Works matching IS 14712350 AND DT 2010 AND VI 11

Results: 173

Association of the rs738409 polymorphism in PNPLA3 with liver damage and the development of nonalcoholic fatty liver disease.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 172, doi. 10.1186/1471-2350-11-172

By:

Hotta, Kikuko;
Yoneda, Masato;
Hyogo, Hideyuki;
Ochi, Hidenori;
Mizusawa, Seiho;
Ueno, Takato;
Chayama, Kazuaki;
Nakajima, Atsushi;
Nakao, Kazuwa;
Sekine, Akihiro

Publication type:

Article

A wide spectrum of clinical and brain MRI findings in patients with SLC19A3 mutations.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 171, doi. 10.1186/1471-2350-11-171

By:

Yamada, Kenichiro;
Miura, Kiyokuni;
Hara, Kenju;
Suzuki, Motomasa;
Nakanishi, Keiko;
Kumagai, Toshiyuki;
Ishihara, Naoko;
Yamada, Yasukazu;
Kuwano, Ryozo;
Tsuji, Shoji;
Wakamatsu, Nobuaki

Publication type:

Article

Exploring multilocus associations of inflammation genes and colorectal cancer risk using hapConstructor.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 170, doi. 10.1186/1471-2350-11-170

By:

Curtin, Karen;
Wolff, Roger K.;
Herrick, Jennifer S;
Abo, Ryan;
Slattery, Martha L.

Publication type:

Article

High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 169, doi. 10.1186/1471-2350-11-169

By:

Papp, Janos;
Kovacs, Marietta Eva;
Solyom, Szilvia;
Kasler, Miklos;
Børresen-Dale, Anne-Lise;
Olah, Edith

Publication type:

Article

Genetic variants in the TIRAP gene are associated with increased risk of sepsis-associated acute lung injury.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 168, doi. 10.1186/1471-2350-11-168

By:

Zhenju Song;
Chaoyang Tong;
Zhan Sun;
Yao Shen;
Chenling Yao;
Jinjun Jiang;
Jun Yin;
Lei Gao;
Yuanlin Song;
Chunxue Bai

Publication type:

Article

Genetic polymorphisms in the endothelial nitric oxide synthase gene correlate with overall survival in advanced non-small-cell lung cancerpatients treated with platinum-based doubletc hemotherapy.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 167, doi. 10.1186/1471-2350-11-167

By:

Fujita, Shiro;
Masago, Katsuhiro;
Hatachi, Yukimasa;
Fukuhara, Akiko;
Hata, Akito;
Kaji, Reiko;
Kim, Young Hak;
Mio, Tadashi;
Mishima, Michiaki;
Katakami, Nobuyuki

Publication type:

Article

Generation Scotland: Donor DNA Databank; A control DNA resource.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 166, doi. 10.1186/1471-2350-11-166

By:

Kerr, Shona M.;
Liewald, David C. M.;
Campbell, Archie;
Taylor, Kerrie;
Wild, Sarah H.;
Newby, David;
Turner, Marc;
Porteous, David J.

Publication type:

Article

A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 165, doi. 10.1186/1471-2350-11-165

By:

Hattersley, Kathryn;
Laurie, Kate J.;
Liebelt, Jan E.;
Gecz, Jozef;
Durkin, Shane R.;
Craig, Jamie E.;
Burdon, Kathryn P.

Publication type:

Article

Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: results of a meta-analysis.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 164, doi. 10.1186/1471-2350-11-164

By:

Kerkhof, Hanneke J. M.;
Meulenbelt, Ingrid;
Carr, Andrew;
Gonzalez, Antonio;
Hart, Deborah;
Hofman, Albert;
Kloppenburg, Margreet;
Lane, Nancy E.;
Loughlin, John;
Nevitt, Michael C.;
Pols, Huibert A. P.;
Rivadeneira, Fernando;
Slagboom, Eline P.;
Spector, Tim D.;
Stolk, Lisette;
Tsezou, Aspasia;
Uitterlinden, André G.;
Valdes, Ana M.;
van Meurs, Joyce B. J.

Publication type:

Article

Significant association between polymorphism of the erythropoietin gene promoter and myelodysplastic syndrome.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 163, doi. 10.1186/1471-2350-11-163

By:

Ma, Wanlong;
Kantarjian, Hagop;
Ke Zhang;
Xi Zhang;
Xiuqiang Wang;
Clifford Chen;
Donahue, Amber C.;
Zhong Zhang;
Chen-Hsiung Yeh;
O'Brien, Susan;
Garcia-Manero, Guillermo;
Caporaso, Neil;
Landgren, Ola;
Albitar, Maher

Publication type:

Article

The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer¿s disease in the Epistasis Project.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 162, doi. 10.1186/1471-2350-11-162

By:

Combarros, Onofre;
Warden, Donald R;
Hammond, Naomi;
Cortina-Borja, Mario;
Belbin, Olivia;
Lehmann, Michael G;
Wilcock, Gordon K;
Brown, Kristelle;
Kehoe, Patrick G.;
Barber, Rachel;
Coto, Eliecer;
Alvarez, Victoria;
Deloukas, Panos;
Gwilliam, Rhian;
Heun, Reinhard;
Kölsch, Heike;
Mateo, Ignacio;
Oulhaj, Abderrahim;
Arias-Vásquez, Alejandro;
Schuur, Maaike

Publication type:

Article

Sequencing of DC-SIGN promoter indicates an association between promoter variation and risk of nasopharyngeal carcinoma in cantonese.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 161, doi. 10.1186/1471-2350-11-161

By:

Ya-Fei Xu;
Wan-Li Liu;
Ju-Qin Dong;
Wen-Sheng Liu;
Qi-Sheng Feng;
Li-Zhen Chen;
Yi-Xin Zeng;
Mu-Sheng Zeng;
Wei-Hua Jia

Publication type:

Article

SNP-SNP interactions dominate the genetic architecture of candidate genes associated with left ventricular mass in african-americans of the GENOA study.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 160, doi. 10.1186/1471-2350-11-160

By:

Meyers, Kristin J.;
Jian Chu;
Mosley, Thomas H.;
Kardia, Sharon L. R.

Publication type:

Article

Polymorphism of SERPINE2 gene is associated with pulmonary emphysema in consecutive autopsy cases.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 159, doi. 10.1186/1471-2350-11-159

By:

Fujimoto, Koichi;
Ikeda, Shinobu;
Arai, Tomio;
Tanaka, Noriko;
Kumasaka, Toshio;
Ishii, Takeo;
Kida, Kozui;
Muramatsu, Masaaki;
Sawabe, Motoji

Publication type:

Article

Association analysis of nine candidate gene polymorphisms in Indian patients with type 2 diabetic retinopathy.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 158, doi. 10.1186/1471-2350-11-158

By:

Balasubbu, Suganthalakshmi;
Sundaresan, Periasamy;
Rajendran, Anand;
Ramasamy, Kim;
Govindarajan, Gowthaman;
Perumalsamy, Namperumalsamy;
Hejtmancik, J. Fielding

Publication type:

Article

Effect of the rs2259816 polymorphism in the HNF1A gene on circulating levels of c-reactive protein and coronary artery disease (the ludwigshafen risk and cardiovascular health study).

Published in:

BMC Medical Genetics, 2010, v. 11, p. 157, doi. 10.1186/1471-2350-11-157

By:

Kleber, Marcus E.;
Grammer, Tanja B.;
Renner, Wilfried;
März, Winfried

Publication type:

Article

Linkage analysis of obesity phenotypes in pre- and post-menopausal women from a United States mid-western population.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 156, doi. 10.1186/1471-2350-11-156

By:

Kelemen, Linda E.;
Atkinson, Elizabeth J.;
de Andrade, Mariza;
Pankratz, V. Shane;
Cunningham, Julie M.;
Wang, Alice;
Hilker, Christopher A.;
Couch, Fergus J.;
Sellers, Thomas A.;
Vachon, Celine M.

Publication type:

Article

Inflammation gene variants and susceptibility to albuminuria in the U.S. population: analysis in the Third National Health and Nutrition Examination Survey (NHANES III), 1991-1994.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 155, doi. 10.1186/1471-2350-11-155

By:

Ned, Renée M.;
Yesupriya, Ajay;
Imperatore, Giuseppina;
Smelser, Diane T.;
Moonesinghe, Ramal;
Chang, Man-huei;
Dowling, Nicole F.

Publication type:

Article

Toll-like receptor gene polymorphisms are associated with susceptibility to Graves' ophthalmopathy in Taiwan males.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 154, doi. 10.1186/1471-2350-11-154

By:

Wen-Ling Liao;
Rong-Hsing Chen;
Hui-Ju Lin;
Yu-Huei Liu;
Wen-Chi Chen;
Yuhsin Tsai;
Lei Wan;
Fuu-Jen Tsai

Publication type:

Article

Chromosomal abnormalities in spontaneous abortion after assisted reproductive treatment.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 153, doi. 10.1186/1471-2350-11-153

By:

Ji Won Kim;
Woo Sik Lee;
Tae Ki Yoon;
Hyun Ha Seok;
Jung Hyun Cho;
You Shin Kim;
Sang Woo Lyu;
Sung Han Shim

Publication type:

Article

Analyses of association between PPAR gamma and EPHX1 polymorphisms and susceptibility to COPD in a Hungarian cohort, a case-control study.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 152, doi. 10.1186/1471-2350-11-152

By:

Penyige, Andras;
Poliska, Szilard;
Csanky, Eszter;
Scholtz, Beata;
Dezso, Balazs;
Schmelczer, Ivan;
Kilty, Iain;
Takacs, Laszlo;
Nagy, Laszlo

Publication type:

Article

Genetic variants in mannose receptor gene (MRC1) confer susceptibility to increased risk of sarcoidosis.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 151, doi. 10.1186/1471-2350-11-151

By:

Hattori, Takeshi;
Konno, Satoshi;
Takahashi, Ayumu;
Isada, Akira;
Shimizu, Kaoruko;
Shimizu, Kenichi;
Taniguchi, Natsuko;
Gao, Peisong;
Yamaguchi, Etsuro;
Hizawa, Nobuyuki;
Huang, Shau-Ku;
Nishimura, Masaharu

Publication type:

Article

The association of the Clock 3111 T/C SNP with lipids and lipoproteins including small dense low-density lipoprotein: results from the Mima study.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 150, doi. 10.1186/1471-2350-11-150

By:

Tsuzaki, Kokoro;
Kotani, Kazuhiko;
Sano, Yoshiko;
Fujiwara, Shinji;
Takahashi, Kaoru;
Sakane, Naoki

Publication type:

Article

Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 145, doi. 10.1186/1471-2350-11-145

By:

Audo, Isabelle;
Bujakowska, Kinga;
Mohand-Saïd, Saddek;
Lancelot, Marie-Elise;
Moskova-Doumanova, Veselina;
Waseem, Naushin H.;
Antonio, Aline;
Sahel, José-Alain;
Bhattacharya, Shomi S.;
Zeitz, Christina

Publication type:

Article

Interaction of functional NPC1 gene Polymorphism with smoking on coronary heart disease.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 149, doi. 10.1186/1471-2350-11-149

By:

Weiwei Ma;
Jing Xu;
Qianqian Wang;
Ying Xin;
Lin Zhang;
Xinxin Zheng;
Hu Wang;
Kai Sun;
Rutai Hui;
Xiaohong Huang

Publication type:

Article

WWOX gene is associated with HDL cholesterol and triglyceride levels.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 148, doi. 10.1186/1471-2350-11-148

By:

Sáez, María E.;
González-Pérez, Antonio;
Martínez-Larrad, María T.;
Gayán, Javier;
Real, Luis M.;
Serrano-Ríos, Manuel;
Ruiz, Agustín

Publication type:

Article

Lack of association of the CIITA -168A→G promoter SNP with myasthenia gravis and its role in autoimmunity.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 147, doi. 10.1186/1471-2350-11-147

By:

Ramanujam, Ryan;
Yaofeng Zhao;
Pirskanen, Ritva;
Hammarström, Lennart

Publication type:

Article

Genetic investigations on 8 patients affected by ring 20 chromosome syndrome.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 146, doi. 10.1186/1471-2350-11-146

By:

Giardino, Daniela;
Vignoli, Aglaia;
Ballarati, Lucia;
Recalcati, Maria Paola;
Russo, Silvia;
Camporeale, Nicole;
Marchi, Margherita;
Finelli, Palma;
Accorsi, Patrizia;
Giordano, Lucio;
La Briola, Francesca;
Chiesa, Valentina;
Canevini, Maria Paola;
Larizza, Lidia

Publication type:

Article

Suggestive evidence of associations between liver X receptor β polymorphisms with type 2 diabetes mellitus and obesity in three cohort studies: HUNT2 (Norway), MONICA (France) and HELENA (Europe).

Published in:

BMC Medical Genetics, 2010, v. 11, p. 144, doi. 10.1186/1471-2350-11-144

By:

Solaas, Karianne;
Legry, Vanessa;
Retterstol, Kjetil;
Berg, Paul R.;
Holven, Kirsten B.;
Ferrières, Jean;
Amouyel, Philippe;
Lien, Sigbjorn;
Romeo, Javier;
Valtueña, Jara;
Widhalm, Kurt;
Ruiz, Jonatan R.;
Dallongeville, Jean;
Tonstad, Serena;
Rootwelt, Helge;
Halvorsen, Bente;
Nenseter, Marit S.;
Birkeland, Kare I.;
Thorsby, Per M.;
Meirhaeghe, Aline

Publication type:

Article

The non-syndromic familial thoracic aortic aneurysms and dissections maps to 15q21 locus.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 143, doi. 10.1186/1471-2350-11-143

By:

Keramati, Ali R.;
Sadeghpour, Anita;
Farahani, Maryam M.;
Chandok, Gurangad;
Mani, Arya

Publication type:

Article

Frameshift mutation hotspot identified in Smith-Magenis syndrome: case report and review of literature.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 142, doi. 10.1186/1471-2350-11-142

By:

Truong, Hoa T.;
Dudding, Tracy;
Blanchard, Christopher L.;
Elsea, Sarah H.

Publication type:

Article

Genes encoding critical transcriptional activators for murine neural tube development and human spina bifida: a case-control study.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 141, doi. 10.1186/1471-2350-11-141

By:

Wei Lu;
Guzman, Adrian R.;
Wei Yang;
Chapa, Claudia J.;
Shaw, Gary M.;
Greene, Robert M.;
Pisano, M. Michele;
Lammer, Edward J.;
Finnell, Richard H.;
Huiping Zhu

Publication type:

Article

The longitudinal association of common susceptibility variants for type 2 diabetes and obesity with fasting glucose level and BMI.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 140, doi. 10.1186/1471-2350-11-140

By:

Webster, Rebecca J.;
Warrington, Nicole M.;
Beilby, John P.;
Frayling, Timothy M.;
Palmer, Lyle J.

Publication type:

Article

A prevalent mutation with founder effect in Spanish Recessive Dystrophic Epidermolysis Bullosa families.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 139, doi. 10.1186/1471-2350-11-139

By:

Cuadrado-Corrales, Natividad;
Sánchez-Jimeno, Carolina;
García, Marta;
Escámez, María-José;
Illera, Nuria;
Hernández-Martín, Ángela;
Trujillo-Tiebas, María-José;
Ayuso, Carmen;
Del Rio, Marcela

Publication type:

Article

Association of CACNG6 polymorphisms with aspirin-intolerance asthmatics in a Korean population.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 138, doi. 10.1186/1471-2350-11-138

By:

Jin Sol Lee;
Jeong-Hyun Kim;
Joon Seol Bae;
Jason Yongha Kim;
Tae Joon Park;
Pasaje, Charisse Flerida;
Byung-Lae Park;
Hyun Sub Cheong;
Soo-Taek Uh;
Jong-Sook Park;
An-Soo Jang;
Mi-Kyeong Kim;
Choi, Inseon S.;
Choon-Sik Park;
Hyoung Doo Shin

Publication type:

Article

Novel association of severe neonatal encephalopathy and Hirschsprung disease in a male with a duplication at the Xq28 region.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 137, doi. 10.1186/1471-2350-11-137

By:

Fernández, Raquel M.;
Núñez-Torres, Rocío;
González-Meneses, Antonio;
Antiñolo, Guillermo;
Borrego, Salud

Publication type:

Article

Variant rs9939609 in the FTO gene is associated with body mass index among Chinese children.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 136, doi. 10.1186/1471-2350-11-136

By:

Hongyun Fang;
Yanping Li;
Songming Du;
Xiaoqi Hu;
Qian Zhang;
Ailing Liu;
Guansheng Ma

Publication type:

Article

Population-based study of genetic variation in individuals with autism spectrum disorders from Croatia.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 134, doi. 10.1186/1471-2350-11-134

By:

Li-San Wang;
Hranilovic, Dubravka;
Kai Wang;
Lindquist, Ingrid E.;
Yurcaba, Lindsay;
Petkovic, Zorana-Bujas;
Gidaya, Nicole;
Jernej, Branimir;
Hakonarson, Hakon;
Bucan, Maja

Publication type:

Article

Association of the eNOS E298D polymorphism and the risk of myocardial infarction in the Greek population.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 133, doi. 10.1186/1471-2350-11-133

By:

Dafni, Chaido;
Drakoulis, Nikolaos;
Landt, Olfert;
Panidis, Dimitris;
Reczko, Martin;
Cokkinos, Dennis V.

Publication type:

Article

Evaluating gene by sex and age interactions on cardiovascular risk factors in Brazilian families.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 132, doi. 10.1186/1471-2350-11-132

By:

Giolo, Suely R.;
Pereira, Alexandre C.;
deAndrade, Mariza;
Krieger, José E.;
Soler, Júlia P.

Publication type:

Article

A SRY-HMG box frame shift mutation inherited from a mosaic father with a mild form of testicular dysgenesis syndrome in Turner syndrome patient.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 131, doi. 10.1186/1471-2350-11-131

By:

Shahid, Mohammad;
Dhillon, Varinderpal S.;
Khalil, Hesham Saleh;
Haque, Shameemul;
Batra, Swaraj;
Husain, Syed Akhtar;
Looijenga, L. H. J.

Publication type:

Article

A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotypecorrelation.

Published in:

2010

By:

Abu-Amero, Khaled K.;
Hellani, Ali M.;
Salih, Mustafa A.;
Seidahmed, Mohammad Z.;
Elmalik, Tageldin S.;
Zidan, Ghassan;
Bosley, Thomas M.

Publication type:

Case Study

A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 130, doi. 10.1186/1471-2350-11-130

By:

Olsson, Malin;
Norgren, Nina;
Obayashi, Konen;
Plante-Bordeneuve, Violaine;
Suhr, Ole B.;
Cederquist, Kristina;
Jonasson, Jenni

Publication type:

Article

A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 129, doi. 10.1186/1471-2350-11-129

By:

Yan Bai;
Zhengmin Wang;
Wenjia Dai;
Qingzhong Li;
Guoling Chen;
Ning Cong;
Minxin Guan;
Huawei Li

Publication type:

Article

Important role of indels in somatic mutations of human cancer genes.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 128, doi. 10.1186/1471-2350-11-128

By:

Haiwang Yang;
Yan Zhong;
Cheng Peng;
Jian-Qun Chen;
Dacheng Tian

Publication type:

Article

E-selectin gene polymorphisms are associated with essential hypertension: a case-control pilot study in a Chinese population.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 127, doi. 10.1186/1471-2350-11-127

By:

Zuoguang Wang;
Ya Liu;
Jieling Liu;
Kuo Liu;
Yuqin Lou;
Jie Wen;
Qiuli Niu;
Shaojun Wen;
Zhaosu Wu

Publication type:

Article

SLC2A10 genetic polymorphism predicts development of peripheral arterial disease in patients with type 2 diabetes. SLC2A10 and PADin type 2 diabetes.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 126, doi. 10.1186/1471-2350-11-126

By:

Yi-Der Jiang;
Yi-Cheng Chang;
Yen-Feng Chiu;
Tien-Jyun Chang;
Hung-Yuan Li;
Wen-Hsing Lin;
Hsiang-Yu Yuan;
Yuan-Tsong Chen;
Lee-Ming Chuang

Publication type:

Article

Associations between genetic variations in theFURIN gene and hypertension.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 124, doi. 10.1186/1471-2350-11-124

By:

Nanfang Li;
Wenli Luo;
Zhang Juhong;
Jin Yang;
Hongmei Wang;
Ling Zhou;
Jianhang Chang

Publication type:

Article

Obesity and diabetes genes are associated with being born small for gestational age: Results from the Auckland Birthweight Collaborative study.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 125, doi. 10.1186/1471-2350-11-125

By:

Morgan, Angharad R.;
Thompson, John M. D.;
Murphy, Rinki;
Black, Peter N.;
Wen-Jiun Lam;
Ferguson, Lynnette R.;
Mitchell, Ed A.

Publication type:

Article

Genome wide screen identifies microsatellite markers associated with acute adverse effects following radiotherapy in cancer patients.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 123, doi. 10.1186/1471-2350-11-123

By:

Michikawa, Yuichi;
Suga, Tomo;
Ishikawa, Atsuko;
Hayashi, Hideki;
Oka, Akira;
Inoko, Hidetoshi;
Iwakawa, Mayumi;
Imai, Takashi

Publication type:

Article