Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected]. - Test2 - elhamkhani - TriplyDB

Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].

Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].

http://www.wikidata.org/entity/Q34318418

about

Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules The RNA-binding proteins FMR1, rasputin and caprin act together with the UBA protein lingerer to restrict tissue growth in Drosophila melanogaster Detection and Quantification of the Fragile X Mental Retardation Protein 1 (FMRP)Subcellular fractionation and localization studies reveal a direct interaction of the fragile X mental retardation protein (FMRP) with nucleolin Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies Comprehensive behavioral analysis of RNG105 (Caprin1) heterozygous mice: Reduced social interaction and attenuated response to novelty RNA granule assembly and disassembly modulated by nuclear factor associated with double-stranded RNA 2 and nuclear factor 45 Increasing our understanding of human cognition through the study of Fragile X Syndrome.Concise review: Fragile X proteins in stem cell maintenance and differentiation Bacterial expression and preliminary crystallographic studies of a 149-residue fragment of human Caprin-1.UVC-induced stress granules in mammalian cells Copy number variable microRNAs in schizophrenia and their neurodevelopmental gene targets.Crystal structure of a dimerization domain of human Caprin-1: insights into the assembly of an evolutionarily conserved ribonucleoprotein complex consisting of Caprin-1, FMRP and G3BP1 Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing Co-regulation of mRNA translation by TDP-43 and Fragile X Syndrome protein FMRP A de novo 11p13 Microduplication in a Patient with Some Features Invoking Silver-Russell Syndrome.The challenges of clinical trials in fragile X syndrome.Fragile X mental retardation protein and synaptic plasticity Localization of mRNAs to the endoplasmic reticulum.The MAP1B case: an old MAP that is new again.Behavioral abnormalities in the Fmr1-KO2 mouse model of fragile X syndrome: The relevance of early life phases.Artificial intelligence in neurodegenerative disease research: use of IBM Watson to identify additional RNA-binding proteins altered in amyotrophic lateral sclerosis.Altered expression of the FMR1 splicing variants landscape in premutation carriers.A novel function for the survival motoneuron protein as a translational regulator

P2860

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P2860

Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].

http://www.wikidata.org/entity/Q34318418

description

2012 nî lūn-bûn

@nan

2012 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Fragile X mental retardation p ...... Protein complexes [corrected].

@ast

Fragile X mental retardation p ...... Protein complexes [corrected].

@en

Fragile X mental retardation p ...... Protein complexes [corrected].

@nl

type

label

Fragile X mental retardation p ...... Protein complexes [corrected].

@ast

Fragile X mental retardation p ...... Protein complexes [corrected].

@en

Fragile X mental retardation p ...... Protein complexes [corrected].

@nl

prefLabel

Fragile X mental retardation p ...... Protein complexes [corrected].

@ast

Fragile X mental retardation p ...... Protein complexes [corrected].

@en

Fragile X mental retardation p ...... Protein complexes [corrected].

@nl

P1433

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P1476

Q34318418-08810DC5-E2D9-416C-A325-D7509B415E0D

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P2860

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P356

Q34318418-2BB57173-8D39-469B-A847-A0366D528027

P407

Q34318418-AE1246B5-CEBE-4525-8CFC-A5458EAC994F

P433

Q34318418-50A5A5FD-54C5-4D86-B4D1-D4E5026FE0AA

P478

Q34318418-CAD2EEB6-88C2-49A3-8D57-5C5A744702A4

P577

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P5875

Q34318418-F90A3B56-2B0B-47FA-9459-AE9230C8CB9C

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Q34318418-F09A1542-1B4C-400B-97C5-B25456E2CD8C

P932

Q34318418-4577E028-432E-49DB-889D-1BECBED14010

P356

JOURNAL.PONE.0039338

P1433

P1476

Fragile X mental retardation p ...... Protein complexes [corrected].

@en

P2093

Alain Y Dury

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

Edouard W Khandjian

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

John W Schrader

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

Paul De Koninck

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

Rachid El Fatimy

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

Samuel Solomon

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

Sandra Tremblay

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

P2860

The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2

The splicing regulator TIA-1 interacts with U1-C to promote U1 snRNP recruitment to 5' splice sites.

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

RNA granule protein 140 (RNG140), a paralog of RNG105 localized to distinct RNA granules in neuronal dendrites in the adult vertebrate brain

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

FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism

Argonaute HITS-CLIP decodes microRNA-mRNA interaction maps

Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation

Distinct structural features of caprin-1 mediate its interaction with G3BP-1 and its induction of phosphorylation of eukaryotic translation initiation factor 2alpha, entry to cytoplasmic stress granules, and selective interaction with a subset of mR

Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes.

P304

e39338

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P31

scholarly article

P356

10.1371/JOURNAL.PONE.0039338

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P407

P433

6

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P478

7

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P577

2012-06-21T00:00:00Z

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P5875

228072040

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P698

22737234

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

P921

ribonucleoprotein

P932

3380850

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