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Jay M. Maniar

Researcher at Stanford University

Publications -  10
Citations -  2236

Jay M. Maniar is an academic researcher from Stanford University. The author has contributed to research in topics: RNA interference & RNA silencing. The author has an hindex of 10, co-authored 10 publications receiving 2065 citations.

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The Energy Sensor AMP-activated Protein Kinase Directly Regulates the Mammalian FOXO3 Transcription Factor

TL;DR: It is found that AMPK directly regulates mammalian FOXO3, a member of the FOXO family of Forkhead transcription factors known to promote resistance to oxidative stress, tumor suppression, and longevity, by phosphorylation by AMPK at six previously unidentified regulatory sites.
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Measurement and Clinical Monitoring of Human Lymphocyte Clonality by Massively Parallel V-D-J Pyrosequencing

TL;DR: It is shown that massively parallel DNA sequencing of rearranged immune receptor loci can provide direct detection and tracking of immune diversity and expanded clonal lymphocyte populations in physiological and pathological contexts.
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Individual Variation in the Germline Ig Gene Repertoire Inferred from Variable Region Gene Rearrangements

TL;DR: The extent of genotypic variation between individuals is highlighted by an individual with aplastic anemia who appears to lack six contiguous IGHD genes on both chromosomes, and these deletions significantly alter the potential expressed IGH repertoire, and possibly immune function, in this individual.
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Amplification of siRNA in Caenorhabditis elegans generates a transgenerational sequence-targeted histone H3 lysine 9 methylation footprint

TL;DR: These results implicate dsRNA-triggered chromatin modification in C. elegans as a programmable and locus-specific response defining a metastable state that can persist through generational boundaries.
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Distinct Phases of siRNA Synthesis in an Endogenous RNAi Pathway in C. elegans Soma

TL;DR: The requirement for two RdRP/Argonaute combinations and initiation by a rare class of uniquely structured siRNAs in this pathway illustrate the caution and flexibility used as biological systems exploit the physiological copying of RNA.