分子疫学研究室


Publications

I. Original Articles


2018

1. Hayashi M, Watanabe A, Muramatsu M, Yamashita N.
Effectiveness of personal genomic testing for disease-prevention behavior when combined with careful consultation with a physician: a preliminary study. BMC Res Notes. 11:223. (2018)

2. Tanisawa K, Hirose N, Arai Y, Shimokata H, Yamada Y, Kawai H, Kojima M, Obuchi S, Hirano H, Suzuki H, Fujiwara Y, Taniguchi Y, Shinkai S, Ihara K, Sugaya M, Higuchi M, Arai T, Mori S, Sawabe M, Sato N, Muramatsu M, Tanaka M.
Inverse association between height-increasing alleles and extreme longevity in Japanese women. J Gerontol A Biol Sci Med Sci. 73:588-595 (2018)

3. Matsuda Y, Tanaka M, Sawabe M, Mori S, Muramatsu M, Mieno MN, Furukawa T, Arai T.
Relationship between pancreatic intraepithelial neoplasias, pancreatic ductal adenocarcinomas, and single nucleotide polymorphisms in autopsied elderly patients. Genes Chromosomes Cancer. 57:12-18 (2018)

4. Udagawa S, Katagiri S, Maekawa S, Takeuchi Y, Komazaki R, Ohtsu A, Sasaki N, Shiba T, Watanabe K, Ishihara K, Sato N, Miyasaka N, Izumi Y.
Effect of Porphyromonas gingivalis infection in the placenta and umbilical cord in pregnant mice with low birth weight. Acta Odontol Scand. 15:1-9 (2018)







2017

1. Sato N, Sudo K, Mori M, Imai C, Muramatsu M, Sugimoto M.
Early gestational maternal low-protein diet diminishes hepatic response to fasting in young adult male mice. Sci Rep. 7:9812 (2017)

2. Dechamethakun S, Muramatsu M.
Long noncoding RNA variations in cardiometabolic diseases. J Hum Genet. 62:97-104 (2017)

3. Dechamethakun S, Sato N, Ikeda S, Sawabe M, Mori S, Yamada Y, Tanaka M, Muramatsu M and Arai T.
Association of Macrophage Capping Protein (CAPG) Arg335His Polymorphism and Cancer Susceptibility in the Elderly Japanese. Journal of Gerontology and Geriatric Research. 6; 417 (2017)

4. Nishi K, Luo H, Nakabayashi K, Doi K, Ishikura S, Iwaihara Y, Yoshida Y, Tanisawa K, Arai T, Mori S, Sawabe M, Muramatsu M, Tanaka M, Sakata T, Shirasawa S, Tsunoda T.
An Alpha-kinase 2 Gene Variant Disrupts Filamentous Actin Localization in the Surface Cells of Colorectal Cancer Spheroids. Anticancer Res. 37:3855-3862. (2017)

5. Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M.
Identification of five genetic variants as novel determinants of type 2 diabetes mellitus in Japanese by exome-wide association studies. Oncotarget. 8:80492-80505. (2017)

6. Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M.
Identification of polymorphisms in 12q24.1, ACAD10, and BRAP as novel genetic determinants of blood pressure in Japanese by exome-wide association studies. Oncotarget 8:43068-43079. (2017)

7. Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M.
Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies. Oncotarget. 8:38950-38961 (2017)

8. Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M.
Identification of rs7350481 at chromosome 11q23.3 as a novel susceptibility locus for metabolic syndrome in Japanese individuals by an exome-wide association study. Oncotarget. 8:39296-39308. (2017)

9. Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M.
Identification of C21orf59 and ATG2A as novel determinants of renal function-related traits in Japanese by exome-wide association studies. Oncotarget. 8:45259-45273. (2017)

10. Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M.
Identification of STXBP2 as a novel susceptibility locus for myocardial infarction in Japanese individuals by an exome-wide association study. Oncotarget. 8:33527-33535. (2017)

11. Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M.
Identification of EGFLAM, SPATC1L and RNASE13 as novel susceptibility loci for aortic aneurysm in Japanese individuals by exome-wide association studies. Int J Mol Med. 39:1091-1100. (2017)

12. Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M.
Identification of six polymorphisms as novel susceptibility loci for ischemic or hemorrhagic stroke by exome-wide association studies. Int J Mol Med. 39:1477-1491. (2017)

13. Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M.
Identification of TNFSF13, SPATC1L, SLC22A25 and SALL4 as novel susceptibility loci for atrial fibrillation by an exome‑wide association study. Mol Med Rep. 16:5823-5832 (2017)

14. Komazaki R, Katagiri S, Takahashi H, Maekawa S, Shiba T, Takeuchi Y, Kitajima Y, Ohtsu A, Udagawa S, Sasaki N, Watanabe K, Sato N, Miyasaka N, Eguchi Y, Anzai K, Izumi Y.
Periodontal pathogenic bacteria, Aggregatibacter actinomycetemcomitans affect non-alcoholic fatty liver disease by altering gut microbiota and glucose metabolism. Sci Rep. 2017 7:13950

15. Zaw KTT, Sato N, Ikeda S, Thu KS, Mieno MN, Arai T, Mori S, Furukawa T, Sasano T, Sawabe M, Tanaka M, Muramatsu M.
Association of ZFHX3 gene variation with atrial fibrillation, cerebral infarction, and lung thromboembolism: An autopsy study. J Cardiol. 70(2):180-184. 2017






2016

1. Thu KS, Sato N, Ikeda S, Naka-Mieno M, Arai T, Mori S, Sawabe M, Muramatsu M, Tanaka M.
Association of polymorphisms of the transporter associated with antigen processing (TAP2) gene with pulmonary tuberculosis in an elderly Japanese population. APMIS. 124:675-80. (2016)

2. Zhou H, Mori S, Ishizaki T, Tanaka M, Tanisawa K, Mieno MN, Sawabe M, Arai T, Muramatsu M, Yamada Y, Ito H.
Genetic risk score based on the lifetime prevalence of femoral fracture in 924 consecutive autopsies of Japanese males. J Bone Miner Metab. 34:685-691 (2016)

3. Tanisawa K, Arai Y, Hirose N, Shimokata H, Yamada Y, Kawai H, Kojima M, Obuchi S, Hirano H, Yoshida H, Suzuki H, Fujiwara Y, Ihara K, Sugaya M, Arai T, Mori S, Sawabe M, Sato N, Muramatsu M, Higuchi M, Liu YW, Kong QP, Tanaka M.
Exome-wide Association Study Identifies CLEC3B Missense Variant p.S106G as Being Associated With Extreme Longevity in East Asian Populations. J Gerontol A Biol Sci Med Sci. [Epub ahead of print] (2016)







2015

1. Yamada M, Sato N, Ikeda S, Arai T, Sawabe M, Mori S, Yamada Y, Muramatsu M, Tanaka M.
Association of the chromodomain helicase DNA-binding protein 4 (CHD4) missense variation p.D140E with cancer: potential interaction with smoking. Genes Chromosomes Cancer 54:122-128 (2015)

2. Nishizawa D, Kasai S, Hasegawa J, Sato N, Yamada H, Tanioka F, Nagashima M, Katoh R, Satoh Y, Tagami M, Ujike H, Ozaki N, Inada T, Iwata N, Sora I, Iyo M, Yamada M, Kondo N, Won MJ, Naruse N, Uehara-Aoyama K, Itokawa M, Ohi K, Hashimoto R, Tanisawa K, Arai T, Mori S, Sawabe M, Naka-Mieno M, Yamada Y, Yamada M, Sato N, Muramatsu M, Tanaka M, Irukayama-Tomobe Y, Saito YC, Sakurai T, Hayashida M, Sugimura H, Ikeda K.
Associations between the orexin (hypocretin) receptor 2 gene polymorphism Val308Ile and nicotine dependence in genome-wide and subsequent association studies. Mol Brain 8:50 (2015)

3. Zhou H, Mori S, Tanaka M, Sawabe M, Arai T, Muramatsu M, Mieno MN, Shinkai S, Yamada Y, Miyachi M, Murakami H, Sanada K, Ito H.
A missense single nucleotide polymorphism, V114I of the Werner syndrome gene, is associated with risk of osteoporosis and femoral fracture in the Japanese population. J Bone Miner Metab. 33:694-700 (2015)

4. Zhou H, Mori S, Ishizaki T, Tanaka M, Tanisawa K, Mieno MN, Sawabe M, Arai T, Muramatsu M, Yamada Y, Ito H.
Genetic risk score based on the lifetime prevalence of femoral fracture in 924 consecutive autopsies of Japanese males. J Bone Miner Metab. [Epub ahead of print] (2015)

5. Maekawa K, Nakamura R, Kaniwa N, Mizusawa S, Kitamoto A, Kitamoto T, Ukaji M, Matsuzawa Y, Sugiyama E, Uchida Y, Kurose K, Ueta M, Sotozono C, Ikeda H, Yagami A, Matsukura S, Kinoshita S, Muramatsu M, Ikezawa Z, Sekine A, Furuya H, Takahashi Y, Matsunaga K, Aihara M, Saito Y; Japan Pharmacogenomics Data Science Consortium.
Development of a simple genotyping method for the HLA-A*31:01-tagging SNP in Japanese. Pharmacogenomics. 16:1689-99 (2015)






2014

1. Dechamethakun S, Ikeda S, Arai T, Sato N, Sawabe M, Muramatsu M.
Associations between the CDKN2A/B, ADTRP and PDGFD Polymorphisms and the Development of Coronary Atherosclerosis in Japanese Patients. J Atheroscler Thromb. 2014 Feb 26. [Epub ahead of print]

2. Zhao C, Ikeda S, Arai T, Naka-Mieno M, Sato N, Muramatsu M, Sawabe M.
Association of the RYR3 gene polymorphisms with atherosclerosis in elderly Japanese population. BMC Cardiovasc Disord. 14:6.2014

3. Parlayan C, Ikeda S, Sato N, Sawabe M, Muramatsu M, Arai T.
Association Analysis of Single Nucleotide Polymorphisms in miR-146a and miR-196a2 on the Prevalence of Cancer in Elderly Japanese: A Case-Control Study. Asian Pacific Journal of Cancer Prevention, 15(5):2101-7. 2014

4. Sato N, Htun NC, Daimon M, Tamiya G, Kato T, Kubota I, Ueno Y, Yamashita H, Fukao A, Kayama T, Muramatsu M.
Likelihood ratio-based integrated personal risk assessment of type 2 diabetes. Endocr J. 61:967-88. 2014

5. Htun NC, Miyaki K, Zhao C, Muramatsu M, Sato N.
Epistasis effects of COMT and MTHFR on inter-individual differences in mental health: under the inverted U-shaped prefrontal dopamine model. Biochem Biophys Res Commun. 451:574-9. 2014


6. Ueta M, Kaniwa N, Sotozono C, Tokunaga K, Saito Y, Sawai H, Miyadera H, Sugiyama E, Maekawa K, Nakamura R, Nagato M, Aihara M, Matsunaga K, Takahashi Y, Furuya H, Muramatsu M, Ikezawa Z, Kinoshita S.
Independent strong association of HLA-A*02:06 and HLA-B*44:03 with cold medicine-related Stevens-Johnson syndrome with severe mucosal involvement. Sci Rep. 4:4862. 2014


7. Honma N, Arai T, Muramatsu M.
Association between colorectal cancer and estrogens. Nihon Rinsho. 72:49-55 2014 (Japanese)



2013

1. Kengia JT, Ko KC, Ikeda S, Hiraishi A, Mieno-Naka M, Arai T, Sato N, Muramatsu M, Sawabe M.
A gene variant in the Atp10d gene associates with atherosclerotic indices in Japanese elderly population. Atherosclerosis. 231:158-62. 2013

2. 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.
Association of the G-protein β3 subunit gene polymorphism with the incidence of cardiovascular disease independent of hypertension: the Funagata study. J Hum Hypertens. 27:612-6. 2013

3. Honma N, Mori S, Zhou H, Ikeda S, Mieno MN, Tanaka N, Takubo K, Arai T, Sawabe M, Muramatsu M, Ito H.
Association between estrogen receptor-β dinucleotide repeat polymorphism and incidence of femoral fracture. J Bone Miner Metab. 31:96-101.2013

4. Honma N, Yamamoto K, Ohnaka K, Morita M, Toyomura K, Kono S, Muramatsu M, Arai T, Ueki T, Tanaka M, Kakeji Y, Maehara Y, Okamura T, Ikejiri K, Futami K, Maekawa T, Yasunami Y, Takenaka K, Ichimiya H, Terasaka R.
Estrogen receptor-β gene polymorphism and colorectal cancer risk: effect modified by body mass index and isoflavone intake. Int J Cancer. 132:951-8. 2013

5. Yatsuga C, Toyohisa D, Fujisawa TX, Nishitani S, Shinohara K, Matsuura N, Ikeda S, Muramatsu M, Hamada A, Tomoda A.
No association between COMT genotype and attention deficit hyperactivity disorder (ADHD) in Japanese children. Brain Dev. S0387-7604(13)00258-1 2013

6. Kaniwa N, Sugiyama E, Saito Y, Kurose K, Maekawa K, Hasegawa R, Furuya H, Ikeda H, Takahashi Y, Muramatsu M, Tohkin M, Ozeki T, Mushiroda T, Kubo M, Kamatani N, Abe M, Yagami A, Ueta M, Sotozono C, Kinoshita S, Ikezawa Z, Matsunaga K, Aihara M.
Japan Pharmacogenomics Data Science Consortium. Specific HLA types are associated with antiepileptic drug-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese subjects. Pharmacogenomics. 14:1821-31. 2013





2012

1. Ikeda S, Tanaka N, Arai T, Chida K, Muramatsu M, Sawabe M. Polymorphisms of LTA, LGALS2, and PSMA6 genes and coronary atherosclerosis: a pathological study of 1503 consecutive autopsy cases. Atherosclerosis. 221:458-60 (2012)

2. Ko MK, Ikeda S, Mieno-Naka M, Arai T, Zaidi SA, Sato N, Muramatsu M, Sawabe M. J Atheroscler Thromb. Association of COMT gene polymorphisms with systemic atherosclerosis in elderly Japanese.19:552-8 (2012)

3. Xi C, Miyaki K, Ikeda S, Song Y, Sinbo T, Muramatsu M. Association of GLUT4 gene variants with HbA1c level in Japanese men. Endocr J.59:677-84 (2012)

4. Ishii T, Hagiwara K, Kamio K, Ikeda S, Arai T, Mieno MN, Kumasaka T, Muramatsu M, Sawabe M, Gemma A, Kida K.
Involvement of surfactant protein D in emphysema revealed by genetic association study. Eur J Hum Genet.20:230-5 (2012)

5. Ishii T, Hagiwara K, Ikeda S, Arai T, Mieno MN, Kumasaka T, Muramatsu M, Sawabe M, Gemma A, Kida K.
Association between genetic variations in surfactant protein d and emphysema, interstitial pneumonia, and lung cancer in a Japanese population. COPD 9:409-16 (2012)

6. Honma N, Yamamoto K, Ohnaka K, Morita M, Toyomura K, Kono S, Muramatsu M, Arai T, Ueki T, Tanaka M, Kakeji Y, Maehara Y, Okamura T, Ikejiri K, Futami K, Maekawa T, Yasunami Y, Takenaka K, Ichimiya H, Terasaka R.
Estrogen receptor-β gene polymorphism and colorectal cancer risk: effect modified by body mass index and isoflavone intake. Int. J, Cancer Epub 2012 Jul 3.

7. Honma N, Mori S, Zhou H, Ikeda S, Mieno MN, Tanaka N, Takubo K, Arai T, Sawabe M, Muramatsu M, Ito H.
Association between estrogen receptor-β dinucleotide repeat polymorphism and incidence of femoral fracture. J Bone Miner Metab.Epub 2012 Sep 5.




2011

1. Polymorphisms of the formylpeptide receptor gene (FPR1) and susceptibility to stomach cancer in 1531 consecutive autopsy cases. Otani T, Ikeda S, Lwin H, Arai T, Muramatsu M, Sawabe M. Biochem Biophys Res Commun. Feb 18;405(3):356-61, 2011

2. Sato N, Yamakawa N, Masuda M, Sudo K, Hatada I, Muramatsu M. 
Genome-Wide DNA Methylation Analysis Reveals Phytoestrogen Modification of Promoter Methylation Patterns during Embryonic Stem Cell Differentiation. PLoS One. Apr 29;6(4):e19278. 2011

3. Matsukura H, Aisaki K, Igarashi K, Matsushima Y, Kanno J, Muramatsu M, Sudo K, Sato N.
Genistein promotes DNA demethylation of the steroidogenic factor 1 (SF-1) promoter in endometrial stromal cells. Biochem Biophys Res Commun. Aug 26;412(2):366-72. 2011

4. Honma N, Arai T, Takubo K, Younes M, Tanaka N, Mieno MN, Tamura K, Ikeda S, Sawabe M, Muramatsu M.
Oestrogen receptor-β CA repeat polymorphism is associated with incidence of colorectal cancer among females. Histopathology. Aug;59(2):216-24. 2011 doi: 10.1111/j.1365-2559.2011.03914.x.

5. Htun N, Miyaki K, Yixuan S, Ikeda S, Shimbo T, Muramatsu M.
Association of the catechol-O-methyl transferase gene Val158Met polymorphism with blood pressure and prevalence of hypertension: Interaction with dietary energy intake Am J Hypertens Sep;24(9):1022-6. 2011

6. Miyaki K, Htun N, Song Y, Ikeda S, Muramatsu M, Shimbo T.
The combined impact of 12 common variants on hypertension in Japanese men considering GWAS results. J Hum Hypertens 2011[Epub ahead of print]

7. Yamada M, Ishii T, Ikeda S, Naka-Mieno M, Tanaka N, Arai T, Kumasaka T, Gemma A, Kida K, Muramatsu M, Sawabe M.
Association of fucosyltransferase 8 (FUT8) polymorphism Thr267Lys with pulmonary emphysema. J Hum Genet. 2011 Oct 20. doi: 10.1038/jhg.2011.118. [Epub ahead of print]

8. Ishii T, Hagiwara K, Kamio K, Ikeda S, Arai T, Mieno MN, Kumasaka T, Muramatsu M, Sawabe M, Gemma A, Kida K.
Involvement of surfactant protein D in emphysema revealed by genetic association study. Eur J Hum Genet. 2011 Sep 21. doi: 10.1038/ejhg.2011.183. [Epub ahead of print]

9. Tohkin M, Kaniwa N, Saito Y, Sugiyama E, Kurose K, Nishikawa J, Hasegawa R, Aihara M, Matsunaga K, Abe M, Furuya H, Takahashi Y, Ikeda H, Muramatsu M, Ueta M, Sotozono C, Kinoshita S, Ikezawa Z.
A whole-genome association study of major determinants for allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients. Pharmacogenomics J. 2011 Sep 13. doi: 10.1038/tpj.2011.41. [Epub ahead of print]




2010

1. Miyaki K, Oo T, Song Y, Lwin H, Tomita Y, Hoshino H, Suzuki N, Muramatsu M.
Association of a cyclin-dependent kinase 5 regulatory subunit-associated protein 1-like 1 (CDKAL1) polymorphism with elevated hemoglobin A1c levels and the prevalence of metabolic syndrome in Japanese men: Interaction with dietary energy intake. Am J Epidemiol. 172:985-991, 2010.

2. Miyaki K, Oo T, Song Y, Lwin H, Tomita Y, Hoshino H, Suzuki N, Muramatsu M. Miyaki et al.
Respond to "Gene x Lifestyle Interactions" Am J Epidemiol. 172:998?999, 2010

3. Zhang L, Miyaki K, Wang W, Muramatsu M.
CYP3A5 polymorphism and sensitivity of Blood Pressure to dietary salt. J Hum Hypertens 24:345-350, 2010

4. Zhang L, Dai Y, Bian L, Wang W, Wang W, Muramatsu M, Hua Q.
Association of the cell death-inducing DNA fragmentation factor alpha-like effector A (CIDEA) gene V115F (G/T) polymorphism with phenotypes of metabolic syndrome in a Chinese population. Diabetes Res Clin Pract. 2010 [Epub ahead of print]

5. Fujimoto K, Ikeda S, Arai T, Tanaka N, Kumasaka T, Ishii T, Kida K, Muramatsu M, Sawabe M.
Polymorphism of SERPINE2 gene is associated with pulmonary emphysema in consecutive autopsy cases BMC Med Genet 11:159, 2010

6. Matsunaga T, Kuwata S, Muramatsu M.
Computational gene knockout reveals transdisease-transgene association structure. J Bioinform Comput Biol. 8:843-66, 2010

7. Kaniwa N, Saito Y, Aihara M, Matsunaga K, Tohkin M, Kurose K, Furuya H, Takahashi Y, Muramatsu M, Kinoshita S, Abe M, Ikeda H, Kashiwagi M, Song Y, Ueta M, Sotozono C, Ikezawa Z, Hasegawa R.
JSAR research group. HLA-B*1511 is a risk factor for carbamazepine-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients. Epilepsia. 51:2461-2465, 2010

8. Ikeda H, Takahashi Y, Yamazaki E, Fujiwara T, Kaniwa N, Saito Y, Aihara M, Kashiwagi M, Muramatsu M.
HLA class I markers in Japanese patients with carbamazepine-induced cutaneous adverse reactions. Epilepsia 51:297-300, 2010

9. Yokoyama K, Urashima M, Ohkido I, Kono T, Yoshida T, Muramatsu M, Niu T, Hosoya T.
L-type voltage-dependent calcium channel alpha subunit 1C is a novel candidate gene associated with secondary hyperparathyroidism: an application of haplotype-based analysis for multiple linked single nucleotide polymorphisms.  Nephron Clin Pract. 115:237-243, 2010

10. 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.
Association of the common fat mass and obesity associated (FTO) gene polymorphism with obesity in a Japanese population. Endocr J. 57:293-301, 2010

11. 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.
Association of the clusterin gene polymorphisms with type 2 diabetes mellitus. Metabolism. 2010 [Epub ahead of print]



2009

1. Sawabe M, Arai T, Araki A, Hosoi T, Kuchiba A, Tanaka N, Naito T, Oda K, Ikeda S, and Muramatsu M. Smoking confers a MTHFR 677C>T genotype-dependent risk for systemic atherosclerosis: Results from a large number of elderly autopsy cases died in a community-based general geriatric hospital. Atherosclerosis and Thrombosis Apr;16:91-104, 2009.

2. Matsunaga T, Yonemori C, Tomita E, Muramatsu M.
Clique-based data mining for related genes in a biomedical database.BMC Bioinformatics. 2009 Jul 1;10:205.

3. Miyaki K, Lwin H, Masaki K, Song Y, Takahashi Y, Muramatsu M, Nakayama T Association between a Polymorphism of Aminolevulinate Dehydrogenase (ALAD) Gene and Blood Lead Levels in Japanese Subjects. Int J Environ Res Public Health 6;999-1009, 2009.

4. Daimon M, Oizumi T, Toriyama S, Karasawa S, Jimbu Y, Wada K, Kameda W, Susa S, Muramatsu M, Kubota I, Kawata S, Kato T. Association of the Ser326Cys polymorphism in the OGG1 gene with type 2 DM. Biochem Biophys Res Commun. 386(1):26-9. 2009

5. Aoki K, Sato N, Yamaguchi A, Kaminuma O, Hosozawa T, Miyatake S.: Regulation of DNA demethylation during maturation of CD4+ naive T cells by the conserved noncoding sequence 1. J Immunol. 182: 7698-707, 2009.



2008

1. Zhang L, Miyaki K, Nakayama T, Muramatsu M.
Cell death-inducing DNA fragmentation factor alpha-like effector A (CIDEA) gene V115F (G-->T) polymorphism is associated with phenotypes of metabolic syndrome in Japanese men. Metabolism 57:502-505, 2008.

2. Takei K, Ikeda S, Arai T, Tanaka N, Muramatsu M, Sawabe M.
Lymphotoxin-alpha polymorphisms and presence of cancer in 1,536 consecutive autopsy cases. BMC Cancer 8:235-240, 2008.

3. Yoshimura M, Kimura T, Ishii M, Ishii K, Matsuura T, Geshi E, Hosokawa M, Muramatsu M.
Functional polymorphisms in carboxylesterase1A2 (CES1A2) gene involves specific protein 1 (Sp1) binding sites. BBRC 369:939-942, 2008.

4. Takeo C, Ugai K, Araki J, Zhang L, Baba M, Ohashi W, Ueno K, Suzuki Y, Amano K, Hirai A, Muramatsu, M.
Pharmacogenetics of hormone replacement therapy for climacteric symptoms. BBRC 374:604-608, 2008.

5. Song Y, Miyaki K, Araki J, Zhang L, Takahashi Y, Nakayama T, Muramatsu M.
Influence of CYP11B2 Gene Polymorphism on the Prevalence of Hypertension and the Blood Pressure in Japanese Men: Interaction with Dietary Salt Intake. J Nutrigenet Nutrigenomics 1:252-258, 2008.

6. Yokoyama K, Shigematsu T, Miyaki K, Hara S, Ohkido I, Hosoya T, Kono T, Yoshida T, Muramatsu M.
Low blood osteoprotegerin levels are a predictor to poor prognosis in Japanese patients on hemodialysis due to diabetic nephropathy. Ther Apher Dial 12:259-260, 2008.

7. Kaniwa N, Saito Y, Aihara M, Matsunaga K, Tohkin M, Kurose K, Sawada JI, Furuya H, Takahashi Y, Muramatsu M, Kinoshita S, Abe M, Ikeda H, Kashiwagi M, Song Y, Ueta M, Sotozono C, Ikezawa Z, Hasegawa R.
HLA-B locus in Japanese patients with anti-epileptics and allopurinol- related Stevens-Johnson syndrome and toxic epidermal necrolysis. Pharmacogenomics. 9:1617-1622, 2008.

8. Shi L, Ogata S, Yu JK, Ohashi J, Yu L, Shi L, Sun H, Lin K, H XQ, Matsushita M, Horai S, Muramatsu M, Chu JY, Tokunaga K.
Distribution of HLA alleles and haplotypes in Jinuo and Wa populations in Southwest China. Hum Immunol 69: 58-65, 2008.

9. 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.
Association of the PIK3C2G gene polymorphisms with type 2 DM in a Japanese Population. BBRC 365:466-471, 2008.

10. Susa S, Daimon M, Sakabe J, Sat H, Oizumi T, Karasawa S, Wada K, Jimbu Y, Kameda W, Emi M, Muramatsu M, Kato T.
A functional polymorphism of the TNF-α gene that is associated with type 2 DM. BBRC 369:943-947, 2008.

11. 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.
Salt consumption-dependent association of the GNB3 gene polymorphism with type 2 DM. BBRC 374:576-580, 2008.

12. Matsukura H, Ikeda S, Yoshimura N, Takazoe M, Muramatsu M.
Genetic polymorphisms of tumour necrosis factor receptor superfamily 1A and 1B affect responses to infliximab in Japanese patients with Crohn’s disease. Aliment Pharmacol Ther 27, 765-770, 2008.



2007

1. Oda K, Tanaka N, Arai T, Araki J, Song Y, Zhang L, Kuchiba A,  Hosoi T, Shirasawa T, Muramatsu M, Sawabe M.
Polymorphisms in pro- and anti-inflammatory cytokine genes and susceptibility to atherosclerosis: a pathological study of 1503 consecutive autopsy cases. Hum Mol Genet. 15;16(6):592-599, 2007.

2. Sakamoto N, Yoshimura M, Kimura T, Toyama K, Sekine-Osajima Y, Watanabe M, Muramatsu M.
Bone morphogenetic protein-7 and interferon-alpha synergistically suppress hepatitis C virus replicon. Biochem Biophys Res Commun. 357:467-473, 2007.

3. Song Y, Miyaki K, Araki J, Zhang L, Omae K, Muramatsu M.
The interaction between the interleukin 6 receptor gene genotype and dietary energy intake on abdominal obesity in Japanese men. Metabolism 56:925-930, 2007.

4. Zhang L, Miyaki K, Araki J, Nakayama T, Muramatsu M.
The relation between nicotinamide N-methyltransferase gene polymorphism and plasma homocysteine concentration in healthy Japanese men. Thromb Res. 121:55-58. 2007

5.Naito T, Sawabe M, Arai T, Chida K, Hamamatsu A, Harada K, Ozawa T, Murayama S, Muramatsu M.
Dyslipidemia is a major determinant of systemic atherosclerosis in the elderly: An autopsy study. Geriatr Gerontol Int. 7:229-237, 2007.

6.Matsunaga T & Muramatsu M.
Disease-related concept mining by knowledge-based two-dimensional gene mapping. J Bioinform Comput Biol 5:1047-1067, 2007.

7.Ogata S, Shi L, Matsushita M, Yu L, Huang XQ, Shi L, Sun H, Ohashi J, Muramatsu M, Tokunaga K, Chu JY.
Polymorphisms of human leucocyte antigen genes in Maonan people in China. Tissue Antigens. 69:154-160 2007.

8. Nagasawa H, Wada M, Arawaka S, Kawanami T, Kurita K, Daimon M, Adachi M, Hosoya T, Emi M, Muramatsu M, Kato T.
A polymorphism of the aldehyde dehydrogenase 2 gene is a risk factor for multiple lacunar infarcts in Japanese men: the Takahata Study. Eur J Neuro. 14:428-434, 2007

9.Sata M, Takabatake N, Inoue S, Shibata Y, Abe S, Machiya J, Wada T, Ji G, Kido T, Matsuura T, Muramatsu M, Kubota I.
Intronic single- nucleotide polymorphisms in Bcl-2 are associated with chronic obstructive pulmonary disease severity. Respirology. 12:34-41. 2007

10. Naito M, Miyaki K, Naito T, Zhang L, Hoshi K, Hara A, Masaki K, Tohyama S, Muramatsu M, Hamajima N, Nakayama T.
Association between vitamin D receptor gene haplotypes and chronic periodontitis among Japanese men. Int J Med Sci. 4: 216-222, 2007



2006

1. Nonomura, N., Tokizane, T., Nakayama, M., Inoue, H., Nishimura, K., Muramatsu,M., and Okuyama, A
. Possible correlation between polymorphism in the tumor necrosis factor-beta gene and the clinicopathogical features of bladder cancer in Japanese patients. International Journal of Urology. 13:971-976. 2006.

2. Tanaka,T., Takahama, K., Kimura, T., Mizuno, T., Nagasaka, M., Iwata, K., Nakano, H., Muramatsu, M., Takazoe, M.
Effect of concurrent elemental diet on infliximab treatment for Crohn’s disease. Journal of Gastroenterology and Hepatology. 21(7):1143-1149. 2006.

3. Daimon, M., Ji, G., Oizumi, T., Kido, T., Baba, M., Jimbu, Y., Kameda, W., Susa, S., Yamaguchi, H., Ohnuma, H., Muramatsu, M., Kato, T.
Association of nephrin gene polymorphisms with type 2 diabetes in a Japanese population: The Funagata study. Diabetes Care. 29:1117-1119. 2006.

4. Kimura, T., Saito, T., Yoshimura, M., Song, Y., Baba, M., Ji, G., Muramatsu, M., Kawata, S.
Association of Transforming Growth Factor-β1 Functional Polymorphisms with Natural Clearance of Hepatitis C Virus. Journal of Infectious Diseases. 193:1371-1374. 2006.

5. Arai, M., Yokosuka, O., Kanda, T., Fukai, K., Imazeki, F., Muramatsu, M., Seki, N., Miyazaki, M., Ochiai, T., Hirasawa, H., Saisho, H.
Serum osteopontin levels in patients with acute liver dysfunction. Scandinavian Journal of Gastroenterology. 41:102-110. 2006.



2005

1. Kato, N., Ji, G., Wang, Y., Baba, M., Hoshida, Y., Otsuka, M., Taniguchi, H., Moriyama, M., Dharel, N., Goto, T., Shao, RX., Matsuura, T., Ishii, K., Shiina, S., Kawabe, T., Muramatsu, M., Omata, M.
Large-scale search of single nucleotide polymorphisms for hepatocellular carcinoma susceptibility genes in patients with hepatitis C. Hepatology 42(4):846-853. 2005.

2. Daimon, M., Kido, T., Baba, M., Oizumi, T., Jimbu, Y., Kameda, W., Yamaguchi, H., Ohnuma, H., Tominaga, M., Muramatsu, M., Kato, T.
Association of the ABCA1 gene polymorphisms with type 2 DM in a Japanese population. Biochemical Biophys Res Commun. 329:205-210. 2005.

3. Matsunaga, T., and Muramatsu M.
Knowledge-based computational search for genes associated with the metabolic syndrome. Bioinformatics. 21:3146-3154. 2005.

4. Daimon, M., Kido, T., Baba, M., Oizumi, T., Jimbu, Y., Kameda, W., Yamaguchi, H., Ohnuma, H., Tominaga, M., Muramatsu, M., Kato, T.
Association of the ABCA1 gene polymorphisms with type 2 DM in a Japanese population. Biochemical Biophys Res Commun. 329:205-210. 2005

5. Song, Y., Araki, J., Zhang, L., Froehlich, T., Sawabe, M., Arai, T., Shirasawa, T., Muramatsu, M..
Haplotyping of TNFα gene promoter using melting temperature analysis: detection of a novel-856 (G/A) mutation. Tissue Antigens.66(4):284-290. 2005.

6. Geshi, E., Kimura, T., Yoshimura, M., Suzuki, H., Koba, S., Sakai, T., Saito, T., Koga, A., Muramatsu, M., Katagiri, T.
A Single Nucleotide Polymorphism in the Carboxylesterase Gene Is Associated with the Responsiveness to Imidapril Medication and the Promoter Activity. Hypertension Research. 28:719-725. 2005.

7. Takabatake, N., Sata, M., Inoue, S., Shibata, Y., Abe, S., Wada, T., Machiya, JI., Ji, G., Matsuura, T., Takeishi, Y., Muramatsu, M., Kubota, I.
A Novel Polymorphism in Secretory Phospholipase A2-IID is Associated with Body Weight Loss in COPD. Am J Respir Crit Care Med. 172(9):1097-1104. 2005.



2004

1. Oda, T., Fukuda, A., Hagiwara, H., Masuho, Y., Muramatsu, M., Hisatake, K., Yamashita, T.
ABT1-associated protein (ABTAP), a novel nuclear protein conserved from yeast to mammals, represses transcriptional activation by ABT1. J Cell Biochem. 93:788-806. 2004.

2. Kitano, H., Oda, K., Kimura, T., Matsuoka, Y., Csete, M., Doyle, J., Muramatsu, M.
Metabolic Syndrome and Robustness Tradeoffs. Diabetes. 53(Suppl.3):S6-S15. 2004.

3. Saito, T., Ji, G., Watanabe, H., Shinzawa, H., Okumoto, K., Hattori, E., Adachi, T., Takeda, T., Sugahara, K., Ito, J., Saito, K., Togashi, H., Ishii, K., Matsuura, T., Inageda, K., Muramatsu, M., Kawata, S.
Genetic variations in humans infected with hepatitis C virus that are associated with differenceds in the course of infection. Biochem Biophys Res Commun. 317:335-341. 2004.

4. Araki, J., Ohashi, J., Muramatsu, M.
Tissue Antigens Application of discordant sib-pair linkage analysis for mapping minorhistocompatibility antigen loci in a novel graft-versus-host-disease model. Tissue Antigens. 64:243-250. 2004.

5. Arai, M., Yokosuka, O., Fukai, K., Imazeki, F., Chiba, T., Sumi, H., Kato, M., Takiguchi, M., Saisho, H., Muramatsu, M., and Seki, N.
Gene expression profilesin liver regeneration with oval cell induction. Biochem Biophys Res Commun. 317:370-376. 2004.

6. Oda, K., Kimura, T., Matsuoka, Y., Funahashi, A., Muramatsu, M., Kitano, H.
Molecular Interaction Map of Macrophage. AfCS Research Reports [http://www.signaling-gateway.org/report/]. 2004.



2003

1. Kimura, T., Yokoyama, T., Matsumura, Y., Yoshiike, N., Date, C., Muramatsu, M., Tanaka, H.
NOS3 genotype dependent correlation between blood pressure and physical activity. Hypertension. 41:355-360. 2003.

2. Saito, K., Yokoyama, T., Yoshiike, N., Date, C., Yamamoto, A., Muramatsu, M., Tanaka, H.
Do the ethanol metabolizing enzymes modify the relationship between alcohol consumption and blood pressure? J Hypertens. 21:1097-1105. 2003.

3. Daimon, M., Ji, G., Saitoh, T., Oizumi, T., Tominaga, M., Nakamura, T., Ishii, K., Matsuura, T., Inageda, K., Matsumine, H., Kido, T., Htay, L., Kamatani, N., Muramatsu, M., Kato, T.
Large-scalesearch of SNPs for type 2 DM susceptibility genes in a Japanese population. Biochem Biophys Res Commun. 302:751-758. 2003.



2002

1. Nanbu-Wakao, R., Morikawa, Y., Matsumura, I., Masuho, Y., Muramatsu, M., Semba, E., Wakao, H.
Stimulation of 3T3-L1 adipogenesis by signal transducer and activator of transcription 5. Mol. Endocrinol. 16. 1565-1576. 2002.



   ~2001

1. Maeda S., Otsuka, M. Hirata, Y. Mitsuno, Y. Yoshida, H. Shiratori, Y. Masuho, Y. Muramatsu, M. Seki, N., and Omata, M. cDNA microarray analysis of Helicobacter pylori-mediated alteration of gene expression in gastric cancer cells. Biochem Biophys Res Commun. 2001;284:443-449.

2. Kato M, Seki N, Sugano S, Hashimoto K, Masuho Y, Muramatsu M., Kaibuchi K, Nakafuku M. Identification of sonic hedgehog-responsive genes using cDNA microarray. Biochem Biophys Res Commun. 2001;289:472-478.

3. Oda T, Muramatsu M, Isogai T, Masuho Y, Asano S, Yamashita T. HSH2: A novel SH2 domain-containing adapter protein involved in tyrosin kinase signaling in hematopoietic cells. Biochem Biophys Res Commun. 2001;288:1078-1086

4. Tokumitsu, H., Muramatsu, M. Ikura, M., and Kobayashi, R. Regulatory mechanism of Ca2+/calmodulin kinase kinase. J. Biol. Chem. 2000;275:20090-20095

5. Okazaki N., Yan J. Yuasa S. Ueno T. Kominami E. Masuho Y. Koga H., and Muramatsu M. . Interaction of the Unc-51-like kinase and microtubule-associated protein light chain 3 related proteins in the brain: possible role of vesicular transport in axonal elongation. Mol Brain Res.2000; 85:1-12.

6. Yano, K., Ueki N. Oda T. Seki N. Masuho, Y., and Muramatsu, M. Identification and characterization of human ZNF274 cDNA, which encodes a novel Kruppel type zinc finger protein having nucleolar targeting ability. Genomics 2000;65:75-80

7. Oda, T., Kayukawa, K. Hagiwara, H. Yudate H. T. Masuho, Y. Murakami, Y. Tamura, T., and Muramatsu, M. A novel TATA-binding protein binding protein ABT1 activates basal transcription and has a yeast homolog that is essential for growth. Mol. Cell. Biol. 2000;20:1407-1418

8. Wakao-Nanbu, R., Fujitani, Y. Masuho, Y. Muramatsu, M., and Wakao, H. Prolactin enhances CCAAT enhancer-binding protein-β (C/REBβ) and peroxisome proliferator-activated receptor γ (PPARγ) messenger RNA expression and stimulates adipogenic conversion of NIH-3T3 cells. Mol. Endocrinol. 2000;14: 307-316

9. Yoshikawa T., Nagasugi, Y. Azuma, T. Kato, M. Sugano, S. Hashimoto, K. Masuho, Y. Muramatsu, M, and Seki, N. Isolation of novel mouse genes differentially expressed in brain using cDNA microarray. Biochem Biophys Res Commun. 2000;275:532-537.

10. Ueki, N., Seki, N. Yano, K. Saito T. Masuho, Y., and Muramatsu, M. Isolation and characterization of a human novel gene (HFB30) which encodes a protein with a RING finger motif. Biochem. Biophys. Acta. 1999;1445:232-236

11. Tokumitsu, H., Takahashi, N. Yano, S. Soderling, T. R., and Muramatsu, M. Substrate recognition of Ca2+/calmodulin-dependent kinase kinase: Role of the Arg-Pro-rich insert. J. Biol. Chem. 1999;274:15803-15810

12. Eto, K., Takahashi, N. Kimura, Y. Masuho, Y. Arai, K. Muramatsu , M., and Tokumitsiu, H. Ca2+/Calmodulin-dependent protein kinase cascade in Caenorhabditis elegans: Implication in transcriptional activation. J. Biol. Chem.1999; 274:22556-22562

13. Yan J., Kuroyanagi H. Tomemori T. Okazaki N. Kuroiwa A., Matsuda Y. Suzuki Y. Ohshima Y. Mitani S. Masuho Y. Shirasawa T., and Muramatsu M. Mouse ULK2, a novel member of the UNC-51-like protein kinases: Unique features of functional domains. Oncogene 1999;18:5850-5859

14. Yan, J., Kuroyanagi, H. Kuroiwa, A. Matsuda, Y. Tokumitsu, H. Tomoda, T. Shirasawa, T., and Muramatsu, M. Identification of mouse ULK1, a novel protein kinase structurally related to C. elegans UNC-51. Biochem. Biophys. Res. Commun. 1998;246:222-227

15. Kuroyanagi, H., Yan, J. Seki, N. Yamanouchi, Y. Suzuki, Y. Takano, T. Muramatsu, M. and Shirasawa, T. Human ULK1, a novel serine/threonine kinase related to UNC-51 of C. elegans: cDNA cloning, expression and chromosomal assignment. Genomics 1998;51:76-85

16. Ueki, N., Oda, T. Kondo, M. Yano, K. Noguchi, T., and Muramatsu, M. Selection system for genes encoding nuclear-targeted proteins. Nat. Biotech. 1998;16:1338-1342

17. Ueki, N., Kondo, M. Seki, N. Yano, K. Oda, T. Masuho, Y., and Muramatsu, M. NOLP: Identification of a novel human nucleolar protein and determination of sequence requirements for nucleolar localization. Biochem. Biophys. Res. Commun. 1998;252:97-102

18. Tokumitsu, H., Wayman, G. A. Muramatsu, M., and Soderling, T. R. Calcium/calmodulin-dependent protein kinase kinase: Identification of regulatory domains. Biochemistry 1997;36:12823-12827

19. Muramatsu, M., Yan, J. Eto, K. Tomoda, T. Yamada, R. and Arai, K. A chimeric serine/threonine kinase receptor system reveals the potential of multiple type II receptors to cooperate with transforming growth factor-? type I receptor. Mol. Biol. Cell 1997;8:469-480 

20. Sasaki, H., Matsuda, M. Lu, Y. Ikuta, K. Matsuyama, S. Hirabayashi, Y. Mitsui, H. Matsumura, T. Muramatsu, M. Tsukada, T. Aizawa, S., and Inoue, T. A fraction unresponsive to growth inhibition by TGF-β among the high-proliferative potential progenitor cells in bone marrow of p53-deficient mice. Leukemia 1997;11:239-244

21. Tomoda, T., Shirasawa, T. Yahagi, Y. Ishii, K. Takagi, H. Furiya, Y. Arai, K. Mori, H., and Muramatsu, M. Transforming growth factor-β is a survival factor for neonate cortical neurons: Coincident expression of type I receptor in developong cerebral cortices. Dev. Biol. 1996;179:79-90

22. Yu, Y-s, Suzuki, Y. Yoshitomo, K. Muramatsu, M. Yamaguchi, N., and Sugano, S. The promoter structure of TGF-β type II receptor revealed by “oligo-capping” method and deletion analysis. Biochem. Biophys. Res. Commun. 1996;225:302-306

23. Watanabe, M., Muramatsu, M. Tsuboi, A., and Arai, K. Differential response of NF-κB1 p105 and NF-κB2 p100 to HTLV-I encoded Tax. FEBS lett. 1994;342:115-118

24. Tsuboi, A., Muramatsu, M. Tsutsumi, A. Arai, K., and Arai, N. Calcineurin activates transcription from the GM-CSF promoter in synergy with either protein kinase C or NF-κB/AP-1 in T cells. Biochem. Biophys. Res. Commun. 1994;199:1064-1072

25. Tomoda, T., Kudo, T. Noma, T. Nakazawa, A. Muramatsu, M, and Arai, K. Molecular cloning of mouse counterpart for human TGF? receptor type I. Biochem. Biophys. Res. Commun. 1994;198:1054-1062

26. Watanabe, M. Muramatsu, M. Hirai, H. Suzuki, T. Fujisawa, J. Yoshida, M. Arai, K., and Arai, N. HTLV-I encoded Tax in association with NF-?B precursor p105 enhances nuclear localization of NF-?B p50 and p65 in transfected cells. Oncogene 1993;8:2949-2958

27. Tomoda, T., Murata, T. Arai, K., and Muramatsu, M. Mutations of 170Glu, a substrate recognition site generate enzymes with altered substrate affinity and biological function. Biochem. Biophys. Acta 1993;1175: 333-342

28. Muramatsu, M., Kaibuchi, K., and Arai, K. Mutations in the autoinhibitory domain of protein kinase C generates enzymes with distinct properties. FEBS lett. 1992;311:75-79

29. Tokumitsu, H., Mizutani, A. Muramatsu, M. Yokota, T. Arai, K., and Hidaka, H. Molecular cloning of rabbit CAP-50, a calcyclin-associated annexin protein. Biochem. Biophys. Res. Commun. 1992;186: 1227-1235.

30. Hirai, H., Fujisawa, J. Suzuki, T. Ueda, K. Muramatsu, M. Tsuboi, A. Arai, N., and Yoshida, M. Transcriptional activator Tax of HTLV-I binds to the NF-kB precursor p105. Oncogene 1992;7:1737-1742

31. Yamamoto, M., Igarashi, T. Muramatsu, M. Fukagawa, M., Motokura, T., and Ogata, E. Hypocalcemia increases and hypercalcemia decreases the steady state level of parathyroid hormone messenger RNA in the rat. J. Clin. Invest. 1989;83:1053-1056

32. Nakano A., and Muramatsu M. A novel GTP binding protein Sar1p, is involved in transport from the endoplasmicreticulum to the Golgi apparatus. J. Cell. Biol. 1989;109:2677-2691

33. Muramatsu, M., Kaibuchi, K., and Arai, K. A protein kinase C cDNA without the regulatory domain is active after transfection in the absence of phorbol ester. Mol. Cell. Biol. 1989;9:831-836

34. Kaibuchi, K., Fukumoto Y. Oku, N. Takai, Y. Arai, K., and Muramatsu, M. Molecular genetic analysis of the regulatory and catalytic domains of protein kinase C. J. Biol. Chem. 1989;264:13489-13496


II. Reviews

2012

1. 佐藤憲子 
「DNA 複製、組換えと修復《デブリン生化学第7 版、第4 章、(上代淑人、渋谷正史、井原康夫監訳)丸善出版、2012.



2011

1. 村松正明 
「遺伝子予防医療に対する期待《 ウェルエイジングのための女性医療 太田博明編pp 269-274 メディカルレビュー社、2011.



2005

1. 村松正明 
遺伝子特許 予防医学事典(松島綱治、酒井敏行、石川 昌、稲寺秀邦編集) 289-290 朝倉書店 2005.



2004

1. 村松正明 
ゲノムと疾患 The Frontiers in Medical Sciences 37-43 南山堂 2004.

2. 馬場昌法、村松正明 
SNPインフォマティクス ゲノム研究実験ハンドブック (辻本豪三、田中利男編)153-160 羊土社 2004.

3. 村松正明 
ファーマコゲノミクスの解析技術と応用 1069-1075 月刊薬事 じほう 2004.

4. 村松正明 
遺伝子の個性を生かした医療に向けて 609-614 科学 岩波書店 2004.

5. 村松正明 
癌関連SNPの探索 戦略と課題 実験医学別冊ポストゲノム研究から診断・治療へ 1927-1931 羊土社 2004.

6. 小田夏奈江、北野宏明、村松正明 
転写因子と糖尿病 1553-1564 臨床検査 2004.



2003

1. 木村友美 村松正明 
SNPsとゲノム創薬 ゲノム創薬の展望[Ⅲ];119 化学フロンティア(12) 化学同人 2003.

2. 木村友美 村松正明 
消化器癌サーベイランスとSNP 消化器癌サーベイランス;302 新興医学出版社;木村 健・藤盛孝博・加藤 洋/編 2003年10月

3. 村松正明 
SNPs研究の現状と展望  特集SNPsと消化器疾患 G.I.Research 11;365-371 先端医学社 2003年11月.



2002

1. 村松正明 
遺伝子の個性を医療に生かす 日経サイエンス別冊 54-61 2002年11月.

2. 木村友美 村松正明 
DNAチップによるSNP解析 癌と化学療法 29(13):2573-2577 2002.


~2001

1. 村松正明 
ゲノム情報系バイオベンチャー ゲノム医学の最先端と世界のバイオベンチャー 96-102 羊土社 2001.

2. 村松正明
遺伝子検査の市場と展望:ポストゲノム時代を迎えて 遺伝子医学 55-59, メディカルドウ社 2001.

3. 村松正明編 
SNP の医療創薬への応用とビジネス展開 Bioベンチャー 羊土社 2001.

4. 村松正明 
日本のベンチャーを取り巻く世界 ゲノム医科学がわかる 93-98, 羊土社 2001.

5. 村松正明 
遺伝子の個人差を医療に生かす 日経サイエンス 28-35 2001年12月号.

6. 村松正明 
ゲノム医学入門 高尿酸値血症と痛風 9:164-168 メディカルレビュ-社 2000.

7. 村松正明
DNA チップによるSNP 解析 SNP 遺伝子多型の戦略 128-135,中山書店 2000.