Takeru Zama

Keio University — Japan

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index973citations19works0.02yr avg
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Research Topics

Cancer-related molecular mechanisms research(4), MicroRNA in disease regulation(3), Circular RNAs in diseases(3), Platelet Disorders and Treatments(2), Antiplatelet Therapy and Cardiovascular Diseases(2)

Publications19 total

Erratum: Polymorphisms in the UGT1A1 gene predict adverse effects of irinotecan in the treatment of gynecologic cancer in Japanese patients
Journal of Human Genetics·2013· 2 citedOpen Access
Subcutaneous Preadipocytes Are Ideal Candidate To Produce A Large Number Of Functional Platelets In a Culture System
Blood·2013
Polymorphisms in the UGT1A1 gene predict adverse effects of irinotecan in the treatment of gynecologic cancer in Japanese patients
Journal of Human Genetics·2013· 26 citedOpen Access
MicroRNA-196a Is a Putative Diagnostic Biomarker and Therapeutic Target for Laryngeal Cancer
PLoS ONE·2013· 82 citedOpen Access
Abstract 4039: miR-196a is a novel diagnostic biomarker and therapeutic target for laryngeal cancer
Cancer Research·2010
Abstract 4089: Regulation of cancer-specific microRNA by aberrant DNA methylation in laryngeal cancer
Cancer Research·2010
MicroRNA Expression Signature in Laryngeal Cancer
Otolaryngology·2009
TNFα‐induced ATF3 expression is bidirectionally regulated by the JNK and ERK pathways in vascular endothelial cells
Genes to Cells·2004· 75 citedOpen Access
A Novel Dual Specificity Phosphatase SKRP1 Interacts with the MAPK Kinase MKK7 and Inactivates the JNK MAPK Pathway
Journal of Biological Chemistry·2002· 46 citedOpen Access
Scaffold Role of a Mitogen-activated Protein Kinase Phosphatase, SKRP1, for the JNK Signaling Pathway
Journal of Biological Chemistry·2002· 54 citedOpen Access
Identification of a Novel Kinesin-related Protein, KRMP1, as a Target for Mitotic Peptidyl-prolyl Isomerase Pin1
Journal of Biological Chemistry·2001· 36 citedOpen Access
Cloning of Human PRP4 Reveals Interaction with Clk1
Journal of Biological Chemistry·2001· 77 citedOpen Access
A fluorescent indicator for visualizing cAMP-induced phosphorylation in vivo
Nature Biotechnology·2000· 190 cited
A family with hereditary factor X deficiency with a point mutation Gla<sup>32</sup> to Gln in the Gla domain (factor X Tokyo)
British Journal of Haematology·1999· 16 citedOpen Access
A polymorphism in a platelet collagen receptor is associated with the receptor density on platelet surface and platelet adhesiveness to collagen under flow conditions
1998
Genetic risk factors for coronary artery disease
The Journal of Japan Atherosclerosis Society·1998· 2 citedOpen Access
A <sup>192</sup> Arg Variant of the Human Paraoxonase <i>(HUMPONA)</i> Gene Polymorphism Is Associated With an Increased Risk for Coronary Artery Disease in the Japanese
Arteriosclerosis Thrombosis and Vascular Biology·1997· 156 citedOpen Access
Coronary Artery Disease and Polymorphisms in a Receptor Mediating Shear Stress–Dependent Platelet Activation
Circulation·1997· 109 cited
Genotype Distribution of Estrogen Receptor Polymorphisms in Men and Postmenopausal Women From Healthy and Coronary Populations and Its Relation to Serum Lipid Levels
Arteriosclerosis Thrombosis and Vascular Biology·1997· 102 citedOpen Access

Frequent Co-authors

Yasuo Ikeda(10), Mitsuru Murata(7), Masatoshi Hagiwara(6), Koichiro Saito(6), Takahiro Kamimoto(6), Ryoko Aoki(5), Yumiko Matsubara(5), Koichi Kawano(5), Nobuo Aoki(5), Akira Hirasawa(5), Gentaro Watanabe(4), Kyozo Ishikawa(4), Koji Inagaki(3), Toshiaki Sugita(3), Satoko Nakajo(3), Keisuke Okubo(3), Koichi Inoue(3), Hideaki Yoshino(2), Hideaki Yoshino(2), Yoko Itō(2)