成富研二 (Naritomi Kenji) - マイポータル

基本情報

学位: 医学博士(鹿児島大学)

J-GLOBAL ID: 200901083463495590
researchmap会員ID: 5000034436

研究キーワード

研究分野

ライフサイエンス / 医化学 /

経歴

2010年4月

- , 琉球大学医学研究科教授
2010年4月

- , University of the Ryukyus, Graduate School of Medicine, Professor
1985年4月

- , 琉球大学医学部医学科教授
1985年4月

- , University of the Ryukyus, Faculty of Medicine, Medicine, Professor
琉球大学医学研究科, 教授

MISC

Lack of C20orf133 and FLRT3 mutations in 43 patients with Kabuki syndrome in Japan

H. Kuniba, M. Tsuda, M. Nakashima, S. Miura, N. Miyake, T. Kondoh, T. Matsumoto, H. Moriuchi, H. Ohashi, K. Kurosawa …

JOURNAL OF MEDICAL GENETICS 45(7) 479-480 2008年7月
No mutation in RAS-MAPK pathway genes in 30 patients with Kabuki syndrome

Hideo Kuniba, Daisuke Sato, Koh-ichiro Yoshiura, Hirofumi Ohashi, Kenji Kurosawa, Noriko Miyake, Tasturo Kondoh, Tadashi Matsumoto, Toshiro Nagai, Nobuhiko Okamoto …

AMERICAN JOURNAL OF MEDICAL GENETICS PART A 146A(14) 1893-1896 2008年7月
Lack of C20orf133 and FLRT3 mutations in 43 patients with Kabuki syndrome in Japan

H. Kuniba, M. Tsuda, M. Nakashima, S. Miura, N. Miyake, T. Kondoh, T. Matsumoto, H. Moriuchi, H. Ohashi, K. Kurosawa …

JOURNAL OF MEDICAL GENETICS 45(7) 479-480 2008年7月
No mutation in RAS-MAPK pathway genes in 30 patients with Kabuki syndrome

Hideo Kuniba, Daisuke Sato, Koh-ichiro Yoshiura, Hirofumi Ohashi, Kenji Kurosawa, Noriko Miyake, Tasturo Kondoh, Tadashi Matsumoto, Toshiro Nagai, Nobuhiko Okamoto …

AMERICAN JOURNAL OF MEDICAL GENETICS PART A 146A(14) 1893-1896 2008年7月
Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome

Tadashi Kaname, Kumiko Yanagi, Yasutsugu Chinen, Yoshio Makita, Nobuhiko Okamoto, Hiroki Maehara, Ichiro Owan, Fuminori Kanaya, Yoshiaki Kubota, Yuichi Oike …

AMERICAN JOURNAL OF HUMAN GENETICS 81(4) 835-841 2007年10月
Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome

Tadashi Kaname, Kumiko Yanagi, Yasutsugu Chinen, Yoshio Makita, Nobuhiko Okamoto, Hiroki Maehara, Ichiro Owan, Fuminori Kanaya, Yoshiaki Kubota, Yuichi Oike …

AMERICAN JOURNAL OF HUMAN GENETICS 81(4) 835-841 2007年10月
Midkine as a novel target for antibody therapy in osteosarcoma

Hiroki Maehara, Tadashi Kaname, Kumiko Yanagi, Hiroaki Hanzawa, Ichiro Owan, Takao Kinjou, Kenji Kadomatsu, Shinya Ikematsu, Teruo Iwamasa, Fuminori Kanaya …

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 358(3) 757-762 2007年7月
Midkine as a novel target for antibody therapy in osteosarcoma

Hiroki Maehara, Tadashi Kaname, Kumiko Yanagi, Hiroaki Hanzawa, Ichiro Owan, Takao Kinjou, Kenji Kadomatsu, Shinya Ikematsu, Teruo Iwamasa, Fuminori Kanaya …

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 358(3) 757-762 2007年7月
Opitz trigonocephaly C syndrome in a boy with a de novo balanced reciprocal translocation t(3;18)(q13.13;q12.1)

Yasutsugu Chinen, Tadashi Kaname, Kumiko Yanagi, Nakamichi Saito, Kenji Naritomi, Takao Ohta

American Journal of Medical Genetics, Part A 140(15) 1655-1657 2006年8月1日
Trigonocephaly in a boy with paternally inherited deletion 22q11.2 syndrome

T Yamamoto, K Sameshima, KI Sekido, N Aida, N Matsumoto, K Naritomi, K Kurosawa

AMERICAN JOURNAL OF MEDICAL GENETICS PART A 140A(12) 1302-1304 2006年6月
Trigonocephaly in a boy with paternally inherited deletion 22q11.2 syndrome

T Yamamoto, K Sameshima, KI Sekido, N Aida, N Matsumoto, K Naritomi, K Kurosawa

AMERICAN JOURNAL OF MEDICAL GENETICS PART A 140A(12) 1302-1304 2006年6月
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.

Tetsuya Niihori, Yoko Aoki, Yoko Narumi, Giovanni Neri, Hélène Cavé, Alain Verloes, Nobuhiko Okamoto, Raoul C M Hennekam, Gabriele Gillessen-Kaesbach, Dagmar Wieczorek …

Nature genetics 38(3) 294-6 2006年3月
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.

Tetsuya Niihori, Yoko Aoki, Yoko Narumi, Giovanni Neri, Hélène Cavé, Alain Verloes, Nobuhiko Okamoto, Raoul C M Hennekam, Gabriele Gillessen-Kaesbach, Dagmar Wieczorek …

Nature genetics 38(3) 294-6 2006年3月
No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients

N Miyake, O Shimokawa, N Harada, N Sosonkina, A Okubo, H Kawara, N Okamoto, H Ohashi, K Kurosawa, K Naritomi …

AMERICAN JOURNAL OF MEDICAL GENETICS PART A 140A(3) 291-293 2006年2月
No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients

N Miyake, O Shimokawa, N Harada, N Sosonkina, A Okubo, H Kawara, N Okamoto, H Ohashi, K Kurosawa, K Naritomi …

AMERICAN JOURNAL OF MEDICAL GENETICS PART A 140A(3) 291-293 2006年2月
Opitz trigonocephaly C syndrome in a boy with a de novo balanced reciprocal translocation t(3;18)(q13.13;q12.1).

Chinen Y, Kaname T, Yanagi K, Saito N, Naritomi K, Ohta T

Am J Med Genet 140A 1655-1657 2006年
Four novel NIPBL mutations in Japanese patients with Cornelia de Lange syndrome [1]

Noriko Miyake, Remco Visser, Akira Kinoshita, Ko-Ichiro Yoshiura, Norio Niikawa, Tatsuro Kondoh, Naomichi Matsumoto, Naoki Harada, Nobuhiko Okamoto, Tohni Sonoda …

American Journal of Medical Genetics 135(1) 103-105 2005年5月15日
Four novel NIPBL mutations in Japanese patients with Cornelia de Lange syndrome

N Miyake, R Visser, A Kinoshita, K Yoshiura, N Niikawa, T Kondoh, N Matsumoto, N Harada, N Okamoto, T Sonoda …

AMERICAN JOURNAL OF MEDICAL GENETICS PART A 135A(1) 103-105 2005年5月
Four novel NIPBL mutations in Japanese patients with Cornelia de Lange syndrome

N Miyake, R Visser, A Kinoshita, K Yoshiura, N Niikawa, T Kondoh, N Matsumoto, N Harada, N Okamoto, T Sonoda …

AMERICAN JOURNAL OF MEDICAL GENETICS PART A 135A(1) 103-105 2005年5月
Four novel NIPBL mutations in Japanese patients with Cornelia de Lange syndrome

N Miyake, R Visser, A Kinoshita, K Yoshiura, N Niikawa, T Kondoh, N Matsumoto, N Harada, N Okamoto, T Sonoda …

AMERICAN JOURNAL OF MEDICAL GENETICS PART A 135A(1) 103-105 2005年5月

もっとみる

書籍等出版物

もっとみる

共同研究・競争的資金等の研究課題

遺伝性疾患データベース開発に関する研究

ＪＳＴ戦略的創造研究推進制度（研究チーム型）（戦略的基礎研究推進事業：ＣＲＥＳＴ） 2007年
Database for Genetic Diseases

JST Basic Research Programs (Core Research for Evolutional Science and Technology :CREST) 2007年
効率の良い遺伝子変異スクリーニング法の開発
Aarskog症候群の責任遺伝子解析
裂手裂足（SHFM1）の責任遺伝子同定と解析
Opitz三角頭蓋症候群の責任遺伝子同定と解析
遺伝性疾患データベース (UR-DBMS)と診断ソフトウェア (Syndrome Finder) の開発
Development of Computer Software for Diagnosis of Malformation Syndormes
Molecular Analysis of the Causative Gene in Split Hand/Foot Syndrome
Molecular Analysis of the Causative Gene in Opitz C Syndromes
日本人遺伝性疾患家系データベース開発に関する研究
奇形症候群診断ソフトウエアの開発に関する研究