Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse-Reference-Cited by-同舟云学术

Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse

Published:2017-09-05 Issue:11 Volume:14 Page:1580-1591
ISSN:1547-6286
Container-title:RNA Biology
language:en
Short-container-title:RNA Biology

Author:

Filippini Alice¹,Bonini Daniela¹,Lacoux Caroline²,Pacini Laura²^ORCID,Zingariello Maria³,Sancillo Laura⁴,Bosisio Daniela⁵,Salvi Valentina⁵,Mingardi Jessica¹,La Via Luca¹,Zalfa Francesca³,Bagni Claudia²⁶⁷,Barbon Alessandro¹^ORCID

Affiliation:

1. Biology and Genetic Division; Department of Molecular and Translational Medicine; University of Brescia; Brescia, Italy

2. Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy

3. Department of Medicine, Campus Bio-Medico University, via Álvaro del Portillo 21, Rome, Italy

4. Department of Medicine and Aging Sciences, Section of Human Morphology, University G. D'Annunzio of Chieti-Pescara, Chieti, Italy

5. Immunology Unit; Department of Molecular and Translational Medicine; University of Brescia; Brescia, Italy

6. VIB Center for the Biology of Disease and Center for Human Genetics, Leuven, Belgium

7. Department of Fundamental Neuroscience, University of Lausanne, Lausanne, Switzerland

Publisher

Informa UK Limited

Subject

Cell Biology,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/15476286.2017.1338232

Reference61 articles.

1. A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE

2. A Decade of Molecular Studies of Fragile X Syndrome

3. Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics

4. Increasing our understanding of human cognition through the study of fragile X syndrome

5. Fragile X Syndrome: From molecular pathology to therapy

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