論文・総説 - 田中　敏博

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  1. Nakajima T, Furukawa T, Hirano Y, Tanaka T, Sakurada H, Takahashi T, Nagai R, Itoh T, Katayama Y, Nakamura Y, Hiraoka M. Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2. Cardiovasc Res. 1999.11; 44 (2): 283-293. ( PubMed )

  2. Mikami M, Yasuda T, Terao A, Nakamura M, Ueno S, Tanabe H, Tanaka T, Onuma T, Goto Y, Kaneko S, Sano A. Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1. Am J Hum Genet. 1999.09; 65 (3): 745-751. ( PubMed )

  3. Tsujikawa M, Kurahashi H, Tanaka T, Nishida K, Shimomura Y, Tano Y, Nakamura Y. Identification of the gene responsible for gelatinous drop-like corneal dystrophy. Nat Genet. 1999.04; 21 (4): 420-423. ( PubMed, DOI )

  4. Tsujikawa M, Kurahashi H, Tanaka T, Okada M, Yamamoto S, Maeda N, Watanabe H, Inoue Y, Kiridoshi A, Matsumoto K, Ohashi Y, Kinoshita S, Shimomura Y, Nakamura Y, Tano Y. Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p. Am J Hum Genet. 1998.10; 63 (4): 1073-1077. ( PubMed, DOI )

  5. Nishiu J, Tanaka T, Nakamura Y. Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and female-specific tissues and its chromosomal localization to 9q22.3. Genomics. 1998.09; 52 (3): 378-381. ( PubMed, DOI )

  6. Itoh T, Tanaka T, Nagai R, Kikuchi K, Ogawa S, Okada S, Yamagata S, Yano K, Yazaki Y, Nakamura Y. Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome. Hum Genet. 1998.09; 103 (3): 290-294. ( PubMed )

  7. Nakajima T, Furukawa T, Tanaka T, Katayama Y, Nagai R, Nakamura Y, Hiraoka M. Novel mechanism of HERG current suppression in LQT2: shift in voltage dependence of HERG inactivation. Circ Res. 1998.08; 83 (4): 415-422. ( PubMed )

  8. Itoh T, Tanaka T, Nagai R, Kamiya T, Sawayama T, Nakayama T, Tomoike H, Sakurada H, Yazaki Y, Nakamura Y. Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome. Hum Genet. 1998.04; 102 (4): 435-439. ( PubMed )

  9. Nishiu J, Tanaka T, Nakamura Y. Isolation and chromosomal mapping of the human homolog of perilipin (PLIN), a rat adipose tissue-specific gene, by differential display method. Genomics. 1998.03; 48 (2): 254-257. ( PubMed, DOI )

  10. Nakagawa H, Koyama K, Tanaka T, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Monden M, Nakamura Y. Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3. Hum Genet. 1998.02; 102 (2): 203-206. ( PubMed )

  11. Yamane-Tanaka Y, Kogawa K, Tanaka T, Nakamura Y, Isomura M. Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population. J Hum Genet. 1998; 43 (3): 165-168. ( PubMed, DOI )

  12. Itoh M, Tsukada S, Orita T, Nishiu J, Tomoike H, Nakamura Y, Tanaka T. Identification by differential display of eight known genes induced during in vivo intimal hyperplasia. J Hum Genet. 1998; 43 (1): 9-13. ( PubMed, DOI )

  13. Tanaka T, Nagai R, Tomoike H, Takata S, Yano K, Yabuta K, Haneda N, Nakano O, Shibata A, Sawayama T, Kasai H, Yazaki Y, Nakamura Y. Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome. Circulation. 1997.02; 95 (3): 565-567. ( PubMed )

  14. Tanaka T, Ogiwara A, Uchiyama I, Takagi T, Yazaki Y, Nakamura Y. Construction of a normalized directionally cloned cDNA library from adult heart and analysis of 3040 clones by partial sequencing. Genomics. 1996.07; 35 (1): 231-235. ( PubMed, DOI )

  15. Tanaka T, Inazawa J, Nakamura Y. Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase (MDH1). Genomics. 1996.02; 32 (1): 128-130. ( PubMed, DOI )

  16. Tanaka T, Inazawa J, Nakamura Y. Molecular cloning of a human cDNA encoding putative cysteine protease (PRSC1) and its chromosome assignment to 14q32.1. Cytogenet Cell Genet. 1996; 74 (1-2): 120-123. ( PubMed )

  17. Chatterjee A, Tanaka T, Parrish JE, Herman GE. Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions. Mamm Genome. 1995.11; 6 (11): 802-804. ( PubMed )

  18. Tanaka T, Okui K, Nakamura Y. Assignment of the human caltractin gene (CALT) to Xq28 by fluorescence in situ hybridization. Genomics. 1994.12; 24 (3): 609-610. ( PubMed )

  19. Tanaka T, Nakahara K, Kato N, Imai T, Yamazaki T, Tomita H, Shimokawa H, Matsuhashi H, Sato N, Matsui M. Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families. Hum Genet. 1994.10; 94 (4): 380-384. ( PubMed )

  20. 須藤毅顕、小林宏明、青木章、田中敏博. 全エクソーム解析による疾患遺伝子の同定-侵襲性歯周炎のNOD2遺伝子の変異の同定- 最新醫學. 2019.01; 74 (2): 207-214.

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