(Q30329219)

18 June 2017

1 reference

title

A structural approach to trinucleotide expansion diseases. (English)

1 reference

18 June 2017

Masino L

1

1 reference

PubMed ID

11719249

18 June 2017

Pastore A

series ordinal

2

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18 June 2017

1 October 2001

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18 June 2017

Brain Research Bulletin

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18 June 2017

56

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18 June 2017

3-4

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18 June 2017

183-189

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Iron-dependent self-assembly of recombinant yeast frataxin: implications for Friedreich ataxia

18 June 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Random coil conformation for extended polyglutamine stretches in aqueous soluble monomeric peptides.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Structure of polyglutamine

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

FMR1 protein: conserved RNP family domains and selective RNA binding

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Accessory factor-bZIP-DNA interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Loss of normal huntingtin function: new developments in Huntington's disease research

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Crystal structure of a dimeric chymotrypsin inhibitor 2 mutant containing an inserted glutamine repeat

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Crystal structure of Escherichia coli CyaY protein reveals a previously unidentified fold for the evolutionarily conserved frataxin family

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Fourteen and counting: unraveling trinucleotide repeat diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Crystal structure of human frataxin

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Friedreich's ataxia protein: phylogenetic evidence for mitochondrial dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

The KH domain occurs in a diverse set of RNA-binding proteins that include the antiterminator NusA and is probably involved in binding to nucleic acid.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

1 reference

7 January 2021

Understanding the molecular basis of fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Peptides containing glutamine repeats as substrates for transglutaminase-catalyzed cross-linking: relevance to diseases of the nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Aberrant protein deposition and neurological disease

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Sequence-specific RNA binding by a Nova KH domain: implications for paraneoplastic disease and the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Amyloid-like inclusions in Huntington's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Poly-L-glutamine forms cation channels: relevance to the pathogenesis of the polyglutamine diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

New tubular single-stranded helix of poly-L-amino acids suggested by molecular mechanics calculations: I. Homopolypeptides in isolated environments

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Three-dimensional structure and stability of the KH domain: molecular insights into the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Towards a structural understanding of Friedreich's ataxia: the solution structure of frataxin

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Reversing neurodegeneration: a promise unfolds

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Molecular pathogenesis of Friedreich ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Protein fate in neurodegenerative proteinopathies: polyglutamine diseases join the (mis)fold

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Trinucleotide repeat DNA structures: dynamic mutations from dynamic DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

1 reference

7 January 2021

Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Glutamine repeats and inherited neurodegenerative diseases: molecular aspects

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Self-assembly of polyglutamine-containing huntingtin fragments into amyloid-like fibrils: implications for Huntington's disease pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Peptide models for inherited neurodegenerative disorders: conformation and aggregation properties of long polyglutamine peptides with and without interruptions

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Folding of oligoglutamines: a theoretical approach based upon thermodynamics and molecular mechanics.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Incorporation of glutamine repeats makes protein oligomerize: implications for neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Polyglutamine diseases: protein cleavage and aggregation.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

Glutamine repeats and neurodegeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900582-2

7 January 2021

10.1016/S0361-9230(01)00582-2

Identifiers

DOI

1 reference

18 June 2017

1 reference

PubMed ID

11719249