(Q28116617)

4 January 2017

title

In vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation protein (English)

1 reference

FMRP translational regulator 1

4 January 2017

main subject

1 reference

Survival of motor neuron 2, centromeric

GOA release 2020-03-11

1 reference

Synaptic functional regulator FMR1

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Christiane Branlant

5

0 references

author name string

Nathalie Piazzon

1

1 reference

4 January 2017

Florence Rage

2

1 reference

4 January 2017

Florence Schlotter

3

1 reference

4 January 2017

Hervé Moine

4

1 reference

4 January 2017

Séverine Massenet

6

1 reference

4 January 2017

language of work or name

English

0 references

publication date

29 February 2008

1 reference

Journal of Biological Chemistry

4 January 2017

published in

1 reference

4 January 2017

volume

283

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4 January 2017

issue

9

1 reference

4 January 2017

page(s)

5598–5610

1 reference

4 January 2017

cites work

Spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Spinal muscular atrophy: a deficiency in a ubiquitous protein; a motor neuron-specific disease

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M707304200

Identification and characterization of a spinal muscular atrophy-determining gene

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M707304200

Correlation between severity and SMN protein level in spinal muscular atrophy

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M707304200

The survival motor neuron protein in spinal muscular atrophy

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M707304200

A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The SMN complex, an assemblyosome of ribonucleoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Characterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Gemin5, a novel WD repeat protein component of the SMN complex that binds Sm proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Purification of native survival of motor neurons complexes and identification of Gemin6 as a novel component

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Identification and characterization of Gemin7, a novel component of the survival of motor neuron complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Gemin8 is a novel component of the survival motor neuron complex and functions in small nuclear ribonucleoprotein assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Unrip is a component of SMN complexes active in snRNP assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Unrip, a factor implicated in cap-independent translation, associates with the cytosolic SMN complex and influences its intracellular localization

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Assisted RNP assembly: SMN and PRMT5 complexes cooperate in the formation of spliceosomal UsnRNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Why do cells need an assembly machine for RNA-protein complexes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Spliceosomal UsnRNP biogenesis, structure and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Specific sequences of the Sm and Sm-like (Lsm) proteins mediate their interaction with the spinal muscular atrophy disease gene product (SMN).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Essential role for the SMN complex in the specificity of snRNP assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Sequence-specific interaction of U1 snRNA with the SMN complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

SMN-mediated assembly of RNPs: a complex story

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

snRNAs contain specific SMN-binding domains that are essential for snRNP assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Specific sequence features, recognized by the SMN complex, identify snRNAs and determine their fate as snRNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The Gemin5 protein of the SMN complex identifies snRNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The SMN complex is associated with snRNPs throughout their cytoplasmic assembly pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

SMN, the spinal muscular atrophy protein, forms a pre-import snRNP complex with snurportin1 and importin beta

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Interaction between the small-nuclear-RNA cap hypermethylase and the spinal muscular atrophy protein, survival of motor neuron

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Coupled in vitro import of U snRNPs and SMN, the spinal muscular atrophy protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Unique Sm core structure of U7 snRNPs: assembly by a specialized SMN complex and the role of a new component, Lsm11, in histone RNA processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Is spinal muscular atrophy the result of defects in motor neuron processes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Chaperoning ribonucleoprotein biogenesis in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Survival motor neuron (SMN) protein: role in neurite outgrowth and neuromuscular maturation during neuronal differentiation and development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

A role for complexes of survival of motor neurons (SMN) protein with gemins and profilin in neurite-like cytoplasmic extensions of cultured nerve cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Localization and translation of mRNA in dendrites and axons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Translating axon guidance cues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

New insights into neuronal regeneration: the role of axonal protein synthesis in pathfinding and axonal extension

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The evolving roles of axonally synthesized proteins in regeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Current advances in local protein synthesis and synaptic plasticity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

SMN interacts with a novel family of hnRNP and spliceosomal proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The fragile X mental retardation protein inhibits translation via interacting with mRNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Analysis of domains affecting intracellular localization of the FMRP protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The mGluR theory of fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Local functions for FMRP in axon growth cone motility and activity-dependent regulation of filopodia and spine synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The fragile X mental retardation protein-RNP granules show an mGluR-dependent localization in the post-synaptic spines

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The methylosome, a 20S complex containing JBP1 and pICln, produces dimethylarginine-modified Sm proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Immunopurification of heterogeneous nuclear ribonucleoprotein particles reveals an assortment of RNA-binding proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Monoclonal antibody characterization of the C proteins of heterogeneous nuclear ribonucleoprotein complexes in vertebrate cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Antibodies to small nuclear RNAs complexed with proteins are produced by patients with systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Brain-derived neurotrophic factor and neurotrophin-3 enhance somatostatin gene expression through a likely direct effect on hypothalamic somatostatin neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The Gemin6-Gemin7 heterodimer from the survival of motor neurons complex has an Sm protein-like structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Transport of fragile X mental retardation protein via granules in neurites of PC12 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Metabotropic glutamate receptor activation regulates fragile x mental retardation protein and FMR1 mRNA localization differentially in dendrites and at synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Automatic and quantitative measurement of protein-protein colocalization in live cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Survival motor neuron protein facilitates assembly of stress granules

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

A Ras-GTPase-activating protein SH3-domain-binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

A novel phosphorylation-dependent RNase activity of GAP-SH3 binding protein: a potential link between signal transduction and RNA stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The RasGAP-associated endoribonuclease G3BP assembles stress granules

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The domain encoded by exon 2 of the survival motor neuron protein mediates nucleic acid binding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

FMR1 protein: conserved RNP family domains and selective RNA binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The C terminus of fragile X mental retardation protein interacts with the multi-domain Ran-binding protein in the microtubule-organising centre

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

A point mutation in the FMR-1 gene associated with fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

SMN, the product of the spinal muscular atrophy gene, binds preferentially to dimethylarginine-containing protein targets

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Coilin methylation regulates nuclear body formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Symmetrical dimethylarginine methylation is required for the localization of SMN in Cajal bodies and pre-mRNA splicing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Identification and characterization of the methyl arginines in the fragile X mental retardation protein Fmrp

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Alternative splicing modulates protein arginine methyltransferase-dependent methylation of fragile X syndrome mental retardation protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

RNA-binding proteins: a lesson in repression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Neuronal RNA granules: movers and makers

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Transcription, translation and fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

A functional interaction between the survival motor neuron complex and RNA polymerase II

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

A novel association of the SMN protein with two major non-ribosomal nucleolar proteins and its implication in spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Molecular composition of IMP1 ribonucleoprotein granules

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Characterization of an RNA granule from developing brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Kinesin transports RNA: isolation and characterization of an RNA-transporting granule

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The composition of Staufen-containing RNA granules from human cells indicates their role in the regulated transport and translation of messenger RNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Characterization of Staufen 1 ribonucleoprotein complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The fragile X mental retardation protein interacts with U-rich RNAs in a yeast three-hybrid system

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

RNA interference: a new mechanism by which FMRP acts in the normal brain? What can Drosophila teach us?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Nuclear export factor family protein participates in cytoplasmic mRNA trafficking.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The MAP1 family of microtubule-associated proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

New insights into fragile X syndrome: from molecules to neurobehaviors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The RNA binding protein FMRP: new connections and missing links.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

The Drosophila fragile X mental retardation protein controls actin dynamics by directly regulating profilin in the brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

p140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Regulators of Rho GTPases in neuronal development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Determinants of the interaction of the spinal muscular atrophy disease protein SMN with the dimethylarginine-modified box H/ACA small nucleolar ribonucleoprotein GAR1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Phosphorylation influences the translation state of FMRP-associated polyribosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M707304200

21 January 2018

Identifiers

DOI

10.1074/JBC.M707304200

0 references

1 reference