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    1. Nakajima, T; Jorde, LB; Ishigami, T; Umemura, S; Emi, M; Lalouel, JM; Inoue, I
      Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Iwasaki, H; Shinohara, Y; Ezura, Y; Ishida, R; Kodaira, M; Kajita, M; Nakajima, T; Shiba, T; Emi, M
      Thirteen single-nucleotide polymorphisms in the human osteopontin gene identified by sequencing of the entire gene in Japanese individuals

      JOURNAL OF HUMAN GENETICS
    3. Shinohara, Y; Ezura, Y; Iwasaki, H; Nakazawa, I; Ishida, R; Kodaira, M; Kajita, M; Shiba, T; Emi, M
      Linkage disequilibrium and haplotype analysis among ten single-nucleotide polymorphisms of interleukin 11 identified by sequencing of the gene

      JOURNAL OF HUMAN GENETICS
    4. Nakazawa, I; Nakajima, T; Ishigami, T; Umemura, S; Emi, M
      Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA)gene

      JOURNAL OF HUMAN GENETICS
    5. Fujiwara, H; Emi, M; Nagai, H; Ohgaki, K; Imoto, I; Akimoto, M; Ogawa, O; Habuchi, T
      Definition of a 1-Mb homozygous deletion at 9q32-q33 in a human bladder-cancer cell line

      JOURNAL OF HUMAN GENETICS
    6. Mine, N; Kurose, K; Nagai, H; Doi, D; Ota, Y; Yoneyama, K; Konishi, H; Araki, T; Emi, M
      Gene fusion involving HMGIC is a frequent aberration in uterine leiomyomas

      JOURNAL OF HUMAN GENETICS
    7. Ota, N; Nakajima, T; Nakazawa, I; Suzuki, T; Hosoi, T; Orimo, H; Inoue, S; Shirai, Y; Emi, M
      A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density

      JOURNAL OF HUMAN GENETICS
    8. Yoshida, S; Fukino, K; Harada, H; Nagai, H; Imoto, I; Inazawa, J; Takahashi, H; Teramoto, A; Emi, M
      The c-Jun NH2-terminal kinase3 (JNK3) gene: genomic structure, chromosomalassignment, and loss of expression in brain tumors

      JOURNAL OF HUMAN GENETICS
    9. Nakazawa, I; Nakajima, T; Harada, H; Ishigami, T; Umemura, S; Emi, M
      Human calcitonin receptor-like receptor for adrenomedullin: genomic structure, eight single-nucleotide polymorphisms, and haplotype analysis

      JOURNAL OF HUMAN GENETICS
    10. Harada, H; Nagai, H; Mine, N; Terada, Y; Fujiwara, H; Mikami, I; Tsuneizumi, M; Yabe, A; Miyazaki, K; Yokota, M; Imoto, I; Inazawa, J; Emi, M
      Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle

      JOURNAL OF HUMAN GENETICS
    11. Harada, H; Nagai, NH; Tsuneizumi, M; Mikami, I; Sugano, S; Emi, M
      Identification of DMC1, a novel gene in the TOC region on 17q25.1 that shows loss of expression in multiple human cancers

      JOURNAL OF HUMAN GENETICS
    12. Keicho, N; Emi, M; Kajita, M; Matsushita, I; Nakata, K; Azuma, A; Ohishi, N; Kudoh, S
      Overestimated frequency of a possible emphysema-susceptibility allele whenmicrosomal epoxide hydrolase is genotyped by the conventional polymerase chain reaction-based method

      JOURNAL OF HUMAN GENETICS
    13. Ishida, R; Ezura, Y; Iwasaki, H; Nakazawa, I; Kajita, M; Kodaira, M; Ito, H; Emi, M
      Linkage disequilibrium and haplotype analysis among four novel single-nucleotide polymorphisms in the human leukemia inhibitory factor (LIF) gene

      JOURNAL OF HUMAN GENETICS
    14. Iwasaki, H; Ota, N; Nakajima, T; Shinohara, Y; Kodaira, M; Kajita, M; Emi, M
      Five novel single-nucleotide polymorphisms of human interferon gamma identified by sequencing the entire gene

      JOURNAL OF HUMAN GENETICS
    15. Hirano, A; Nagai, H; Harada, H; Terada, Y; Haga, S; Kajiwara, T; Emi, M
      Nine novel single-nucleotide polymorphisms in the integrin beta 4 (ITGB4) gene in the Japanese population

      JOURNAL OF HUMAN GENETICS
    16. Kajita, M; Iwasaki, H; Ota, N; Shinohara, Y; Kodaira, M; Nakajima, T; Emi, M
      Novel single nucleotide polymorphisms of the human colony-stimulating factor 2 (CSF2) gene identified by sequencing the entire gene

      JOURNAL OF HUMAN GENETICS
    17. Shinohara, Y; Iwasaki, H; Ota, N; Nakajima, T; Kodaira, M; Kajita, M; Shiba, T; Emi, M
      Novel single nucleotide polymorphisms of the human nuclear factor kappa-B 2 gene identified by sequencing the entire gene

      JOURNAL OF HUMAN GENETICS
    18. Hirano, A; Emi, M; Tsuneizumi, M; Utada, Y; Yoshimoto, M; Kasumi, F; Akiyama, F; Sakamoto, G; Haga, S; Kajiwara, T; Nakamura, Y
      Allelic losses of loci at 3p25.1, 8p22, 13q12, 17p13.3, and 22q13 correlate with postoperative recurrence in breast cancer

      CLINICAL CANCER RESEARCH
    19. Tsuneizumi, M; Emi, M; Nagai, H; Harada, H; Sakamoto, G; Kasumi, F; Inoue, S; Kazui, T; Nakamura, Y
      Overrepresentation of the EBAG9 gene at 8q23 associated with early-stage breast cancers

      CLINICAL CANCER RESEARCH
    20. Kurose, K; Mine, N; Iida, A; Nagai, H; Harada, H; Araki, T; Emi, M
      Three aberrant splicing variants of the HMGIC gene transcribed in uterine leiomyomas

      GENES CHROMOSOMES & CANCER
    21. Mikami, I; Harada, H; Nagai, H; Tsuneizumi, M; Nobe, Y; Koizumi, K; Sugano, S; Tanaka, S; Emi, M
      Down-regulation in multiple human cancers of a novel gene, DMHC, from 17q25.1 that encodes an integral membrane protein

      JAPANESE JOURNAL OF CANCER RESEARCH
    22. Mine, N; Kurose, K; Konishi, H; Araki, T; Nagai, H; Emi, M
      Fusion of a sequence from HEI10 (14q11) to the HMGIC gene at 12q15 in a uterine leiomyoma

      JAPANESE JOURNAL OF CANCER RESEARCH
    23. Haga, S; Emi, M; Hirano, A; Utada, Y; Kajiwara, T; Akiyama, F; Sakamoto, G; Takahashi, K; Tada, T; Kasumi, F; Miki, Y; Nakamura, Y
      Association of allelic losses at 3p25.1, 13q12, or 17p13.3 with poor prognosis in breast cancers with lymph node metastasis

      JAPANESE JOURNAL OF CANCER RESEARCH
    24. Yokota, T; Nagai, H; Harada, H; Mine, N; Terada, Y; Fujiwara, H; Yabe, A; Miyazaki, K; Emi, M
      Identification, tissue expression, and chromosomal position of a novel gene encoding human ubiquitin-conjugating enzyme E2-230k

      GENE
    25. Gemma, A; Hosoya, Y; Seike, M; Uematsu, K; Kurimoto, F; Hibino, S; Yoshimura, A; Shibuya, M; Kudoh, S; Emi, M
      Genomic structure of the human MAD2 gene and mutation analysis in human lung and breast cancers

      LUNG CANCER
    26. Nagai, H; Kim, YS; Lee, KT; Chu, MY; Konishi, N; Fujimoto, J; Baba, M; Matsubara, K; Emi, M
      Inactivation of SSI-1, a JAK/STAT inhibitor, in human hepatocellular carcinomas, as revealed by two-dimensional electrophoresis

      JOURNAL OF HEPATOLOGY
    27. Terada, Y; Imoto, I; Nagai, H; Suwa, K; Momoi, M; Tajiri, T; Onda, M; Inazawa, J; Emi, M
      An 8-cM interstitial deletion on 4q21-q22 in DNA from an infant with hepatoblastoma overlaps with a commonly deleted region in adult liver cancers

      AMERICAN JOURNAL OF MEDICAL GENETICS
    28. Kitamura, Y; Shimizu, K; Ito, K; Tanaka, S; Emi, M
      Allelotyping of follicular thyroid carcinoma: Frequent allelic losses in chromosome arms 7q, 11p, and 22q

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    29. Ogawa, S; Emi, M; Shiraki, M; Hosoi, T; Ouchi, Y; Inoue, S
      Association of estrogen receptor beta (ESR2) gene polymorphism with blood pressure

      JOURNAL OF HUMAN GENETICS
    30. Miyao, M; Hosoi, T; Emi, M; Nakajima, T; Inoue, S; Hoshino, S; Shiraki, M; Orimo, H; Ouchi, Y
      Association of hone mineral density with a dinucleotide repeat polymorphism at the calcitonin (CT) locus

      JOURNAL OF HUMAN GENETICS
    31. Nakajima, T; Iwaki, K; Hamakubo, T; Kodama, T; Emi, M
      Genomic structure of the gene encoding human 3-hydroxy-3-methyl-glutaryl coenzyme A reductase: comparison of exon/intron organization of sterol-sensing domains among four related genes

      JOURNAL OF HUMAN GENETICS
    32. Nakajima, T; Iwaki, K; Kodama, T; Inazawa, J; Emi, M
      Genomic structure and chromosomal mapping of the human Site-1 protease (S1P) gene

      JOURNAL OF HUMAN GENETICS
    33. Orimo, H; Nakajima, E; Yamamoto, M; Ikejima, M; Emi, M; Shimada, T
      Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability

      JOURNAL OF HUMAN GENETICS
    34. Wu, LL; Hopkins, PN; Xin, YP; Stephenson, SH; Williams, RR; Nobe, Y; Kajita, M; Nakajima, T; Emi, M
      Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities

      JOURNAL OF HUMAN GENETICS
    35. Yokota, T; Nakata, T; Minami, S; Inazawa, J; Emi, M
      Genomic organization and chromosomal mapping of ELKS, a gene rearranged ina papillary thyroid carcinoma

      JOURNAL OF HUMAN GENETICS
    36. Fukino, K; Teramoto, A; Adachi, K; Takahashi, H; Emi, M
      A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL gene

      JOURNAL OF HUMAN GENETICS
    37. Utada, Y; Emi, M; Yoshimoto, M; Kasumi, F; Akiyama, F; Sakamoto, G; Haga, S; Kajiwara, T; Nakamura, Y
      Allelic loss at 1p34-36 predicts poor prognosis in node-negative breast cancer

      CLINICAL CANCER RESEARCH
    38. Kitamura, Y; Shimizu, K; Tanaka, S; Ito, K; Emi, M
      Association of allelic loss on 1q, 4p, 7q, 9p, 9q, and 16q with postoperative death in papillary thyroid carcinoma

      CLINICAL CANCER RESEARCH
    39. Bando, K; Nagai, H; Matsumoto, S; Koyama, M; Kawamura, N; Tajiri, T; Onda, M; Emi, M
      Identification of a I-Mb common region at 16q24.I-24.2 deleted in hepatocellular carcinoma

      GENES CHROMOSOMES & CANCER
    40. Kitamura, Y; Shimizu, K; Tanaka, S; Ito, K; Emi, M
      Allelotyping of anaplastic thyroid carcinoma: Frequent allelic losses on 1q, 9p, 11, 17, 19p, and 22q

      GENES CHROMOSOMES & CANCER
    41. Kurose, K; Mine, N; Doi, D; Ota, Y; Yoneyama, K; Konishi, H; Araki, T; Emi, M
      Novel gene fusion of COX6C at 8q22-23 to HMGIC at 12q15 in a uterine leiomyoma

      GENES CHROMOSOMES & CANCER
    42. Nishimine, M; Konishi, N; Yamamoto, K; Nagai, H; Emi, M; Kirita, T; Sugimura, M
      Epigenetic alterations in methylation in oral squamous cell carcinoma celllines detected by two-dimensional gel electrophoresis

      INTERNATIONAL JOURNAL OF ONCOLOGY
    43. Utada, Y; Haga, S; Kajiwara, T; Kasumi, F; Sakamoto, G; Nakamura, Y; Emi, M
      Mapping of target regions of allelic loss in primary breast cancers to 1-cM intervals on genomic contigs at 6q21 and 6q25.3

      JAPANESE JOURNAL OF CANCER RESEARCH
    44. Iida, A; Emi, M; Matsuoka, R; Hiratsuka, E; Okui, K; Ohashi, H; Inazawa, J; Fukushima, Y; Imai, T; Nakamura, Y
      Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient withleft-right axis malformation

      HUMAN GENETICS
    45. Matsumoto, S; Minobe, K; Utada, Y; Furukawa, K; Onda, M; Sakamoto, G; Kasumi, F; Nakamura, Y; Emi, M
      Loss of heterozygosity at 3p24-p25 as a prognostic factor in breast cancer

      CANCER LETTERS
    46. Tsukamoto, K; Orimo, H; Hosoi, T; Miyao, M; Ota, N; Nakajima, T; Yoshida, H; Watanabe, S; Suzuki, T; Emi, M
      Association of bone mineral density with polymorphism of the human calcium-sensing receptor locus

      CALCIFIED TISSUE INTERNATIONAL
    47. Koyama, M; Nagai, H; Bando, K; Matsumoto, S; Tajiri, T; Onda, M; Ito, M; Moriyama, Y; Emi, M
      New target region of allelic loss in hepatocellular carcinomas within a 1-cM interval on chromosome 6q23

      JOURNAL OF HEPATOLOGY
    48. Utada, Y; Haga, S; Kajiwara, T; Kasumi, F; Sakamoto, G; Nakamura, Y; Emi, M
      Allelic loss at the 8p22 region as a prognostic factor in large and estrogen receptor negative breast carcinomas

      CANCER
    49. Ikeda, K; Sato, M; Tsutsumi, O; Tsuchiya, F; Tsuneizumi, M; Emi, M; Imoto, I; Inazawa, J; Muramatsu, M; Inoue, S
      Promoter analysis and chromosomal mapping of human EBAG9 gene

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    50. Ogawa, S; Hosoi, T; Shiraki, M; Orimo, H; Emi, M; Muramatsu, M; Ouchi, Y; Inoue, S
      Association of estrogen receptor beta gene polymorphism with bone mineral density

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    51. Keicho, N; Ohashi, J; Tamiya, G; Nakata, K; Taguchi, Y; Azuma, A; Ohishi, N; Emi, M; Park, MH; Inoko, H; Tokunaga, K; Kudoh, S
      Fine localization of a major disease-susceptibility locus for diffuse panbronchiolitis

      AMERICAN JOURNAL OF HUMAN GENETICS
    52. Hopkins, PN; Wu, LL; Stephenson, SH; Xin, YP; Katsumata, H; Nobe, Y; Nakajima, T; Hirayama, T; Emi, M; Williams, RR
      A novel LDLR mutation, H190Y, in a Utah kindred with familial Hypercholesterolemia

      JOURNAL OF HUMAN GENETICS
    53. Nakajima, T; Hamakubo, T; Kodama, T; Inazawa, J; Emi, M
      Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) gene

      JOURNAL OF HUMAN GENETICS
    54. Iwaki, K; Nakajima, T; Ota, N; Emi, M
      A common Ile796Val polymorphism of the human SREBP cleavage-activating protein (SCAP) gene

      JOURNAL OF HUMAN GENETICS
    55. Nakajima, T; Ota, N; Kodama, T; Emi, M
      Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the SREBP cleavage-activating protein (SCAP) locus

      JOURNAL OF HUMAN GENETICS
    56. Mine, N; Bando, K; Utada, Y; Nagai, H; Araki, T; Emi, M
      Two single nucleotide polymorphisms of the hSNF5/INI1 gene

      JOURNAL OF HUMAN GENETICS
    57. Tsukamoto, K; Yoshida, H; Watanabe, S; Suzuki, T; Miyao, M; Hosoi, T; Orimo, H; Emi, M
      Association of radial bone mineral density with CA repeat polymorphism at the interleukin 6 locus in postmenopausal Japanese women

      JOURNAL OF HUMAN GENETICS
    58. Emi, M; Keicho, N; Tokunaga, K; Katsumata, H; Souma, S; Nakata, K; Taguchi, Y; Ohishi, N; Azuma, A; Kudoh, S
      Association of diffuse panbronchiolitis with microsatellite polymorphism of the human interleukin 8 (IL-8) gene

      JOURNAL OF HUMAN GENETICS
    59. Kitamura, Y; Minobe, K; Nakata, T; Shimizu, K; Tanaka, S; Fujimori, M; Yokoyama, S; Ito, K; Onda, M; Emi, M
      Ret/PTC3 is the most frequent form of gene rearrangement in papillary thyroid carcinomas in Japan

      JOURNAL OF HUMAN GENETICS
    60. Ota, N; Nakajima, T; Shirai, Y; Emi, M
      Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the human nuclear factor kappa-beta subunit 1 (NFKB1) locus

      JOURNAL OF HUMAN GENETICS
    61. Emi, M; Yoshimoto, M; Sato, T; Matsumoto, S; Utada, Y; Ito, I; Minobe, K; Iwase, T; Katagiri, T; Bando, K; Akiyama, F; Harada, Y; Fukino, K; Sakamoto, G; Matsushima, M; Iida, A; Tada, T; Saito, H; Miki, Y; Kasumi, F; Nakamura, Y
      Allelic loss at 1p34, 13q12, 17p13.3, and 17q21.1 correlates with poor postoperative prognosis in breast cancer

      GENES CHROMOSOMES & CANCER
    62. Bando, K; Nagai, H; Matsumoto, S; Koyama, M; Kawamura, N; Onda, M; Emi, M
      Identification of a 1-cM region of common deletion on 4q35 associated withprogression of hepatocellular carcinoma

      GENES CHROMOSOMES & CANCER
    63. Nakata, T; Kitamura, Y; Shimizu, K; Tanaka, S; Fujimori, M; Yokoyama, S; Ito, K; Emi, M
      Fusion of a novel gene, ELKS, to RET due to translocation t(10;12)(q11;p13) in a papillary thyroid carcinoma

      GENES CHROMOSOMES & CANCER
    64. Ohgaki, K; Iida, A; Ogawa, O; Kubota, Y; Akimoto, M; Emi, M
      Localization of tumor suppressor gene associated with distant metastasis of urinary bladder cancer to a 1-Mb interval on 8p22

      GENES CHROMOSOMES & CANCER
    65. Fukino, K; Iida, A; Teramoto, A; Sakamoto, G; Kasumi, F; Nakamura, Y; Emi, M
      Frequent allelic loss at the TOC locus on 17q25.1 in primary breast cancers

      GENES CHROMOSOMES & CANCER
    66. Ueda, T; Emi, M; Suzuki, H; Komiya, A; Akakura, K; Ichikawa, I; Watanabe, M; Shiraishi, T; Masai, M; Igarashi, T; Ito, H
      Identification of a I-cM region of common deletion on 13q14 associated with human prostate cancer

      GENES CHROMOSOMES & CANCER
    67. Keicho, N; Emi, M; Nakata, K; Taguchi, Y; Azuma, A; Tokunaga, K; Ohishi, N; Kudoh, S
      Promoter variation of tumour necrosis factor-alpha gene: possible high risk for chronic bronchitis but not diffuse panbronchiolitis

      RESPIRATORY MEDICINE
    68. Koyama, M; Nagai, H; Bando, K; Ito, M; Moriyama, Y; Emi, M
      Localization of a target region of allelic loss to a 1-cM interval on chromosome 16p.13.13 in hepatocellular carcinoma

      JAPANESE JOURNAL OF CANCER RESEARCH
    69. Ohgaki, K; Minobe, K; Kurose, K; Iida, A; Habuchi, T; Ogawa, O; Kubota, Y; Akimoto, M; Emi, M
      Two target regions of allelic loss on chromosome 9 in urinary-bladder cancer

      JAPANESE JOURNAL OF CANCER RESEARCH
    70. Kawamura, N; Nagai, H; Bando, K; Koyama, M; Matsumoto, S; Tajiri, T; Onda, M; Fujimoto, J; Ueki, T; Konishi, N; Shiba, T; Emi, M
      PTEN/MMAC1 mutations in hepatocellular carcinomas: Somatic inactivation ofboth alleles in tumors

      JAPANESE JOURNAL OF CANCER RESEARCH
    71. Orimo, H; Nakajima, E; Ikejima, M; Emi, M; Shimada, T
      Frameshift mutations and a length polymorphism in the hMSH3 gene and the spectrum of microsatellite instability in sporadic colon cancer

      JAPANESE JOURNAL OF CANCER RESEARCH
    72. Nagai, H; Kim, YS; Yasuda, T; Ohmachi, Y; Yokouchi, H; Monden, M; Emi, M; Konishi, N; Nogami, M; Okumura, K; Matsubara, K
      A novel sperm-specific hypomethylation sequence is a demethylation hotspotin human hepatocellular carcinomas

      GENE
    73. Ota, N; Hunt, SC; Nakajima, T; Suzuki, T; Hosoi, T; Orimo, H; Shirai, Y; Emi, M
      Linkage of interleukin 6 locus to human osteopenia by sibling pair analysis

      HUMAN GENETICS
    74. Minobea, K; Bando, K; Fukino, K; Soma, S; Kasumi, F; Sakamoto, G; Furukawa, K; Higuchi, K; Onda, M; Nakamura, Y; Emi, M
      Somatic mutation of the PTEN/MMAC1 gene in breast cancers with microsatellite instability

      CANCER LETTERS
    75. Fukino, K; Kitamura, Y; Sanno, N; Teramoto, A; Emi, M
      Analysis of the MEN1 gene in sporadic pituitary adenomas from Japanese patients

      CANCER LETTERS
    76. Tsukamoto, K; Yoshimoto, M; Kasumi, F; Akiyama, F; Sakamoto, G; Nakamura, Y; Emi, M
      Frequent multiplication of chromosome 1q in non-invasive and papillotubular carcinoma of the breast

      CANCER LETTERS
    77. Yokota, T; Yoshimoto, M; Akiyama, F; Sakamoto, G; Kasumi, F; Nakamura, Y; Emi, M
      Frequent multiplication of chromosomal region 8q24.1 associated with aggressive histologic types of breast cancers

      CANCER LETTERS
    78. Nakajima, T; Ota, N; Shirai, Y; Hata, A; Yoshida, H; Suzuki, T; Hosoi, T; Orimo, H; Emi, M
      Ethnic difference in contribution of Sp1 site variation of COLIA1 gene in genetic predisposition to osteoporosis

      CALCIFIED TISSUE INTERNATIONAL
    79. Nobe, Y; Emi, M; Katsumata, H; Nakajima, T; Hirayama, T; Wu, LL; Stephenson, SH; Hopkins, PN; Williams, RR
      Familial hypercholesterolemia in Utah kindred with novel 2412-6 ins G mutations in exon 17 of the LDL receptor gene

      JAPANESE HEART JOURNAL
    80. Katsumata, H; Emi, M; Nobe, Y; Nakajima, T; Hirayama, T; Wu, LL; Stephenson, SH; Hopkins, PN; Williams, RR
      Familial hypercholesterolemia in Utah kindred with novel R103W mutations in exon 4 of the LDL receptor gene

      JAPANESE HEART JOURNAL
    81. Yokota, T; Yoshimoto, M; Akiyama, F; Sakamoto, G; Kasumi, F; Nakamura, Y; Emi, M
      Localization of a tumor suppressor gene associated with the progression ofhuman breast carcinoma within a 1-cM interval of 8p22-p23.1

      CANCER
    82. Noguchi, S; Kasugai, T; Miki, Y; Fukutomi, T; Emi, M; Nomizu, T
      Clinicopathologic analysis of BRCA1- or BRCA2-associated hereditary breastcarcinoma in Japanese women

      CANCER
    83. Kurose, K; Araki, T; Matsunaka, T; Takada, Y; Emi, M
      Variant manifestation of Cowden disease in Japan: Hamartomatous polyposis of the digestive tract with mutation of the PTEN gene

      AMERICAN JOURNAL OF HUMAN GENETICS
    84. Keicho, N; Tokunaga, K; Nakata, K; Taguchi, Y; Azuma, A; Tanabe, K; Matsushita, M; Emi, M; Ohishi, N; Kudoh, S
      Contribution of TAP genes to genetic predisposition for diffuse panbronchiolitis

      TISSUE ANTIGENS
    85. TSUKAMOTO K; EMI M
      A POLYMORPHIC CA REPEAT SEQUENCE AT THE HUMAN CALCITONIN LOCUS

      JOURNAL OF HUMAN GENETICS
    86. TSUKAMOTO K; HARUTA K; SHIBA T; EMI M
      ISOLATION AND MAPPING OF A POLYMORPHIC CA REPEAT SEQUENCE AT THE HUMAN INTERLEUKIN-6 LOCUS

      JOURNAL OF HUMAN GENETICS
    87. TSUKAMOTO K; INOUE S; HOSOI T; ORIMO H; EMI M
      ISOLATION AND RADIATION HYBRID MAPPING OF DINUCLEOTIDE REPEAT POLYMORPHISM AT THE HUMAN ESTROGEN-RECEPTOR BETA-LOCUS

      JOURNAL OF HUMAN GENETICS
    88. WATANABE I; TSUKAMOTO K; SHIBA T; EMI M
      ISOLATION AND RADIATION HYBRID MAPPING OF DINUCLEOTIDE REPEAT POLYMORPHISM AT THE HUMAN MATRIX GLA PROTEIN (MGP) LOCUS

      JOURNAL OF HUMAN GENETICS
    89. Hirayama, T; Yamaki, E; Hata, A; Tsuji, M; Hashimoto, K; Yamamoto, M; Emi, M
      Five familial hypercholesterolemic kindreds in Japan with novel mutations of the LDL receptor gene

      JOURNAL OF HUMAN GENETICS
    90. Tsukamoto, K; Ohta, N; Shirai, Y; Emi, M
      A highly polymorphic CA repeat marker at the human tumor necrosis factor alpha (TNFA alpha) locus

      JOURNAL OF HUMAN GENETICS
    91. Tsukamoto, K; Watanabe, I; Shiba, T; Emi, M
      Isolation and radiation hybrid mapping of a dinucleotide repeat polymorphism at the human calcium-sensing receptor (CASR) locus

      JOURNAL OF HUMAN GENETICS
    92. Tsukamoto, K; Watanabe, I; Shiba, T; Emi, M
      Isolation of a polymorphic CA repeat sequence at the human progesterone receptor (PGR) locus

      JOURNAL OF HUMAN GENETICS
    93. Tsukamoto, K; Ohta, N; Shirai, Y; Emi, M
      A highly polymorphic CA repeat marker at the human interleukin 6 receptor (IL6R) locus

      JOURNAL OF HUMAN GENETICS
    94. KEICHO N; TOKUNAGA K; NAKATA K; TAGUCHI Y; AZUMA A; BANNAI M; EMI M; OHISHI N; YAZAKI Y; KUDOH S
      CONTRIBUTION OF HLA GENES TO GENETIC PREDISPOSITION IN DIFFUSE PANBRONCHIOLITIS

      American journal of respiratory and critical care medicine
    95. OHGAKI K; IIDA A; KASUMI F; SAKAMOTO G; AKIMOTO M; NAKAMURA Y; EMI M
      MAPPING OF A NEW TARGET REGION OF ALLELIC LOSS TO A 6-CM INTERVAL AT 21Q21 IN PRIMARY BREAST CANCERS

      Genes chromosomes & cancer (Print)
    96. IIDA A; KUROSE K; ISOBE R; AKIYAMA F; SAKAMOTO G; YOSHIMOTO M; KASUMI F; NAKAMURA Y; EMI M
      MAPPING OF A NEW TARGET REGION OF ALLELIC LOSS TO A 2-CM INTERVAL AT 22Q13.1 IN PRIMARY BREAST-CANCER

      Genes, chromosomes & cancer
    97. NAKATA T; YOSHIMOTO M; KASUMI F; AKIYAMA F; SAKAMOTO G; NAKAMURA Y; EMI M
      IDENTIFICATION OF A NEW COMMONLY DELETED REGION WITHIN A 2-CM INTERVAL OF CHROMOSOME 11P11 IN BREAST CANCERS

      European journal of cancer
    98. KAMIGAKI M; TSUJI M; ISHII J; HATA A; CHIBA H; AKITA H; HIRAYAMA T; EMI M
      FAMILIAL HYPERCHOLESTEROLEMIA WITH CHOLESTERYL ESTER TRANSFER PROTEIN-DEFICIENCY

      Internal medicine
    99. KUROSE K; BANDO K; FUKINO K; SUGISAKI Y; ARAKI T; EMI M
      SOMATIC MUTATIONS OF THE PTEN MMAC1 GENE IN 15 JAPANESE ENDOMETRIAL CANCERS - EVIDENCE FOR INACTIVATION OF BOTH ALLELES/

      Japanese journal of cancer research
    100. KUROSE K; IIDA A; ARAKI T; SAKAMOTO G; KASUMI F; NAKAMURA Y; EMI M
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      Japanese journal of cancer research


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/06/20 alle ore 01:47:31