Výsledky vyhledávání - Arpit Mehta
- Zobrazuji výsledky 1 - 4 z 4
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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... Autor Chiara Pastori, Veronica J. Peschansky, Deborah Barbouth, Arpit Mehta, José Silva, Claes Wahlestedt
Vydáno 2013Artigo -
2
Whole exome sequencing of rare variants in <i>EIF4G1</i> and <i>VPS35</i> in Parkinson disease Autor 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
Vydáno 2013Artigo -
3
Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform Autor 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
Vydáno 2011Artigo -
4
Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease Autor 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
Vydáno 2019Artigo
Vyhledávací nástroje:
Související témata
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