Literature DB >> 25259928

SnapShot: FMRP interacting proteins.

Emanuela Pasciuto1, Claudia Bagni2.   

Abstract

The Fragile X syndrome, caused by the absence or mutation of fragile X mental retardation protein, FMRP, is a the common component of inherited intellectual disability and autism. This SnapShot surveys the protein interaction partners of FMRP, focusing on the cellular pathways in which they are involved.
Copyright © 2014 Elsevier Inc. All rights reserved.

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Year:  2014        PMID： 25259928     DOI： 10.1016/j.cell.2014.08.036

Source DB:  PubMed          Journal:  Cell        ISSN： 0092-8674            Impact factor:   41.582


  17 in total

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Journal:  Neurochem Res       Date:  2017-02-04       Impact factor: 3.996

2.  Function of FMRP Domains in Regulating Distinct Roles of Neuronal Protein Synthesis.

Authors:  Michelle Ninochka D'Souza; Sarayu Ramakrishna; Bindushree K Radhakrishna; Vishwaja Jhaveri; Sreenath Ravindran; Lahari Yeramala; Deepak Nair; Dasaradhi Palakodeti; Ravi S Muddashetty
Journal:  Mol Neurobiol       Date:  2022-10-01       Impact factor: 5.682

Review 3.  The molecular biology of FMRP: new insights into fragile X syndrome.

Authors:  Joel D Richter; Xinyu Zhao
Journal:  Nat Rev Neurosci       Date:  2021-02-19       Impact factor: 38.755

4.  Maturation Delay of Human GABAergic Neurogenesis in Fragile X Syndrome Pluripotent Stem Cells.

Authors:  Ai Zhang; Irina Sokolova; Alain Domissy; Joshua Davis; Lee Rao; Kagistia Hana Utami; Yanling Wang; Randi J Hagerman; Mahmoud A Pouladi; Pietro Sanna; Michael J Boland; Jeanne F Loring
Journal:  Stem Cells Transl Med       Date:  2022-06-22       Impact factor: 7.655

5.  Phenotypic and molecular convergence of 2q23.1 deletion syndrome with other neurodevelopmental syndromes associated with autism spectrum disorder.

Authors:  Sureni V Mullegama; Joseph T Alaimo; Li Chen; Sarah H Elsea
Journal:  Int J Mol Sci       Date:  2015-04-07       Impact factor: 5.923

6.  Autism spectrum disorders: emerging mechanisms and mechanism-based treatment.

Authors:  Hansen Wang; Laurie C Doering
Journal:  Front Cell Neurosci       Date:  2015-05-12       Impact factor: 5.505

7.  Fragile X mental retardation protein: from autism to neurodegenerative disease.

Authors:  Hansen Wang
Journal:  Front Cell Neurosci       Date:  2015-02-12       Impact factor: 5.505

8.  GABAB receptor upregulates fragile X mental retardation protein expression in neurons.

Authors:  Wenhua Zhang; Chanjuan Xu; Haijun Tu; Yunyun Wang; Qian Sun; Ping Hu; Yongjian Hu; Philippe Rondard; Jianfeng Liu
Journal:  Sci Rep       Date:  2015-05-28       Impact factor: 4.379

Review 9.  An "Omic" Overview of Fragile X Syndrome.

Authors:  Olivier Dionne; François Corbin
Journal:  Biology (Basel)       Date:  2021-05-13

10.  Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes.

Authors:  Beata Stepniak; Anne Kästner; Giulia Poggi; Marina Mitjans; Martin Begemann; Annette Hartmann; Sandra Van der Auwera; Farahnaz Sananbenesi; Dilja Krueger-Burg; Gabriela Matuszko; Cornelia Brosi; Georg Homuth; Henry Völzke; Fritz Benseler; Claudia Bagni; Utz Fischer; Alexander Dityatev; Hans-Jörgen Grabe; Dan Rujescu; Andre Fischer; Hannelore Ehrenreich
Journal:  EMBO Mol Med       Date:  2015-12       Impact factor: 12.137
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