Papers - Murata, Mitsuru

液体クロマトグラフィータンデム質量分析法による尿中エストロゲン　3分画同時定量のための基礎的検討

MURATA MITSURU

臨床血液 55 ( 9 )  2014

Joint Work

血栓形成傾向の検出を目指す新たな検査法T-TASに関する検討　いわゆる血液ドロドロ・サラサラ検査について

森木 隆典, 広瀬 寛, 田中 由紀子, 齋藤 圭美, 神吉 正子, 村田 満, 河邉 博史

慶應保健研究 31 ( 1 ) 59 - 65 2013.08

Joint Work

Measurement of reference intervals for urinary free adrenal steroid levels in Japanese newborn infants by using stable isotope dilution gas chromatography/mass spectrometry.

Koyama Y, Homma K, Miwa M, Ikeda K,MURATA MITSURU, Hasegawa T

Clin Chim Acta  2013

Joint Work

Studies of a microchip flow-chamber system to characterize whole blood thrombogenicity in healthy individuals.

Yamaguchi Y, Moriki T, Igari A, Matsubara Y, Ohnishi T, Hosokawa K,MURATA MITSURU

Thromb Res  2013

Joint Work

The future directions of clinical hematology in 2013 - hemostatic and thrombotic diseases- overview.

MURATA MITSURU

Rinsho Ketsueki  2013

Single Work

OP9 bone marrow stroma cells differentiate into megakaryocytes and platelets.

Matsubara Y, Ono Y, Suzuki H, Arai F, Suda T, MURATA MITSURU, Ikeda Y

PLoS One  2013

Joint Work

Persistent parvovirus B19 infection resulting in red cell aplasia after allogeneic hematopoietic stem cell transplantation.

Koda Y, Mori T, Kato J, Kohashi S, Kikuchi T, Mitsuhashi T, MURATA MITSURU, Uemura T, Handa M, Okamoto S

Transpl Infect Dis  2013

Joint Work

新規多項目自動血球分析装置ＸＮ-1000の性能評価

谷田部陽子、荒井智子、片桐尚子、清水長子、林文明、近藤民章、三ツ橋雄之、村田 満

日本検査血液学会雑誌 14 ( 1 ) 34 - 40 2013

Joint Work

POCT対応全自動蛍光免疫測定装置ミュータンスワコーi30によるプロカルシトニンの測定

上條裕美子、野口昌代、柴田綾子、菊池春人、村田 満

JJCLA  2013

Joint Work

POC対応血糖測定機器の比較検討

酒井昭子、野口昌代、柴田綾子、菊池春人、村田 満

JJCLA  2013

Joint Work

Development of the Program for Quality Control of Multi-item Automatic Analyzers ~The First Report: A Monitoring Program for Measuring the Results of Qurality Coutrol Samples~

早川富夫、渡部直美、大竹和子、石田浩二，石橋みどり、大竹皓子、菊池春人，村田満

日本臨床検査自動化学会会誌 33 ( 1 ) 38-45 2008

Research paper (scientific journal), Joint Work

血栓症-危険因子としての遺伝的背景

松原 由美子，　村田　満

成人病と生活習慣病 36 ( 2 ) 230-233 2006.02

Research paper (scientific journal), Joint Work

アテローム破綻に血小板はどこまで関与しているのか？

松原 由美子，　村田　満

Vascular Medicine 1 ( 2 ) 178-184 2005.10

Research paper (scientific journal), Joint Work

Factor XII Shizuoka, a novel mutation (Ala392Thr) identified and characterized in a patient with congenital coagulation factor XII deficiency

OGUCHI SHUJIIshii KeikoMoriki TakanoriTakeshita EikoMurata MitsuruIkeda Yasuo>Watanabe Kiyoaki

Thrombosis Research 115 ( 3 ) 191-197 2005.01

Research paper (scientific journal), Single Work

　View Summary

We identified a novel mutation (Ala392Thr) in the factor XII (FXII) gene of a patient with congenital FXII deficiency, designated Factor XII Shizuoka. The proband was an asymptomatic 63-year-old Japanese male with an abnormal coagulation test, discovered by chance during preoperative testing. The FXII activity was under 3% and antigen level was under 10%. Sequence analysis of the proband's FXII gene revealed a homozygous nucleotide substitution G to A in exon 10, resulting in the amino acid substitution Ala392 to Thr in the catalytic domain. We constructed the mutant FXII cDNA in an expression plasmid vector and transfected it into Chinese hamster ovary (CHO) cells. The recombinant wild-type FXII antigen was detected in the culture medium by immunoprecipitation assay, but the mutant FXII (A392T) was not observed. Both the wild-type FXII and A392T cell lysates, however, contained equivalent levels of FXII antigen and FXII mRNA, as estimated by Western blotting and quantitative reverse transcriptase-polymerase chain reaction (RT-PCR), respectively. These findings suggest that the Ala392 to Thr substitution impairs intracellular protein processing and causes a cross-reacting material -negative FXII deficiency.

重症患者における貧血と輸血．Anemia and blood transfusion in critically III patients.

松原　由美子，　村田 満

JAMA 日本語版  ( 2月 ) 109-119 2004.02

Research paper (scientific journal), Joint Work

Relation between development of nephropathy and the p22phox C242T and receptor for advanced glycation end product G1704T gene polymorphisms in type 2 diabetic patients.

Matsunaga-Irie Seiko, Maruyama Taro, Yamamoto Yukihiro, Motohashi Yoshiko, Hirose Hiroshi, Shimada Akira, Murata Mitsuru, Saruta Takao

Diabetes Care 27 ( 2 ) 303-307 2004.02

Research paper (scientific journal), Joint Work

Role of genetic factors (CETP gene Taq IB polymorphism and Apo A-1 gene MSP I polymorphism) in serum HDL-C levels in women.

Motohashi Yoshiko, Maruyama Taro, Murata Mitsuru, Nakano Satomi, Maruyama Chizuko, Kyotani Shingo, Tsushima Motoo, Saruta Takao.

Nutr Metab Cardiovasc Dis 14 ( 1 ) 6-14 2004.02

Research paper (scientific journal), Joint Work

虚血性脳血管障害と関係する遺伝子多型解析．

石井　啓子，　小口　修司，　竹下　栄子，　村田 満，　　　伊東　大介，　棚橋　紀夫，　福内　靖男，　斉藤　郁夫，　池田　康夫，　渡辺　清明

臨床病理 52 ( 1 ) 22-27 2004.01

Research paper (scientific journal), Joint Work

Detection of von Willebrand factor - cleaving protease (ADAMTS-13) in human platelets.

Suzuki Misako, Murata Mitsuru, Matsubara Yumiko, Uchida Toshihiro, Ishihara Hiroaki, Shibano Toshiro, Ashida Shin-ichiro, Soejima Kenji, Okada Yasunori, Ikeda Yasuo

Biochem Biophys Res Commun 313 ( 1 ) 212-216 2004.01

Research paper (scientific journal), Joint Work

The ratio of serum paraoxonase/arylesterase activity using an improved assay for arylesterase activity to discriminate PON1 (R192) from PON1 (Q192).

Nakanishi Mamoru, Takanami Yoshikazu, Maruyama Taro, Murata Mitsuru, Motohashi Yoshiko, Nakano Satomi, Uchida Kagehiro, Maruyama Chizuko, Kyotani Shingo, Tsushima Motoo

Journal of Atherosclerosis and Thrombosis 10 ( 6 ) 337-342 2003.12

Research paper (scientific journal), Joint Work