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1
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0023104845
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Variable number of tandem repeat (VNTR) markers for human gene mapping
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Nakamura Y. Leppert M, O'Connell P, Wolff R, Holm T, Culver M, Martin C, Fujimoto E, Hoff M, Kumlin E, et al: Variable number of tandem repeat (VNTR) markers for human gene mapping. Science 1987; 235: 1616-1622
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Hoff, M.9
Kumlin, E.10
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2
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0023244033
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Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17
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Barker D, Wright E, Nguyen K, Cannon L, Fain P, Goldgar D, Bishop DT, Carey J, Baty B, et al: Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17. Science 1987; 236: 1100-1102
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Goldgar, D.6
Bishop, D.T.7
Carey, J.8
Baty, B.9
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3
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0023572211
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The gene for familial polyposis coli maps to the long arm of chromosome 5
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Leppert M, Dobbs M, Scambler P, O'Connell P, Nakamura Y, Stauffer D, Woodward S, Burt R, Hughes J, Gardner E, et al. The gene for familial polyposis coli maps to the long arm of chromosome 5. Science 1987; 238: 1411-1413
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Science
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Stauffer, D.6
Woodward, S.7
Burt, R.8
Hughes, J.9
Gardner, E.10
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4
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0023828816
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Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma
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Larsson C, Skogseid B, Oberg K, Nakamura Y, Nordenskjold M: Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature 1988; 332: 85-87
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(1988)
Nature
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Larsson, C.1
Skogseid, B.2
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Nakamura, Y.4
Nordenskjold, M.5
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5
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0023751357
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Mapping of mutation causing Friedreich's ataxia to human chromosome 9
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Chamberlain S, Shaw J, Rowland A, Wallis J, South S, Nakamura Y, von Gabain A, Farrall M, Williamson R: Mapping of mutation causing Friedreich's ataxia to human chromosome 9. Nature 1988; 334: 248-250
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Nature
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Von Gabain, A.7
Farrall, M.8
Williamson, R.9
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6
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0025961417
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Presymptomatic screening for multiple endocrine neoplasia type 2A with linked DNA markers
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The MEN 2A International Collaborative Group
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Mathew CG, Easton DF, Nakamura Y, Ponder BA: Presymptomatic screening for multiple endocrine neoplasia type 2A with linked DNA markers. The MEN 2A International Collaborative Group. Lancet 1991; 337: 7-11
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Mathew, C.G.1
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Ponder, B.A.4
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7
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0023748414
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Genetic alterations during colorectal-tumor development
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Vogelstein B, Fearon ER, Hamilton SR, Kern SE, Preisinger AC, Leppert M, Nakamura Y, White R, Smits AM, Bos JL: Genetic alterations during colorectal-tumor development. N Engl J Med 1988; 319: 525-532
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N Engl J Med
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White, R.8
Smits, A.M.9
Bos, J.L.10
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8
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0024514647
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Allelotype of colorectal carcinomas
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Vogelstein B, Fearon ER, Kern SE, Hamilton SR, Preisinger AC, Nakamura Y, White R: Allelotype of colorectal carcinomas. Science 1989; 244: 207-211
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(1989)
Science
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Vogelstein, B.1
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Preisinger, A.C.5
Nakamura, Y.6
White, R.7
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9
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0024536654
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Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas
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Baker SJ, Fearon ER, Nigro JM, Hamilton SR, Preisinger AC, Jessup JM, vanTuinen P, Ledbetter DH, Barker DF, Nakamura Y. et al: Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas. Science 1989; 244: 217-221
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Science
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Baker, S.J.1
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Jessup, J.M.6
VanTuinen, P.7
Ledbetter, D.H.8
Barker, D.F.9
Nakamura, Y.10
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10
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0025354907
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Genetic analysis of an inherited predisposition to colon cancer in a family with a variable number of adenomatous polyps
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Leppert M, Burt R, Hughes JP, Samowitz W, Nakamura Y, Woodward S, Gardner E, Lalouel JM, White R: Genetic analysis of an inherited predisposition to colon cancer in a family with a variable number of adenomatous polyps. N Engl J Med 1990; 322: 904-908
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Nakamura, Y.5
Woodward, S.6
Gardner, E.7
Lalouel, J.M.8
White, R.9
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11
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0025909734
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Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers
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Kinzler KW, Nilbert MC, Vogelstein B, Bryan TM, Levy DB, Smith KJ, Preisinger AC, Hamilton SR, Hedge P, Markham A, et al: Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers. Science 1991; 251: 1366-1370
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Markham, A.10
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0025817880
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Kinzler KW, Nilbert MC, Su LK, Vogelstein B, Bryan TM, Levy DB, Smith KJ, Preisinger AC, Hedge P, McKechnie D, et al: Identification of FAP locus genes from chromosome 5q21. Science 1991; 253: 661-665
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Smith, K.J.7
Preisinger, A.C.8
Hedge, P.9
McKechnie, D.10
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13
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0025899162
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Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients
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Nishisho I, Nakamura Y, Miyoshi Y, Miki Y, Ando H, Horii A, Koyama K, Utsunomiya J, Baba S, Hedge P: Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. Science 1991; 253: 665-669
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Nishisho, I.1
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Horii, A.6
Koyama, K.7
Utsunomiya, J.8
Baba, S.9
Hedge, P.10
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14
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11944252481
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Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients
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Miyoshi Y, Ando H, Nagase H, Nishisho I, Horii A, Miki Y, Mori T, Utsunomiya J, Baba S, Petersen G, et al: Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients. Proc Natl Acad Sci USA 1992; 89: 4452-4456
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Baba, S.9
Petersen, G.10
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15
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0027366136
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A novel metalloprotease/disintegrin-like gene at 17q21.3 is somatically rearranged in two primary breast cancers
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Emi M, Katagiri T, Harada Y, Saito H, Inazawa J, Ito I, Kasumi F, Nakamura Y: A novel metalloprotease/disintegrin-like gene at 17q21.3 is somatically rearranged in two primary breast cancers. Nat Genet 1993; 5: 151-157
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Kasumi, F.7
Nakamura, Y.8
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16
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0030058209
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Mutation analysis in the BRCA2 gene in primary breast cancers
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Miki Y, Katagiri T, Kasumi F, Yoshimoto T, Nakamura Y: Mutation analysis in the BRCA2 gene in primary breast cancers. Nat Genet 1996; 13: 245-247
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Nat Genet
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Miki, Y.1
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17
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0034088858
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AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1
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Satoh S, Daigo Y, Furukawa Y, Kato T, Miwa N, Nishiwaki T, Kawasoe T, Ishiguro H, Fujita M, Tokino T, et al: AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1. Nat Genet 2000; 24: 245-250
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Fujita, M.9
Tokino, T.10
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18
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0034594978
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A ribonucleotide reductase gene involved in a p53 dependent cell-cycle checkpoint for DNA damage
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Tanaka H, Arakawa H, Yamaguchi T, Shiraishi K, Fukuda S, Matsui K, Takei Y, Nakamura Y: A ribonucleotide reductase gene involved in a p53 dependent cell-cycle checkpoint for DNA damage. Nature 2000; 404: 42-49
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Nature
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Tanaka, H.1
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Takei, Y.7
Nakamura, Y.8
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19
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0034664733
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p53AIP1, a potential mediator of p53-dependent apoptosis, and its regulation by Ser-46-phosphorylated p53
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Oda K, Arakawa H, Tanaka T, Matsuda K, Tanikawa C, Mori T, Nishimori H, Tamai K, Tokino T, Nakamura Y, et al: p53AIP1, a potential mediator of p53-dependent apoptosis, and its regulation by Ser-46-phosphorylated p53. Cell 2000; 102: 849-862
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Nishimori, H.7
Tamai, K.8
Tokino, T.9
Nakamura, Y.10
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20
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0029906919
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Isolation of a novel GPI-anchored gene specifically regulated by p53; Correlation between its expression and anti-cancer drug sensitivity
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Furuhata T, Tokino T, Urano T, Nakamura Y: Isolation of a novel GPI-anchored gene specifically regulated by p53; correlation between its expression and anti-cancer drug sensitivity. Oncogene 1996; 13: 1965-1970
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Oncogene
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Furuhata, T.1
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Nakamura, Y.4
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21
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0030756159
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Cloning of P2XM, a novel human P2X receptor gene regulated by p53
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Urano T, Nishimori H, Han HJ, Furuhata T, Kimura Y, Nakamura Y, Tokino T: Cloning of P2XM, a novel human P2X receptor gene regulated by p53. Cancer Res 1997; 57: 3281-3287
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Cancer Res
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Nakamura, Y.6
Tokino, T.7
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22
-
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9844261161
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A novel brain-specific p53-target gene, BAI1, containing thrombospondin type1 repeats inhibits experimental angiogenesis
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Nishimori H, Shiratsuchi T, Urano T, Kimura Y, Kiyono K, Tatsumi K, Yoshida S, Ono M, Kuwano M, Nakamura Y, et al: A novel brain-specific p53-target gene, BAI1, containing thrombospondin type1 repeats inhibits experimental angiogenesis. Oncogene 1997; 15: 2145-2150
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Oncogene
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Tatsumi, K.6
Yoshida, S.7
Ono, M.8
Kuwano, M.9
Nakamura, Y.10
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23
-
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0031833909
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CSR, a scavenger receptor-like protein with a protective role against cellular damage caused by UV irradiation and oxidative stress
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Han HJ, Tokino T, Nakamura Y: CSR, a scavenger receptor-like protein with a protective role against cellular damage caused by UV irradiation and oxidative stress. Hum Mol Genet 1998; 7: 1039-1046
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Hum Mol Genet
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Han, H.J.1
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24
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0032746791
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Isolation and characterization of a novel TP53-inducible gene. TP53TG3
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Ng CC, Koyama K, Okamura S, Kondoh H, Takei Y, Nakamura Y: Isolation and characterization of a novel TP53-inducible gene. TP53TG3. Genes Chromosmes Cancer 1999; 26: 329-335
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Genes Chromosmes Cancer
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Nakamura, Y.6
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25
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0034660875
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Identification of fractalkine, a CX3C-type chemokine, as a direct target of p53
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Shiraishi K, Fukuda S, Mori T, Matsuda K, Yamaguchi T, Tanikawa C, Ogawa M, Nakamura Y, Arakawa H: Identification of fractalkine, a CX3C-type chemokine, as a direct target of p53. Cancer Res 2000; 60: 3722-3726
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Cancer Res
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Tanikawa, C.6
Ogawa, M.7
Nakamura, Y.8
Arakawa, H.9
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26
-
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0027364850
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Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31 33
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Toda T, Segawa M, Nomura Y, Nonaka I, Masuda K, Ishihara T, Sakai M, Tomita I, Origuchi Y, Suzuki M, et al: Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31 33. Nat Genet 1993; 5: 283-286
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Sakai, M.7
Tomita, I.8
Origuchi, Y.9
Suzuki, M.10
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27
-
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17344372572
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Positional cloning of the gene for Nijmegen breakage syndrome
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Matsuura S, Tauchi H, Nakamura A, Kondo N, Sakamoto S, Endo S, Smeets D, Solder B, Belohradsky BH, Der Kaloustian VM, et al: Positional cloning of the gene for Nijmegen breakage syndrome. Nat Genet 1998; 19: 179-181
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Nat Genet
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Matsuura, S.1
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Smeets, D.7
Solder, B.8
Belohradsky, B.H.9
Der Kaloustian, V.M.10
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28
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0031859977
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Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine
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Okawa A, Nakamura I, Goto S, Moriya H, Nakamura Y, Ikegawa S: Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine. Nat Genet 1998; 19: 271-273
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(1998)
Nat Genet
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Okawa, A.1
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Ikegawa, S.6
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29
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0032560851
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An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
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Kobayashi K, Nakahori Y, Miyake M, Matsumura K, Kondo-Iida E, Nomura Y, Segawa M, Yoshioka M, Saito K, Osawa M, et al: An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature 1998; 394: 388-392
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Yoshioka, M.8
Saito, K.9
Osawa, M.10
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30
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0032900158
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Identification of the gene responsible for gelatinous drop-like corneal dystrophy
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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; 21: 420-423
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(1999)
Nat Genet
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Tsujikawa, M.1
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Tano, Y.6
Nakamura, Y.7
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