Papers - MATSUSHITA, Tadashi
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Identification of amino acid residues responsible for von Willebrand factor binding to sulfatide by charged-to-alanine-scanning mutagenesis. Reviewed
Nakayama T, Matsushita T, Yamamoto K, Mutsuga N, Kojima T, Katsumi A, Nakao N, Sadler JE, Naoe T, Saito H
Int J Hematol Vol. 87 page： 363-370 2008
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Prognostic implication and biological roles of RhoH in acute myeloid leukaemia. Reviewed
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. Vol. 81 page： 454-460 2008
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Ablation of angiotensin IV receptor attenuates hypofibrinolysis via PAI-1 downregulation and reduces occlusive arterial thrombosis. Reviewed
Numaguchi Y, Ishii M, Kubota R, Morita Y, Yamamoto K, Matsushita T, Okumura K, Murohara T
Arterioscler Thromb Vasc Biol. Vol. 29 page： 2102-2108 2009
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A novel missense mutation causing abnormal LMAN1 in a Japanese patient with combined deficiency of factor V and factor VIII. Reviewed
Yamada T, Fujimori Y, Suzuki A, Miyawaki Y, Takagi A, Murate T, Sano M, Matsushita T, Saito H, Kojima T
Am J Hematol. Vol. 84 page： 738-742 2009
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Definite diagnosis in Japanese patients with protein C deficiency by identification of causative PROC mutations. Reviewed
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. Vol. 89 page： 555-557 2009
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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. Reviewed
Okada H, Kunishima S, Hamaguchi M, Takagi A, Yamamoto K, Takamatsu J, Matsushita T, Saito H, Kojima T, Yamazaki T.
Thromb Res. Vol. 125 page： e246-250 2010
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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. Reviewed
Tanizaki R, Nomura Y, Miyata Y, Minami Y, Abe A, Hanamura A, Sawa M, Murata M, Kiyoi H, Matsushita T, Naoe T.
Cancer Sci. Vol. 101 page： 631-638 2010
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Heterozygous antithrombin deficiency improves in vivo haemostasis in factor VIII-deficient mice. Reviewed
Bolliger D, Szlam F, Suzuki N, Matsushita T, Tanaka KA
Thromb Haemost. Vol. 103 page： 1233-1238 2010
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Severe hemophilia A in a Japanese female caused by an F8-intron 22 inversion associated with skewed X chromosome inactivation. Reviewed
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. Vol. 92 page： 405-408 2010
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Impaired secretion of carboxyl-terminal truncated factor VII due to an F7 nonsense mutation associated with FVII deficiency. Reviewed
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. Vol. 125 page： 262-266 2010
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Successful fertility management of a patient with factor V deficiency: planned transfusion of fresh frozen plasma under infertility treatment. Reviewed
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. Vol. 95 page： 2124.e5-7 2011
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Pitavastatin-induced angiogenesis and arteriogenesis is mediated by Notch1 in a murine hindlimb ischemia model without induction of VEGF. Reviewed
Kikuchi R, Takeshita K, Uchida Y, Kondo M, Cheng XW, Nakayama T, Yamamoto K, Matsushita T, Liao JK, Murohara T.
Lab Invest. Vol. 91 page： 691-703 2011
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Virus-associated hemophagocytic syndrome caused by pandemic swine-origin influenza A (H1N1) in a patient after unrelated bone marrow transplantation. Reviewed
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. Vol. 51 page： 63-65 2011
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FLT/ITD regulates leukemia cell adhesion thruough α4β1 integrin ando Pyk2 signalling. Reviewed
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. Vol. 86 page： 191-198 2011
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A novel ENG mutation causing impaired co-translational processing of endoglin associated with hereditary hemorrhagic telangiectasia. Reviewed
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. Vol. 129 page： e200-208 2012
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Increased von Willebrand Factor to ADAMTS13 ratio as a predictor of thrombotic complications following a major hepatectomy. Reviewed
Kobayashi S, Yokoyama Y, Matsushita T, Kainuma M, Ebata T, Igami T, Sugawara G, Takahashi Y, Nagino M.
Arch Surg. Vol. 147 page： 909-917 2012
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Thrombosis from a prothrombin mutation conveying antithrombin resistance. Reviewed
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. Vol. 366 page： 2390-2396 2012
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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. Reviewed
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. Vol. 10 page： 81-89 2012
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Stress augments insulin resistance and prothrombotic state: role of visceral adipose-derived monocyte chemoattractant protein-1. Reviewed
Uchida Y, Takeshita K, Yamamoto K, Kikuchi R, Nakayama T, Nomura M, Cheng XW, Egashira K, Matsushita T, Nakamura H, Murohara T.
Diabetes. Vol. 61 page： 1552-1561 2012
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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 Vol. 120 ( 4 ) page： 482 - 491 2024.10