Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment
出版年份 2017 全文链接
标题
Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment
作者
关键词
-
出版物
eLife
Volume 6, Issue -, Pages -
出版商
eLife Sciences Organisation, Ltd.
发表日期
2017-07-11
DOI
10.7554/elife.25730
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。- First-in-man study with a novel PEGylated recombinant human insulin-like growth factor-I
- (2017) H. Kletzl et al. GROWTH HORMONE & IGF RESEARCH
- Animal Models of Speech and Vocal Communication Deficits Associated With Psychiatric Disorders
- (2016) Genevieve Konopka et al. BIOLOGICAL PSYCHIATRY
- Essential Roles for ARID1B in Dendritic Arborization and Spine Morphology of Developing Pyramidal Neurons
- (2016) Minhan Ka et al. JOURNAL OF NEUROSCIENCE
- Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group
- (2016) L Schmaal et al. MOLECULAR PSYCHIATRY
- CHD8 haploinsufficiency results in autistic-like phenotypes in mice
- (2016) Yuta Katayama et al. NATURE
- De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature
- (2015) Yongguo Yu et al. BMC GENOMICS
- FoxP1 orchestration of ASD-relevant signaling pathways in the striatum
- (2015) Daniel J. Araujo et al. GENES & DEVELOPMENT
- Dentate gyrus volume and memory performance in major depressive disorder
- (2015) Scott Travis et al. JOURNAL OF AFFECTIVE DISORDERS
- HISAT: a fast spliced aligner with low memory requirements
- (2015) Daehwan Kim et al. NATURE METHODS
- Mammalian SWI/SNF chromatin remodeling complexes and cancer: Mechanistic insights gained from human genomics
- (2015) C. Kadoch et al. Science Advances
- TheARID1Bphenotype: What we have learned so far
- (2014) Gijs W.E. Santen et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Tissue-specific SMARCA4 binding at active and repressed regulatory elements during embryogenesis
- (2014) C. Attanasio et al. GENOME RESEARCH
- The P7C3 class of neuroprotective compounds exerts antidepressant efficacy in mice by increasing hippocampal neurogenesis
- (2014) A K Walker et al. MOLECULAR PSYCHIATRY
- Large-scale discovery of novel genetic causes of developmental disorders
- (2014) T. W. Fitzgerald et al. NATURE
- Functional recovery with recombinant human IGF1 treatment in a mouse model of Rett Syndrome
- (2014) Jorge Castro et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
- (2013) Y. Liao et al. BIOINFORMATICS
- A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling
- (2013) Dagmar Wieczorek et al. HUMAN MOLECULAR GENETICS
- Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients
- (2013) Gijs W.E. Santen et al. HUMAN MUTATION
- Decreased hippocampal volume and increased anxiety in a transgenic mouse model expressing the human CYP2C19 gene
- (2013) A Persson et al. MOLECULAR PSYCHIATRY
- From neural development to cognition: unexpected roles for chromatin
- (2013) Jehnna L. Ronan et al. NATURE REVIEWS GENETICS
- Hippocampal Granule Neuron Number and Dentate Gyrus Volume in Antidepressant-Treated and Untreated Major Depression
- (2013) Maura Boldrini et al. NEUROPSYCHOPHARMACOLOGY
- Haploinsufficiency of ARID1B , a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability
- (2012) Juliane Hoyer et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Autism-related behavioral abnormalities in synapsin knockout mice
- (2012) Barbara Greco et al. BEHAVIOURAL BRAIN RESEARCH
- GENCODE: The reference human genome annotation for The ENCODE Project
- (2012) J. Harrow et al. GENOME RESEARCH
- Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome
- (2012) Gijs W E Santen et al. NATURE GENETICS
- Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome
- (2012) Yoshinori Tsurusaki et al. NATURE GENETICS
- Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
- (2012) B. J. O'Roak et al. SCIENCE
- Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B
- (2011) C Halgren et al. CLINICAL GENETICS
- Abnormal Speech Spectrum and Increased Pitch Variability in Young Autistic Children
- (2011) Yoram S. Bonneh et al. Frontiers in Human Neuroscience
- Chromatin remodelling during development
- (2010) Lena Ho et al. NATURE
- Behavioural phenotyping assays for mouse models of autism
- (2010) Jill L. Silverman et al. NATURE REVIEWS NEUROSCIENCE
- Is this the Coffin-Siris syndrome or the BOD syndrome?
- (2009) Ariel Brautbar et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- edgeR: a Bioconductor package for differential expression analysis of digital gene expression data
- (2009) M. D. Robinson et al. BIOINFORMATICS
- Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice
- (2009) Daniela Tropea et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- AutDB: a gene reference resource for autism research
- (2008) Saumyendra N. Basu et al. NUCLEIC ACIDS RESEARCH
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started