(Q38345118)

2 September 2017

A study of the distributional characteristics of FMR1 transcript levels in 238 individuals (English)

1 reference

2 September 2017

Emily G Allen

1

1 reference

2 September 2017

Weiya He

series ordinal

2

1 reference

2 September 2017

Maneesha Yadav-Shah

series ordinal

3

1 reference

2 September 2017

Stephanie L Sherman

series ordinal

4

1 reference

2 September 2017

language of work or name

1 reference

3 February 2004

1 reference

2 September 2017

1 reference

2 September 2017

114

1 reference

2 September 2017

5

1 reference

2 September 2017

439-447

1 reference

https://scigraph.springernature.com/pub.10.1007/s00439-004-1086-x

2 September 2017

0 references

cites work

FMR1 protein: conserved RNP family domains and selective RNA binding

1 reference

12 December 2020

Clinical involvement and protein expression in individuals with the FMR1 premutation.

1 reference

12 December 2020

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome

1 reference

12 December 2020

Translational suppression by trinucleotide repeat expansion at FMR1.

1 reference

12 December 2020

Triplet repeats, RNA secondary structure and toxic gain-of-function models for pathogenesis

1 reference

12 December 2020

The fragile X premutation: into the phenotypic fold

1 reference

12 December 2020

Characterization and expression of a cDNA encoding the human androgen receptor

1 reference

12 December 2020

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

12 December 2020

Methylation of ZNF261 as an assay for determining X chromosome inactivation patterns

1 reference

12 December 2020

FMR1 and the fragile X syndrome: human genome epidemiology review

1 reference

12 December 2020

Transcription of the FMR1 gene in individuals with fragile X syndrome

1 reference

12 December 2020

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

1 reference

12 December 2020

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

1 reference

12 December 2020

RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila

1 reference

12 December 2020

Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction.

1 reference

12 December 2020

Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.

1 reference

12 December 2020

Premature ovarian failure in the fragile X syndrome

1 reference

12 December 2020

Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test.

1 reference

12 December 2020

Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers

1 reference

12 December 2020

10.1007/S00439-004-1086-X

Identifiers

DOI

1 reference

Dimensions Publication ID

2 September 2017

0 references

1 reference