Risultati della ricerca - Arpit Mehta
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1
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 Chiara Pastori, Veronica J. Peschansky, Deborah Barbouth, Arpit Mehta, José Silva, Claes Wahlestedt
Pubblicazione 2013Artigo -
2
Whole exome sequencing of rare variants in <i>EIF4G1</i> and <i>VPS35</i> in Parkinson disease di Karen Nuytemans, Güney Bademci, Vanessa Inchausti, Amy Dressen, Daniel D. Kinnamon, Arpit Mehta, Liyong Wang, Stephan Züchner, Gary W. Beecham, Eden R. Martin, William K. Scott, Jeffery M. Vance
Pubblicazione 2013Artigo -
3
Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform di Dale J. Hedges, Toumy Guettouche, Shan Yang, Güney Bademci, Ashley Diaz, Ashley Andersen, William Hulme, Sara B. Linker, Arpit Mehta, Yvonne J. K. Edwards, Gary W. Beecham, Eden R. Martin, Margaret A. Pericak‐Vance, Stephan Züchner, Jeffery M. Vance, John R. Gilbert
Pubblicazione 2011Artigo -
4
Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease di Juan I. Young, Sathesh K. Sivasankaran, Lily Wang, Aleena Ali, Arpit Mehta, David A. Davis, Derek M. Dykxhoorn, Carol K. Petito, Gary W. Beecham, Eden R. Martin, Deborah C. Mash, Margaret A. Pericak‐Vance, William K. Scott, Thomas J. Montine, Jeffery M. Vance
Pubblicazione 2019Artigo
Strumenti per la ricerca:
Soggetti correlati
Biology
Gene
Genetics
Genome
Genotype
Neuroscience
Allele
Ataxia
Computational biology
Computer science
DNA methylation
DNA sequencing
Differentially methylated regions
Disease
Dorsal motor nucleus
Epigenetics
Exome
Exome sequencing
FMR1
Fragile X syndrome
Gene expression
Gene silencing
Genetic association
Genotyping
Indel
Internal medicine
Locus (genetics)
Long non-coding RNA
Medicine
Methylation