論文 - 松下 正
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Identification of amino acid residues responsible for von Willebrand factor binding to sulfatide by charged-to-alanine-scanning mutagenesis. 査読有り
Nakayama T, Matsushita T, Yamamoto K, Mutsuga N, Kojima T, Katsumi A, Nakao N, Sadler JE, Naoe T, Saito H
Int J Hematol 87 巻 頁： 363-370 2008年
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Prognostic implication and biological roles of RhoH in acute myeloid leukaemia. 査読有り
Iwasaki T, Katsumi A, Kiyoi H, Tanizaki R, Ishikawa Y, Ozeki K, Kobayashi M, Abe A, Matsushita T, Watanabe T, Amano M, Kojima T, Kaibuchi K, Naoe T
Eur J Haematol. 81 巻 頁： 454-460 2008年
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Ablation of angiotensin IV receptor attenuates hypofibrinolysis via PAI-1 downregulation and reduces occlusive arterial thrombosis. 査読有り
Numaguchi Y, Ishii M, Kubota R, Morita Y, Yamamoto K, Matsushita T, Okumura K, Murohara T
Arterioscler Thromb Vasc Biol. 29 巻 頁： 2102-2108 2009年
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A novel missense mutation causing abnormal LMAN1 in a Japanese patient with combined deficiency of factor V and factor VIII. 査読有り
Yamada T, Fujimori Y, Suzuki A, Miyawaki Y, Takagi A, Murate T, Sano M, Matsushita T, Saito H, Kojima T
Am J Hematol. 84 巻 頁： 738-742 2009年
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Definite diagnosis in Japanese patients with protein C deficiency by identification of causative PROC mutations. 査読有り
Takagi A, Tanaka R, Nakashima D, Fujimori Y, Yamada T, Okumura K, Murate T, Yamada M, Horikoshi Y, Yamamoto K, Katsumi A, Matsushita T, Naoe T, Kojima T.
Int J Hematol. 89 巻 頁： 555-557 2009年
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A novel splice site mutation in intron C of PROS1 leads to markedly reduced mutant mRNA level, absence of thrombin-sensitive region, and impaired secretion and cofactor activity of mutant protein S. 査読有り
Okada H, Kunishima S, Hamaguchi M, Takagi A, Yamamoto K, Takamatsu J, Matsushita T, Saito H, Kojima T, Yamazaki T.
Thromb Res. 125 巻 頁： e246-250 2010年
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Irrespective of CD34 expression, lineage-committed cell fraction reconstitutes and re-establishes transformed Philadelphia chromosome-positive leukemia in NOD/SCID/IL-2Rgammac-/- mice. 査読有り
Tanizaki R, Nomura Y, Miyata Y, Minami Y, Abe A, Hanamura A, Sawa M, Murata M, Kiyoi H, Matsushita T, Naoe T.
Cancer Sci. 101 巻 頁： 631-638 2010年
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Heterozygous antithrombin deficiency improves in vivo haemostasis in factor VIII-deficient mice. 査読有り
Bolliger D, Szlam F, Suzuki N, Matsushita T, Tanaka KA
Thromb Haemost. 103 巻 頁： 1233-1238 2010年
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Severe hemophilia A in a Japanese female caused by an F8-intron 22 inversion associated with skewed X chromosome inactivation. 査読有り
Miyawaki Y, Suzuki A, Fujimori Y, Takagi A, Murate T, Suzuki N, Katsumi A, Naoe T, Yamamoto K, Matsushita T, Takamatsu J, Kojima T.
Int J Hematol. 92 巻 頁： 405-408 2010年
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Impaired secretion of carboxyl-terminal truncated factor VII due to an F7 nonsense mutation associated with FVII deficiency. 査読有り
Tanaka R, Nakashima D, Suzuki A, Miyawaki Y, Fujimori Y, Yamada T, Takagi A, Murate T, Yamamoto K, Katsumi A, Matsushita T, Naoe T, Kojima T.
Thromb Res. 125 巻 頁： 262-266 2010年
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Successful fertility management of a patient with factor V deficiency: planned transfusion of fresh frozen plasma under infertility treatment. 査読有り
Iwase A, Goto M, Manabe S, Hirokawa W, Kobayashi H, Nakahara T, Takikawa S, Kotani T, Sumigama S, Tsuda H, Nakayama T, Suzuki N, Matsushita T, Kikkawa F.
Fertil Steril. 95 巻 頁： 2124.e5-7 2011年
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Pitavastatin-induced angiogenesis and arteriogenesis is mediated by Notch1 in a murine hindlimb ischemia model without induction of VEGF. 査読有り
Kikuchi R, Takeshita K, Uchida Y, Kondo M, Cheng XW, Nakayama T, Yamamoto K, Matsushita T, Liao JK, Murohara T.
Lab Invest. 91 巻 頁： 691-703 2011年
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Virus-associated hemophagocytic syndrome caused by pandemic swine-origin influenza A (H1N1) in a patient after unrelated bone marrow transplantation. 査読有り
Katsumi A, Nishida T, Murata M, Terakura S, Shimada K, Saito S, Kobayashi M, Kodaira A, Shibata S, Oda I, Yagi T, Kiyoi H, Matsushita T, Kojima T, Naoe T.
J Clin Exp Hematop. 51 巻 頁： 63-65 2011年
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FLT/ITD regulates leukemia cell adhesion thruough α4β1 integrin ando Pyk2 signalling. 査読有り
Katsumi A, Kiyoi H, Abe A, Tanizaki R, Iwasaki T, Kobayashi M, Matsushita T, Kaibuchi K, Senga T, Kojima T, Kohno T, Hamaguchi M, Naoe T.
Eur J Haematol. 86 巻 頁： 191-198 2011年
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A novel ENG mutation causing impaired co-translational processing of endoglin associated with hereditary hemorrhagic telangiectasia. 査読有り
Suzuki A, Nakashima D, Miyawaki Y, Fujita J, Maki A, Fujimori Y, Takagi A, Murate T, Teranishi M, Matsushita T, Saito H, Kojima T.
Thromb Res. 129 巻 頁： e200-208 2012年
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Increased von Willebrand Factor to ADAMTS13 ratio as a predictor of thrombotic complications following a major hepatectomy. 査読有り
Kobayashi S, Yokoyama Y, Matsushita T, Kainuma M, Ebata T, Igami T, Sugawara G, Takahashi Y, Nagino M.
Arch Surg. 147 巻 頁： 909-917 2012年
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Thrombosis from a prothrombin mutation conveying antithrombin resistance. 査読有り
Miyawaki Y, Suzuki A, Fujita J, Maki A, Okuyama E, Murata M, Takagi A, Murate T, Kunishima S, Sakai M, Okamoto K, Matsushita T, Naoe T, Saito H, Kojima T.
N Engl J Med. 366 巻 頁： 2390-2396 2012年
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Recombinant factor VIIa analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: a randomized controlled trial. 査読有り
de Paula EV, Kavakli K, Mahlangu J, Ayob Y, Lentz SR, Morfini M, Nemes L, Šalek SZ, Shima M, Windyga J, Ehrenforth S, Chuansumrit A
J Thromb Haemost. 10 巻 頁： 81-89 2012年
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Stress augments insulin resistance and prothrombotic state: role of visceral adipose-derived monocyte chemoattractant protein-1. 査読有り
Uchida Y, Takeshita K, Yamamoto K, Kikuchi R, Nakayama T, Nomura M, Cheng XW, Egashira K, Matsushita T, Nakamura H, Murohara T.
Diabetes. 61 巻 頁： 1552-1561 2012年
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Seki, Y; Ogawa, Y; Kikuchi, T; Sakaida, E; Mizuta, Y; Kitagawa, T; Takemura, K; Miyaguchi, Y; Nogami, K; Matsushita, T
INTERNATIONAL JOURNAL OF HEMATOLOGY 120 巻 ( 4 ) 頁： 482 - 491 2024年10月