Risultati della ricerca - 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... di 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 di 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 di 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 di 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 di 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 di 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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