Rieko Matsuoka, Ph.D. - Publications

Affiliations: 
2006 Temple University, Philadelphia, PA, United States 
Area:
community ecology, macroecology

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Year Citation  Score
2018 Matsushita Y, Furutani Y, Matsuoka R, Furukawa T. Hot water extract of Agaricus blazei Murrill specifically inhibits growth and induces apoptosis in human pancreatic cancer cells. Bmc Complementary and Alternative Medicine. 18: 319. PMID 30514293 DOI: 10.1186/s12906-018-2385-4  0.36
2016 Chida A, Inai K, Sato H, Shimada E, Nishizawa T, Shimada M, Furutani M, Furutani Y, Kawamura Y, Sugimoto M, Ishihara J, Fujiwara M, Soga T, Kawana M, Fuji S, ... ... Matsuoka R, et al. Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy. Heart and Vessels. PMID 27885498 DOI: 10.1007/s00380-016-0920-0  0.4
2016 Izumi G, Hayama E, Yamazawa H, Inai K, Shimada M, Furutani M, Nishizawa T, Furutani Y, Matsuoka R, Nakanishi T. Compound Mutations Cause Increased Cardiac Events in Children with Long QT Syndrome: Can the Sequence Homology-Based Tools be Applied for Prediction of Phenotypic Severity? Pediatric Cardiology. 1-9. DOI: 10.1007/s00246-016-1378-7  0.4
2015 Takeuchi D, Furutani M, Harada Y, Furutani Y, Inai K, Nakanishi T, Matsuoka R. High prevalence of cardiovascular risk factors in children and adolescents with Williams-Beuren syndrome. Bmc Pediatrics. 15: 126. PMID 26384008 DOI: 10.1186/s12887-015-0445-1  0.4
2014 Dhandapany PS, Razzaque MA, Muthusami U, Kunnoth S, Edwards JJ, Mulero-Navarro S, Riess I, Pardo S, Sheng J, Rani DS, Rani B, Govindaraj P, Flex E, Yokota T, Furutani M, ... ... Matsuoka R, et al. RAF1 mutations in childhood-onset dilated cardiomyopathy. Nature Genetics. 46: 635-9. PMID 24777450 DOI: 10.1038/ng.2963  0.4
2014 Yoshimura K, Kitagawa H, Fujiki R, Tanabe M, Takezawa S, Takada I, Yamaoka I, Yonezawa M, Kondo T, Furutani Y, Yagi H, Yoshinaga S, Masuda T, Fukuda T, Yamamoto Y, ... ... Matsuoka R, et al. Retraction for Yoshimura et al., Distinct function of 2 chromatin remodeling complexes that share a common subunit, Williams syndrome transcription factor (WSTF). Proceedings of the National Academy of Sciences of the United States of America. 111: 2398. PMID 24449918 DOI: 10.1073/pnas.1323397111  0.4
2014 Chida A, Sato H, Shintani M, Nakayama T, Kawamura Y, Furutani Y, Inai K, Saji T, Matsuoka R, Nonoyama S, Nakanishi T. Soluble ST2 and N-terminal pro-brain natriuretic peptide combination. Useful biomarker for predicting outcome of childhoodpulmonary arterial hypertension. Circulation Journal : Official Journal of the Japanese Circulation Society. 78: 436-42. PMID 24304538 DOI: DN/JST.JSTAGE/circj/CJ-13-1033  0.4
2013 Fujita E, Nakanishi T, Nishizawa T, Hagiwara N, Matsuoka R. Mutations in the cardiac troponin T gene show various prognoses in Japanese patients with hypertrophic cardiomyopathy. Heart and Vessels. 28: 785-94. PMID 23494605 DOI: 10.1007/s00380-013-0332-3  0.4
2013 Dong S, Furutani Y, Kimura S, Zhu Y, Kawabata K, Furutani M, Nishikawa T, Tanaka T, Masaki T, Matsuoka R, Kiyama R. Brefeldin A is an estrogenic, Erk1/2-activating component in the extract of Agaricus blazei mycelia. Journal of Agricultural and Food Chemistry. 61: 128-36. PMID 23215459 DOI: 10.1021/jf304546a  0.4
2013 Sakata M, Yücel Z, Shinozawa K, Hagita N, Imai M, Furutani M, Matsuoka R. An inference engine for estimating outside states of clinical test items Acm Transactions On Management Information Systems. 4. DOI: 10.1145/2517084  0.4
2012 Yee KK, Yagi H, Matsuoka R, Nakanishi T, Furukawa T. Transrepression activity of T-box1 in a gene regulation network in mouse cells. Gene. 510: 162-70. PMID 22982415 DOI: 10.1016/j.gene.2012.09.017  0.4
2012 Chida A, Shintani M, Yagi H, Fujiwara M, Kojima Y, Sato H, Imamura S, Yokozawa M, Onodera N, Horigome H, Kobayashi T, Hatai Y, Nakayama T, Fukushima H, Nishiyama M, ... ... Matsuoka R, et al. Outcomes of childhood pulmonary arterial hypertension in BMPR2 and ALK1 mutation carriers. The American Journal of Cardiology. 110: 586-93. PMID 22632830 DOI: 10.1016/j.amjcard.2012.04.035  0.4
2012 Takagaki Y, Yamagishi H, Matsuoka R. Factors involved in signal transduction during vertebrate myogenesis. International Review of Cell and Molecular Biology. 296: 187-272. PMID 22559940 DOI: 10.1016/B978-0-12-394307-1.00004-7  0.4
2012 Kodo K, Nishizawa T, Furutani M, Arai S, Ishihara K, Oda M, Makino S, Fukuda K, Takahashi T, Matsuoka R, Nakanishi T, Yamagishi H. Genetic analysis of essential cardiac transcription factors in 256 patients with non-syndromic congenital heart defects. Circulation Journal : Official Journal of the Japanese Circulation Society. 76: 1703-11. PMID 22498567 DOI: JST.JSTAGE/circj/CJ-11-1389  0.4
2012 Razzaque MA, Komoike Y, Nishizawa T, Inai K, Furutani M, Higashinakagawa T, Matsuoka R. Characterization of a novel KRAS mutation identified in Noonan syndrome. American Journal of Medical Genetics. Part A. 158: 524-32. PMID 22302539 DOI: 10.1002/ajmg.a.34419  0.4
2012 Dong S, Furutani Y, Suto Y, Furutani M, Zhu Y, Yoneyama M, Kato T, Itabe H, Nishikawa T, Tomimatsu H, Tanaka T, Kasanuki H, Masaki T, Kiyama R, Matsuoka R. Estrogen-like activity and dual roles in cell signaling of an Agaricus blazei Murrill mycelia-dikaryon extract. Microbiological Research. 167: 231-7. PMID 22015258 DOI: 10.1016/j.micres.2011.09.003  0.4
2011 Maeda J, Yamagishi H, Furutani Y, Kamisago M, Waragai T, Oana S, Kajino H, Matsuura H, Mori K, Matsuoka R, Nakanishi T. The impact of cardiac surgery in patients with trisomy 18 and trisomy 13 in Japan. American Journal of Medical Genetics. Part A. 155: 2641-6. PMID 21990245 DOI: 10.1002/ajmg.a.34285  0.4
2011 Tsutsumi Y, Kosaki R, Itoh Y, Tsukamoto K, Matsuoka R, Shintani M, Nosaka S, Masaki H, Iizuka Y. Vein of Galen aneurysmal malformation associated with an endoglin gene mutation. Pediatrics. 128: e1307-10. PMID 21987708 DOI: 10.1542/peds.2010-0961  0.4
2011 Hayakawa EH, Furutani M, Matsuoka R, Takakuwa Y. Comparison of protein behavior between wild-type and G601S hERG in living cells by fluorescence correlation spectroscopy. The Journal of Physiological Sciences : Jps. 61: 313-9. PMID 21573751 DOI: 10.1007/s12576-011-0150-2  0.4
2011 Yamada O, Ozaki K, Furukawa T, Machida M, Wang YH, Motoji T, Mitsuishi T, Akiyama M, Yamada H, Kawauchi K, Matsuoka R. Activation of STAT5 confers imatinib resistance on leukemic cells through the transcription of TERT and MDR1. Cellular Signalling. 23: 1119-27. PMID 21356308 DOI: 10.1016/j.cellsig.2011.02.005  0.4
2011 Unuma K, Harada K, Furutani M, Furutani Y, Nakajima M, Nakanishi T, Matsuoka R, Yoshida K. Multiple stenotic arteriopathy in a 72-year-old female with Williams syndrome. Journal of Clinical Pathology. 64: 368-70. PMID 21212057 DOI: 10.1136/jcp.2010.085803  0.4
2011 Okubo T, Kawamura A, Takahashi J, Yagi H, Morishima M, Matsuoka R, Takada S. Ripply3, a Tbx1 repressor, is required for development of the pharyngeal apparatus and its derivatives in mice. Development (Cambridge, England). 138: 339-48. PMID 21177346 DOI: 10.1242/dev.054056  0.4
2011 Chang B, Nishizawa T, Furutani M, Fujiki A, Tani M, Kawaguchi M, Ibuki K, Hirono K, Taneichi H, Uese K, Onuma Y, Bowles NE, Ichida F, Inoue H, Matsuoka R, et al. Identification of a novel TPM1 mutation in a family with left ventricular noncompaction and sudden death. Molecular Genetics and Metabolism. 102: 200-6. PMID 20965760 DOI: 10.1016/j.ymgme.2010.09.009  0.4
2011 Machida M, Takagaki Y, Matsuoka R, Kawaguchi N. Proteomic comparison of spherical aggregates and adherent cells of cardiac stem cells. International Journal of Cardiology. 153: 296-305. PMID 20864193 DOI: 10.1016/j.ijcard.2010.08.049  0.4
2011 Nakanishi T, Sun F, Momma K, Matsuoka R. Dilatation of the rat ductus arteriosus by nicorandil Therapeutic Research. 32: 273.  0.4
2010 Kawaguchi N, Smith AJ, Waring CD, Hasan MK, Miyamoto S, Matsuoka R, Ellison GM. c-kitpos GATA-4 high rat cardiac stem cells foster adult cardiomyocyte survival through IGF-1 paracrine signalling. Plos One. 5: e14297. PMID 21179204 DOI: 10.1371/journal.pone.0014297  0.4
2010 Yamada O, Ozaki K, Nakatake M, Kakiuchi Y, Akiyama M, Mitsuishi T, Kawauchi K, Matsuoka R. Akt and PKC are involved not only in upregulation of telomerase activity but also in cell differentiation-related function via mTORC2 in leukemia cells. Histochemistry and Cell Biology. 134: 555-63. PMID 21086135 DOI: 10.1007/s00418-010-0764-0  0.4
2010 Sun F, Hayama E, Katsube Y, Matsuoka R, Nakanishi T. The role of the large-conductance voltage-dependent and calcium-activated potassium (BK(Ca)) channels in the regulation of rat ductus arteriosus tone. Heart and Vessels. 25: 556-64. PMID 20936291 DOI: 10.1007/s00380-010-0008-1  0.4
2010 Ri G, Ohno S, Furutani M, Furutani Y, Tsukahara T, Hagita N, Haruyama H, Nakamura S, Yamamoto T, Matsuoka R. An indication for correlation between the serum ADA level and gastric cancer risk. Anticancer Research. 30: 2347-9. PMID 20651391  0.4
2010 Kawaguchi N, Nakao R, Yamaguchi M, Ogawa D, Matsuoka R. TGF-beta superfamily regulates a switch that mediates differentiation either into adipocytes or myocytes in left atrium derived pluripotent cells (LA-PCS). Biochemical and Biophysical Research Communications. 396: 619-25. PMID 20420809 DOI: 10.1016/j.bbrc.2010.04.123  0.4
2010 Kamrul Hasan M, Komoike Y, Tsunesumi S, Nakao R, Nagao H, Matsuoka R, Kawaguchi N. Myogenic differentiation in atrium-derived adult cardiac pluripotent cells and the transcriptional regulation of GATA4 and myogenin on ANP promoter. Genes to Cells : Devoted to Molecular & Cellular Mechanisms. 15: 439-54. PMID 20384792 DOI: 10.1111/j.1365-2443.2010.01394.x  0.4
2010 Hosseinkhani H, Hosseinkhani M, Hattori S, Matsuoka R, Kawaguchi N. Micro and nano-scale in vitro 3D culture system for cardiac stem cells. Journal of Biomedical Materials Research. Part A. 94: 1-8. PMID 20014298 DOI: 10.1002/jbm.a.32676  0.4
2010 Miyamoto S, Kawaguchi N, Ellison GM, Matsuoka R, Shin'Oka T, Kurosawa H. Characterization of long-term cultured c-kit+ cardiac stem cells derived from adult rat hearts Stem Cells and Development. 19: 105-116. PMID 19580375 DOI: 10.1089/scd.2009.0041  0.4
2010 Abe A, Hagita N, Furutani M, Furutani Y, Matsuoka R. An interface for medical diagnosis support: From the viewpoint of chance discovery International Journal of Advanced Intelligence Paradigms. 2: 283-302. DOI: 10.1504/IJAIP.2010.030540  0.4
2010 Mori M, Tsukahara T, Shinozawa K, Hagita N, Furutani M, Furutani Y, Matsuoka R. Medical diagnosis support system for disease prevention and its interface 2010 4th International Conference On Bioinformatics and Biomedical Engineering, Icbbe 2010. DOI: 10.1109/ICBBE.2010.5515539  0.4
2010 Abe A, Hagita N, Furutani M, Furutani Y, Matsuoka R. Categorized and integrated data mining of medical data from the viewpoint of chance discovery Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 6278: 307-314. DOI: 10.1007/978-3-642-15393-8_35  0.4
2009 Ri G, Ohno S, Yamamoto T, Ito E, Furutani M, Furutani Y, Umeda Y, Tsukahara T, Hagita N, Matsuoka R. Serum levels of CA15-3, KL-6 and BCA225 are positively correlated with each other in the general population Anticancer Research. 29: 4239-4242. PMID 19846980  0.4
2009 Tang S, Hoshida H, Kamisago M, Yagi H, Momma K, Matsuoka R. Phenotype-genotype correlation in a patient with co-occurrence of Marfan and LEOPARD syndromes American Journal of Medical Genetics, Part A. 149: 2216-2219. PMID 19725129 DOI: 10.1002/ajmg.a.32735  0.4
2009 Kodo K, Nishizawa T, Furutani M, Arai S, Yamamura E, Joo K, Takahashi T, Matsuoka R, Yamagishi H. GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling. Proceedings of the National Academy of Sciences of the United States of America. 106: 13933-8. PMID 19666519 DOI: 10.1073/pnas.0904744106  0.4
2009 Yoshimura K, Kitagawa H, Fujiki R, Tanabe M, Takezawa S, Takada I, Yamaoka I, Yonezawa M, Kondo T, Furutani Y, Yagi H, Yoshinaga S, Masuda T, Fukuda T, Yamamoto Y, ... ... Matsuoka R, et al. Distinct function of 2 chromatin remodeling complexes that share a common subunit, Williams syndrome transcription factor (WSTF). Proceedings of the National Academy of Sciences of the United States of America. 106: 9280-5. PMID 19470456 DOI: 10.1073/pnas.0901184106  0.4
2009 Shintani M, Yagi H, Nakayama T, Saji T, Matsuoka R. A new nonsense mutation of SMAD8 associated with pulmonary arterial hypertension. Journal of Medical Genetics. 46: 331-7. PMID 19211612 DOI: 10.1136/jmg.2008.062703  0.4
2009 Iwasaki Y, Horigome H, Takahashi-Igari M, Kato Y, Razzaque AM, Matsuoka R. Coronary artery dilatation in LEOPARD syndrome. A child case and literature review Congenital Heart Disease. 4: 38-41. PMID 19207402 DOI: 10.1111/j.1747-0803.2008.00243.x  0.4
2009 Shinozawa K, Hagita N, Furutani M, Matsuoka R. A data mining method for finding hidden relationship in blood and urine examination items for health check Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 5633: 44-50. DOI: 10.1007/978-3-642-03067-3_5  0.4
2008 Fujiwara M, Yagi H, Matsuoka R, Saji T. Analysis of genetic mutation and modifier genes in pulmonary arterial hypertension Nippon Rinsho. Japanese Journal of Clinical Medicine. 66: 2071-2075. PMID 19051722  0.4
2008 Yamamoto T, Dowa Y, Ueda H, Kawataki M, Asou T, Sasaki Y, Harada N, Matsumoto N, Matsuoka R, Kurosawa K. Tetralogy of Fallot associated with pulmonary atresia and major aortopulmonary collateral arteries in a patient with interstitial deletion of 16q21-q22.1 American Journal of Medical Genetics, Part A. 146: 1575-1580. PMID 18470894 DOI: 10.1002/ajmg.a.32204  0.4
2008 Páez MT, Yamamoto T, Hayashi KI, Yasuda T, Harada N, Matsumoto N, Kurosawa K, Furutani Y, Asakawa S, Shimizu N, Matsuoka R. Two patients with atypical interstitial deletions of 8p23.1: Mapping of phenotypical traits American Journal of Medical Genetics, Part A. 146: 1158-1165. PMID 18393291 DOI: 10.1002/ajmg.a.32205  0.4
2008 Yamada O, Ozaki K, Nakatake M, Akiyama M, Kawauchi K, Matsuoka R. Multistep regulation of telomerase during differentiation of HL60 cells Journal of Leukocyte Biology. 83: 1240-1248. PMID 18276798 DOI: 10.1189/jlb.1207848  0.4
2008 Fujiwara M, Yagi H, Matsuoka R, Akimoto K, Furutani M, Imamura SI, Uehara R, Nakayama T, Takao A, Nakazawa M, Saji T. Implications of mutations of activin receptor-like kinase 1 gene (ALK1) in addition to bone morphogenetic protein receptor II gene (BMPR2) in children with pulmonary arterial hypertension Circulation Journal. 72: 127-133. PMID 18159113 DOI: 10.1253/circj.72.127  0.4
2008 Abe A, Hagita N, Furutani M, Furutani Y, Matsuoka R. Exceptions as chance for computational chance discovery Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 5178: 750-757. DOI: 10.1007/978-3-540-85565-1-93  0.4
2008 Abe A, Hagita N, Furutani M, Furutani Y, Matsuoka R. Data mining of multi-categorized data Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 4944: 182-195. DOI: 10.1007/978-3-540-68416-9_15  0.4
2007 Matsuoka R. GATA4 mutation and congenital cardiovascular diseases: Importance of phenotype and genetic background clarification Journal of Molecular and Cellular Cardiology. 43: 667-669. PMID 17961590 DOI: 10.1016/j.yjmcc.2007.08.017  0.4
2007 Razzaque MA, Nishizawa T, Komoike Y, Yagi H, Furutani M, Amo R, Kamisago M, Momma K, Katayama H, Nakagawa M, Fujiwara Y, Matsushima M, Mizuno K, Tokuyama M, Hirota H, ... ... Matsuoka R, et al. Germline gain-of-function mutations in RAF1 cause Noonan syndrome Nature Genetics. 39: 1013-1017. PMID 17603482 DOI: 10.1038/ng2078  0.4
2007 Matsushita Y, Furukawa T, Kasanuki H, Nishibatake M, Kurihara Y, Ikeda A, Kamatani N, Takeshima H, Matsuoka R. Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathy Journal of Human Genetics. 52: 543-548. PMID 17476457 DOI: 10.1007/s10038-007-0149-y  0.4
2007 Wu C, Hayama E, Imamura SI, Matsuoka R, Nakanishi T. Developmental changes in the expression of voltage-gated potassium channels in the ductus arteriosus of the fetal rat Heart and Vessels. 22: 34-40. PMID 17285444 DOI: 10.1007/s00380-006-0926-0  0.4
2007 Abe A, Hagita N, Furutani M, Furutani Y, Matsuoka R. Possibility of integrated data mining of clinical data Data Science Journal. 6: S104-S115. DOI: 10.2481/dsj.6.S104  0.4
2007 Fujiwara M, Saji T, Nakayama T, Akimoto K, Furutani M, Imamura S, Takao A, Nakazawa M, Matsuoka R. Mutation Analysis of BMPR2 and other Genes in Japanese Patients with Pediatric Primary Pulmonary Hypertension Cardiovascular Development and Congenital Malformations: Molecular & Genetic Mechanisms. 282-284. DOI: 10.1002/9780470988664.ch69  0.4
2007 Momiyama Y, Furutani M, Suzuki Y, Imamura S, Hosokawa K, Atsumi Y, Matsuoka K, Kimura M, Kasanuki H, Ohsuzu F, Matsuoka R. Mitochondrial 16189 DNA Variant and left Ventricular Hypertrophy in Diabetes Mellitus Cardiovascular Development and Congenital Malformations: Molecular & Genetic Mechanisms. 279-281. DOI: 10.1002/9780470988664.ch68  0.4
2007 Kamisago M, Hirayama-Yamada K, Kato T, Imamura S, Joo K, Ando M, Takao A, Momma K, Nakazawa M, Matsuoka R. Novel Gene Mutations in Patients with Left Ventricular Noncompaction and Evidence for Genetic Heterogeneity Cardiovascular Development and Congenital Malformations: Molecular & Genetic Mechanisms. 277-278. DOI: 10.1002/9780470988664.ch67  0.4
2007 Matsuoka R. T-Box Gene Family and Congenital Cardiovascular Anomalies Cardiovascular Development and Congenital Malformations: Molecular & Genetic Mechanisms. 235-237. DOI: 10.1002/9780470988664.ch58  0.4
2007 Minamisawa S, Matsuoka R. Sarcolipin, a Novel Regulator of Calcium Cycling, is Preferentially Expressed in the Murine and Human Atrium Cardiovascular Development and Congenital Malformations: Molecular & Genetic Mechanisms. 196-198. DOI: 10.1002/9780470988664.ch49  0.4
2006 Hayama E, Imamura SI, Wu C, Nakazawa M, Matsuoka R, Nakanishi T. Analysis of voltage-gated potassium channel β1 subunits in the porcine neonatal ductus arteriosus Pediatric Research. 59: 167-174. DOI: 10.1203/01.pdr.0000196736.89742.c1  0.4
2005 Matsuoka R. Mutations of transcription factors in human with heart disease for understanding the development and mechanisms of congenital cardiovascular heart disease Advances in Experimental Medicine and Biology. 565: 349-357. PMID 16106988  0.4
2005 Hirayama-Yamada K, Kamisago M, Akimoto K, Aotsuka H, Nakamura Y, Tomita H, Furutani M, Imamura SI, Takao A, Nakazawa M, Matsuoka R. Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect American Journal of Medical Genetics. 135: 47-52. PMID 15810002 DOI: 10.1002/ajmg.a.30684  0.4
2005 Bassuk AG, Craig D, Jalali A, Mukhopadhyay A, Kim F, Charrow J, Gulbu U, Epstein LG, Bowman R, McLone D, Yagi H, Matsuoka R, Stephan DA, Kessler JA. The genetics of tethered cord syndrome. American Journal of Medical Genetics. Part A. 132: 450-3. PMID 15558749 DOI: 10.1002/ajmg.a.30439  0.4
2004 Minamisawa S, Oshikawa J, Takeshima H, Hoshijima M, Wang Y, Chien KR, Ishikawa Y, Matsuoka R. Junctophilin type 2 is associated with caveolin-3 and is down-regulated in the hypertrophic and dilated cardiomyopathies Biochemical and Biophysical Research Communications. 325: 852-856. PMID 15541368 DOI: 10.1016/j.bbrc.2004.10.107  0.4
2004 Tatsuguchi M, Hiratsuka E, Machida S, Nishikawa T, Imamura S, Shimizu S, Nishimura M, Komuro I, Furutani Y, Furutani M, Nagao H, Komatsu K, Kasanuki H, Matsuoka R. Swimming exercise in infancy has beneficial effect on the hearts in cardiomyopathic Syrian hamsters. Journal of Muscle Research and Cell Motility. 25: 69-76. PMID 15160490 DOI: 10.1023/B:JURE.0000021353.82449.9e  0.4
2004 Matsuoka R. Study of the vertebrate MHC multigene family during heart development Advances in Experimental Medicine and Biology. 538: 17-30. PMID 15098651  0.4
2004 Chen CS, Matsuoka R, Arai S, Momiyama Y, Murakami H, Kuno SY, Ishikawa K, Nakada K, Tawata M, Hayashi JI. Determination of Normal Ranges of Mitochondrial Respiratory Activities by mtDNA Transfer from 54 Human Subjects to mtDNA-less HeLa Cells for Identification of the Pathogenicities of Mutated mtDNAs Journal of Biochemistry. 135: 237-243. PMID 15047726 DOI: 10.1093/jb/mvh028  0.4
2003 Momiyama Y, Furutani M, Suzuki Y, Ohmori R, Imamura SI, Mokubo A, Asahina T, Murata C, Kato K, Anazawa S, Hosokawa K, Atsumi Y, Matsuoka K, Kimura M, Kasanuki H, ... ... Matsuoka R, et al. A mitochondrial DNA variant associated with left ventricular hypertrophy in diabetes Biochemical and Biophysical Research Communications. 312: 858-864. PMID 14680844 DOI: 10.1016/j.bbrc.2003.10.195  0.4
2003 Minamisawa S, Hiratsuka E, Ruiz-Lozano P, Machida S, Furutani Y, Nishimura M, Takao A, Yanagisawa K, Momma K, Saeki Y, Matsuoka R. Ectopic expression of an embryonic skeletal myosin heavy chain in human fetal and Syrian hamster hearts Journal of Muscle Research and Cell Motility. 24: 399-406. PMID 14677642 DOI: 10.1023/A:1027302924443  0.4
2003 Yagi H, Furutani Y, Hamada H, Sasaki T, Asakawa S, Minoshima S, Ichida F, Joo K, Kimura M, Imamura S, Kamatani N, Momma K, Takao A, Nakazawa M, Shimizu N, ... Matsuoka R, et al. Role of TBX1 in human del22q11.2 syndrome. Lancet. 362: 1366-73. PMID 14585638 DOI: 10.1016/S0140-6736(03)14632-6  0.4
2003 Hirota H, Matsuoka R, Chen XN, Salandanan LS, Lincoln A, Rose FE, Sunahara M, Osawa M, Bellugi U, Korenberg JR. Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 5: 311-21. PMID 12865760 DOI: 10.1097/01.GIM.0000076975.10224.67  0.4
2003 Garg V, Kathiriya IS, Barnes R, Schluterman MK, King IN, Butler CA, Rothrock CR, Eapen RS, Hirayama-Yamada K, Joo K, Matsuoka R, Cohen JC, Srivastava D. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature. 424: 443-7. PMID 12845333 DOI: 10.1038/nature01827  0.4
2003 Minamisawa S, Sato Y, Tatsuguchi Y, Fujino T, Imamura SI, Uetsuka Y, Nakazawa M, Matsuoka R. Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy Biochemical and Biophysical Research Communications. 304: 1-4. PMID 12705874 DOI: 10.1016/S0006-291X(03)00526-6  0.4
2003 Hidai C, Masako O, Ikeda H, Nagashima H, Matsuoka R, Quertermous T, Kasanuki H, Kokubun S, Kawana M. FGF-1 enhanced cardiogenesis in differentiating embryonal carcinoma cell cultures, which was opposite to the effect of FGF-2 Journal of Molecular and Cellular Cardiology. 35: 421-425. PMID 12689822 DOI: 10.1016/S0022-2828(03)00019-1  0.4
2003 Tatsuguchi M, Furutani M, Hinagata J, Tanaka T, Furutani Y, Imamura S, Kawana M, Masaki T, Kasanuki H, Sawamura T, Matsuoka R. Oxidized LDL receptor gene (OLR1) is associated with the risk of myocardial infarction. Biochemical and Biophysical Research Communications. 303: 247-50. PMID 12646194 DOI: 10.1016/S0006-291X(03)00326-7  0.4
2003 Minamisawa S, Wang Y, Chen J, Ishikawa Y, Chien KR, Matsuoka R. Atrial chamber-specific expression of sarcolipin is regulated during development and hypertrophic remodeling Journal of Biological Chemistry. 278: 9570-9575. PMID 12645548 DOI: 10.1074/jbc.M213132200  0.4
2003 Kato T, Kosaka K, Kimura M, Imamura SI, Yamada O, Iwai K, Ando M, Joh-o K, Kuroe K, Ohtake A, Takao A, Momma K, Matsuoka R. Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-β Genetics in Medicine. 5: 113-119. PMID 12644781 DOI: 10.1097/01.GIM.0000056828.03164.30  0.4
2003 Miura M, Yamagishi H, Morikawa Y, Matsuoka R. Congenital long QT syndrome and 2:1 atrioventricular block with a mutation of the SCN5A gene Pediatric Cardiology. 24: 70-72. PMID 12574983 DOI: 10.1007/s00246-002-0169-5  0.4
2002 Machida S, Noda S, Takao A, Nakazawa M, Matsuoka R. Expression of slow skeletal myosin heavy chain 2 gene in Purkinje fiber cells in chick heart Biology of the Cell. 94: 389-399. PMID 12500945 DOI: 10.1016/S0248-4900(02)00010-2  0.4
2002 Nakanishi K, Nakata Y, Kanazawa F, Imamura SI, Matsuoka R, Osada H, Kawai T, Uenoyama M, Aurues T, Ikeda T. Changes in myosin heavy chain and its localization in rat heart in association with hypobaric hypoxia-induced pulmonary hypertension Journal of Pathology. 197: 380-387. PMID 12115885 DOI: 10.1002/path.1132  0.4
2002 Matsuoka R, Kasanuki H. Diabetes. deafness .conduction abnormality. cardiomyopathy Nippon Rinsho. Japanese Journal of Clinical Medicine. 60: 662-666. PMID 12013968  0.4
2001 Natarajan A, Yamagishi H, Ahmad F, Li D, Roberts R, Matsuoka R, Hill S, Srivastava D. Human eHAND, but not dHAND, is down-regulated in cardiomyopathies Journal of Molecular and Cellular Cardiology. 33: 1607-1614. PMID 11549340 DOI: 10.1006/jmcc.2001.1434  0.4
2001 Momma K, Takao A, Matsuoka R, Imai Y, Muto A, Osawa M, Takayama M. Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 3: 56-60. PMID 11339379  0.4
2001 Ogita T, Hashimoto E, Yamasaki M, Nakaoka T, Matsuoka R, Kira Y, Fujita T. Hypoxic induction of adrenomedullin in cultured human umbilical vein endothelial cells Journal of Hypertension. 19: 603-608. PMID 11327636 DOI: 10.1097/00004872-200103001-00013  0.4
2001 Aomi Y, Chen CS, Nakada K, Ito S, Isobe K, Murakami H, Kuno SY, Tawata M, Matsuoka R, Mizusawa H, Hayashi JI. Cytoplasmic transfer of platelet mtDNA from elderly patients with Parkinson's disease to mtDNA-less HeLa cells restores complete mitochondrial respiratory function Biochemical and Biophysical Research Communications. 280: 265-273. PMID 11162509 DOI: 10.1006/bbrc.2000.4113  0.4
2000 Korenberg JR, Chen XN, Hirota H, Lai Z, Bellugi U, Burian D, Roe B, Matsuoka R. VI. Genome structure and cognitive map of Williams syndrome. Journal of Cognitive Neuroscience. 12: 89-107. PMID 10953236  0.4
2000 Ohta H, Tokimasa S, Zou Z, Funaki S, Kurahashi H, Takahashi Y, Kimura M, Matsuoka R, Horie M, Hara J, Shimada K, Takihara Y. Structure and chromosomal localization of the RAE28/HPH1 gene, a human homologue of the polyhomeotic gene. Dna Sequence : the Journal of Dna Sequencing and Mapping. 11: 61-73. PMID 10902910 DOI: 10.3109/10425170009033970  0.4
2000 Maeda J, Yamagishi H, Matsuoka R, Ishihara J, Tokumura M, Fukushima H, Ueda H, Takahashi E, Yoshiba S, Kojima Y. Frequent association of 22q11.2 deletion with tetralogy of Fallot American Journal of Medical Genetics. 92: 269-272. PMID 10842294 DOI: 10.1002/(SICI)1096-8628(20000605)92:4<269::AID-AJMG9>3.0.CO;2-L  0.4
2000 Iida A, Emi M, Matsuoka R, Hiratsuka E, Okui K, Ohashi H, Inazawa J, Fukushima Y, Imai T, Nakamura Y. Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient with left-right axis malformation Human Genetics. 106: 277-287. PMID 10798355 DOI: 10.1007/s004390051038  0.4
2000 Machida S, Noda S, Furutani Y, Takao A, Momma K, Matsuoka R. Complete sequence and characterization of chick ventricular myosin heavy chain in the developing atria Biochimica Et Biophysica Acta - Gene Structure and Expression. 1490: 333-341. PMID 10684978 DOI: 10.1016/S0167-4781(99)00247-X  0.4
2000 Machida S, Matsuoka R, Noda S, Hiratsuka E, Takagaki Y, Oana S, Furutani Y, Nakajima H, Takao A, Momma K. Evidence for the expression of neonatal skeletal myosin heavy chain in primary myocardium and cardiac conduction tissue in the developing chick heart Developmental Dynamics. 217: 37-49. PMID 10679928 DOI: 10.1002/(SICI)1097-0177(200001)217:1<37::AID-DVDY4>3.0.CO;2-3  0.4
2000 Imamura SI, Nishikawa T, Hiratsuka E, Takao A, Matsuoka R. Behavior of smooth muscle cells during arterial ductal closure at birth Journal of Histochemistry and Cytochemistry. 48: 35-44. PMID 10653584  0.4
1999 Kamisago M, Kimura M, Furutani Y, Furutani M, Takao A, Momma K, Matsuoka R. Assignment of human desert hedgehog gene (DHH) to chromosome band 12q13.1 by in situ hybridization Cytogenetics and Cell Genetics. 87: 117-118. PMID 10640830  0.4
1999 Hachida M, Lu H, Zhang X, Saito S, Furutani Y, Matsuoka R, Hoshi H, Koyanagi H. Inhibitory effect of triptolide on platelet derived growth factor-A and coronary arteriosclerosis after heart transplantation Transplantation Proceedings. 31: 2719-2723. PMID 10578264 DOI: 10.1016/S0041-1345(99)00539-4  0.4
1999 Sugama S, Namihira T, Matsuoka R, Taira N, Eto Y, Maekawa K. Psychiatric inpatients and chromosome deletions within 22q11.2 Journal of Neurology Neurosurgery and Psychiatry. 67: 803-806. PMID 10567504  0.4
1999 Momma K, Ando M, Matsuoka R, Joo K. Interruption of the aortic arch associated with deletion of chromosome 22q11 is associated with a subarterial and doubly committed ventricular septal defect in Japanese patients Cardiology in the Young. 9: 463-467. PMID 10535824  0.4
1999 Sakurai H, Imamura SI, Furutani Y, Takao A, Momma K, Matsuoka R. Unique Expression Patterns of Myosin Heavy Chain Genes in the Ductus Arteriosus and Uterus of Rabbits Journal of Veterinary Medical Science. 61: 1049-1054. PMID 10535512  0.4
1999 Furutani M, Trudeau MC, Hagiwara N, Seki A, Gong Q, Zhou Z, Imamura S, Nagashima H, Kasanuki H, Takao A, Momma K, January CT, Robertson GA, Matsuoka R. Novel mechanism associated with an inherited cardiac arrhythmia: defective protein trafficking by the mutant HERG (G601S) potassium channel. Circulation. 99: 2290-4. PMID 10226095  0.4
1996 Matsuoka R, Sawamura T, Yamada K, Yoshida M, Furutani Y, Ikura T, Shiraki T, Hoshikawa H, Shimada K, Tanzawa K, Masaki T. Human endothelin converting enzyme gene (ECE1) mapped to chromosomal region 1p36.1. Cytogenetics and Cell Genetics. 72: 322-4. PMID 8641140 DOI: 10.1159/000134214  0.36
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