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1581por McEwen, Lisa M., Morin, Alexander M., Edgar, Rachel D., MacIsaac, Julia L., Jones, Meaghan J., Dow, William H., Rosero-Bixby, Luis, Kobor, Michael S., Rehkopf, David H.“…METHODS: In a cross-sectional subsample of the Costa Rican Longevity and Healthy Aging Study, we compared whole blood DNA methylation profiles of residents from Nicoya (n = 48) and non-Nicoya (other Costa Rican regions, n = 47) using the Infinium HumanMethylation450 microarray. RESULTS: We observed a number of differences that may be markers of delayed aging, such as bioinformatically derived differential CD8+ T cell proportions. …”
Publicado 2017
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1582por Wang, Xiaohua, Long, Yan, Wang, Nian, Zou, Jun, Ding, Guangda, Broadley, Martin R., White, Philip J., Yuan, Pan, Zhang, Qianwen, Luo, Ziliang, Liu, Peifa, Zhao, Hua, Zhang, Ying, Cai, Hongmei, King, Graham J., Xu, Fangsen, Meng, Jinling, Shi, Lei“…We genotyped Tapidor (European), Ningyou7 (Chinese) and their progenitors with the Brassica 60 K Illumina Infinium SNP array and mapped a total of 29,347 SNP markers onto the reference genome of Darmor-bzh. …”
Publicado 2017
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1583por Yamada, Yoshiji, Sakuma, Jun, Takeuchi, Ichiro, Yasukochi, Yoshiki, Kato, Kimihiko, Oguri, Mitsutoshi, Fujimaki, Tetsuo, Horibe, Hideki, Muramatsu, Masaaki, Sawabe, Motoji, Fujiwara, Yoshinori, Taniguchi, Yu, Obuchi, Shuichi, Kawai, Hisashi, Shinkai, Shoji, Mori, Seijiro, Arai, Tomio, Tanaka, Masashi“…The exome-wide association studies were performed with 12,698 individuals (3488 subjects with coronary artery disease including 2438 with myocardial infarction, 9210 controls) and with the use of the Illumina HumanExome-12 DNA Analysis or Infinium Exome-24 BeadChip. The relation of allele frequencies for 41,339 single nucleotide polymorphisms that passed quality control to coronary artery disease or myocardial infarction was examined with Fisher's exact test. …”
Publicado 2017
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1584por Smith, Eric, Palethorpe, Helen M., Hayden, Annette L., Young, Joanne P., Underwood, Timothy J., Drew, Paul A.“…We measured the DNA methylation profiles of 10 TDFs from OAC with 12 NDF from normal oesophageal mucosa using Infinium HumanMethylation450 Beadchips and found they differed in multidimensional scaling analysis. …”
Publicado 2017
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1585por Sailer, Verena, Gevensleben, Heidrun, Dietrich, Joern, Goltz, Diane, Kristiansen, Glen, Bootz, Friedrich, Dietrich, Dimo“…In the present study, the clinical performance of PITX2 methylation was validated in a HNSCC cohort by means of an independent analytical platform (Infinium HumanMethylation450 BeadChip, Illumina, Inc.). …”
Publicado 2017
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1586por Yamada, Yoshiji, Sakuma, Jun, Takeuchi, Ichiro, Yasukochi, Yoshiki, Kato, Kimihiko, Oguri, Mitsutoshi, Fujimaki, Tetsuo, Horibe, Hideki, Muramatsu, Masaaki, Sawabe, Motoji, Fujiwara, Yoshinori, Taniguchi, Yu, Obuchi, Shuichi, Kawai, Hisashi, Shinkai, Shoji, Mori, Seijiro, Arai, Tomio, Tanaka, Masashi“…Exome-wide association studies were performed with Illumina HumanExome-12 DNA Analysis BeadChip or Infinium Exome-24 BeadChip arrays. The relation of genotypes of single nucleotide polymorphisms to body mass index was examined by linear regression analysis, and that of allele frequencies of single nucleotide polymorphisms to obesity or metabolic syndrome was evaluated with Fisher's exact test. …”
Publicado 2017
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1587por Yamada, Yoshiji, Sakuma, Jun, Takeuchi, Ichiro, Yasukochi, Yoshiki, Kato, Kimihiko, Oguri, Mitsutoshi, Fujimaki, Tetsuo, Horibe, Hideki, Muramatsu, Masaaki, Sawabe, Motoji, Fujiwara, Yoshinori, Taniguchi, Yu, Obuchi, Shuichi, Kawai, Hisashi, Shinkai, Shoji, Mori, Seijiro, Arai, Tomio, Tanaka, Masashi“…The exome-wide association studies were performed with the use of Illumina HumanExome-12 DNA Analysis BeadChip or Infinium Exome-24 BeadChip arrays and with 14,678 subjects, including 8215 individuals with hypertension and 6463 controls. …”
Publicado 2017
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1588por Guastafierro, T., Bacalini, M. G., Marcoccia, A., Gentilini, D., Pisoni, S., Di Blasio, A. M., Corsi, A., Franceschi, C., Raimondo, D., Spanò, A., Garagnani, P., Bondanini, F.“…RESULTS: To address whether epigenetic changes can be associated with Werner syndrome phenotype, we analysed genome-wide DNA methylation profile using the Infinium MethylationEPIC BeadChip in the whole blood from three patients affected by Werner syndrome compared with three age- and sex-matched healthy controls. …”
Publicado 2017
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1589por Jones, David B., Jerry, Dean R., Khatkar, Mehar S., Raadsma, Herman W., Steen, Hein van der, Prochaska, Jeffrey, Forêt, Sylvain, Zenger, Kyall R.“…This study describes the development of a comprehensive set of genomic gene-based resources including the identification and validation of 234,452 putative single nucleotide polymorphisms in-silico, of which 8,967 high value SNPs were incorporated into a commercially available Illumina Infinium ShrimpLD-24 v1.0 genotyping array. A framework genetic linkage map was constructed and combined with locus ordering by disequilibrium methodology to generate an integrated genetic map containing 4,817 SNPs, which spanned a total of 4552.5 cM and covered an estimated 98.12% of the genome. …”
Publicado 2017
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1590por Funata, Sayaka, Matsusaka, Keisuke, Yamanaka, Ryota, Yamamoto, Shogo, Okabe, Atsushi, Fukuyo, Masaki, Aburatani, Hiroyuki, Fukayama, Masashi, Kaneda, Atsushi“…Herein, we performed comprehensive analysis of epigenomic alteration during EBV infection, by Infinium HumanMethylation 450K BeadChip for DNA methylation and ChIP-sequencing for histone modification alteration during EBV infection into gastric cancer cell line MKN7. …”
Publicado 2017
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1591por Hnoonual, Areerat, Thammachote, Weerin, Tim-Aroon, Thipwimol, Rojnueangnit, Kitiwan, Hansakunachai, Tippawan, Sombuntham, Tasanawat, Roongpraiwan, Rawiwan, Worachotekamjorn, Juthamas, Chuthapisith, Jariya, Fucharoen, Suthat, Wattanasirichaigoon, Duangrurdee, Ruangdaraganon, Nichara, Limprasert, Pornprot, Jinawath, Natini“…The aims of this study were to identify known and novel ASD associated-CNVs and to evaluate the diagnostic yield of CMA in Thai patients with ASD. The Infinium CytoSNP-850K BeadChip was used to detect CNVs in 114 Thai patients comprised of 68 retrospective ASD patients (group 1) with the use of CMA as a second line test and 46 prospective ASD and developmental delay patients (group 2) with the use of CMA as the first-tier test. …”
Publicado 2017
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1592por Morris, John A, Tsai, Pei‐Chien, Joehanes, Roby, Zheng, Jie, Trajanoska, Katerina, Soerensen, Mette, Forgetta, Vincenzo, Castillo‐Fernandez, Juan Edgar, Frost, Morten, Spector, Tim D, Christensen, Kaare, Christiansen, Lene, Rivadeneira, Fernando, Tobias, Jonathan H, Evans, David M, Kiel, Douglas P, Hsu, Yi‐Hsiang, Richards, J Brent, Bell, Jordana T“…We undertook a large‐scale BMD EWAS using the Infinium HumanMethylation450 array to measure site‐specific DNA methylation in up to 5515 European‐descent individuals (N(Discovery )= 4614, N(Validation )= 901). …”
Publicado 2017
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1593por Jorgensen, Chad, Luo, Ming-Cheng, Ramasamy, Ramesh, Dawson, Mathew, Gill, Bikram S., Korol, Abraham B., Distelfeld, Assaf, Dvorak, Jan“…‘Langdon’ x wild emmer accession PI 428082 from this region was developed and genotyped with the Illumina 90K single nucleotide polymorphism Infinium assay. A genetic map comprising 2,650 segregating markers was constructed. …”
Publicado 2017
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1594por Walton, Esther, Cecil, Charlotte A.M., Suderman, Matthew, Liu, Jingyu, Turner, Jessica A., Calhoun, Vince, Ehrlich, Stefan, Relton, Caroline L., Barker, Edward D.“…METHODS: Analyses were based on a subsample (n = 109 males) from the Avon Longitudinal Study of Parents and Children, which included measures of prenatal risk, DNA methylation (Infinium Illumina 450k), T1‐weighted brain scans and psychopathology in early adulthood (age 18–21). …”
Publicado 2017
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1595por Heckerman, David, Traynor, Bryan J., Picca, Anna, Calvani, Riccardo, Marzetti, Emanuele, Hernandez, Dena, Nalls, Michael, Arepali, Sampath, Ferrucci, Luigi, Landi, Francesco“…Genotyping was accomplished on Infinium Human610-QUAD version 1. In the ilSIRENTE population, genetic variants in ZNF295 and C2CD2 (rs928874 and rs1788355) on chromosome 21q22.3, were significantly associated with the 4-meter gait speed (rs928874, p = 5.61 × 10(−8); rs1788355, p = 5.73 × 10(−8)). …”
Publicado 2017
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1596por Montalvo-Ortiz, Janitza L, Zhang, Huiping, Chen, Chao, Liu, Chunyu, Coccaro, Emil F“…Peripheral blood DNA methylome was profiled using the Illumina Infinium HumanMethylation450 Beadchip. Intermittent explosive disorder-associated genome-wide DNA methylation changes were analyzed using the CpGassoc R package, with covariates age, sex, and race being adjusted. …”
Publicado 2017
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1597por Breton, Carrie V., Gao, Lu, Yao, Jin, Siegmund, Kimberly D., Lurmann, Fred, Gilliland, Frank“…We investigated the effects of prenatal particulate matter (PM) exposure on DNA methylation of 178,309 promoter regions in 240 newborns using the Infinium HumanMethylation450 BeadChip, using a generalized linear regression model with a quasi-binomial link family, adjusted for gender, plate, and cell types. …”
Publicado 2016
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1598por van den Dungen, Myrthe W., Murk, Albertinka J., Kampman, Ellen, Steegenga, Wilma T., Kok, Dieuwertje E.“…Clinical parameters related to e.g. hormone levels and liver enzymes were measured as biomarkers for adverse health effects. The Infinium 450K BeadChip was used to assess DNA methylation in a representative subset of 34 men. …”
Publicado 2017
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1599por Rodríguez-Paredes, Manuel, Bormann, Felix, Raddatz, Günter, Gutekunst, Julian, Lucena-Porcel, Carlota, Köhler, Florian, Wurzer, Elisabeth, Schmidt, Katrin, Gallinat, Stefan, Wenck, Horst, Röwert-Huber, Joachim, Denisova, Evgeniya, Feuerbach, Lars, Park, Jeongbin, Brors, Benedikt, Herpel, Esther, Nindl, Ingo, Hofmann, Thomas G., Winnefeld, Marc, Lyko, Frank“…Despite various efforts to characterize these lesions molecularly, the etiology of AK and its progression to cSCC remain partially understood. Here, we use Infinium MethylationEPIC BeadChips to interrogate the DNA methylation status in healthy, AK and cSCC epidermis samples. …”
Publicado 2018
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1600por Forest, Marie, O'Donnell, Kieran J., Voisin, Greg, Gaudreau, Helene, MacIsaac, Julia L., McEwen, Lisa M., Silveira, Patricia P., Steiner, Meir, Kobor, Michael S., Meaney, Michael J., Greenwood, Celia M.T.“…Here, we used data from two studies, three tissue types, and multiple time points to assess the stability of DNA methylation measured with the Illumina Infinium HumanMethylation450 BeadChip array. Redundancy analysis enabled visual assessment of agreement of replicate samples overall and showed good agreement after removing effects of tissue type, age, and sex. …”
Publicado 2018
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