标题
Increased gene expression of FOXP1 in patients with autism spectrum disorders
作者
关键词
Autism, FOXP1, Expression microarray, Genetics, Lymphoblastoid cell line
出版物
Molecular Autism
Volume 4, Issue 1, Pages 23
出版商
Springer Nature
发表日期
2013-07-01
DOI
10.1186/2040-2392-4-23
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。- Forkhead box protein p1 is a transcriptional repressor of immune signaling in the CNS: implications for transcriptional dysregulation in Huntington disease
- (2012) Bin Tang et al. HUMAN MOLECULAR GENETICS
- Genome-wide expression profiling of schizophrenia using a large combined cohort
- (2012) M Mistry et al. MOLECULAR PSYCHIATRY
- Characteristics and Predictive Value of Blood Transcriptome Signature in Males with Autism Spectrum Disorders
- (2012) Sek Won Kong et al. PLoS One
- Prevalence of Autism Spectrum Disorders in a Total Population Sample
- (2011) Young Shin Kim et al. AMERICAN JOURNAL OF PSYCHIATRY
- Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1
- (2011) Anne Gregor et al. BMC Medical Genetics
- Genetic basis of autism: is there a way forward?
- (2011) Valsamma Eapen CURRENT OPINION IN PSYCHIATRY
- Links between genetics and pathophysiology in the autism spectrum disorders
- (2011) Richard Holt et al. EMBO Molecular Medicine
- MicroRNA miR-9 Modifies Motor Neuron Columns by a Tuning Regulation of FoxP1 Levels in Developing Spinal Cords
- (2011) G. Otaegi et al. JOURNAL OF NEUROSCIENCE
- Imprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells
- (2011) E Gardiner et al. MOLECULAR PSYCHIATRY
- Modelling schizophrenia using human induced pluripotent stem cells
- (2011) Kristen J. Brennand et al. NATURE
- Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
- (2011) Brian J O'Roak et al. NATURE GENETICS
- The conundrums of understanding genetic risks for autism spectrum disorders
- (2011) Matthew W State et al. NATURE NEUROSCIENCE
- Gene expression studies in autism: Moving from the genome to the transcriptome and beyond
- (2011) Irina Voineagu NEUROBIOLOGY OF DISEASE
- Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder
- (2011) Eriko Fujita et al. NEUROSCIENCE LETTERS
- Expression profiling in neuropsychiatric disorders: Emphasis on glutamate receptors in bipolar disorder
- (2011) Stephen D. Ginsberg et al. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
- Gene expression analysis in lymphoblasts derived from patients with autism spectrum disorder
- (2011) Yuka Yasuda et al. Molecular Autism
- De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment
- (2010) Fadi F. Hamdan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Sex difference in the rates and co-occurring conditions of psychiatric symptoms in incoming college students in Taiwan
- (2010) Yi-Ling Chien et al. COMPREHENSIVE PSYCHIATRY
- Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
- (2010) Denise Horn et al. HUMAN MUTATION
- Genetic Advances in the Study of Speech and Language Disorders
- (2010) D.F. Newbury et al. NEURON
- Cellular and mitochondrial glutathione redox imbalance in lymphoblastoid cells derived from children with autism
- (2009) S. Jill James et al. FASEB JOURNAL
- Prevalence of Parent-Reported Diagnosis of Autism Spectrum Disorder Among Children in the US, 2007
- (2009) M. D. Kogan et al. PEDIATRICS
- Gene Expression Profiling of Lymphoblasts from Autistic and Nonaffected Sib Pairs: Altered Pathways in Neuronal Development and Steroid Biosynthesis
- (2009) Valerie W. Hu et al. PLoS One
- Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan
- (2009) Wei-Hsien Chien et al. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
- Behavioral problems and parenting style among Taiwanese children with autism and their siblings
- (2009) Susan Shur-Fen Gau et al. PSYCHIATRY AND CLINICAL NEUROSCIENCES
- Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
- (2008) Maricela Alarcón et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism
- (2008) Dan E. Arking et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders
- (2008) Betul Bakkaloglu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A Discriminating Messenger RNA Signature for Bipolar Disorder Formed by an Aberrant Expression of Inflammatory Genes in Monocytes
- (2008) Roos C. Padmos et al. ARCHIVES OF GENERAL PSYCHIATRY
- Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism
- (2008) Zohreh Talebizadeh et al. Autism Research
- Methylation Mediated Silencing of MicroRNA-1 Gene and Its Role in Hepatocellular Carcinogenesis
- (2008) J. Datta et al. CANCER RESEARCH
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