The -974C>A (rs3087459) gene polymorphism in the endothelin gene (EDN1) is associated with risk of developing acute coronary syndrome in Mexican patients (English)
- New search for: Vargas-Alarcon, G.
- New search for: Vallejo, M.
- New search for: Posadas-Romero, C.
- New search for: Juarez-Rojas, J. G.
- New search for: Martinez-Rios, M. A.
- New search for: Pena-Duque, M. A.
- New search for: Carrillo-Sanchez, S.
- New search for: Perez-Mendez, O.
- New search for: Fragoso, J. M.
- New search for: Vargas-Alarcon, G.
- New search for: Vallejo, M.
- New search for: Posadas-Romero, C.
- New search for: Juarez-Rojas, J. G.
- New search for: Martinez-Rios, M. A.
- New search for: Pena-Duque, M. A.
- New search for: Carrillo-Sanchez, S.
- New search for: Perez-Mendez, O.
- New search for: Fragoso, J. M.
In:
GENE -AMSTERDAM-
;
542
, 2
;
258-262
;
2014
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ISSN:
- Article (Journal) / Print
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Title:The -974C>A (rs3087459) gene polymorphism in the endothelin gene (EDN1) is associated with risk of developing acute coronary syndrome in Mexican patients
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Contributors:Vargas-Alarcon, G. ( author ) / Vallejo, M. ( author ) / Posadas-Romero, C. ( author ) / Juarez-Rojas, J. G. ( author ) / Martinez-Rios, M. A. ( author ) / Pena-Duque, M. A. ( author ) / Carrillo-Sanchez, S. ( author ) / Perez-Mendez, O. ( author ) / Fragoso, J. M. ( author )
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Published in:GENE -AMSTERDAM- ; 542, 2 ; 258-262
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Publisher:
- New search for: Elsevier Science B.V., Amsterdam.
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Publication date:2014-01-01
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Size:5 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 572.86
- Further information on Dewey Decimal Classification
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Classification:
DDC: 572.86 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 542, Issue 2
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 89
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Computational identification and analysis of functional polymorphisms involved in the activation and detoxification genes implicated in endometriosisPanda, Roshni / P.K., Suresh et al. | 2014
- 98
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Conservation and divergence in the frog immunome: pyrosequencing and de novo assembly of immune tissue transcriptomesSavage, Anna E. / Kiemnec-Tyburczy, Karen M. / Ellison, Amy R. / Fleischer, Robert C. / Zamudio, Kelly R. et al. | 2014
- 109
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Down-regulation of miR-199b associated with imatinib drug resistance in 9q34.1 deleted BCR/ABL positive CML patientsJoshi, Dolly / Chandrakala, S. / Korgaonkar, Seema / Ghosh, Kanjaksha / Vundinti, Babu Rao et al. | 2014
- 113
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Characterization of a stearoyl-acyl carrier protein desaturase gene from potential biofuel plant, Pongamia pinnata L.Ramesh, Aadi Moolam / Kesari, Vigya / Rangan, Latha et al. | 2014
- 122
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High expression of heat shock protein 90 alpha and its significance in human acute leukemia cellsTian, Wen-Liang / He, Fei / Fu, Xue / Lin, Jun-Tang / Tang, Ping / Huang, Yu-Min / Guo, Rong / Sun, Ling et al. | 2014
- 129
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Association of VDR-gene variants with factors related to the metabolic syndrome, type 2 diabetes and vitamin D deficiencyAl-Daghri, Nasser M. / Al-Attas, Omar S. / Alkharfy, Khalid M. / Khan, Nasiruddin / Mohammed, Abdul Khader / Vinodson, Benjamin / Ansari, Mohammed Ghouse Ahmed / Alenad, Amal / Alokail, Majed S. et al. | 2014
- 134
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Sp1 transcriptionally regulates BRK1 expression in non-small cell lung cancer cellsLi, Meng / Ling, Bing / Xiao, Ting / Tan, Jinjing / An, Ning / Han, Naijun / Guo, Suping / Cheng, Shujun / Zhang, Kaitai et al. | 2014
- 141
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Progranulin polymorphism rs5848 is associated with increased risk of Alzheimer's diseaseSheng, Jinghao / Su, Liling / Xu, Zhengping / Chen, Guangdi et al. | 2014
- 146
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Mitogenomic circumscription of a novel percomorph fish clade mainly comprising “Syngnathoidei” (Teleostei)Song, Ha Yeun / Mabuchi, Kohji / Satoh, Takashi P. / Moore, Jon A. / Yamanoue, Yusuke / Miya, Masaki / Nishida, Mutsumi et al. | 2014
- 156
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Morpho-molecular analysis as a prognostic model for repulsive feedback of the medicinal plant “Andrographis paniculata” to allogamyValdiani, Alireza / Talei, Daryush / Javanmard, Arash / Tan, Soon Guan / Kadir, Mihdzar Abdul / Maziah, Mahmood et al. | 2014
- 168
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The effect of variants in the promoter of BMPER on the intramuscular fat deposition in longissimus dorsi muscle of pigsLiu, Zhi / Sun, Wenxing / Zhao, Yongyan / Xu, Chunying / Fu, Yingying / Li, Yan / Chen, Jie et al. | 2014
- 173
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Sox9 and Hif-2α regulate TUBB3 gene expression and affect ovarian cancer aggressivenessRaspaglio, Giuseppina / Petrillo, Marco / Martinelli, Enrica / Li Puma, Domenica Donatella / Mariani, Marisa / De Donato, Marta / Filippetti, Flavia / Mozzetti, Simona / Prislei, Silvia / Zannoni, Gian Franco et al. | 2014
- 173
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Sox9 and Hif-2a regulate TUBB3 gene expression and affect ovarian cancer aggressivenessRaspaglio, G. / Petrillo, M. / Martinelli, E. / Li Puma, D. D. / Mariani, M. / De Donato, M. / Filippetti, F. / Mozzetti, S. / Prislei, S. / Zannoni, G. F. et al. | 2014
- 182
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The LIM domain protein FHL1C interacts with tight junction protein ZO-1 contributing to the epithelial–mesenchymal transition (EMT) of a breast adenocarcinoma cell lineZhao, Jun-Long / Liang, Shi-Qian / Fu, Wei / Zhu, Bing-Ke / Li, San-Zhong / Han, Hua / Qin, Hong-Yan et al. | 2014
- 190
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Assembly and annotation of full mitochondrial genomes for the corn rootworm species, Diabrotica virgifera virgifera and Diabrotica barberi (Insecta: Coleoptera: Chrysomelidae), using Next Generation Sequence dataCoates, Brad S. et al. | 2014
- 198
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Map-based analysis of the tenacious glume gene Tg-B1 of wild emmer and its role in wheat domesticationFaris, Justin D. / Zhang, Zengcui / Chao, Shiaoman et al. | 2014
- 209
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Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patientsVozzi, D. / Morgan, A. / Vuckovic, D. / D'Eustacchio, A. / Abdulhadi, K. / Rubinato, E. / Badii, R. / Gasparini, P. / Girotto, G. et al. | 2014
- 217
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Hyper-IgD and periodic fever syndrome: a new MVK mutation (p.R277G) associated with a severe phenotypeSantos, Joana A. / Aróstegui, Juan I. / Brito, Maria J. / Neves, Conceição / Conde, Marta et al. | 2014
- 221
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Identification of Tf1 integration events in S. pombe under nonselective conditionsCherry, Kristina E. / Hearn, Willis E. / Seshie, Osborne Y.K. / Singleton, Teresa L. et al. | 2014
- 232
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Core promoter regulates the expression of cathepsin B gene in the fat body of Bombyx moriCai, Xiang-Yun / Yu, Jie / Yu, Hai-Yan / Liu, Yan-Wei / Fang, Yin / Ren, Zi-Xu / Jia, Jun-Qiang / Zhang, Guo-Zheng / Guo, Xi-Jie / Jin, Byung-Rae et al. | 2014
- 240
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Taiwanese aborigines: genetic heterogeneity and paternal contribution to OceaniaZeng, Zhaoshu / Rowold, Diane J. / Garcia-Bertrand, Ralph / Calderon, Silvia / Regueiro, Maria / Li, Li / Zhong, Mingxia / Herrera, Rene J. et al. | 2014
- 248
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The relation between hairpin formation by mitochondrial WANCY tRNAs and the occurrence of the light strand replication origin in LepidosauriaSeligmann, Hervé / Labra, Antonieta et al. | 2014
- 258
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The −974C>A (rs3087459) gene polymorphism in the endothelin gene (EDN1) is associated with risk of developing acute coronary syndrome in Mexican patientsVargas-Alarcon, Gilberto / Vallejo, Maite / Posadas-Romero, Carlos / Juarez-Rojas, Juan G. / Martinez-Rios, Marco Antonio / Peña-Duque, Marco Antonio / Carrillo-Sanchez, Silvia / Perez-Mendez, Oscar / Fragoso, José Manuel et al. | 2013
- 263
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Chromosome microarray analysis: a case report of infertile brothers with CATSPER gene deletionJaiswal, Deepika / Singh, Vertika / Dwivedi, U.S. / Trivedi, Sameer / Singh, Kiran et al. | 2014
- 266
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Prenatal skeletal dysplasia phenotype in severe MLII alpha/beta with novel GNPTAB mutationAggarwal, Shagun / Coutinho, Maria Francisca / Dalal, Ashwin B. / Mohamed Nurul Jain, S.Jamal / Prata, Maria João / Alves, Sandra et al. | 2014
- 269
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A new missense mutation in FGF23 gene in a male with hyperostosis–hyperphosphatemia syndrome (HHS)Abbasi, Farzaneh / Ghafouri-Fard, Soudeh / Javaheri, Mona / Dideban, Abdullah / Ebrahimi, Ayoub / Ebrahim-Habibi, Azadeh et al. | 2014
- iv
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Editorial Board| 2012