Facile FMR1 mRNA structure regulation by interruptions in CGG repeats (Q24801535)

4

object named as

Wlodzimierz J Krzyzosiak

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author name string

Marek Napierala

1

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Daniel Michalowski

2

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Mateusz de Mezer

The fragile-X premutation: a maturing perspective

3

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language of work or name

English

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publication date

2005

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published in

Nucleic Acids Research

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volume

33

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issue

2

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page(s)

451-63

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cites work

1 reference

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Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population

7 April 2017

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

7 April 2017

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

7 April 2017

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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

7 April 2017

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Repetitive sequences that shape the human transcriptome

7 April 2017

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Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element

28 September 2017

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The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer

28 September 2017

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The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter

28 September 2017

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RNA structure of trinucleotide repeats associated with human neurological diseases

28 September 2017

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The X chromosome and fragile X mental retardation

28 September 2017

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Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations.

28 September 2017

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The non-Watson-Crick base pairs and their associated isostericity matrices

28 September 2017

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Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes.

28 September 2017

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The fragile X premutation: into the phenotypic fold

28 September 2017

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

28 September 2017

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Transcription of the FMR1 gene in individuals with fragile X syndrome

28 September 2017

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

28 September 2017

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T7 RNA polymerase produces 5' end heterogeneity during in vitro transcription from certain templates

28 September 2017

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The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure

28 September 2017

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Length of uninterrupted CGG repeats determines instability in the FMR1 gene

28 September 2017

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The fragile X premutation in carriers and its effect on mutation size in offspring

28 September 2017

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28 September 2017

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28 September 2017

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A proton-coupled conformational switch of Escherichia coli 5S ribosomal RNA

28 September 2017

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Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation

28 September 2017

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Effects of Mg2 , K , and H on an equilibrium between alternative conformations of an RNA pseudoknot

28 September 2017

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Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome

30 May 2018

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Population incidence and segregation ratios in the Martin-Bell syndrome

30 May 2018

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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

30 May 2018

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Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

30 May 2018

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Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome

30 May 2018

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

28 November 2018

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Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles

28 November 2018

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

28 November 2018

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Translational suppression by trinucleotide repeat expansion at FMR1.

28 November 2018

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Characterization of the lead(II)-induced cleavages in tRNAs in solution and effect of the Y-base removal in yeast tRNAPhe

28 November 2018

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[Effect of protonation of nucleic acid bases on the energy of formation of the Watson-Crick pairs]

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12 December 2020

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CUG Repeats Present in Myotonin Kinase RNA Form Metastable “Slippery” Hairpins

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