标题
CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 23, Issue 12, Pages 3228-3238
出版商
Oxford University Press (OUP)
发表日期
2014-01-25
DOI
10.1093/hmg/ddu032
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- 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 syndromeâFrom 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
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now