa S, kodama T, Aburatani H, et al. Genetic analysis of a Japanese family with normotriglyceridemic abetalipoproteinemia indicates a lack of linkage to the apolipoprotein B gene. Biochem Biophys Res Commun 182: 99-104. 1992
  • Goradia TM, Stanton VP Jr, Cui XF, Aburatani H, et al. Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. Genomics 10: 748-55, 1991
  • Gogos JA, Aburatani H, et al. Detection of single base mismatches of thymine and cytosine residues by potassium permanganate and hydroxylamine in the presence of tetralkylammonium salts. Nucleic Acids Res. 18(23): 6807-6814. 1990
  • 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. Proc Natl Acad Sci U S A. 87(23): 9133-9137. 1990
  • Ishikawa T, Aburatani H, et al. A functional retinoic acid receptor encoded by the gene on human chromosome 12.Mol Endocrinol. 4(6): 837-844. 1990
  • Aburatani H, et al. Single base substitution between human intestinal and hepatic apolipoprotein B mRNA detected by ribonuclease cleavage analysis. J Biochem (Tokyo).105(6): 911-915. 1989
  • Ohno M, Aburatani H, et al. A neonatal case of apolipoprotein C-II deficiency. Eur J Pediatr. 148(6): 550-552. 1989
  • Shimano H, Aburatani H, et al. Down-regulation of hepatic LDL receptor protein and messenger RNA in fasted rabbits. J Biochem (Tokyo). 104(5): 712-716. 1988
  • Aburatani H, et al. Increased levels of messenger ribonucleic acid for apolipoprotein E in the spleen of probucol-treated rabbits. Am J Cardiol. 62(3): 60B-65B. 1988
  • Aburatani H, et al. A study of DNA polymorphism in the apolipoprotein B gene in a Japanese population. Atherosclerosis 72: 71-76. 1988
  • Aburatani H, et al. Deoxyribonucleic Acid (DNA) Polymorphism in the Apolipoprotein AI Gene:A Study in a Japanese Population. Japanese Journal of Medicine, 27: 26-59. 1988
  • Aburatani H, et al. Apolipoprotein B-gene polymorphism and myocardial infarction. New England J Med, 317: 52-53. 1987
  • Matsumoto A, Aburatani H, et al. Cloning and regulation of rat apolipoprotein B mRNA. Biochem Biophys Res Comm 142: 92-99. 1987
  • Ishikawa T, Aburatani H, et al. Primary intrahepatic sclerosing cholangitis with inflamatory bowel disease. Acta Patol.Jpn. 37: 1637-1643. 1987
  • Takashima Y, Kodama T, Aburatani H, et al. Normotriglycedemic Abetalipoproteinemia in Infancy: An isolated Apolipoproteinemia B-100 Deficiency. Pediartrics, 75, 541-546. 1985
  • Aburatani H, et al. Analysis of Apolipoproteins B100 and B48 by Sodium Dodesyl Sulfate Polyacrylamide Gradient Gel Electrophoresis. Biochem. 94: 1241-1245. 1983
  • Kodama T, Akanuma Y, Okazaki M and Aburatani H, et al. Abnormalities in plasma lipoprotein in familial partial lecithin:cholesterol acyltransferase deficiency. Biochim Biophys Acta, 752:407-415. 1983