Loss of Drosophila FMRP leads to alterations in energy metabolism and mitochondrial function-Reference-Cited by-同舟云学术

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Loss of Drosophila FMRP leads to alterations in energy metabolism and mitochondrial function

Published:2017-11-02 Issue:1 Volume:27 Page:95-106
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Weisz Eliana D¹,Towheed Atif²,Monyak Rachel E¹,Toth Meridith S¹,Wallace Douglas C¹²³,Jongens Thomas A¹

Affiliation:

1. Department of Genetics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA,

2. Center for Mitochondrial and Epigenomic Medicine, The Children’s Hospital of Philadelphia, Philadelphia, PA 19104, USA

3. Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA

Funder

National Institutes of Health

FRAXA Research Foundation

United Mitochondrial Disease Foundation

University of Pennsylvania

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/27/1/95/24325637/ddx387.pdf

Reference62 articles.

1. Fragile X syndrome and model organisms: identifying potential routes of therapeutic intervention;Bhogal;Dis. Model. Mech,2010

2. Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes;Bardoni;Curr. Opin. Genet. Dev,2002

3. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991

4. Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome;Bell;Cell,1991

5. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome;Oberlé;Science,1991

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5. Species-specific FMRP regulation of RACK1 is critical for prenatal cortical development;Neuron;2023-12

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