Differential increases of specificFMR1mRNA isoforms in premutation carriers

A Chromatin-Dependent Role of the Fragile X Mental Retardation Protein FMRP in the DNA Damage Response

(2014) Roman Alpatov et al.   CELL

The MAP1B case: An old MAP that is new again

(2014) David Villarroel-Campos et al.   Developmental Neurobiology

Fragile X Mental Retardation Protein Regulates Translation by Binding Directly to the Ribosome

(2014) Eileen Chen et al.   MOLECULAR CELL

Fragile X mental retardation protein controls synaptic vesicle exocytosis by modulating N-type calcium channel density

(2014) Laurent Ferron et al.   Nature Communications

FMR1CGG expansions: Prevalence and sex ratios

(2013) Matthew J. Maenner et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome

(2013) Randi Hagerman et al.   LANCET NEUROLOGY

Reduced excitatory amino acid transporter 1 and metabotropic glutamate receptor 5 expression in the cerebellum of fragile X mental retardation gene 1 premutation carriers with fragile X-associated tremor/ataxia syndrome

(2013) Dalyir I. Pretto et al.   NEUROBIOLOGY OF AGING

Fmr1 Transcript Isoforms: Association with Polyribosomes; Regional and Developmental Expression in Mouse Brain

(2013) David M. Brackett et al.   PLoS One

Nuclear Fragile X Mental Retardation Protein Is localized to Cajal Bodies

(2013) Alain Y. Dury et al.   PLoS Genetics

Sequencing the unsequenceable: Expanded CGG-repeat alleles of the fragile X gene

(2012) E. W. Loomis et al.   GENOME RESEARCH

Regulation of N-type Voltage-Gated Calcium Channels and Presynaptic Function by Cyclin-Dependent Kinase 5

(2012) Susan C. Su et al.   NEURON

BC1-FMRP interaction is modulated by 2′-O-methylation: RNA-binding activity of the tudor domain and translational regulation at synapses

(2012) Caroline Lacoux et al.   NUCLEIC ACIDS RESEARCH

FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States

(2012) Flora Tassone et al.   Genome Medicine

Analysis of the Fragile X mental retardation protein isoforms 1, 2 and 3 interactions with the G-quadruplex forming semaphorin 3F mRNA

(2011) Timothy L. Evans et al.   Molecular BioSystems

Spinal muscular atrophy: A new player joins the battle forSMN2exon 7 splicing

(2010) Simona Pedrotti et al.   CELL CYCLE

Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients

(2010) Chantal Sellier et al.   EMBO JOURNAL

A flexible and efficient template format for circular consensus sequencing and SNP detection

(2010) K. J. Travers et al.   NUCLEIC ACIDS RESEARCH

Structural Studies of the Tandem Tudor Domains of Fragile X Mental Retardation Related Proteins FXR1 and FXR2

(2010) Melanie A. Adams-Cioaba et al.   PLoS One

Recombinant bacterial expression and purification of human fragile X mental retardation protein isoform 1

(2010) Timothy L. Evans et al.   PROTEIN EXPRESSION AND PURIFICATION

Functional status of men with the fragile X premutation, with and without the tremor/ataxia syndrome (FXTAS)

(2009) Angela G. Brega et al.   INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY

Examination of FMR1 transcript and protein levels among 74 premutation carriers

(2009) Emmanuel Peprah et al.   JOURNAL OF HUMAN GENETICS

Tissue and developmental regulation of fragile X mental retardation 1 exon 12 and 15 isoforms

(2009) Wen Xie et al.   NEUROBIOLOGY OF DISEASE

Structure and function of KH domains

(2008) Roberto Valverde et al.   FEBS Journal

GPS 2.0, a Tool to Predict Kinase-specific Phosphorylation Sites in Hierarchy

(2008) Yu Xue et al.   MOLECULAR & CELLULAR PROTEOMICS

Sam68 Regulates a Set of Alternatively Spliced Exons during Neurogenesis

(2008) G. Chawla et al.   MOLECULAR AND CELLULAR BIOLOGY

Real-Time DNA Sequencing from Single Polymerase Molecules

(2008) J. Eid et al.   SCIENCE