Resultados de búsqueda - Mehta, Arpit
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Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-asso... por Pastori, Chiara, Peschansky, Veronica J., Barbouth, Deborah, Mehta, Arpit, Silva, Jose P., Wahlestedt, Claes
Publicado 2013Texto -
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Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease por Nuytemans, Karen, Bademci, Guney, Inchausti, Vanessa, Dressen, Amy, Kinnamon, Daniel D., Mehta, Arpit, Wang, Liyong, Züchner, Stephan, Beecham, Gary W., Martin, Eden R., Scott, William K., Vance, Jeffery M.
Publicado 2013Texto -
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Regulation of AKT signaling by Id1 controls t(8;21) leukemia initiation and progression por Wang, Lan, Man, Na, Sun, Xiao-Jian, Tan, Yurong, Cao, Marta Garcia, Liu, Fan, Hatlen, Megan, Xu, Haiming, Huang, Gang, Mattlin, Meredith, Mehta, Arpit, Rampersaud, Evadnie, Benezra, Robert, Nimer, Stephen D.
Publicado 2015Texto -
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Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform por Hedges, Dale J., Guettouche, Toumy, Yang, Shan, Bademci, Guney, Diaz, Ashley, Andersen, Ashley, Hulme, William F., Linker, Sara, Mehta, Arpit, Edwards, Yvonne J. K., Beecham, Gary W., Martin, Eden R., Pericak-Vance, Margaret A., Zuchner, Stephan, Vance, Jeffery M., Gilbert, John R.
Publicado 2011Texto -
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Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease por Young, Juan I., Sivasankaran, Sathesh K., Wang, Lily, Ali, Aleena, Mehta, Arpit, Davis, David A., Dykxhoorn, Derek M., Petito, Carol K., Beecham, Gary W., Martin, Eden R., Mash, Deborah C., Pericak-Vance, Margaret, Scott, William K., Montine, Thomas J., Vance, Jeffery M.
Publicado 2019Texto