Resultados da pesquisa - Mehta, Arpit

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

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Next-generation sequencing of mitochondrial targeted AAV transfer of human ND4 in mice Por Yu, Hong, Mehta, Arpit, Wang, Gaofeng, Hauswirth, William W., Chiodo, Vince, Boye, Sanford L., Guy, John

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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.

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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.

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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.

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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.

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