A novel G168X mutation and a recurrent 730-731delCT mutation of the porphobilinogen deaminase gene in Japanese patients with acute intermittent porphyria. , Blood Cells Mol Dis, 51(2) 130-131, 2013

Susa S, Daimon M, Kato T, Maeda N

Multiple Authorship (Only Japanese)

Association of the G-protein β3 subunit gene polymorphism with the incidence of cardiovascular disease independent of hypertension: the Funagata study. , J Hum Hypertens., 27(10) 612-616, 2013

Daimon M, Sato H, Kaino W, Tada K, Takase K, Karasawa S, Wada K, Kameda W, Susa S, Oizumi T, Kayama T, Muramatsu M, Kato T

Multiple Authorship (Only Japanese)

Lower physical activity is a risk factor for a clustering of metabolic risk factors in non-obese and obese Japanese subjects: the Takahata study, Endocr J, 60(5) 617-628, 2013

Kaino W, Daimon M, Sasaki S, Karasawa S, Takase K, Tada K, Wada K, Kameda W, Susa S, Oizumi T, Fukao A, Kubota I, Kayama T, Kato T

Multiple Authorship (Only Japanese)

Serum glycerophosphate levels are increased in Japanese men with type 2 diabetes., Intern Med, 51(6) 545-551, 2012

Daimon M, Soga T, Hozawa A, Oizumi T, Kaino W, Takase K, Karasawa S, Jimbu Y, Wada K, Kameda W, Susa S, Kayama T, Saito K, Tomita M, Kato T

Multiple Authorship (Only Japanese)

Higher plasma renin activity is a risk factor for total mortality in older Japanese individuals: the Takahata study. , Metabolism, 61(6) 815-822, 2012

Daimon M, Soga T, Hozawa A, Oizumi T, Kaino W, Takase K, Karasawa S, Jimbu Y, Wada K, Kameda W, Susa S, Kayama T, Saito K, Tomita M, Kato T

Multiple Authorship (Only Japanese)

Association of the clusterin gene polymorphisms with type 2 diabetes mellitus. , Metabolism, 60(6) 815-822, 2012

Daimon M, Oizumi T, Karasawa S, Kaino W, Takase K, Tada K, Jimbu Y, Wada K, Kameda W, Susa S, Muramatsu M, Kubota I, Kawata S, Kato T

Multiple Authorship (Only Japanese)

Thyroid dysfunction in patients treated with tyrosine kinase inhibitors, sunitinib, sorafenib and axitinib, for metastatic renal cell carcinoma. , Jpn J Clin Oncol. , 42(8) 742-747, 2012

Daimon M, Kato T, Kaino W, Takase K, Karasawa S, Wada K, Kameda W, Susa S, Oizumi T, Tomita Y, Kato T

Multiple Authorship (Only Japanese)

Association of the common fat mass and obesity associated (FTO) gene polymorphism with obesity in a Japanese population. , Endocr J , 57(4) 293-301, 2010

Karasawa S, Daimon M, Sasaki S, Toriyama S, Oizumi T, Susa S, Kameda W, Wada K, Muramatsu M, Fukao A, Kubota I, Kawata S, Kayama T, Kato T

Multiple Authorship (Only Japanese)

Hemoglobin A1c in predicting progression to diabetes. , Diabetes Res Clin Pract. , 87(1) 126-131, 2010

9. Nakagami T, Tajima N, Oizumi T, Karasawa S, Wada K, Kameda W, Susa S, Kato T, Daimon M

Multiple Authorship (Only Japanese)

Association of the Ser326Cys polymorphism in the OGG1 gene with type 2 DM. , iochem Biophys Res Commun., 386(1) 26-29, 2009

Daimon M, Oizumi T, Toriyama S, Karasawa S, Jimbu Y, Wada K, Kameda W, Susa S, Muramatsu M, Kubota I, Kawata S, Kato T

Multiple Authorship (Only Japanese)

A functional polymorphism of the TNF-alpha gene that is associated with type 2 DM, Biochem Biophys Res Commun. , 369(3) 943-947, 2008

Susa shinji

Multiple Authorship (Including Foreigners)

Salt consumption-dependent association of the GNB3 gene polymorphism with type 2 DM., Biochem Biophys Res Commun. , 374(3) 576-580, 2008

Daimon M, Sato H, Sasaki S, Toriyama S, Emi M, Muramatsu M, Hunt SC, Hopkins PN, Karasawa S, Wada K, Jimbu Y, Kameda W, Susa S, Oizumi T, Fukao A, Kubota I, Kawata S, Kato T

Multiple Authorship (Only Japanese)

Association of the PIK3C2G gene polymorphisms with type 2 DM in a Japanese population. , Biochem Biophys Res Commun., 365(3) 466-471, 2008

Daimon M, Sato H, Oizumi T, Toriyama S, Saito T, Karasawa S, Jimbu Y, Wada K, Kameda W, Susa S, Yamaguchi H, Emi M, Muramatsu M, Kubota I, Kawata S, Kato T

Multiple Authorship (Only Japanese)

Impaired glucose tolerance is a risk factor for stroke in a Japanese sample--the Funagata study. , Metabolism., 57(3) 333-338, 2008

Oizumi T, Daimon M, Jimbu Y, Wada K, Kameda W, Susa S, Yamaguchi H, Ohnuma H, Tominaga M, Kato T

Multiple Authorship (Only Japanese)

hrelin infused into the portal vein inhibits glucose-stimulated insulin secretion in Wistar rats. , Peptides, 29(7) 1241-1246, 2008

Cui C, Ohnuma H, Daimon M, Susa S, Yamaguchi H, Kameda W, Jimbu Y, Oizumi T, Kato T

Multiple Authorship (Only Japanese)

proposal for the cutoff point of waist circumference for the diagnosis of metabolic syndrome in the Japanese population., Circ J, 70(12) 801-806, 2006

Oizumi T, Daimon M, Wada K, Jimbu Y, Kameda W, Susa S, Yamaguchi H, Ohnuma H, Kato T

Multiple Authorship (Only Japanese)

Association of nephrin gene polymorphisms with type 2 diabetes in a Japanese population: The Funagata study. , Diabetes Care., 29(5) 1117-1119, 2006

Daimon M, Ji G, Oizumi T, Kido T, Baba M, Jimbu Y, Kameda W, Susa S, Yamaguchi H, Ohnuma H, Muramatsu M, Kato T

Multiple Authorship (Only Japanese)

Extracellular alkalosis activates ERK mitogen-activated protein kinase of vascular smooth muscle cells through NADPH-mediated formation of reactive oxygen species., FEBS Letter, 554(3) 399-402, 2003.11

Susa S, Wakabayashi I

Multiple Authorship (Including Foreigners)

The long, but not the short, presequence of human coproporphyrinogen oxidase is essential for its import and sorting to mitochondria., Tohoku J. Exp. Med., 200(1) 39-45, 2003.05

Susa S, Daimon M, Ono H, Li S, Yoshida T, Kato T

Multiple Authorship (Including Foreigners)

Lymphoid enhancer factor 1 makes cells resistant to transforming growth factor beta-induced repression of c-myc. , Cancer Res. , 63(4) 801-806, 2003

Sasaki T, Suzuki H, Yagi K, Furuhashi M, Yao R, Susa S, Noda T, Arai Y, Miyazono K, Kato M

Multiple Authorship (Only Japanese)

Heme inhibits the mitochondrial import of coproporphyrinogen oxidase., Blood, 100(13) 4678-4679, 2002.12

Susa S, Daimon M, Ono H, Li S, Yoshida T, Kato T

Multiple Authorship (Including Foreigners)

Platelet-derived growth factor BB-induced p38 mitogen-activated protein kinase activation causes cell growth, but not apoptosis, in vascular smooth muscle cells., Endocr J, 48(4) 433-442, 2001

Yamaguchi H, Igarashi M, Hirata A, Susa S, Ohnuma H, Tominaga M, Daimon M, Kato T

Multiple Authorship (Only Japanese)

Characterization of platelet-derived growth factor-induced p38 mitogen-activated protein kinase activation in vascular smooth muscle cells., Eur J Clin Invest., 31(8) 672-680, 2001

Yamaguchi H, Igarashi M, Hirata A, Tsuchiya H, Susa S, Tominaga M, Daimon M, Kato T

Multiple Authorship (Only Japanese)

Neonatal-onset hereditary coproporphyria with male pseudohermaphrodism. , Blood, 98(13) 3871-3873, 2001

2. Takeuchi H, Kondo M, Daimon M, Susa S, Ueoka K, Uemura O, Togari H

Multiple Authorship (Only Japanese)

Hypoceruloplasminemia in neurological diseases. , Intern Med, 40(6) 548-549, 2001

25. Moriai S, Daimon M, Susa S, Kurimura M, Kawanami T, Kurita K, Kato T

Multiple Authorship (Only Japanese)

Increase in serum ceruloplasmin with aging is not observed in type 2 diabetes. , Endocr J, 47(3) 215-219, 2000

Daimon M, Susa S, Hasegawa K, Yamaguchi H, Kimura M, Ohnuma H, Eguchi H, Igarashi M, Manaka H, Kato T

Multiple Authorship (Only Japanese)

A novel mutation of the ceruloplasmin gene in a patient with heteroallelic ceruloplasmin gene mutation (HypoCPGM). , Tohoku J Exp Med., 191(3) 119-125, 2000

27. Daimon M, Susa S, Ohizumi T, Moriai S, Kawanami T, Hirata A, Yamaguchi H, Ohnuma H, Igarashi M, Kato T

Multiple Authorship (Only Japanese)

Acute intermittent porphyria with central pontine myelinolysis and cortical laminar necrosis., Neuroradiology, 41(11) 835-839, 1999.11

Susa S, Daimon M, Morita Y, Kitagawa M, Hirata A, Manaka H, Sasaki H, Kato T

Multiple Authorship (Including Foreigners)

Fine structure of the human translocation protein 1 (HTP1/TLOC1) gene. , IUBMB Life., 48(6) 619-624, 1999

Daimon M, Susa S, Kato T

Multiple Authorship (Only Japanese)

Hypoceruloplasminaemia with heteroallelic caeruloplasmin gene mutation: MRI of the brain., Neuroradiology, 41(3) 185-187, 1999

Daimon M, Moriai S, Susa S, Yamatani K, Hosoya T, Kato T

Multiple Authorship (Only Japanese)

A case of myasthenia graris caused by D-penicillamine therapy, Nippon Naika Gakkai Zasshi, 87(12) 2513-2515, 1998.12

Single Author

Identification of a novel mutation of the CPO gene in a Japanese hereditary coproporphyria family., Am. J. Med. Genet., 80(3) 204-206, 1998.11

Susa S, Daimon M, Kondo H, Kondo M, Yamatani K, Sasaki H

Multiple Authorship (Including Foreigners)

A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family., J. Hum. Genet, 43(3) 182-184, 1998.09

Susa S, Daimon M, Yamamori I, Kondo M, Yamatani K, Sasaki H, Kato T

Multiple Authorship (Only Japanese)

Hyperglycemia is a factor for an increase in serum ceruloplasmin in type 2 diabetes. , Diabetes Care, 21(9) 1525-1528, 1998

30. Daimon M, Susa S, Yamatani K, Manaka H, Hama K, Kimura M, Ohnuma H, Kato T

Multiple Authorship (Only Japanese)

Identification of a human cDNA homologue to the Drosophila translocation protein 1 (Dtrp1). , Biochem Biophys Res Commun, 230(1) 100-104, 1997

Daimon M, Susa S, Suzuki K, Kato T, Yamatani K, Sasaki H

Multiple Authorship (Only Japanese)