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Devon M. Chenette

Researcher at New York University

Publications -  11
Citations -  365

Devon M. Chenette is an academic researcher from New York University. The author has contributed to research in topics: Myocyte & Regeneration (biology). The author has an hindex of 7, co-authored 11 publications receiving 246 citations. Previous affiliations of Devon M. Chenette include Yale University.

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mTORC1/2 inhibition preserves ovarian function and fertility during genotoxic chemotherapy

TL;DR: It is shown that mTOR inhibition preserves the ovarian reserve, primordial follicle counts, serum anti-Mullerian hormone levels, and fertility, indicating a potentially effective and readily accessible pharmacologic approach to fertility preservation during conventional chemotherapy.
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Physiological networks and disease functions of RNA-binding protein AUF1.

TL;DR: AUF1 has been implicated in controlling a variety of physiological functions through its ability to regulate the expression of numerous mRNAs containing 3′‐UTR AREs, thereby coordinating functionally related pathways.
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Functional Genome-wide Screen Identifies Pathways Restricting Central Nervous System Axonal Regeneration

TL;DR: A comprehensive functional screen reveals multiple pathways restricting axonal regeneration and neurological recovery after injury and validates a cell-autonomous restriction of regeneration by Rab27.
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RNA-binding protein AUF1 promotes myogenesis by regulating MEF2C expression levels.

TL;DR: Investigating the function of AUF1 in skeletal muscle differentiation found that it associated with the 3′ untranslated region (UTR) of Mef2c mRNA and promoted MEF2C translation without affecting Mef 2c mRNA stability, and proposed that MEf2C is a key effector of the myogenesis program promoted by AUF 1.
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Targeted mRNA Decay by RNA Binding Protein AUF1 Regulates Adult Muscle Stem Cell Fate, Promoting Skeletal Muscle Integrity

TL;DR: Control of ARE-mRNAs containing 3' AU-rich elements by AUF1 represents a mechanism for adult stem cell regulation and is implicated in human skeletal muscle wasting diseases.