AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats. - Wikidata - awgldk - TriplyDB

AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats.

AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats.

http://www.wikidata.org/entity/Q35049830

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Unique AGG Interruption in the CGG Repeats of the FMR1 Gene Exclusively Found in Asians Linked to a Specific SNP Haplotype Defining the role of the CGGBP1 protein in FMR1 gene expression.Of Men and Mice: Modeling the Fragile X Syndrome.

P2860

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P2860

AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats.

http://www.wikidata.org/entity/Q35049830

description

2013 nî lūn-bûn

@nan

2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

@zh-hk

2013年論文

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2013年論文

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2013年论文

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name

AGG/CCT interruptions affect n ...... ength CGG/CCG triplet repeats.

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AGG/CCT interruptions affect n ...... ength CGG/CCG triplet repeats.

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AGG/CCT interruptions affect n ...... ength CGG/CCG triplet repeats.

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AGG/CCT interruptions affect n ...... ength CGG/CCG triplet repeats.

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AGG/CCT interruptions affect n ...... ength CGG/CCG triplet repeats.

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1471-2091-14-33

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BMC Biochemistry

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AGG/CCT interruptions affect n ...... ength CGG/CCG triplet repeats.

@en

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Catherine B Volle

http://www.w3.org/2001/XMLSchema#string

Sarah Delaney

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P2860

Crystal structure of the nucleosome core particle at 2.8 A resolution

Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function

Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles

Hydroxyl radical "footprinting": high-resolution information about DNA-protein contacts and application to lambda repressor and Cro protein

Facile FMR1 mRNA structure regulation by interruptions in CGG repeats

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

A decade of molecular studies of fragile X syndrome

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

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

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

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1471-2091-14-33

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33

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10.1186/1471-2091-14-33

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14

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2013-11-22T00:00:00Z

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258827225

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