『徳島大学 教育・研究者情報データベース (EDB)』---[学外] /
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登録情報

抽出条件

REF=閲覧 Journal of Human Genetics (日本人類遺伝学会)

登録情報の数

有効な情報: 58件 + 無効な情報: 5件 = 全ての情報: 63件

全ての有効な情報 (58件)
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[組織](著作の帰属する組織)による分類 :
閲覧 閲覧 徳島大学 …(1)
閲覧 閲覧 徳島大学 …(1)
閲覧 (未定義) …(51)
[年月日](発行年月日)による分類
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抽出結果のリスト

排列順: 項目表示:
閲覧 Toyomasa Katagiri, F Kasumi, M Yoshimoto, K Asaishi, R Abe, A Tsuchiya, M Sugano, T Nomizu, S Takai, M Yoneda, K Nanba, M Makita, H Okazaki, K Hirata, M Okazaki, Y Furutsuma, Y Morishita, Y Iino, T Karino, T Fukutomi, H Ayabe, S Hara, T Kajiwara, S Houga, T Shimizu, M Toda, Y Yamasaki, T Uchida, K Kunitomo, H Sonoo, J Kurebayashi, K Shimotuma, Y Nakamura and Y. Miki : High proportion of missense mutations of the BRCA1 and BRCA2 genes in Japanese breast cancer families., Journal of Human Genetics, Vol.43, No.1, 42-48, 1998..[誌名] ...
閲覧 Toyomasa Katagiri, M Futamura and Y. Nakamura : A Gln/Arg polymorphism at codon 349 of the hBUBR1 gene., Journal of Human Genetics, Vol.44, No.2, 131-2, 1999..[誌名] ...
閲覧 M Kato, K Yano, F Matsuo, H Saito, Toyomasa Katagiri, H Kurumizaka, M Yoshimoto, F Kasumi, F Akiyama, G Sakamoto, H Nagawa, Y Nakamura and Y Miki : Identification of Rad51 alteration in patients with bilateral breast cancer, Journal of Human Genetics, Vol.45, No.3, 133-137, 2000..[誌名] ...
閲覧 Keiko Ohsugi, Keiko Kobayashi, Kouji Itou, Hitoshi Sakuraba and Noriko Sakuragawa : Enzymatic corrections for cells derived from Fabry disease patients by a recombinant adenovirus vector., Journal of Human Genetics, Vol.45, No.1, 1-5, 2000..[誌名] ...
閲覧 Kyoko Takiguchi, Kouji Itou, Michie Shimmoto, Pinar T. Ozand, Hirofumi Doi and Hitoshi Sakuraba : Structural and functional study of K453E mutant protective protein/cathepsin A causing the late infantile form of galactosialidosis., Journal of Human Genetics, Vol.45, No.4, 200-206, 2000..[誌名] ...
閲覧 Yasunori Naganawa, Kouji Itou, Michie Shimmoto, Kyoko Takiguchi, Hirofumi Doi, Yuzuru Nishizawa, Takayoshi Kobayashi, Sachiko Kamei, Alexey V. Pshezhetsky, M. Potier and Hitoshi Sakuraba : Molecular and structural studies of Japanese patients with sialidosis type 1., Journal of Human Genetics, Vol.45, No.4, 241-249, 2000..[誌名] ...
閲覧 Toshikatsu Shinka, Takushi Naroda, Takamichi Tamura, Kenji Sasahara and Yutaka Nakahori : A rapid and simple method for sex identification by heteroduplex analysis, using denaturing high-performance liquid chromatography (DHPLC), Journal of Human Genetics, Vol.46, No.5, 263-266, 2001..[誌名] ...
閲覧 Juwon Lee, E Svetlana Kotliarova, A Ashraf Ewis, Akio Hida, Toshikatsu Shinka, Yoko Kuroki, Katsushi Tokunaga and Yutaka Nakahori : Y chromosome compound haplotypes with the microsatellite markers DXYS265, DXYS266, and DXYS241, Journal of Human Genetics, Vol.46, No.2, 80-84, 2001..[誌名] ...
閲覧 Ya-Ping Qian, Zheng-Tao Chu, Qin Dai, Can-Dong Wei, Jia-You Chu, Atsushi Tajima and Satoshi Horai : Mitochondrial DNA polymorphisms in Yunnan nationalities in China., Journal of Human Genetics, Vol.46, No.4, 211-220, 2001..[誌名] ...
閲覧 S Kure, K Kojima, T Kudo, K Kanno, Y Aoki, Y Suzuki, Toshikatsu Shinka, Y Sakata, K Narisawa and Y Matsubara : Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemia, Journal of Human Genetics, Vol.46, No.7, 378-384, 2001..[誌名] ...
閲覧 Kouji Itou, Yasunori Naganawa, Fumiko Matuzawa, Seiichi Aikawa, Hirofumi Doi, Naokazu Sasagasako, Takeshi Yamada, Jun-ichi Kira, Takuro Kobayashi, Alexey V. Pshezhetsky and Hitoshi Sakuraba : Novel missense mutaitions in the human lysosomal sialidase gene in sialidosis patients and prediction of structural alterations of mutant enzymes., Journal of Human Genetics, Vol.47, No.1, 29-37, 2002..[誌名] ...
閲覧 G Johannes W Janssen, Issei Imoto, Jun Inoue, Yutaka Shimada, Masakazu Ueda, Masayuki Imamura, R Claus Bartram and Johji Inazawa : MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas., Journal of Human Genetics, Vol.47, No.9, 460-464, 2002..[誌名] ...
閲覧 AA Ewis, J Lee, Toshikatsu Shinka and Yutaka Nakahori : Microdeletions of a Y-specific marker, Yfm1, and implications for a role in spermatogenesis, Journal of Human Genetics, Vol.47, No.5, 257-261, 2002..[誌名] ...
閲覧 Ashraf A. Ewis, Juwon W. Lee, Yoko Kuroki, Toshikatsu Shinka and Yutaka Nakahori : Yfm1, a multicopy marker specific for the Y chromosome and beneficial for forensic, population, genetic, and spermatogenesis-related studies, Journal of Human Genetics, Vol.47, No.10, 523-528, 2002..[誌名] ...
閲覧 Mingshun Li, Kinya Ishikawa, Shuta Toru, Hiroyuki Tomimitsu, Minoru Takashima, Jun Goto, Yoshihisa Takiyama, Hidenao Sasaki, Issei Imoto, Johji Inazawa, Tatsushi Toda, Ichiro Kanazawa and Hidehiro Mizusawa : Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan., Journal of Human Genetics, Vol.48, No.3, 111-118, 2003..[誌名] ...
閲覧 K Ochi, Y Daigo, Toyomasa Katagiri, A Saito-Hisaminato, T Tsunoda, Y Toyama, H Matsumoto and Y Nakamura : Expression profiles of two types of human knee-joint cartilage, Journal of Human Genetics, Vol.48, No.4, 177-182, 2003..[誌名] ...
閲覧 Wei Yu, Jun Inoue, Issei Imoto, Yoshinobu Matsuo, Abraham Karpas and Johji Inazawa : GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell lines., Journal of Human Genetics, Vol.48, No.6, 331-335, 2003..[誌名] ...
閲覧 Akiko Misawa, Hajime Hosoi, Issei Imoto, Tomoko Iehara, Tohru Sugimoto and Johji Inazawa : Translocation (1;22)(p36;q11.2) with concurrent del(22)(q11.2) resulted in homozygous deletion of SNF5/INI1 in a newly established cell line derived from extrarenal rhabdoid tumor., Journal of Human Genetics, Vol.49, No.10, 586-589, 2004..[誌名] ...
閲覧 Atsushi Tajima, Masanori Hayami, Katsushi Tokunaga, Takeo Juji, Masafumi Matsuo, Sangkot Marzuki, Keiichi Omoto and Satoshi Horai : Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages., Journal of Human Genetics, Vol.49, No.4, 187-193, 2004..[誌名] ...
閲覧 Atsushi Tajima, Kazuyuki Hamaguchi, Hideo Terao, Ayako Oribe, M Victor Perrotta, Amoros Carlos Baez, R Jose Arias, Hironobu Yoshimatsu, Toshiie Sakata and Satoshi Horai : Genetic background of people in the Dominican Republic with or without obese type 2 diabetes revealed by mitochondrial DNA polymorphism., Journal of Human Genetics, Vol.49, No.9, 495-499, 2004..[誌名] ...
閲覧 Kouhei Ishiwari, Masaharu Kotani, Minoru Suzuki, Elena Pumbo, Akemi Suzuki, Toshihide Kobayashi, Tamaki Ueno, Tomoko Fukushige, Tamotsu Kanzaki, Masato Imada, Kouji Itou, Shinji Akioka, Youichi Tajima and Hitoshi Sakuraba : Clinical, biochemical, and cytochemical studies on a Japanese Salla disease case associated with a renal disorder., Journal of Human Genetics, Vol.49, No.12, 656-663, 2004..[誌名] ...
閲覧 Hong-Tao Yan, Toshikatsu Shinka, Keigo Kinoshita, Youichi Sato, Mayumi Umeno, Gang Chen, Keiko Tsuji, Yukiko Unemi, Xin-Jun Yang, Teruaki Iwamoto and Yutaka Nakahori : Molecular analysis of TBL1Y, a Y-linked homologue of TBL1X related with X-linked late-onset sensorineural deafness, Journal of Human Genetics, Vol.50, No.4, 175-181, 2005..[誌名] ...
閲覧 Mai Murata-Ohsawa, Masaharu Kotani, Youichi Tajima, Daisuke Tsuji, Yasuhiro Ishibashi, Aya Kuroki, Kouji Itou, Kazuhiko Watabe, Kazunori Sango, Shoji Yamanaka and Hitoshi Sakuraba : Establishment of immortalized Schwann cells from Sandhoff mice and corrective effect of recombinant human β-hexosaminidase A on the accumulated GM2 ganglioside., Journal of Human Genetics, Vol.50, No.9, 460-467, 2005..[誌名] ...
閲覧 Parvaneh Keshavarz, Hiroshi Inoue, Yukiko Yamashita, Kiyoshi Kunika, Toshihito Tanahashi, Naoto Nakamura, Toshikazu Yoshikawa, Natsuo Yasui, Hiroshi Shiota and Mitsuo Itakura : No evidence for association of ENPP1(PC-1)K121Q variant with risk of Type 2 diabetes in a Japanese population., Journal of Human Genetics, Vol.51, No.6, 559-566, 2006..[誌名] ...
閲覧 Hitoshi Sakuraba, Mai Murata-Ohsawa, Ikuo Kawashima, Youichi Tajima, Masaharu Kotani, Toshio Ohshima, Yasunori Chiba, Minako Takashiba, Yoshifumi Jigami, Tomoko Fukushige, Tamotsu Kanzaki and Kouji Itou : Comparison of the effects of agalsidase alfa and agalsidase beta on cultured human Fabry fibroblasts and Fabry mice., Journal of Human Genetics, Vol.51, No.3, 180-188, 2006..[誌名] ...
閲覧 Boris Krischek, Akira Narita, Hiroyuki Akagawa, Hidetoshi Kasuya, Atsushi Tajima, Hideaki Onda, Taku Yoneyama, Tomokatsu Hori and Ituro Inoue : Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?, Journal of Human Genetics, Vol.51, No.5, 491-494, 2006..[誌名] ...
閲覧 Kiyoshi Kunika, Toshihito Tanahashi, Eiji Kudo, Noriko Mizusawa, Eiichiro Ichiishi, Naoto Nakamura, Toshikazu Yoshikawa, Takashi Yamaoka, Hiroaki Yasumo, Kazue Tsugaw, Maki Moritani, Hiroshi Inoue and Mitsuo Itakura : Effect of +36T > C in intron 1 on the glutamine: fructose-6-phosphate amidotransferase 1 gene and its contribution to type 2 diabetes in different populations., Journal of Human Genetics, Vol.51, No.12, 1100-1109, 2006..[誌名] ...
閲覧 Shin Hayashi, Shozo Honda, Maki Minaguchi, Yoshio Makita, Nobuhiko Okamoto, Rika Kosaki, Torayuki Okuyama, Issei Imoto, Shuki Mizutani and Johji Inazawa : Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis., Journal of Human Genetics, Vol.52, No.5, 397-405, 2007..[誌名] ...
閲覧 Youichi Tajima, Fumiko Matsuzawa, Sei-ichi Aikawa, Toshika Okumiya, Michiru Yoshimizu, Takahiro Tsukimura, Masahiko Ikekita, Seiichi Tsujino, Akihiko Tsuji, Tim Edmunds and Hitoshi Sakuraba : Structural and biochemical studies on Pompe disease and a "pseudodeficiency of acid α-glucosidase", Journal of Human Genetics, Vol.52, No.11, 898-906, 2007..[誌名] ...
閲覧 Yukiko Yamashita, Hiroshi Inoue, Keshavarz Parvaneh, Katsuyuki Miyawaki, Yuka Yamaguchi, Maki Moritani, Kiyoshi Kunika, Naoto Nakamura, Toshikazu Yoshikawa, Natsuo Yasui, Hiroshi Shiota, Toshihito Tanahashi and Mitsuo Itakura : SNPs in the KCNJ11-ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese population., Journal of Human Genetics, Vol.52, No.10, 781-793, 2007..[誌名] ...
閲覧 Yoichiro Kamatani, Koichi Matsuda, Tetsuya Ohishi, Shigeru Ohtsubo, Keiko Yamazaki, Aritoshi Iida, Naoya Hosono, Michiaki Kubo, Wako Yumura, Kosaku Nitta, Toyomasa Katagiri, Yasushi Kawaguchi, Naoyuki Kamatani and Yusuke Nakamura : Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population., Journal of Human Genetics, Vol.53, No.1, 64-73, 2008..[誌名] ...
閲覧 Yoichiro Takata, Hiroshi Inoue, Aya Sato, Kazue Tsugawa, Katsutoshi Miyatake, Daisuke Hamada, Fumio Shinomiya, Shunji Nakano, Natsuo Yasui, Toshihito Tanahashi and Mitsuo Itakura : Replication of reported genetic associations of PADI4, FCRL3, SLC22A4 and RUNX1 genes with rheumatoid arthritis: results of an independent Japanese population and evidence from meta-analysis of East Asian studies., Journal of Human Genetics, Vol.53, No.2, 163-173, 2008..[誌名] ...
閲覧 Kiyoshi Kunika, Toshihito Tanahashi, Shusuke Numata, Shu-ichi Ueno, Tetsuro Ohmori, Naoto Nakamura, Kazue Tsugawa, Katsuyuki Miyawaki, Maki Moritani, Hiroshi Inoue and Mitsuo Itakura : Common coding variant in the TCF7L2 gene and study of the association with type 2 diabetes in Japanese subjects, Journal of Human Genetics, Vol.53, No.11-12, 972-982, 2008..[誌名] ...
閲覧 (種別) : Moto Kajiwara, Tomohiro Terada, Ken Ogasawara, Junko Iwano, Toshiya Katsura, Atsushi Fukatsu, Toshio Doi and Ken-ichi Inui : Identification of multidrug and toxin extrusion (MATE1 and MATE2-K) variants with complete loss of transport activity., Journal of Human Genetics, Vol.54, No.1, 40-46, (発行所), (都市), Jan. 2009..[誌名] ...
閲覧 (種別) : Kazuaki Miyake, Woosung Yang, Kazuo Hara, Kazuki Yasuda, Yukio Horikawa, Haruhiko Osawa, Hiroto Furuta, Maggie Cy Ng, Yushi Hirota, Hiroyuki Mori, Keisuke Ido, Kazuya Yamagata, Yoshinori Hinokio, Yoshitomo Oka, Naoko Iwasaki, Yasuhiko Iwamoto, Yuichiro Yamada, Yutaka Seino, Hiroshi Maegawa, Atsunori Kashiwagi, He-Yao Wang, Toshihito Tanahashi, Naoto Nakamura, Jun Takeda, Eiichi Maeda, Ken Yamamoto, Katsushi Tokunaga, Ronald Cw Ma, Wing-Yee So, Juliana Cn Chan, Naoyuki Kamatani, Hideichi Makino, Kishio Nanjo, Takashi Kadowaki and Masato Kasuga : Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association., Journal of Human Genetics, Vol.54, No.4, 236-241, (発行所), (都市), Feb. 2009..[誌名] ...
閲覧 Ohata Takako, Tsuchiya Atsushi, Watanabe Maiko, Sumida Tomohisa and Takada Fumio : Physicians' opinion for 'new' genetic testing in Japan, Journal of Human Genetics, Vol.54, 203-208, 2009..[誌名] ...
閲覧 Kazuhiro Fujita, Masashi Sanada, Hiroshi Harada, Hiraku Mori, Haruo Niikura, Mitsuhiro Omine, Johji Inazawa and Issei Imoto : Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemia., Journal of Human Genetics, Vol.54, No.6, 355-359, 2009..[誌名] ...
閲覧 Siew-Kee Low, Kazuma Kiyotani, Taisei Mushiroda, Yataro Daigo, Yusuke Nakamura and Hitoshi Zembutsu : Association study of genetic polymorphism in ABCC4 with cyclophosphamide-induced adverse drug reactions in breast cancer patients., Journal of Human Genetics, Vol.54, No.10, 564-571, 2009..[誌名] ...
閲覧 Kazuhiko Nakabayashi, Gen Komaki, Atsushi Tajima, Tetsuya Ando, Mayuko Ishikawa, Junko Nomoto, Kenichiro Hata, Akira Oka, Hidetoshi Inoko, Takehiko Sasazuki, (JGRED) Genetic Research Group for Eating Disorders Japanese and Senji Shirasawa : Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers., Journal of Human Genetics, Vol.54, No.9, 531-537, 2009..[誌名] ...
閲覧 Shozo Honda, O Koji Orii, Junya Kobayashi, Shin Hayashi, Atsushi Imamura, Issei Imoto, Eiji Nakagawa, Yu-ichi Goto and Johji Inazawa : Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation., Journal of Human Genetics, Vol.55, No.4, 244-247, 2010..[誌名] ...
閲覧 Shozo Honda, Shin Hayashi, Issei Imoto, Jun Toyama, Hitoshi Okazawa, Eiji Nakagawa, Yu-Ichi Goto and Johji Inazawa : Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis., Journal of Human Genetics, Vol.55, No.9, 590-599, 2010..[誌名] ...
閲覧 Koichi Akiyama, Akira Narita, Hirofumi Nakaoka, Tailin Cui, Tomoko Takahashi, Katsuhito Yasuno, Atsushi Tajima, Boris Krischek, Ken Yamamoto, Hidetoshi Kasuya, Akira Hata and Ituro Inoue : Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms., Journal of Human Genetics, Vol.55, No.10, 656-661, 2010..[誌名] ...
閲覧 Sosuke Adachi, Atsushi Tajima, Jinhua Quan, Kazufumi Haino, Kosuke Yoshihara, Hideaki Masuzaki, Hidetaka Katabuchi, Kenichiro Ikuma, Hiroshi Suginami, Nao Nishida, Ryozo Kuwano, Yuji Okazaki, Yoshiya Kawamura, Tsukasa Sasaki, Katsushi Tokunaga, Ituro Inoue and Kenichi Tanaka : Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population., Journal of Human Genetics, Vol.55, No.12, 816-821, 2010..[誌名] ...
閲覧 Masakatsu Yanagimachi, Takako Miyamae, Takuya Naruto, Takuma Hara, Masako Kikuchi, Ryoki Hara, Tomoyuki Imagawa, Masaaki Mori, Tetsuji Kaneko, Hiroaki Goto, Satoshi Morita, Nobuhisa Mizuki, Akinori Kimura and Shumpei Yokota : Association of HLA-A*02:06 and HLA-DRB1*04:05 with clinical subtypes of juvenile idiopathic arthritis., Journal of Human Genetics, Vol.56, No.3, 196-199, 2010..[誌名] ...
閲覧 Shin Hayashi, Issei Imoto, Yoshinori Aizu, Nobuhiko Okamoto, Seiji Mizuno, Kenji Kurosawa, Nana Okamoto, Shozo Honda, Satoshi Araki, Shuki Mizutani, Hironao Numabe, Shinji Saitoh, Tomoki Kosho, Yoshimitsu Fukushima, Hiroshi Mitsubuchi, Fumio Endo, Yasutsugu Chinen, Rika Kosaki, Torayuki Okuyama, Hirotaka Ohki, Hiroshi Yoshihashi, Masae Ono, Fumio Takada, Hiroaki Ono, Mariko Yagi, Hiroshi Matsumoto, Yoshio Makita, Akira Hata and Johji Inazawa : Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies., Journal of Human Genetics, Vol.56, No.2, 110-124, 2011..[誌名] ...
閲覧 Kazuhiko Nakabayashi, Atsushi Tajima, Ken Yamamoto, Atsushi Takahashi, Kenichiro Hata, Yasuo Takashima, Midori Koyanagi, Hirofumi Nakaoka, Takashi Akamizu, Naofumi Ishikawa, Sumihisa Kubota, Shiro Maeda, Tatsuhiko Tsunoda, Michiaki Kubo, Naoyuki Kamatani, Yusuke Nakamura, Takehiko Sasazuki and Senji Shirasawa : Identification of independent risk loci for Graves' disease within the MHC in the Japanese population., Journal of Human Genetics, Vol.56, No.11, 772-778, 2011..[誌名] ...
閲覧 Shozo Honda, Shigeko Satomura, Shin Hayashi, Issei Imoto, Eiji Nakagawa, Yu-ichi Goto and Johji Inazawa : Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation., Journal of Human Genetics, Vol.57, No.1, 73-77, 2011..[誌名] ...
閲覧 Nana Okamoto, Shin Hayashi, Ayako Masui, Rika Kosaki, Izumi Oguri, Tomoko Hasegawa, Issei Imoto, Yoshio Makita, Akira Hata, Keiji Moriyama and Johji Inazawa : Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion., Journal of Human Genetics, Vol.57, No.3, 191-196, 2012..[誌名] ...
閲覧 Masato Obayashi, Kinya Ishikawa, Yuishin Izumi, Makoto Takahashi, Yusuke Niimi, Nozomu Sato, Osamu Onodera, Ryuji Kaji, Masatoyo Nishizawa and Hidehiro Mizusawa : Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage., Journal of Human Genetics, Vol.57, No.3, 202-206, 2012..[誌名] ...
閲覧 Yutaka Nakahori, Youichi Sato, ASHRAF ABDEL AZIM EWIS, Teruaki Iwamoto, Toshikatsu Shinka, Shiari Nozawa, Miki Yoshiike, Xin-Jun Yang, Masako Sei, Mikio Namiki, Eitetsu Kou, Naoki Ito, Kiyoshi Komatsu, Kiyomi Matsumiya and Yasuo Nakagome : Climatic influence on the reproductive characteristics of Japanese males, Journal of Human Genetics, Vol.57, No.6, 375-378, 2012..[誌名] ...
閲覧 Shusuke Numata : A commentary on the gender-specific association of TSNAX/DISC1 locus for schizophrenia and bipolar affective disorder in South Indian population., Journal of Human Genetics, Vol.57, No.8, 475-476, 2012..[誌名] ...
閲覧 Seham Elgazzar, Hitoshi Zembutsu, Atsushi Takahashi, Michiaki Kubo, Fuminori Aki, Koichi Hirata, Yuichi Takatsuka, Minoru Okazaki, Shozo Ohsumi, Takashi Yamakawa, Mitsunori Sasa, Toyomasa Katagiri, Yoshio Miki and Yusuke Nakamura : A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese., Journal of Human Genetics, Vol.57, No.12, 766-771, 2012..[誌名] ...
閲覧 Japanese Archipelago Human Population Genetics Consortium, Timothy Jinam, Nao Nishida, Momoki Hirai, Shoji Kawamura, Hiroki Oota, Kazuo Umetsu, Ryosuke Kimura, Jun Ohashi, Atsushi Tajima, Toshimichi Yamamoto, Hideyuki Tanabe, Shuhei Mano, Yumiko Suto, Tadashi Kaname, Kenji Naritomi, Kumiko Yanagi, Norio Niikawa, Keiichi Omoto, Katsushi Tokunaga and Naruya Saitou : The history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations., Journal of Human Genetics, Vol.57, No.12, 787-795, 2012..[誌名] ...
閲覧 Kazuma Kiyotani and Toyomasa Katagiri : A commentary on Analysis of ZNF350/ZBRK1 promoter variants and breast cancer susceptibility in non-BRCA1/2 French Canadian breast cancer families., Journal of Human Genetics, Vol.58, No.2, 58, 2012..[誌名] ...
閲覧 Yuki Hata, Hirofumi Nakaoka, Kosuke Yoshihara, Sosuke Adachi, Kazufumi Haino, Masayuki Yamaguchi, Nobumichi Nishikawa, Katsunori Kashima, Tetsuro Yahata, Atsushi Tajima, Atsushi Watanabe, Shigeo Akira, Kazuyoshi Hosomichi, Ituro Inoue and Kenichi Tanaka : A nonsynonymous variant of IL1A is associated with endometriosis in Japanese population., Journal of Human Genetics, Vol.58, No.8, 517-520, 2013..[誌名] ...
閲覧 Tiaki Daniela Uehara, Shin Hayashi, Nobuhiko Okamoto, Seiji Mizuno, Yasutsugu Chinen, Rika Kosaki, Tomoki Kosho, Kenji Kurosawa, Hiroshi Matsumoto, Hiroshi Mitsubuchi, Hironao Numabe, Shinji Saitoh, Yoshio Makita, Akira Hata, Issei Imoto and Johji Inazawa : SNP array screening of cryptic genomic imbalances in 450 Japanese subjects with intellectual disability and multiple congenital anomalies previously negative for large rearrangements., Journal of Human Genetics, Vol.61, No.4, 335-343, 2016..[誌名] ...
閲覧 Youichi Sato, Atsushi Tajima, Motoki Katsurayama, Shiari Nozawa, Miki Yoshiike, Eitetsue Koh, Jiro Kanaya, Mikio Namiki, Kiyomi Matsumiya, Akira Tsujimura, Kiyoshi Komatsu, Naoki Itoh, Jiro Eguchi, Issei Imoto, Aiko Yamauchi and Teruaki Iwamoto : A replication study of a candidate locus for follicle-stimulating hormone levels and association analysis for semen quality traits in Japanese men, Journal of Human Genetics, Vol.61, No.11, 911-915, 2016..[誌名] ...
閲覧 Youichi Sato, Atsushi Tajima, Misaki Kiguchi, Suzu Kogusuri, Aki Fujii, Takehiro Sato, Shiari Nozawa, Miki Yoshiike, Makiko Mieno, Kosuke Kojo, Masahiro Uchida, Haruki Tsuchiya, Kazumitu Yamasaki, Issei Imoto and Teruaki Iwamoto : Genome-wide association study of semen volume, sperm concentration, testis size, and plasma inhibin B levels, Journal of Human Genetics, Vol.65, No.8, 683-691, 2020..[誌名] ...

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