Результати пошуку - Arpit Mehta
- Показ 1 - 4 результатів із 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... за авторством Chiara Pastori, Veronica J. Peschansky, Deborah Barbouth, Arpit Mehta, José Silva, Claes Wahlestedt
Опубліковано 2013Artigo -
2
Whole exome sequencing of rare variants in <i>EIF4G1</i> and <i>VPS35</i> in Parkinson disease за авторством 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
Опубліковано 2013Artigo -
3
Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform за авторством 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
Опубліковано 2011Artigo -
4
Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease за авторством 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
Опубліковано 2019Artigo
Інструменти для пошуку:
Пов'язані теми
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