Literature DB >> 21739597

The FRAXopathies: definition, overview, and update.

Filomena Pirozzi1, Elisabetta Tabolacci, Giovanni Neri.   

Abstract

The fragile X syndrome, fragile X tremor ataxia syndrome, and premature ovarian insufficiency are conditions related to the X chromosome folate-sensitive fragile site FRAXA. Therefore, we propose that they are considered as a family of disorders under the general designation of FRAXopathies. The present review will outline the main clinical and molecular features of these disorders, with special emphasis on the pathogenic mechanisms that lead to distinct phenotypes, starting from related mutations. The understanding of these mechanisms is already generating promising therapeutic approaches.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21739597     DOI: 10.1002/ajmg.a.34113

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  13 in total

1.  Defining the role of the CGGBP1 protein in FMR1 gene expression.

Authors:  Martina Goracci; Stella Lanni; Giorgia Mancano; Federica Palumbo; Pietro Chiurazzi; Giovanni Neri; Elisabetta Tabolacci
Journal:  Eur J Hum Genet       Date:  2015-08-26       Impact factor: 4.246

2.  Prevalence of CGG expansions of the FMR1 gene in a US population-based sample.

Authors:  Marsha Mailick Seltzer; Mei Wang Baker; Jinkuk Hong; Matthew Maenner; Jan Greenberg; Daniel Mandel
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2012-05-22       Impact factor: 3.568

Review 3.  Genetics of androgen metabolism in women with infertility and hypoandrogenism.

Authors:  Aya Shohat-Tal; Aritro Sen; David H Barad; Vitaly Kushnir; Norbert Gleicher
Journal:  Nat Rev Endocrinol       Date:  2015-05-05       Impact factor: 43.330

4.  New kid on the ID block: neural functions of the Nab2/ZC3H14 class of Cys₃His tandem zinc-finger polyadenosine RNA binding proteins.

Authors:  Seth Kelly; Changhui Pak; Masoud Garshasbi; Andreas Kuss; Anita H Corbett; Kenneth Moberg
Journal:  RNA Biol       Date:  2012-05-01       Impact factor: 4.652

5.  The FMR1 promoter is selectively hydroxymethylated in primary neurons of fragile X syndrome patients.

Authors:  Rustam Esanov; Nadja S Andrade; Sarah Bennison; Claes Wahlestedt; Zane Zeier
Journal:  Hum Mol Genet       Date:  2016-11-15       Impact factor: 6.150

6.  Tremor-Ataxia syndrome and primary ovarian insufficiency in an FMR1 premutation carrier.

Authors:  Wilmar Saldarriaga-Gil; Tatiana Rodriguez-Guerrero; Andres Fandiño-Losada; Julian Ramirez-Cheyne
Journal:  Colomb Med (Cali)       Date:  2017-09-30

Review 7.  Regulation of Adult Neurogenesis by the Fragile X Family of RNA Binding Proteins.

Authors:  Natalie E Patzlaff; Minjie Shen; Xinyu Zhao
Journal:  Brain Plast       Date:  2018-08-10

8.  FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 Gene.

Authors:  Esperanza Fernández; Elena Gennaro; Filomena Pirozzi; Chiara Baldo; Francesca Forzano; Licia Turolla; Francesca Faravelli; Denise Gastaldo; Domenico Coviello; Marina Grasso; Claudia Bagni
Journal:  Front Genet       Date:  2018-11-02       Impact factor: 4.599

9.  Role of CTCF protein in regulating FMR1 locus transcription.

Authors:  Stella Lanni; Martina Goracci; Loredana Borrelli; Giorgia Mancano; Pietro Chiurazzi; Umberto Moscato; Fabrizio Ferrè; Manuela Helmer-Citterich; Elisabetta Tabolacci; Giovanni Neri
Journal:  PLoS Genet       Date:  2013-07-18       Impact factor: 5.917

Review 10.  Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome.

Authors:  Elisabetta Tabolacci; Federica Palumbo; Veronica Nobile; Giovanni Neri
Journal:  Genes (Basel)       Date:  2016-08-17       Impact factor: 4.096

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