Literature DB >> 10331604

In vivo footprinting analysis of the FMR1 gene: proposals concerning gene regulation in high-functioning males.

S Schwemmle.   

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Year:  1999        PMID： 10331604

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  4 in total

1.  Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defect.

Authors:  R W Burman; P A Yates; L D Green; P B Jacky; M S Turker; B W Popovich
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

2.  Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?

Authors:  U Salat; B Bardoni; D Wöhrle; P Steinbach
Journal:  J Med Genet       Date:  2000-11       Impact factor: 6.318

3.  Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine.

Authors:  Roberta Pietrobono; Maria Grazia Pomponi; Elisabetta Tabolacci; Ben Oostra; Pietro Chiurazzi; Giovanni Neri
Journal:  Nucleic Acids Res       Date:  2002-07-15       Impact factor: 16.971

Review 4.  Human pluripotent stem cell models of Fragile X syndrome.

Authors:  Anita Bhattacharyya; Xinyu Zhao
Journal:  Mol Cell Neurosci       Date:  2015-11-27       Impact factor: 4.314
  4 in total

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