Cytoplasmic FMRP interacting protein 1/2 (CYFIP1/2) expression analysis in autism
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Title
Cytoplasmic FMRP interacting protein 1/2 (CYFIP1/2) expression analysis in autism
Authors
Keywords
CYFIP1, CYFIP2, Autism
Journal
METABOLIC BRAIN DISEASE
Volume 33, Issue 4, Pages 1353-1358
Publisher
Springer Nature
Online
2018-05-11
DOI
10.1007/s11011-018-0249-8
References
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Related references
Note: Only part of the references are listed.- Association study of the vesicular monoamine transporter 1 ( VMAT1 ) gene with autism in an Iranian population
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- (2016) Sachin Suresh Tiwari et al. BRAIN
- Peripheral brain-derived neurotrophic factor in autism spectrum disorder: a systematic review and meta-analysis
- (2016) Zhen Zheng et al. Scientific Reports
- A Putative Blood-Based Biomarker for Autism Spectrum Disorder-Associated Ileocolitis
- (2016) Stephen J. Walker et al. Scientific Reports
- Common Regulatory Variants ofCYFIP1Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism
- (2015) Jian Wang et al. ANNALS OF HUMAN GENETICS
- Perspective Biological Markers for Autism Spectrum Disorders: Advantages of the Use of Receiver Operating Characteristic Curves in Evaluating Marker Sensitivity and Specificity
- (2015) Provvidenza M. Abruzzo et al. DISEASE MARKERS
- Fragile X mental retardation protein (FMRP) interacting proteins exhibit different expression patterns during development
- (2015) C.M. Bonaccorso et al. INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE
- Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR
- (2014) A Oguro-Ando et al. MOLECULAR PSYCHIATRY
- CYFIP family proteins between autism and intellectual disability: links with Fragile X syndrome
- (2014) Sabiha Abekhoukh et al. Frontiers in Cellular Neuroscience
- Erratum: The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines
- (2014) M Pathania et al. Translational Psychiatry
- Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders
- (2011) Dan Levy et al. NEURON
- A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder
- (2009) Bert van der Zwaag et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
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