(Q28583305)

31 January 2017

1 reference

Europe PubMed Central

title

Molecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targets (English)

1 reference

smooth endoplasmic reticulum cisterna

31 January 2017

main subject

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Gene Ontology release 2020-05-02

Gene Ontology ID

GO:0120082

rough endoplasmic reticulum cisterna

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Gene Ontology release 2020-05-02

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1 reference

Walter E. Kaufmann

1

1 reference

31 January 2017

Sonia Cohen

series ordinal

2

1 reference

31 January 2017

Hong-Tao Sun

series ordinal

3

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31 January 2017

George Ho

series ordinal

4

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31 January 2017

language of work or name

1 reference

1 May 2002

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Microscopy Research and Technique

31 January 2017

published in

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31 January 2017

volume

57

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31 January 2017

issue

3

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31 January 2017

page(s)

135–144

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FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome

31 January 2017

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Evidence that fragile X mental retardation protein is a negative regulator of translation

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The fragile X mental retardation protein inhibits translation via interacting with mRNA

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A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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Rapid antibody test for fragile X syndrome.

21 January 2018

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Association of FMRP with ribosomal precursor particles in the nucleolus

21 January 2018

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Noninvasive test for fragile X syndrome, using hair root analysis

21 January 2018

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Cortisol and social stressors in children with fragile X: a pilot study

21 January 2018

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21 January 2018

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21 January 2018

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Reduced mRNA for G3BP in fragile X cells: evidence of FMR1 gene regulation

21 January 2018

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