研究者詳細 - 土岐　力

論文 - 土岐　力

分割表示 >> ／全件表示135 件中 1 - 135 件目

Landscape of driver mutations and their clinical effects on Down syndrome-related myeloid neoplasms.

Sato T, Yoshida K, Toki T, Kanezaki R, Terui K, Saiki R, Ojima M, Ochi Y, Mizuno S, Yoshihara M, Uechi T, Kenmochi N, Tanaka S, Matsubayashi J, Kisai K, Kudo K, Yuzawa K, Takahashi Y, Tanaka T, Yamamoto Y, Kobayashi A, Kamio T, Sasaki S, Shiraishi Y, Chiba K, Tanaka H, Muramatsu H, Hama A, Hasegawa D, Sato A, Koh K, Karakawa S, Kobayashi M, Hara J, Taneyama Y, Imai C, Hasegawa D, Fujita N, Yoshitomi M, Iwamoto S, Yamato G, Saida S, Kiyokawa N, Deguchi T, Ito M, Matsuo H, Adachi S Prof, Hayashi Y, Taga T, Moriya Saito A, Horibe K, Watanabe K, Tomizawa D, Miyano S, Takahashi S, Ogawa S, Ito E

Blood 143 ( 25 ) 2627 - 2643 2024年03月

Transient erythroblastopenia due to a GATA1 variant in an infant female.

Yamashita M, Tomoda T, Mizuo A, Isoda T, Egawa M, Yoshida M, Toki T, Kudo K, Terui K, Ito E, Morio T, Takagi M

Pediatric blood & cancer 71 ( 3 ) e30834 2024年03月

Antileukemic effect of azacitidine, a DNA methyltransferase inhibitor, on cell lines of myeloid leukemia associated with Down syndrome.

Tanaka T, Kudo K, Kanezaki R, Yuzawa K, Toki T, Okuse R, Kobayashi A, Sato T, Kamio T, Terui K, Ito E

Experimental hematology 132 104179 2024年02月

Early-onset Marfan syndrome with a novel missense mutation: A case report.

Soma K, Kitagawa Y, Toki T, Miura F, Shimada J, Sato T, Kudo K, Otani K, Takahashi T, Terui K

Journal of cardiology cases 27 ( 6 ) 283 - 286 2023年06月

Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond-Blackfan anaemia

Akie Kobayashi, Ryusei Ohtaka, Tsutomu Toki, Junichi Hara, Hideki Muramatsu, Rika Kanezaki, Yuka Takahashi, Tomohiko Sato, Takuya Kamio, Ko Kudo, Shinya Sasaki, Taro Yoshida, Taiju Utsugisawa, Hitoshi Kanno, Kenichi Yoshida, Yasuhito Nannya, Yoshiyuki Takahashi, Seiji Kojima, Satoru Miyano, Seishi Ogawa, Kiminori Terui, Etsuro Ito

eJHaem 3 163 - 167 2022年12月

Mechanism of KIT gene regulation by GATA1 lacking the N-terminal domain in Down syndrome-related myeloid disorders.

Kanezaki R, Toki T, Terui K, Sato T, Kobayashi A, Kudo K, Kamio T, Sasaki S, Kawaguchi K, Watanabe K, Ito E

Scientific reports 12 ( 1 ) 20587 2022年11月

BRAF V600E-positive cells as molecular markers of bone marrow disease in pediatric Langerhans cell histiocytosis.

Kudo K, Toki T, Kanezaki R, Tanaka T, Kamio T, Sato T, Sasaki S, Imamura M, Imai C, Ando K, Kakuda H, Doi T, Kawaguchi H, Irie M, Sasahara Y, Tamura A, Hasegawa D, Itakura Y, Watanabe K, Sakamoto K, Shioda Y, Kato M, Kudo K, Fukano R, Sato A, Yagasaki H, Kanegane H, Kato I, Umeda K, Adachi S, Kataoka T, Kurose A, Nakazawa A, Terui K, Ito E

Haematologica - ( 7 ) 1719 - 1725 2022年03月

Childhood acute myeloid leukemia with 5q deletion and HNRNPH1-MLLT10 fusion: The first case report.

Kudo K, Kubota Y, Toki T, Kanezaki R, Kobayashi A, Sato T, Kamio T, Sasaki S, Shiba N, Tomizawa D, Adachi S, Yoshida K, Ogawa S, Seki M, Takita J, Terui K

Blood advances 6 ( 10 ) 3162 - 3166 2022年02月

A Case of Congenital Leukemia With MYB-GATA1 Fusion Gene in a Female Patient.

Ozono S, Yano S, Oishi S, Mitsuo M, Nakagawa S, Toki T, Terui K, Ito E

Journal of pediatric hematology/oncology 44 ( 1 ) e250 - e252 2022年01月

長期に渡る繰り返す紫斑と低γグロブリン血症を主症状とした肢端紅痛症

唐沢貴生, 橋本峻, 佐藤理子, 藤田真司, 相澤知美, 津川浩二, 土岐力, 金崎里香, 佐藤知彦, 工藤耕, 照井君典, 田中完

弘前医学 72 ( 1-4 ) 80 - 83 2022年

Ribosomal protein L5 facilitates rDNA-bundled condensate and nucleolar assembly

伊藤由馬, 徳永万喜洋, 原口徳子, 粟津暁紀, 落合博, 土岐力, 伊藤悦朗, 中尾光善, 斉藤典子

Life Sci Alliance 5 ( 7 ) 2022年

Association of Multiple Gene Polymorphisms Including Homozygous NUDT15 R139C With Thiopurine Intolerance During the Treatment of Acute Lymphoblastic Leukemia.

Kudo K, Sato T, Takahashi Y, Yuzawa K, Kobayashi A, Kamio T, Sasaki S, Shimada J, Otani K, Tusjimoto S, Kato M, Toki T, Terui K, Ito E

Journal of pediatric hematology/oncology 43 ( 8 ) e1173 - e1176 2021年11月

Post-induction MRD by FCM and GATA1-PCR are significant prognostic factors for myeloid leukemia of Down syndrome.

Taga T, Tanaka S, Hasegawa D, Terui K, Toki T, Iwamoto S, Hiramatsu H, Miyamura T, Hashii Y, Moritake H, Nakayama H, Takahashi H, Shimada A, Taki T, Ito E, Hama A, Ito M, Koh K, Hasegawa D, Saito AM, Adachi S, Tomizawa D

Leukemia 35 ( 9 ) 2508 - 2516 2021年09月

Usefulness of functional splicing analysis to confirm precise disease pathogenesis in Diamond-Blackfan anemia caused by intronic variants in RPS19.

Takafuji S, Mori T, Nishimura N, Yamamoto N, Uemura S, Nozu K, Terui K, Toki T, Ito E, Muramatsu H, Takahashi Y, Matsuo M, Yamamura T, Iijima K

Pediatric hematology and oncology 38 ( 6 ) 515 - 527 2021年09月

Predictive factors for the development of leukemia in patients with transient abnormal myelopoiesis and Down syndrome.

Yamato G, Deguchi T, Terui K, Toki T, Watanabe T, Imaizumi T, Hama A, Iwamoto S, Hasegawa D, Ueda T, Yokosuka T, Tanaka S, Yanagisawa R, Koh K, Saito AM, Horibe K, Hayashi Y, Adachi S, Mizutani S, Taga T, Ito E, Watanabe K, Muramatsu H

Leukemia 35 ( 5 ) 1480 - 1484 2021年05月

Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia.

Koyamaishi S, Kamio T, Kobayashi A, Sato T, Kudo K, Sasaki S, Kanezaki R, Hasegawa D, Muramatsu H, Takahashi Y, Sasahara Y, Hiramatsu H, Kakuda H, Tanaka M, Ishimura M, Nishi M, Ishiguro A, Yabe H, Sarashina T, Yamamoto M, Yuza Y, Hyakuna N, Yoshida K, Kanno H, Ohga S, Ohara A, Kojima S, Miyano S, Ogawa S, Toki T, Terui K, Ito E

Bone marrow transplantation 56 ( 5 ) 1013 - 1020 2021年05月

Down syndrome-related transient abnormal myelopoiesis is attributed to a specific erythro-megakaryocytic subpopulation with GATA1 mutation.

Nishinaka-Arai Y, Niwa A, Matsuo S, Kazuki Y, Yakura Y, Hiroma T, Toki T, Sakuma T, Yamamoto T, Ito E, Oshimura M, Nakahata T, Saito MK

Haematologica 106 ( 2 ) 635 - 640 2021年02月

Enzymatic Changes in Red Blood Cells of Diamond-Blackfan Anemia.

Utsugisawa T, Uchiyama T, Toki T, Shimojima-Yamamoto K, Ohga S, Ito E, Kanno H

The Tohoku journal of experimental medicine 255 ( 1 ) 49 - 55 2021年

遺伝性骨髄不全症候群の新知見

伊藤悦朗, 土岐力, 神尾卓哉, 照井君典

臨床血液 62 ( 10 ) 1455 - 1464 2021年

Outcome of colorectal cancer in Diamond-Blackfan syndrome with a ribosomal protein S19 mutation.

Kazuya Kimura, Kazuhiro Shimazu, Tsutomu Toki et al.

Clinical journal of gastroenterology 13 ( 6 ) 1173 - 1177 2020年12月

Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21

Kentaro Yuzawa, Kiminori Terui, Tsutomu Toki, Rika Kanezaki, Akie Kobayashi, Tomohiko Sato, Takuya Kamio, Ko Kudo, Shinya Sasaki, Mikiya Endo, Shuichi Ozono, Keiko Nomura, Etsuro Ito

Pediatric Blood & Cancer 67 ( 4 ) e28188 2020年02月

Highly sensitive detection of GATA1 mutations in patients with myeloid leukemia associated with Down syndrome by combining Sanger and targeted next generation sequencing

Kiminori Terui, Tsutomu Toki, Takashi Taga, Shotaro Iwamoto, Takako Miyamura, Daisuke Hasegawa, Hiroshi Moritake, Asahito Hama, Kentaro Nakashima, Rika Kanezaki, Ko Kudo, Akiko M. Saito, Keizo Horibe, Souichi Adachi, Daisuke Tomizawa, Etsuro Ito

Genes, Chromosomes and Cancer 59 ( 3 ) 160 - 167 2019年10月

Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome

Yasuo Kubota, Kumiko Uryu, Tatsuya Ito, Masafumi Seki, Tomoko Kawai, Tomoya Isobe, Tadayuki Kumagai, Tsutomu Toki, Kenichi Yoshida, Hiromichi Suzuki, Keisuke Kataoka, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Kentaro Ohki, Nobutaka Kiyokawa, Jiro Kagawa, Satoru Miyano, Akira Oka, Yasuhide Hayashi, Seishi Ogawa, Kiminori Terui, Atsushi Sato, Kenichiro Hata, Etsuro Ito, Junko Takita

Cancer Science 110 ( 10 ) 3358 - 3367 2019年09月

Resistance of t(17;19)‐acute lymphoblastic leukemia cell lines to multiagents in induction therapy

Atsushi Watanabe, Takeshi Inukai, Keiko Kagami, Masako Abe, Masatoshi Takagi, Takashi Fukushima, Hiroko Fukushima, Toru Nanmoku, Kiminori Terui, Tatsuya Ito, Tsutomu Toki, Etsuro Ito, Junya Fujimura, Hiroaki Goto, Mikiya Endo, Thomas Look, Mark Kamps, Masayoshi Minegishi, Junko Takita, Toshiya Inaba, Hiroyuki Takahashi, Akira Ohara, Daisuke Harama, Tamao Shinohara, Shinpei Somazu, Hiroko Oshiro, Koshi Akahane, Kumiko Goi, Kanji Sugita

Cancer Medicine 8 ( 11 ) 5274 - 5288 2019年07月

MYH7 mutation identified by next-generation sequencing in three infant siblings with bi-ventricular noncompaction presenting with restrictive hemodynamics: A report of three siblings with a severe phenotype and poor prognosis.

Miura F, Shimada J, Kitagawa Y, Otani K, Sato T, Toki T, Takahashi T, Yonesaka S, Mizukami H, Ito E

Journal of cardiology cases 19 ( 4 ) 140 - 143 2019年04月

Comprehensive genetic analyses of relapsed B-cell precursor acute lymphoblastic leukemia in children

Kubo Kaori, Kudo Ko, Toki Tsutomu, Ito Etsuro, Ikeda Fumika, Ito Tatsuya, Kobayashi Akie, Sato Tomohiko, Kamio Takuya, Sasaki Shinya

Hirosaki Medical Journal 70 ( 1 ) 13 - 23 2019年

Effective response to azacitidine in a child with a second relapse of myeloid leukemia associated with Down syndrome after bone marrow transplantation.

S. Uemura, T. Mori, C. Nagano, S. Takafuji, N. Nishimura, T. Toki, K. Terui, E. Ito, K. Iijima

Pediatric blood & cancer 65 ( 12 ) e27414 - e27414 2018年12月

Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation

Ko Kudo, Hiroo Ueno, Tomohiko Sato, Kaori Kubo, Rika Kanezaki, Akie Kobayashi, Takuya Kamio, Shinya Sasaki, Kiminori Terui, Akira Kurose, Kenichi Yoshida, Yusuke Shiozawa, Tsutomu Toki, Seishi Ogawa, Etsuro Ito

Genes, Chromosomes and Cancer 57 ( 12 ) 665 - 669 2018年10月

Effective response to azacitidine in a child with a second relapse of myeloid leukemia associated with Down syndrome after bone marrow transplantation

Suguru Uemura, Takeshi Mori, China Nagano, Satoru Takafuji, Noriyuki Nishimura, Tsutomu Toki, Kiminori Terui, Etsuro Ito, Kazumoto Iijima

Pediatric Blood & Cancer 65 ( 12 ) e27414 2018年09月

De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome.

Toki T, Yoshida K, Wang R, Nakamura S, Maekawa T, Goi K, Katoh MC, Mizuno S, Sugiyama F, Kanezaki R, Uechi T, Nakajima Y, Sato Y, Okuno Y, Sato-Otsubo A, Shiozawa Y, Kataoka K, Shiraishi Y, Sanada M, Chiba K, Tanaka H, Terui K, Sato T, Kamio T, Sakaguchi H, Ohga S, Kuramitsu M, Hamaguchi I, Ohara A, Kanno H, Miyano S, Kojima S, Ishiguro A, Sugita K, Kenmochi N, Takahashi S, Eto K, Ogawa S, Ito E

American journal of human genetics 103 ( 3 ) 440 - 447 2018年09月

Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.

Sonoda M, Ishimura M, Ichimiya Y, Terashi E, Eguchi K, Sakai Y, Takada H, Hama A, Kanno H, Toki T, Ito E, Ohga S

International journal of hematology 108 ( 2 ) 228 - 231 2018年08月

Correction to: Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.

Sonoda M, Ishimura M, Ichimiya Y, Terashi E, Eguchi K, Sakai Y, Takada H, Hama A, Kanno H, Toki T, Ito E, Ohga S

International journal of hematology 108 ( 2 ) 236 - 236 2018年08月

綜説 Diamond-Blackfan貧血の診断的ターゲットおよびエクソームシーケンス解析

土岐力, 伊藤悦朗

小児科 59 ( 8 ) 1203 - 1212 2018年07月

本邦におけるDiamond-Blackfan貧血の診断的ターゲットおよびエクソームシーケンス解析

土岐力, 伊藤悦朗

臨床血液 59 ( 7 ) 945 - 952 2018年

Purification of leukemic blast cells from blood smears using laser microdissection.

Matsuo H, Shiga S, Imai T, Kamikubo Y, Toki T, Terui K, Ito E, Adachi S

International journal of hematology 106 ( 1 ) 55 - 59 2017年07月

Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing.

Takuya Ichimura, Kenichi Yoshida, Yusuke Okuno, Toshiaki Yujiri, Kozo Nagai, Masanori Nishi, Yuichi Shiraishi, Hiroo Ueno, Tsutomu Toki, Kenichi Chiba, Hiroko Tanaka, Hideki Muramatsu, Toshiro Hara, Hitoshi Kanno, Seiji Kojima, Satoru Miyano, Etsuro Ito, Seishi Ogawa, Shouichi Ohga

International journal of hematology 105 ( 4 ) 515 - 520 2017年04月

Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia.

Fumika Ikeda, Kenichi Yoshida, Tsutomu Toki, Tamayo Uechi, Shiori Ishida, Yukari Nakajima, Yoji Sasahara, Yusuke Okuno, Rika Kanezaki, Kiminori Terui, Takuya Kamio, Akie Kobayashi, Takashi Fujita, Aiko Sato-Otsubo, Yuichi Shiraishi, Hiroko Tanaka, Kenichi Chiba, Hideki Muramatsu, Hitoshi Kanno, Shouichi Ohga, Akira Ohara, Seiji Kojima, Naoya Kenmochi, Satoru Miyano, Seishi Ogawa, Etsuro Ito

Haematologica 102 ( 3 ) e93 - e96 2017年03月

感染を契機に診断に至ったRPL11の遺伝子変異陽性Diamond-Blackfan anemiaの11歳男児例(原著論文/症例報告)

新居敏, 藤野寿典, 赤澤嶺, 田尻雄二朗, 高野良彦, 土岐力, 他

小児科臨床 69 ( 8 ) 1416 - 1420 2016年08月

Erythrocyte glutathione is a novel biomarker of Diamond-Blackfan anemia.

Utsugisawa T, Uchiyama T, Toki T, Ogura H, Aoki T, Hamaguchi I, Ishiguro A, Ohara A, Kojima S, Ohga S, Ito E, Kanno H

Blood cells, molecules & diseases 59 31 - 36 2016年07月

Systematic Cellular Disease Models Reveal Synergistic Interaction of Trisomy 21 and GATA1 Mutations in Hematopoietic Abnormalities.

Banno K, Omori S, Hirata K, Nawa N, Nakagawa N, Nishimura K, Ohtaka M, Nakanishi M, Sakuma T, Yamamoto T, Toki T, Ito E, Yamamoto T, Kokubu C, Takeda J, Taniguchi H, Arahori H, Wada K, Kitabatake Y, Ozono K

Cell reports 15 ( 6 ) 1228 - 1241 2016年05月

ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan.

Ikeda F, Toki T, Kanezaki R, Terui K, Yoshida K, Kanno H, Ohga S, Ohara A, Kojima S, Ogawa S, Ito E

International journal of hematology 103 ( 1 ) 112 - 114 2016年01月

遺伝性骨髄不全症研究の最近の進歩

伊藤悦朗, 土岐力, 照井君典

臨床血液 57 ( 7 ) 882 - 890 2016年

Transient myeloproliferative disorder with partial trisomy 21.

Takahide Takahashi, Akira Inoue, Junko Yoshimoto, Kiichiro Kanamitsu, Tomohiko Taki, Masahide Imada, Mutsuko Yamada, Shinsuke Ninomiya, Tsutomu Toki, Kiminori Terui, Etsuro Ito, Akira Shimada

Pediatric blood & cancer 62 ( 11 ) 2021 - 2024 2015年11月

Preserved High Probability of Overall Survival with Significant Reduction of Chemotherapy for Myeloid Leukemia in Down Syndrome: A Nationwide Prospective Study in Japan

Takashi Taga, Tomoyuki Watanabe, Daisuke Tomizawa, Kazuko Kudo, Kiminori Terui, Hiroshi Moritake, Akitoshi Kinoshita, Shotaro Iwamoto MD, Hideki Nakayama MD, Hiroyuki Takahashi MD, Akira Shimada MD, Tomohiko Taki, Tsutomu Toki, Etsuro Ito, Hiroaki Goto, Katsuyoshi Koh, Akiko M. Saito, Keizo Horibe, Tatsutoshi Nakahata, Akio Tawa, Souichi Adachi

Pediatric Blood & Cancer 63 ( 2 ) 248 - 254 2015年10月

Transient myeloproliferative disorder with partial trisomy 21

Takahide Takahashi, Akira Inoue, Junko Yoshimoto, Kiichiro Kanamitsu, Tomohiko Taki, Masahide Imada, Mutsuko Yamada, Shinsuke Ninomiya, Tsutomu Toki, Kiminori Terui, Etsuro Ito, Akira Shimada

Pediatric Blood & Cancer 62 ( 11 ) 2021 - 2024 2015年07月

Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal children.

Rintaro Ono, Daisuke Hasegawa, Shinsuke Hirabayashi, Takahiro Kamiya, Kenichi Yoshida, Satoko Yonekawa, Chitose Ogawa, Ryota Hosoya, Tsutomu Toki, Kiminori Terui, Etsuro Ito, Atsushi Manabe

European journal of pediatrics 174 ( 4 ) 525 - 531 2015年04月

ダイアモンド・ブラックファン貧血の病態分子機構

土岐力, 伊藤悦朗

臨床血液 56 ( 7 ) 867 - 876 2015年

ダウン症候群に伴うTAM発症の分子機構

金崎里香, 土岐力, 伊藤悦朗

日本産婦人科・新生児血液学会誌 25 49 - 54 2015年

Loss of function mutations inRPL27andRPS27identified by whole-exome sequencing in Diamond-Blackfan anaemia

RuNan Wang, Kenichi Yoshida, Tsutomu Toki, Takafumi Sawada, Tamayo Uechi, Yusuke Okuno, Aiko Sato-Otsubo, Kazuko Kudo, Isamu Kamimaki, Rika Kanezaki, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Kiminori Terui, Tomohiko Sato, Yuji Iribe, Shouichi Ohga, Madoka Kuramitsu, Isao Hamaguchi, Akira Ohara, Junichi Hara, Kumiko Goi, Kousaku Matsubara, Kenichi Koike, Akira Ishiguro, Yasuhiro Okamoto, Kenichiro Watanabe, Hitoshi Kanno, Seiji Kojima, Satoru Miyano, Naoya Kenmochi, Seishi Ogawa, Etsuro Ito

British Journal of Haematology 168 ( 6 ) 854 - 864 2014年11月

Down syndrome-associated haematopoiesis abnormalities created by chromosome transfer and genome editing technologies.

Kazuki Y, Yakura Y, Abe S, Osaki M, Kajitani N, Kazuki K, Takehara S, Honma K, Suemori H, Yamazaki S, Sakuma T, Toki T, Shimizu R, Nakauchi H, Yamamoto T, Oshimura M

Scientific reports 4 6136 2014年08月

Gene alterations involving the CRLF2-JAK pathway and recurrent gene deletions in Down syndrome-associated acute lymphoblastic leukemia in Japan

Isamu Hanada, Kiminori Terui, Fumika Ikeda, Tsutomu Toki, Rika Kanezaki, Tomohiko Sato, Takuya Kamio, Ko Kudo, Shinya Sasaki, Yoshihiro Takahashi, Yasuhide Hayashi, Takeshi Inukai, Seiji Kojima, Kenichi Koike, Yoshiyuki Kosaka, Masao Kobayashi, Masue Imaizumi, Tetsuo Mitsui, Hiroki Hori, Junichi Hara, Keizo Horibe, Jun-ichi Nagai, Hiroaki Goto, Etsuro Ito

Genes, Chromosomes and Cancer 53 ( 11 ) 902 - 910 2014年07月

非ダウン症小児急性巨核芽球性白血病にみとめられた新規GATA1インフレーム変異

王汝南, 金崎里香, 土岐力, 照井君典, 佐々木伸也, 工藤耕, 神尾卓哉, 佐藤知彦, 池田史圭, 荒木亮, 落合英俊, 伊藤悦朗

弘前医学 65 ( 2-4 ) 227 - 237 2014年

特集造血器腫瘍のゲノム解析４.Down syndrome associated myeloid disorders

伊藤悦朗, 土岐力

血液フロンティア 24 ( 1 ) 47 - 53 2013年12月

The landscape of somatic mutations in Down syndrome-related myeloid disorders.

Yoshida K, Toki T, Okuno Y, Kanezaki R, Shiraishi Y, Sato-Otsubo A, Sanada M, Park MJ, Terui K, Suzuki H, Kon A, Nagata Y, Sato Y, Wang R, Shiba N, Chiba K, Tanaka H, Hama A, Muramatsu H, Hasegawa D, Nakamura K, Kanegane H, Tsukamoto K, Adachi S, Kawakami K, Kato K, Nishimura R, Izraeli S, Hayashi Y, Miyano S, Kojima S, Ito E, Ogawa S

Nature genetics 45 ( 11 ) 1293 - + 2013年11月

Clonal selection in xenografted TAM recapitulates the evolutionary process of myeloid leukemia in Down syndrome

Satoshi Saida, Ken-ichiro Watanabe, Aiko Sato-Otsubo, Kiminori Terui, Kenichi Yoshida, Yusuke Okuno, Tsutomu Toki, RuNan Wang, Yuichi Shiraishi, Satoru Miyano, Itaru Kato, Tatsuya Morishima, Hisanori Fujino, Katsutsugu Umeda, Hidefumi Hiramatsu, Souichi Adachi, Etsuro Ito, Seishi Ogawa, Mamoru Ito, Tatsutoshi Nakahata, Toshio Heike

Blood 121 ( 21 ) 4377 - 4387 2013年05月

Naturally occurring oncogenic GATA1 mutants with internal deletions in transient abnormal myelopoiesis in Down syndrome

Tsutomu Toki, Rika Kanezaki, Eri Kobayashi, Hiroshi Kaneko, Mikiko Suzuki, RuNan Wang, Kiminori Terui, Hirokazu Kanegane, Miho Maeda, Mikiya Endo, Tatsuki Mizuochi, Souichi Adachi, Yasuhide Hayashi, Masayuki Yamamoto, Ritsuko Shimizu, Etsuro Ito

Blood 121 ( 16 ) 3181 - 3184 2013年04月

Down syndrome associated myeloid disorders

土岐力

血液フロンティア 24 47 - 53 2013年

新生児科医のためのTAM診療ガイドラインTAM発症の分子機構

照井君典, 土岐力

日本周産期・新生児医学会雑誌 49 20 - 22 2013年

ダウン症候群関連急性リンパ性白血病におけるJAK2およびCRLF2遺伝子異常

照井君典, 土岐力

日本小児血液・がん学会雑誌 50 11 - 14 2013年

A novel mutation of ribosomal protein S10 gene in a Japanese patient with diamond-Blackfan anemia.

Yazaki M, Kamei M, Ito Y, Konno Y, Wang R, Toki T, Ito E

Journal of pediatric hematology/oncology 34 ( 4 ) 293 - 295 2012年05月

[Transient myeloproliferative disorder in Down syndrome].

Ito E, Toki T

Nihon rinsho. Japanese journal of clinical medicine 70 Suppl 2 687 - 91 2012年04月

Identification of TRIB1 R107L gain-of-function mutation in human acute megakaryocytic leukemia

Takashi Yokoyama, Tsutomu Toki, Yoshihiro Aoki, Rika Kanezaki, Myoung-ja Park, Yohei Kanno, Tomoko Takahara, Yukari Yamazaki, Etsuro Ito, Yasuhide Hayashi, Takuro Nakamura

Blood 119 ( 11 ) 2608 - 2611 2012年03月

Extensive gene deletions in Japanese patients with Diamond-Blackfan anemia

Madoka Kuramitsu, Aiko Sato-Otsubo, Tomohiro Morio, Masatoshi Takagi, Tsutomu Toki, Kiminori Terui, RuNan Wang, Hitoshi Kanno, Shouichi Ohga, Akira Ohara, Seiji Kojima, Toshiyuki Kitoh, Kumiko Goi, Kazuko Kudo, Tadashi Matsubayashi, Nobuo Mizue, Michio Ozeki, Atsuko Masumi, Haruka Momose, Kazuya Takizawa, Takuo Mizukami, Kazunari Yamaguchi, Seishi Ogawa, Etsuro Ito, Isao Hamaguchi

Blood 119 ( 10 ) 2376 - 2384 2012年03月

Down症に伴う骨髄増殖症

土岐力

日本臨床 70 687 - 91 2012年

Nrf2 regulates ferroportin 1-mediated iron efflux and counteracts lipopolysaccharide-induced ferroportin 1 mRNA suppression in macrophages.

Harada N, Kanayama M, Maruyama A, Yoshida A, Tazumi K, Hosoya T, Mimura J, Toki T, Maher JM, Yamamoto M, Itoh K

Archives of biochemistry and biophysics 508 ( 1 ) 101 - 109 2011年04月

一過性骨髄異常増殖症(TAM)発症の分子機構

土岐力

日本小児血液学会雑誌 25 171 - 8 2011年

Down syndrome and GATA1 mutations in transient abnormal myeloproliferative disorder: mutation classes correlate with progression to myeloid leukemia

Rika Kanezaki, Tsutomu Toki, Kiminori Terui, Gang Xu, RuNan Wang, Akira Shimada, Asahito Hama, Hirokazu Kanegane, Kiyoshi Kawakami, Mikiya Endo, Daisuke Hasegawa, Kazuhiro Kogawa, Souichi Adachi, Yasuhiko Ikeda, Shotaro Iwamoto, Takashi Taga, Yoshiyuki Kosaka, Seiji Kojima, Yasuhide Hayashi, Etsuro Ito

Blood 116 ( 22 ) 4631 - 4638 2010年11月

Selective KIT inhibitor KI-328 and HSP90 inhibitor show different potency against the type of KIT mutations recurrently identified in acute myeloid leukemia.

Tsujimura A, Kiyoi H, Shiotsu Y, Ishikawa Y, Mori Y, Ishida H, Toki T, Ito E, Naoe T

International journal of hematology 92 ( 4 ) 624 - 633 2010年11月

Molecular pathogenesis in Diamond-Blackfan anemia.

Ito E, Konno Y, Toki T, Terui K

International journal of hematology 92 ( 3 ) 413 - 418 2010年10月

典型例とは異なる緩徐な臨床経過を示し、リボソームタンパク遺伝子RPL11の変異の検出により診断したDiamond-Blackfan貧血の1例

佐野弘純, 朴明子, 外松学, 今野友貴, 土岐力, 伊藤悦朗, 林泰秀

日本小児血液学会雑誌 24 ( 4 ) 225 - 228 2010年08月

Mutations in the ribosomal protein genes in Japanese patients with Diamond-Blackfan anemia.

Konno Y, Toki T, Tandai S, Xu G, Wang R, Terui K, Ohga S, Hara T, Hama A, Kojima S, Hasegawa D, Kosaka Y, Yanagisawa R, Koike K, Kanai R, Imai T, Hongo T, Park MJ, Sugita K, Ito E

Haematologica 95 ( 8 ) 1293 - 1299 2010年08月

Exposure to a MRI-type high-strength static magnetic field stimulates megakaryocytic/erythroid hematopoiesis in CD34+ cells from human placental and umbilical cord blood.

Monzen S, Takahashi K, Toki T, Ito E, Sakurai T, Miyakoshi J, Kashiwakura I

Bioelectromagnetics 30 ( 4 ) 280 - 285 2009年05月

The key role of stem cell factor/KIT signaling in the proliferation of blast cells from Down syndrome-related leukemia

土岐力

Leukemia 23 ( 1 ) 95 - 103 2009年

小児科領域の血液疾患一過性骨髄増殖性疾患

土岐力, 照井君典

日本検査血液学会雑誌 10 457 - 464 2009年

一過性骨髄増殖症.小児疾患診療のための病態生理

土岐力, 照井君典

小児内科増刊号 41 1183 - 1186 2009年

一過性骨髄増殖症

土岐力

小児疾患診療のための病態生理小児内科増刊号 41 1183 - 1186 2009年

Construction of an expression system for aqualysin I in Escherichia coli that gives a markedly improved yield of the enzyme protein.

Sakaguchi M, Niimiya K, Takezawa M, Toki T, Sugahara Y, Kawakita M

Bioscience, biotechnology, and biochemistry 72 ( 8 ) 2012 - 2018 2008年08月

Functional analysis of JAK3 mutations in transient myeloproliferative disorder and acute megakaryoblastic leukaemia accompanying Down syndrome.

Sato T, Toki T, Kanezaki R, Xu G, Terui K, Kanegane H, Miura M, Adachi S, Migita M, Morinaga S, Nakano T, Endo M, Kojima S, Kiyoi H, Mano H, Ito E

British journal of haematology 141 ( 5 ) 681 - 688 2008年06月

Edaravone inhibits the expression of vascular endothelial growth factor in human astrocytes exposed to hypoxia.

Ishikawa A, Yoshida H, Metoki N, Toki T, Imaizumi T, Matsumiya T, Yamashita K, Taima K, Satoh K

Neuroscience research 59 ( 4 ) 406 - 412 2007年12月

Correction of immunodeficiency associated with NEMO mutation by umbilical cord blood transplantation using a reduced-intensity conditioning regimen.

Tono C, Takahashi Y, Terui K, Sasaki S, Kamio T, Tandai S, Sato T, Kudo K, Toki T, Tachibana N, Yoshioka T, Nakahata T, Morio T, Nishikomori R, Ito E.

Bone Marrow Transplantation 39 ( 12 ) 801 - 804 2007年04月

[The molecular mechanism of leukemogenesis in Down syndrome-related acute megakaryocytic leukemia].

Ito E, Toki T

Nihon rinsho. Japanese journal of clinical medicine 65 Suppl 1 136 - 140 2007年01月

Development of acute megakaryoblastic leukemia from a minor clone in a Down syndrome patient with clinically overt transient myeloproliferative disorder.

Xu G, Kato K, Toki T, Takahashi Y, Terui K, Ito E

Journal of pediatric hematology/oncology 28 ( 10 ) 696 - 698 2006年10月

Physical association of the patient-specific GATA1 mutants with RUNX1 in acute megakaryoblastic leukemia accompanying Down syndrome.

Xu G, Kanezaki R, Toki T, Watanabe S, Takahashi Y, Terui K, Kitabayashi I, Ito E.

Leukemia 20 ( 6 ) 1002 - 1008 2006年06月

Cloning and characterization of the novel chimeric gene p53/FXR2 in the acute megakaryoblastic leukemia cell line CMK11-5.

Kanezaki R, Toki T, Xu G, Narayanan R, Ito E

The Tohoku journal of experimental medicine 209 ( 3 ) 169 - 180 2006年

JAK2 Val617Phe activating tyrosine kinase mutation in juvenile myelomonocytic leukemia.

Tono C, Xu G, Toki T, Takahashi Y, Sasaki S, Terui K, Ito E.

Leukemia 19 ( 10 ) 1843 - 1844 2005年10月

Roxithromycin is an inhibitor of human coronary artery smooth muscle cells proliferation: a potential ability to prevent coronary heart disease.

Tomita H, Osanai T, Toki T, Maeda N, Murakami R, Chen Z, Yamabe H, Osawa H, Yasujima M, Okumura K

Atherosclerosis 182 ( 1 ) 87 - 95 2005年09月

The proto-oncogene ERG in megakaryoblastic leukemias.

Rainis L, Toki T, Pimanda JE, Rosenthal E, Machol K, Strehl S, Göttgens B, Ito E, Izraeli S

Cancer research 65 ( 17 ) 7596 - 7602 2005年09月

Troglitazone and 15-deoxy-delta(12,14)-prostaglandin J2 inhibit shear-induced coupling factor 6 release in endothelial cells.

Tomita H, Osanai T, Toki T, Sasaki S, Maeda N, Murakami R, Magota K, Yasujima M, Okumura K

Cardiovascular research 67 ( 1 ) 134 - 141 2005年07月

KCNJ2 mutation in intractable ventricular arrhythmia with Andersen's syndrome.

Takahashi T, Tandai S, Toki T, Sato T, Eto S, Sato A, Ueda T, Sato S, Ichinose K, Ito E, Yonesaka S

Pediatrics international : official journal of the Japan Pediatric Society 47 ( 2 ) 220 - 223 2005年04月

Transgenic expression of BACH1 transcription factor results in megakaryocytic impairment.

Toki T, Katsuoka F, Kanezaki R, Xu G, Kurotaki H, Sun J, Kamio T, Watanabe S, Tandai S, Terui K, Yagihashi S, Komatsu N, Igarashi K, Yamamoto M, Ito E

Blood 105 ( 8 ) 3100 - 3108 2005年04月

The GATA1 mutation in an adult patient with acute megakaryoblastic leukemia not accompanying Down syndrome.

Harigae H, Xu G, Sugawara T, Ishikawa I, Toki T, Ito E

Blood 103 ( 8 ) 3242 - 3243 2004年04月

21q11-21領域からの一過性骨髄異常増殖症の原因遺伝子単離の試み

石崎典子, 金崎里香, 土岐力, 伊藤悦朗

弘前医学 55 ( 3-4 ) 83 - 94 2004年03月

Fetal origin of the GATA1 mutation in identical twins with transient myeloproliferative disorder and acute megakaryoblastic leukemia accompanying Down syndrome.

Shimada A, Xu G, Toki T, Kimura H, Hayashi Y, Ito E

Blood 103 ( 1 ) 366 2004年01月

21q11-21 領域からの一過性骨髄異常増殖症の原因遺伝子単離の試み

石崎典子, 金崎里香, 土岐力, 伊藤悦朗

弘前医学 55 ( 3-4 ) 83 - 94 2004年

Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients.

Uyeda T, Takahashi T, Eto S, Sato T, Xu G, Kanezaki R, Toki T, Yonesaka S, Ito E

Journal of human genetics 49 ( 8 ) 404 - 407 2004年

B-cell-specific transcription factor BACH2 modifies the cytotoxic effects of anticancer drugs.

Kamio T, Toki T, Kanezaki R, Sasaki S, Tandai S, Terui K, Ikebe D, Igarashi K, Ito E

Blood 102 ( 9 ) 3317 - 3322 2003年11月

Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndrome.

Xu G, Nagano M, Kanezaki R, Toki T, Hayashi Y, Taketani T, Taki T, Mitui T, Koike K, Kato K, Imaizumi M, Sekine I, Ikeda Y, Hanada R, Sako M, Kudo K, Kojima S, Ohneda O, Yamamoto M, Ito E

Blood 102 ( 8 ) 2960 - 2968 2003年10月

Glycogen synthase kinase-3beta phosphorylates synphilin-1 in vitro.

Tanji K, Toki T, Tamo W, Imaizumi T, Matsumiya T, Mori F, Takahashi H, Satoh K, Wakabayashi K

Neuropathology : official journal of the Japanese Society of Neuropathology 23 ( 3 ) 199 - 202 2003年09月

B細胞特異的転写因子BACH2によるBCL-2関連遺伝子A1の発現抑制機構

丹代(山田) 諭, 佐藤秀子, 金崎里香, 土岐力, 五十嵐和彦, 伊藤悦朗

弘前醫學 54 ( 1 ) 8 - 20 2002年

Transcription factor BACH1 is recruited to the nucleus by its novel alternative spliced isoform.

R Kanezaki, T Toki, M Yokoyama, K Yomogida, K Sugiyama, M Yamamoto, K Igarashi, E Ito

The Journal of biological chemistry 276 ( 10 ) 7278 - 7284 2001年03月

Desferrioxamine, an iron chelator, upregulates cyclooxygenase-2 expression and prostaglandin production in a human macrophage cell line.

K Tanji, T Imaizumi, T Matsumiya, H Itaya, K Fujimoto, X Cui, T Toki, E Ito, H Yoshida, K Wakabayashi, K Satoh

Biochimica et biophysica acta 1530 ( 2-3 ) 227 - 235 2001年02月

B細胞特異的転写因子BACH2の標的遺伝子の同定

佐藤秀子, 佐々木伸也, 金崎里香, 土岐力, 伊藤悦朗

弘前醫學 53 ( 2 ) 73 - 81 2001年

Expression of transcription factors during megakaryocytic differentiation of CD34+ cells from human cord blood induced by thrombopoietin.

K Terui, Y Takahashi, J Kitazawa, T Toki, M Yokoyama, E Ito

The Tohoku journal of experimental medicine 192 ( 4 ) 259 - 273 2000年12月

Functional characterization of the two alternative promoters of human p45 NF-E2 gene.

T Toki, K Arai, K Terui, N Komatsu, M Yokoyama, F Katsuoka, M Yamamoto, E Ito

Experimental hematology 28 ( 10 ) 1113 - 1119 2000年10月

Cloning and expression of human B cell-specific transcription factor BACH2 mapped to chromosome 6q15.

S Sasaki, E Ito, T Toki, T Maekawa, R Kanezaki, T Umenai, A Muto, H Nagai, T Kinoshita, M Yamamoto, J Inazawa, M M Taketo, T Nakahata, K Igarashi, M Yokoyama

Oncogene 19 ( 33 ) 3739 - 3749 2000年08月

Expression of Transcription Factors during Megakaryocytic Differentiation of CD34+ Cells from Human Cord Blood Induced by Thrombopoietin

Terui Kiminori, Takahashi Yoshihiro, Kitazawa Junichi, Toki Tsutomu, Yokoyama Masaru, Ito Etsuro

The Tohoku Journal of Experimental Medicine 192 ( 4 ) 259 - 273 2000年

Molecular cloning and functional characterization of a new Cap'n' collar family transcription factor Nrf3.

A Kobayashi, E Ito, T Toki, K Kogame, S Takahashi, K Igarashi, N Hayashi, M Yamamoto

The Journal of biological chemistry 274 ( 10 ) 6443 - 6452 1999年03月

Erythroid accelerating factor detected in serum from rats with drug induced hemolysis.

M Kasai, M Yokoyama, T Toki, H Maruyama, K Satoh, E Itoh

The Tohoku journal of experimental medicine 186 ( 4 ) 279 - 289 1998年12月

Progression from myelodysplastic syndrome with monosomy 7 to acute monoblastic leukemia with MLL gene rearrangement.

J Kitazawa, T Umenai, E Ito, K Arai, H Otomo, T Toki, M Seto, R Ueda, M Yokoyama

International journal of hematology 67 ( 1 ) 23 - 26 1998年01月

Structure and chromosome mapping of the human small maf-genes MAFG and MAFK.

T Iwata, K Kogame, T Toki, M Yokoyama, M Yamamoto, E Ito

Cytogenetics and cell genetics 82 ( 1-2 ) 88 - 90 1998年

Erythroid Accelerating Factor Detected in Serum from Rats with Drug Induced Hemolysis.

Kasai Mikio, Yokoyama Masaru, Toki Tsutomu, Maruyama Hidekazu, Satoh Kei, Itoh Etsuro

The Tohoku Journal of Experimental Medicine 186 ( 4 ) 279 - 289 1998年

再生不良性貧血小児の予後因子の検討

貝塚理子, 井上リカルド進常, 土岐力, 他

日本小児血液学会雑誌 11 ( 2 ) 84 - 87 1997年04月

過去30年間に経験した再生不良性貧血小児の予後および予後因子の検討

貝塚理子, 井上リカルド進常, 土岐力, 伊藤悦朗, 横山碓

日本小児血液学会雑誌 11 ( 2 ) 79 - 83 1997年04月

Human small Maf proteins form heterodimers with CNC family transcription factors and recognize the NF-E2 motif.

T Toki, J Itoh, J Kitazawa, K Arai, K Hatakeyama, J Akasaka, K Igarashi, N Nomura, M Yokoyama, M Yamamoto, E Ito

Oncogene 14 ( 16 ) 1901 - 1910 1997年04月

再生不良性貧血小児の予後因子の検討

貝塚理子, 井上リカルド進常, 土岐力, 伊藤悦朗, 横山〓

日本小児血液学会雑誌 11 ( 2 ) 84 - 87 1997年

過去３０年間に経験した再生不良性貧血小児の予後および予後因子の検討

貝塚理子, 井上リカルド進常, 土岐力, 伊藤悦朗, 横山〓

日本小児血液学会雑誌 11 ( 2 ) 79 - 83 1997年

Expression of erythroid-specific genes in megakaryoblastic disorders.

E Ito, M Kasai, T Toki, K Arai, M Yokoyama

Leukemia & lymphoma 23 ( 5-6 ) 545 - 550 1996年11月

乳児白血病の臨床解析 : 予後因子の検討

荒井宏治, 伊藤悦郎, 土岐力, 他

日本小児血液学会雑誌 10 ( 5 ) 344 - 350 1996年10月

Abundant expression of erythroid transcription factor P45 NF-E2 mRNA in human peripheral granurocytes.

T Toki, J Itoh, K Arai, J Kitazawa, M Yokoyama, K Igarashi, M Yamamoto, E Ito

Biochemical and biophysical research communications 219 ( 3 ) 760 - 765 1996年02月

乳児白血病の臨床解析　予後因子の検討

荒井宏治, 伊藤悦朗, 土岐力, 照井君典, 安斎由紀子, 岡敏明, 石川順一, 工藤亨, 武田武夫, 立花直樹, 高野長邦, 渡辺新, 横山新吉, 今泉益栄, 菊田敦, 田中篤, 横山雄

日本小児血液学会雑誌 10 ( 5 ) 344 - 350 1996年

赤血球特異的転写因子と造血

伊藤悦朗, 土岐力

日本小児血液学会雑誌 10 ( 1 ) 8 - 17 1996年

神経疾患児の貧血　とくに抗てんかん剤の影響について

塩谷陸子, 小野寺典夫, 土岐　力, 他

弘前医学 46 254 - 259 1995年12月

Expression of erythroid-specific genes in acute megakaryoblastic leukaemia and transient myeloproliferative disorder in Down's syndrome.

E Ito, M Kasai, Y Hayashi, T Toki, et al

British journal of haematology 90 ( 3 ) 607 - 614 1995年07月

Erythroid transcription factor GATA-1 is abundantly transcribed in mouse testis.

E Ito, T Toki, H Ishihara, et al.

Nature 362 ( 6419 ) 466 - 468 1993年04月

Expression of a lineage specific transcriptional factor GATA-1 in leukaemic blasts from patients with infantile leukaemia.

E Ito, T Toki, K Arai, K Kawauchi, H Tsuda, M Yokoyama

British journal of haematology 80 ( 4 ) 561 - 563 1992年04月

赤血球造血刺激後の細胞内種々酵素活性の変動 in vivoおよびin vitroにおける検討

土岐　力, 横山　碓

日本小児血液学会誌 5 ( 2 ) 145 - 150 1991年05月

赤血球造血刺激後の細胞内種々酵素活性の変動　Ｉｎ　ｖｉｖｏおよびｉｎ　ｖｉｔｒｏにおける検討

土岐力, 横山雄

日本小児血液学会雑誌 5 ( 2 ) 145 - 150 1991年

中学生における血小板数異常と鉄欠乏性貧血治療に伴う血小板数・粒度分布の変動

須藤善雅, 越前屋竹寅, 綛谷啓之 , 他

日本小児血液学会誌 4 ( 4 ) 342 - 347 1990年04月

中学生における血小板数異常と鉄欠乏性貧血治療に伴う血小板数・粒度分布の変動

須藤善雅, 越前屋竹寅, 綛谷啓之, 荒井宏治, 土岐力, 河内暁一, 佐藤雄一, 横山〓

日本小児血液学会雑誌 4 ( 4 ) 342 - 347 1990年

Cyclosporin AとPrednisoloneの併用が有効であった重症再生不良性貧血の1例

伊東亮助, 河内暁一, 土岐　力, 他

臨床血液 30 ( 12 ) 2157 - 2162 1989年12月

赤血球造血に対するホルモンの効果

綛谷啓之, 土岐　力, 横山　碓

日本小児血液学会誌 3 ( 4 ) 325 - 332 1989年04月

種々血液疾患における赤血球GOTの変動と病態について

小瀧力, 伊東亮助, 綛谷啓之, 他

日本小児血液学会誌 2 325 - 330 1989年01月

Cyclosporin AとPrednisoloneの併用が有効であった重症再生不良性貧血の1例

伊東亮助, 河内暁一, 土岐力, 葛西幹雄, 荒井宏治, 斎藤俊光, 宮野孝一, 佐藤雄一, 横山〓

臨床血液 30 ( 12 ) 2157 - 2162 1989年

赤血球造血刺激後の細胞内cyclic nucleotides量の変化

土岐力, 綛谷裕之, 荒井宏治, 横山〓

日本小児血液学会雑誌 3 ( 4 ) 345 - 350 1989年

赤血球造血に対するホルモンの効果

綛谷啓之, 土岐力, 横山〓

日本小児血液学会雑誌 3 ( 4 ) 325 - 332 1989年

　前のページ-次のページ　

<土岐 力>

論文 - 土岐 力

<土岐　力>

論文 - 土岐　力