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
about
Inclusion of Scar/WAVE3 in a similar complex to Scar/WAVE1 and 2CRMP-2 is involved in kinesin-1-dependent transport of the Sra-1/WAVE1 complex and axon formationHem-1 complexes are essential for Rac activation, actin polymerization, and myosin regulation during neutrophil chemotaxisNYAP: a phosphoprotein family that links PI3K to WAVE1 signalling in neuronsIdentification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking dupliconsNIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).Evolutionarily conserved human targets of adenosine to inosine RNA editingThe comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Age-related gene-specific changes of A-to-I mRNA editing in the human brainFragile X syndrome: loss of local mRNA regulation alters synaptic development and functionDysregulation and restoration of translational homeostasis in fragile X syndromeThe FMRP regulon: from targets to disease convergenceFragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice.Alzheimer-related decrease in CYFIP2 links amyloid production to tau hyperphosphorylation and memory loss.Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in miceThe amino-terminal structure of human fragile X mental retardation protein obtained using precipitant-immobilized imprinted polymersThe neurobiology of the Prader-Willi phenotype of fragile X syndromeSubcellular fractionation and localization studies reveal a direct interaction of the fragile X mental retardation protein (FMRP) with nucleolinKissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes.Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodiesIndependent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizuresIn vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation proteinThe fragile X gene and its functionMechanism of regulation of WAVE1-induced actin nucleation by Rac1 and NckFrom mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndromeAbi1 is essential for the formation and activation of a WAVE2 signalling complexRNA and microRNAs in fragile X mental retardationThe fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif.Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structureUp-regulated cytoplasmic FMRP-interacting protein 1 in intractable temporal lobe epilepsy patients and a rat modelMolecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targetsABI2-deficient mice exhibit defective cell migration, aberrant dendritic spine morphogenesis, and deficits in learning and memoryCYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formationSystematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts.Transcript diversification in the nervous system: a to I RNA editing in CNS function and disease developmentFragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2PFilopodia formation in the absence of functional WAVE- and Arp2/3-complexes.Cyfip1 is a putative invasion suppressor in epithelial cancers.Visual search of neuropil-enriched RNAs from brain in situ hybridization data through the image analysis pipeline hippo-ATESC.Transport of Drosophila fragile X mental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein.
P2860
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P248
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P2860
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
description
2001 nî lūn-bûn
@nan
2001 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@ast
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@en
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@en-gb
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@nl
type
label
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@ast
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@en
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@en-gb
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@nl
prefLabel
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@ast
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@en
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@en-gb
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@nl
P2860
P50
P921
P3181
P356
P1476
A highly conserved protein fam ...... lated proteins FXR1P and FXR2P
@en
P2093
P2860
P304
P3181
P356
10.1073/PNAS.151231598
P407
P577
2001-07-03T00:00:00Z