Literature DB >> 25713352

Profile of Stephen T. Warren.

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Year:  2015        PMID： 25713352      PMCID： PMC4364191          DOI： 10.1073/pnas.1502201112

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   11.205


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  8 in total

1.  Reversible inhibition of PSD-95 mRNA translation by miR-125a, FMRP phosphorylation, and mGluR signaling.

Authors:  Ravi S Muddashetty; Vijayalaxmi C Nalavadi; Christina Gross; Xiaodi Yao; Lei Xing; Oskar Laur; Stephen T Warren; Gary J Bassell
Journal:  Mol Cell       Date:  2011-06-10       Impact factor: 17.970

2.  Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures.

Authors:  Leila K Myrick; Pan-Yue Deng; Hideharu Hashimoto; Young Mi Oh; Yongcheol Cho; Mickael J Poidevin; Joshua A Suhl; Jeannie Visootsak; Valeria Cavalli; Peng Jin; Xiaodong Cheng; Stephen T Warren; Vitaly A Klyachko
Journal:  Proc Natl Acad Sci U S A       Date:  2015-01-05       Impact factor: 11.205

3.  The fragile X site in somatic cell hybrids: an approach for molecular cloning of fragile sites.

Authors:  S T Warren; F Zhang; G R Licameli; J F Peters
Journal:  Science       Date:  1987-07-24       Impact factor: 47.728

4.  Elevated spontaneous mutation rate in Bloom syndrome fibroblasts.

Authors:  S T Warren; R A Schultz; C C Chang; M H Wade; J E Trosko
Journal:  Proc Natl Acad Sci U S A       Date:  1981-05       Impact factor: 11.205

5.  Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

Authors:  A J Verkerk; M Pieretti; J S Sutcliffe; Y H Fu; D P Kuhl; A Pizzuti; O Reiner; S Richards; M F Victoria; F P Zhang
Journal:  Cell       Date:  1991-05-31       Impact factor: 41.582

6.  FMR1 protein: conserved RNP family domains and selective RNA binding.

Authors:  C T Ashley; K D Wilkinson; D Reines; S T Warren
Journal:  Science       Date:  1993-10-22       Impact factor: 47.728

7.  FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association.

Authors:  Y Feng; D Absher; D E Eberhart; V Brown; H E Malter; S T Warren
Journal:  Mol Cell       Date:  1997-12       Impact factor: 17.970

Review 8.  The mGluR theory of fragile X mental retardation.

Authors:  Mark F Bear; Kimberly M Huber; Stephen T Warren
Journal:  Trends Neurosci       Date:  2004-07       Impact factor: 13.837
  8 in total
  1 in total

1.  Stephen T. Warren: Human geneticist who advanced understanding of mutational mechanisms and developmental disorders.

Authors:  David L Nelson; C Thomas Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  2021-08-24       Impact factor: 11.205
  1 in total

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