CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size

Mouse Models of Fragile X-Associated Tremor Ataxia

(2016) Robert F. Berman et al.   JOURNAL OF INVESTIGATIVE MEDICINE

Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms

(2013) Paul Hagerman   ACTA NEUROPATHOLOGICA

FMR1CGG expansions: Prevalence and sex ratios

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

Abnormal dendrite and spine morphology in primary visual cortex in the CGG knock-in mouse model of the fragile X premutation

(2012) Robert F. Berman et al.   EPILEPSIA

Influence of the fragile X mental retardation (FMR1) gene on the brain and working memory in men with normal FMR1 alleles

(2012) Jun Yi Wang et al.   NEUROIMAGE

FXTAS: New insights and the need for revised diagnostic criteria

(2012) E. Apartis et al.   NEUROLOGY

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

(2012) Flora Tassone et al.   Genome Medicine

Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice

(2011) Michael R. Hunsaker et al.   ACTA NEUROPATHOLOGICA

Motor deficits on a ladder rung task in male and female adolescent and adult CGG knock-in mice

(2011) Michael R. Hunsaker et al.   BEHAVIOURAL BRAIN RESEARCH

Quantitative measurement of FMRP in blood platelets as a new screening test for fragile X syndrome

(2011) M Lessard et al.   CLINICAL GENETICS

Initiation of Translation of the FMR1 mRNA Occurs Predominantly through 5′-End-Dependent Ribosomal Scanning

(2011) Anna L. Ludwig et al.   JOURNAL OF MOLECULAR BIOLOGY

Rare Intranuclear Inclusions in the Brains of 3 Older Adult Males With Fragile X Syndrome: Implications for the Spectrum of Fragile X-Associated Disorders

(2011) Michael R. Hunsaker et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

FMRP Regulates the Transition from Radial Glial Cells to Intermediate Progenitor Cells during Neocortical Development

(2011) R. Saffary et al.   JOURNAL OF NEUROSCIENCE

A mouse model of the fragile X premutation: Effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis

(2011) Mei Qin et al.   NEUROBIOLOGY OF DISEASE

Female CGG knock-in mice modeling the fragile X premutation are impaired on a skilled forelimb reaching task

(2011) Amanda A. Diep et al.   NEUROBIOLOGY OF LEARNING AND MEMORY

New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS)

(2011) Jorge L. Juncos et al.   NEUROGENETICS

Fibromyalgia in fragile X mental retardation 1 gene premutation carriers

(2011) M. A. Leehey et al.   RHEUMATOLOGY

FMR1 and the Continuum of Primary Ovarian Insufficiency

(2011) Shannon Sullivan et al.   SEMINARS IN REPRODUCTIVE MEDICINE

Temporal ordering deficits in female CGG KI mice heterozygous for the fragile X premutation

(2010) Michael R. Hunsaker et al.   BEHAVIOURAL BRAIN RESEARCH

Ubiquitin-positive intranuclear inclusions in neuronal and glial cells in a mouse model of the fragile X premutation

(2010) H. Jürgen Wenzel et al.   BRAIN RESEARCH

FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: Insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States

(2010) Feras M Hantash et al.   GENETICS IN MEDICINE

Fragile X Mental Retardation Protein Regulates Proliferation and Differentiation of Adult Neural Stem/Progenitor Cells

(2010) Yuping Luo et al.   PLoS Genetics

Progressive spatial processing deficits in a mouse model of the fragile X premutation.

(2009) Michael R. Hunsaker et al.   BEHAVIORAL NEUROSCIENCE

Fragile X syndrome—From genes to cognition

(2009) A. Schneider et al.   Developmental Disabilities Research Reviews

Fibroblast phenotype in male carriers of FMR1 premutation alleles

(2009) Dolores Garcia-Arocena et al.   HUMAN MOLECULAR GENETICS

Ectopic expression of CGG containing mRNA is neurotoxic in mammals

(2009) V. Hashem et al.   HUMAN MOLECULAR GENETICS

Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration

(2009) Y. Chen et al.   HUMAN MOLECULAR GENETICS

Examination of FMR1 transcript and protein levels among 74 premutation carriers

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

A Quantitative ELISA Assay for the Fragile X Mental Retardation 1 Protein

(2009) Christine Iwahashi et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome

(2008) Judith R. Brouwer et al.   JOURNAL OF NEUROCHEMISTRY

Advances in the Treatment of Fragile X Syndrome

(2008) R. J. Hagerman et al.   PEDIATRICS

Altered hypothalamus–pituitary–adrenal gland axis regulation in the expanded CGG-repeat mouse model for fragile X-associated tremor/ataxia syndrome

(2008) J.R. Brouwer et al.   PSYCHONEUROENDOCRINOLOGY