Fmr1-Deficiency Impacts Body Composition, Skeleton, and Bone Microstructure in a Mouse Model of Fragile X Syndrome-Reference-Cited by-同舟云学术

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Fmr1-Deficiency Impacts Body Composition, Skeleton, and Bone Microstructure in a Mouse Model of Fragile X Syndrome

Published:2019-10-02 Issue: Volume:10 Page:
ISSN:1664-2392
Container-title:Frontiers in Endocrinology
language:
Short-container-title:Front. Endocrinol.

Author:

Leboucher Antoine,Bermudez-Martin Patricia,Mouska Xavier,Amri Ez-Zoubir,Pisani Didier F.,Davidovic Laetitia

Funder

FRAXA Research Foundation

Agence Nationale de la Recherche

Publisher

Frontiers Media SA

Subject

Endocrinology, Diabetes and Metabolism

Reference37 articles.

1. Genetics and pathophysiology of mental retardation;Chelly;Eur J Hum Genet.,2006

2. The genetic landscape of intellectual disability arising from chromosome X;Gecz;Trends Genet,2009

3. The fragile X prevalence paradox;Hagerman;J Med Genet,2008

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

5. The pathophysiology of fragile x syndrome;Penagarikano;Annu Rev Genom Hum Genet,2007

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1. Effects of Soy Protein Isolate on Fragile X Phenotypes in Mice;Nutrients;2024-01-18

2. Increased body weight in mice with fragile X messenger ribonucleoprotein 1 (Fmr1) gene mutation is associated with hypothalamic dysfunction;Scientific Reports;2023-08-04

3. Fragile X Messenger Ribonucleoprotein 1 (FMR1), a novel inhibitor of osteoblast/osteocyte differentiation, regulates bone formation, mass, and strength in young and aged male and female mice;Bone Research;2023-05-17

4. Evaluating the effect of R-Baclofen and LP-211 on autistic behavior of the BTBR and Fmr1-KO mouse models;Frontiers in Neuroscience;2023-03-30

5. Bioinformatics identification and experimental validation of m6A-related diagnostic biomarkers in the subtype classification of blood monocytes from postmenopausal osteoporosis patients;Frontiers in Endocrinology;2023-03-08

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