Keijiro Suzuki - My portal

Profile Information

Affiliation: Part-time Lecturer, School of Medicine, Iwate Medical University School of Medicine, Iwate Medical University

Degree: Doctor of Medicine(Yamagata University)

J-GLOBAL ID: 200901005277499509
researchmap Member ID: 5000060372

External link: http://sites.google.com/site/imudlmcoagl/

Research Interests

Research Areas

Education

- 1998

Yamagata University
- 1998

Hematology, Graduate School, Division of Medicine, Yamagata University
- 1993

Faculty of Medicine, Yamagata University
- 1993

Faculty of Medicine, Yamagata University

Papers

Compound heterozygous mutations (p.Leu13Pro and p.Tyr294*) associated with factor VII deficiency cause impaired secretion through ineffective translocation and extensive intracellular degradation of factor VII

Keijiro Suzuki, Takeshi Sugawara, Yoji Ishida, Akira Suwabe

THROMBOSIS RESEARCH, 131(2) 166-172, Feb, 2013 Peer-reviewed
Factor XII Ofunato: Lys346Asn mutation associated with blood coagulation factor XII deficiency causes impaired secretion through a proteasome-mediated degradation

Keijiro Suzuki, Kazunori Murai, Akira Suwabe, Yoji Ishida

THROMBOSIS RESEARCH, 125(5) 438-443, May, 2010 Peer-reviewed
Clinical significance of high-Km 5 '-nucleotidase (cN-II) mRNA expression in high-risk myelodysplastic syndrome

Keijiro Suzuki, Takeshi Sugawara, Tatsuo Oyake, Toshiyuki Uchiyama, Yusei Aoki, Yasuhiko Tsukushi, Shima Onodera, Shigeki Ito, Kazunori Murai, Yoji Ishida

LEUKEMIA RESEARCH, 31(10) 1343-1349, Oct, 2007 Peer-reviewed
Aberrant maspin expression in gallbladder epithelium is associated with intestinal metaplasia in patients with cholelithiasis

C Maesawa, S Ogasawara, A Yashima-Abo, T Kimura, K Kotani, S Masuda, Y Nagata, T Iwaya, K Suzuki, T Oyake …

JOURNAL OF CLINICAL PATHOLOGY, 59(3) 328-330, Mar, 2006
Platelet glycoprotein Ib alpha polymorphisms affect the interaction with von Willebrand factor under flow conditions

Y Matsubara, M Murata, T Hayashi, K Suzuki, Y Okamura, M Handa, H Ishihara, T Shibano, Y Ikeda

BRITISH JOURNAL OF HAEMATOLOGY, 128(4) 533-539, Feb, 2005
Clinical and biological significance of CD56 antigen expression in acute promyelocytic leukemia

S Ito, Y Ishida, T Oyake, M Satoh, Y Aoki, S Kowata, T Uchiyama, S Enomoto, T Sugawara, H Numaoka …

LEUKEMIA & LYMPHOMA, 45(9) 1783-1789, Sep, 2004
Uncommon karyotypic abnormality, t(11;19)(q23;p13.3), in a patient with blastic phase of chronic myeloid leukemia

K Suzuki, T Sugawara, S Kowata, T Utsugizawa, S Ito, K Murai, Y Ishida

CANCER GENETICS AND CYTOGENETICS, 150(2) 159-163, Apr, 2004

Misc.

先天性血液凝固第Ⅶ因子欠乏症患者に認められたヘテロ接合体変異(p.Arg337Cys)と遺伝子多型性(p.Arg413Gln)のハプロタイプ解析

鈴木啓二朗, 吉岡智子, 小原丈裕, 諏訪部章

臨床病理 = The official journal of Japanese Society of Laboratory Medicine : 日本臨床検査医学会誌, 64(4) 380-386, Apr, 2016
Molecular diagnostics and pathogenesis of hereditary blood coagulation factor deficiency

SUZUKI Keijiro, SUWABE Akira

58(12) 1232-1232, Dec 25, 2010

Professional Memberships

Works

Research Projects

Risk analysis and management of delayed reactions after autologous blood donation

Grants-in-Aid for Scientific Research, Grant-in-Aid for Scientific Research (C), Japan Society for the Promotion of Science, Apr, 2017 - Mar, 2023
先天性凝固因子欠乏症の分子病態

共同研究, 2006
血管内皮細胞における凝固線溶因子の発現調節

共同研究
先天性血小板機能異常症の分子病態

その他の研究制度
molecular pathogenesis of congenital blood coagulation factor deficiency

Cooperative Research
regulation of hemostasis and fiblinolysis on vascular endothelial cell

Cooperative Research
molecular pathology of hereditary platelet disorders

Cooperative Research