Rho GTPase Regulators and Effectors in Autism Spectrum Disorders: Animal Models and Insights for Therapeutics
Published 2020 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Rho GTPase Regulators and Effectors in Autism Spectrum Disorders: Animal Models and Insights for Therapeutics
Authors
Keywords
-
Journal
Cells
Volume 9, Issue 4, Pages 835
Publisher
MDPI AG
Online
2020-04-01
DOI
10.3390/cells9040835
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders
- (2020) Sónia Barbosa et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Two Autism/Dyslexia Linked Variations of DOCK4 Disrupt the Gene Function on Rac1/Rap1 Activation, Neurite Outgrowth, and Synapse Development
- (2020) Miaoqi Huang et al. Frontiers in Cellular Neuroscience
- Behavioral training rescues motor deficits in Cyfip1 haploinsufficiency mouse model of autism spectrum disorders
- (2019) Sven O. Bachmann et al. Translational Psychiatry
- Trio Haploinsufficiency Causes Neurodevelopmental Disease-Associated Deficits
- (2019) Sara Marie Katrancha et al. Cell Reports
- Autism and Schizophrenia-Associated CYFIP1 Regulates the Balance of Synaptic Excitation and Inhibition
- (2019) Elizabeth C. Davenport et al. Cell Reports
- Regulators of Rho GTPases in the Nervous System: Molecular Implication in Axon Guidance and Neurological Disorders
- (2019) Sadig Niftullayev et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- (2019) Nirmal Vadgama et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- The influence of neuroinflammation in Autism Spectrum Disorder
- (2019) Samantha M. Matta et al. BRAIN BEHAVIOR AND IMMUNITY
- Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes
- (2019) Juan Xiong et al. Frontiers in Neuroscience
- p190RhoGAPs, the ARHGAP35- and ARHGAP5-Encoded Proteins, in Health and Disease
- (2019) Héraud et al. Cells
- DOCK8 is expressed in microglia, and it regulates microglial activity during neurodegeneration in murine disease models
- (2019) Kazuhiko Namekata et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The autism- and schizophrenia-associated protein CYFIP1 regulates bilateral brain connectivity and behaviour
- (2019) Nuria Domínguez-Iturza et al. Nature Communications
- Cyfip1 haploinsufficient rats show white matter changes, myelin thinning, abnormal oligodendrocytes and behavioural inflexibility
- (2019) Ana I. Silva et al. Nature Communications
- CYFIP1 overexpression increases fear response in mice but does not affect social or repetitive behavioral phenotypes
- (2019) Catherine Fricano-Kugler et al. Molecular Autism
- Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks
- (2019) Elizabeth K. Ruzzo et al. CELL
- Characterization of intellectual disability and autism comorbidity through gene panel sequencing
- (2019) Maria C. Aspromonte et al. HUMAN MUTATION
- Autism-like social deficit generated by Dock4 deficiency is rescued by restoration of Rac1 activity and NMDA receptor function
- (2019) Daji Guo et al. MOLECULAR PSYCHIATRY
- Biochemical and Morphological Characterization of a Guanine Nucleotide Exchange Factor ARHGEF9 in Mouse Tissues
- (2018) Kyoko Ibaraki et al. ACTA HISTOCHEMICA ET CYTOCHEMICA
- De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures
- (2018) Yoko Ito et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Rho GTPases in Intellectual Disability: From Genetics to Therapeutic Opportunities
- (2018) Valentina Zamboni et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Cytoplasmic FMRP interacting protein 1/2 (CYFIP1/2) expression analysis in autism
- (2018) Rezvan Noroozi et al. METABOLIC BRAIN DISEASE
- Dendritic spine actin cytoskeleton in autism spectrum disorder
- (2018) Merja Joensuu et al. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
- Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders
- (2018) Danijela Krgovic et al. Scientific Reports
- Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder
- (2018) Atsushi Takata et al. Cell Reports
- Impairment of social behaviors in Arhgef10 knockout mice
- (2018) Dai-Hua Lu et al. Molecular Autism
- Synaptic Plasticity and Excitation-Inhibition Balance in the Dentate Gyrus: Insights from In Vivo Recordings in Neuroligin-1, Neuroligin-2, and Collybistin Knockouts
- (2018) Peter Jedlicka et al. NEURAL PLASTICITY
- The Autism-Related Protein PX-RICS Mediates GABAergic Synaptic Plasticity in Hippocampal Neurons and Emotional Learning in Mice
- (2018) Tsutomu Nakamura et al. EBioMedicine
- Autism spectrum disorder in females with ARHGEF9 alterations and a random pattern of X chromosome inactivation
- (2018) Mahmoud Aarabi et al. European Journal of Medical Genetics
- PAK2 Haploinsufficiency Results in Synaptic Cytoskeleton Impairment and Autism-Related Behavior
- (2018) Yan Wang et al. Cell Reports
- Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes
- (2018) Hui Guo et al. GENETICS IN MEDICINE
- OCRL Deficiency Impairs Endolysosomal Function in a Humanized Mouse Model for Lowe Syndrome and Dent Disease
- (2018) Beatrice Paola Festa et al. HUMAN MOLECULAR GENETICS
- Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model
- (2018) Hui Guo et al. Molecular Autism
- The Evolutionary Landscape of Dbl-Like RhoGEF Families: Adapting Eukaryotic Cells to Environmental Signals
- (2017) Philippe Fort et al. Genome Biology and Evolution
- Rho GTPase signaling complexes in cell migration and invasion
- (2017) Campbell D. Lawson et al. JOURNAL OF CELL BIOLOGY
- Protein Kinase A Deregulation in the Medial Prefrontal Cortex Impairs Working Memory in Murine Oligophrenin-1 Deficiency
- (2017) Chun-Lei Zhang et al. JOURNAL OF NEUROSCIENCE
- Rho GTPase-activating proteins: Regulators of Rho GTPase activity in neuronal development and CNS diseases
- (2017) Guo-Hui Huang et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders
- (2017) Jinchen Li et al. MOLECULAR PSYCHIATRY
- Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
- (2017) Holly A F Stessman et al. NATURE GENETICS
- Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
- (2017) Madeleine R Geisheker et al. NATURE NEUROSCIENCE
- Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
- (2017) Ryan K C Yuen et al. NATURE NEUROSCIENCE
- WAVE1 in neurons expressing the D1 dopamine receptor regulates cellular and behavioral actions of cocaine
- (2017) Ilaria Ceglia et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- p190RhoGAP proteins contain pseudoGTPase domains
- (2017) Amy L. Stiegler et al. Nature Communications
- p190-B RhoGAP and intracellular cytokine signals balance hematopoietic stem and progenitor cell self-renewal and differentiation
- (2017) Ashwini Hinge et al. Nature Communications
- An autism spectrum disorder-related de novo mutation hotspot discovered in the GEF1 domain of Trio
- (2017) Anastasiia Sadybekov et al. Nature Communications
- Rho GTPases as therapeutic targets in Alzheimer’s disease
- (2017) Byron J. Aguilar et al. Alzheimers Research & Therapy
- Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders
- (2017) Joseph T. Glessner et al. Genome Medicine
- RhoGEF9 splice isoforms influence neuronal maturation and synapse formation downstream of α2 GABAA receptors
- (2017) Claire de Groot et al. PLoS Genetics
- Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA
- (2016) Tychele N. Turner et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Novel features of 3q29 deletion syndrome: Results from the 3q29 registry
- (2016) Megan R. Glassford et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders
- (2016) Chiara Picinelli et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Morphological and behavioral characterization of adult mice deficient for SrGAP3
- (2016) Jonathan Bertram et al. CELL AND TISSUE RESEARCH
- Neocortex expansion in development and evolution — from cell biology to single genes
- (2016) Michaela Wilsch-Bräuninger et al. CURRENT OPINION IN NEUROBIOLOGY
- Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder
- (2016) Gifty Bhat et al. European Journal of Medical Genetics
- Oligophrenin-1 regulates number, morphology and synaptic properties of adult-born inhibitory interneurons in the olfactory bulb
- (2016) Nelly Redolfi et al. HUMAN MOLECULAR GENETICS
- Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability
- (2016) Hamid Meziane et al. HUMAN MOLECULAR GENETICS
- Deciphering the Molecular and Functional Basis of RHOGAP Family Proteins
- (2016) Ehsan Amin et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Cyfip1 Regulates Presynaptic Activity during Development
- (2016) Kuangfu Hsiao et al. JOURNAL OF NEUROSCIENCE
- Comprehensive molecular testing in patients with high functioning autism spectrum disorder
- (2016) Maria Isabel Alvarez-Mora et al. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
- Regulating Rho GTPases and their regulators
- (2016) Richard G. Hodge et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Vicarious trial and error
- (2016) A. David Redish NATURE REVIEWS NEUROSCIENCE
- IRSp53/BAIAP2 in dendritic spine development, NMDA receptor regulation, and psychiatric disorders
- (2016) Jaeseung Kang et al. NEUROPHARMACOLOGY
- Astrocytes and Microglia and Their Potential Link with Autism Spectrum Disorders
- (2016) Francesco Petrelli et al. Frontiers in Cellular Neuroscience
- PX-RICS-deficient mice mimic autism spectrum disorder in Jacobsen syndrome through impaired GABAA receptor trafficking
- (2016) Tsutomu Nakamura et al. Nature Communications
- De novo genic mutations among a Chinese autism spectrum disorder cohort
- (2016) Tianyun Wang et al. Nature Communications
- MYO9B gene polymorphisms are associated with the risk of inflammatory bowel diseases
- (2016) Ming-Jie Wang et al. Oncotarget
- The Contribution of Mosaic Variants to Autism Spectrum Disorder
- (2016) Donald Freed et al. PLoS Genetics
- MicroRNA-132 Interact with p250GAP/Cdc42 Pathway in the Hippocampal Neuronal Culture Model of Acquired Epilepsy and Associated with Epileptogenesis Process
- (2016) Jinxian Yuan et al. NEURAL PLASTICITY
- A pilot study on commonality and specificity of copy number variants in schizophrenia and bipolar disorder
- (2016) J Chen et al. Translational Psychiatry
- A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
- (2016) M. Florio et al. Science Advances
- Common Regulatory Variants ofCYFIP1Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism
- (2015) Jian Wang et al. ANNALS OF HUMAN GENETICS
- Parental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficient mice
- (2015) Leeyup Chung et al. BRAIN RESEARCH
- Trio gene is required for mouse learning ability
- (2015) Wen Zong et al. BRAIN RESEARCH
- Loss of Either Rac1 or Rac3 GTPase Differentially Affects the Behavior of Mutant Mice and the Development of Functional GABAergic Networks
- (2015) Roberta Pennucci et al. CEREBRAL CORTEX
- Collybistin binds and inhibits mTORC1 signaling: a potential novel mechanism contributing to intellectual disability and autism
- (2015) Camila Oliveira Freitas Machado et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A single PXXP motif in the C-terminal region of srGAP3 mediates binding to multiple SH3 domains
- (2015) Silvia Wuertenberger et al. FEBS LETTERS
- 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
- The 15q11.2 BP1–BP2 Microdeletion Syndrome: A Review
- (2015) Devin Cox et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Heritability of autism spectrum disorders: a meta-analysis of twin studies
- (2015) Beata Tick et al. JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY
- From the genetic architecture to synaptic plasticity in autism spectrum disorder
- (2015) Thomas Bourgeron NATURE REVIEWS NEUROSCIENCE
- Rac1 plays an essential role in axon growth and guidance and in neuronal survival in the central and peripheral nervous systems
- (2015) Zhong L. Hua et al. Neural Development
- Low load for disruptive mutations in autism genes and their biased transmission
- (2015) Ivan Iossifov et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Synaptic P-Rex1 signaling regulates hippocampal long-term depression and autism-like social behavior
- (2015) Jun Li et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion
- (2015) M. Florio et al. SCIENCE
- Regulating Rac in the Nervous System: Molecular Function and Disease Implication of Rac GEFs and GAPs
- (2015) Yanyang Bai et al. Biomed Research International
- Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample
- (2015) Emma Colvert et al. JAMA Psychiatry
- Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants
- (2015) Anthony J. Griswold et al. Molecular Autism
- Evidence for autism spectrum disorder in Jacobsen syndrome: identification of a candidate gene in distal 11q
- (2014) Natacha Akshoomoff et al. GENETICS IN MEDICINE
- Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders
- (2014) Regina Waltes et al. HUMAN GENETICS
- Dendritic Cell Motility and T Cell Activation Requires Regulation of Rho-Cofilin Signaling by the Rho-GTPase Activating Protein Myosin IXb
- (2014) Y. Xu et al. JOURNAL OF IMMUNOLOGY
- Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population
- (2014) Shuang Liang et al. Journal of Zhejiang University-SCIENCE B
- Synaptic, transcriptional and chromatin genes disrupted in autism
- (2014) Silvia De Rubeis et al. NATURE
- The contribution of de novo coding mutations to autism spectrum disorder
- (2014) Ivan Iossifov et al. NATURE
- Oligophrenin-1 (OPHN1), a Gene Involved in X-Linked Intellectual Disability, Undergoes RNA Editing and Alternative Splicing during Human Brain Development
- (2014) Sabina Barresi et al. PLoS One
- Dock GEFs and their therapeutic potential: Neuroprotection and axon regeneration
- (2014) Kazuhiko Namekata et al. PROGRESS IN RETINAL AND EYE RESEARCH
- Rho family GTPases: key players in neuronal development, neuronal survival, and neurodegeneration
- (2014) Trisha R. Stankiewicz et al. Frontiers in Cellular Neuroscience
- 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
- Dysfunction ofSHANK2andCHRNA7in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci
- (2013) B Chilian et al. CLINICAL GENETICS
- Immune regulatory functions of DOCK family proteins in health and disease
- (2013) Akihiko Nishikimi et al. EXPERIMENTAL CELL RESEARCH
- The Atypical Guanine Nucleotide Exchange Factor Dock4 Regulates Neurite Differentiation through Modulation of Rac1 GTPase and Actin Dynamics
- (2013) Yangui Xiao et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Type 1 Inositol Trisphosphate Receptor Regulates Cerebellar Circuits by Maintaining the Spine Morphology of Purkinje Cells in Adult Mice
- (2013) T. Sugawara et al. JOURNAL OF NEUROSCIENCE
- Neuronal Rac1 Is Required for Learning-Evoked Neurogenesis
- (2013) U. Haditsch et al. JOURNAL OF NEUROSCIENCE
- p190-B RhoGAP regulates the functional composition of the mesenchymal microenvironment
- (2013) R Raman et al. LEUKEMIA
- Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations
- (2013) C Toma et al. MOLECULAR PSYCHIATRY
- Activity-dependent neuronal signalling and autism spectrum disorder
- (2013) Daniel H. Ebert et al. NATURE
- Progress toward treatments for synaptic defects in autism
- (2013) Richard Delorme et al. NATURE MEDICINE
- CYFIP1 Coordinates mRNA Translation and Cytoskeleton Remodeling to Ensure Proper Dendritic Spine Formation
- (2013) Silvia De Rubeis et al. NEURON
- Lack of the presynaptic RhoGAP protein oligophrenin1 leads to cognitive disabilities through dysregulation of the cAMP/PKA signalling pathway
- (2013) M. Khelfaoui et al. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES
- The Inverse F-BAR Domain Protein srGAP2 Acts through srGAP3 to Modulate Neuronal Differentiation and Neurite Outgrowth of Mouse Neuroblastoma Cells
- (2013) Yue Ma et al. PLoS One
- IP3R1 deficiency in the cerebellum/brainstem causes basal ganglia-independent dystonia by triggering tonic Purkinje cell firings in mice
- (2013) Chihiro Hisatsune et al. Frontiers in Neural Circuits
- Prevalence of autism in mainland China, Hong Kong and Taiwan: a systematic review and meta-analysis
- (2013) Xiang Sun et al. Molecular Autism
- SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
- (2013) Brett S Abrahams et al. Molecular Autism
- Duplication ofOCRLand adjacent genes associated with autism but not Lowe syndrome
- (2012) Richard J. Schroer et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Global Prevalence of Autism and Other Pervasive Developmental Disorders
- (2012) Mayada Elsabbagh et al. Autism Research
- DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses
- (2012) Y. Harada et al. BLOOD
- Myo9b and RICS Modulate Dendritic Morphology of Cortical Neurons
- (2012) Hui Long et al. CEREBRAL CORTEX
- Srgap3−/− mice present a neurodevelopmental disorder with schizophrenia-related intermediate phenotypes
- (2012) Robert Waltereit et al. FASEB JOURNAL
- The cellular function of srGAP3 and its role in neuronal morphogenesis
- (2012) Claire Bacon et al. MECHANISMS OF DEVELOPMENT
- De Novo Gene Disruptions in Children on the Autistic Spectrum
- (2012) Ivan Iossifov et al. NEURON
- Haploinsufficiency of Cyfip1 Produces Fragile X-Like Phenotypes in Mice
- (2012) Ozlem Bozdagi et al. PLoS One
- Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
- (2012) Claire S. Leblond et al. PLoS Genetics
- Prevalence of Autism Spectrum Disorders in a Total Population Sample
- (2011) Young Shin Kim et al. AMERICAN JOURNAL OF PSYCHIATRY
- Rac1-Dependent Cell Cycle Exit of MGE Precursors and GABAergic Interneuron Migration to the Cortex
- (2011) Marina Vidaki et al. CEREBRAL CORTEX
- Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE
- (2011) Patricia B.S. Celestino-Soper et al. HUMAN MOLECULAR GENETICS
- The RhoG/ELMO1/Dock180 Signaling Module Is Required for Spine Morphogenesis in Hippocampal Neurons
- (2011) Jeong-Yoon Kim et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Identification of a Negative Regulatory Region for the Exchange Activity and Characterization of T332I Mutant of Rho Guanine Nucleotide Exchange Factor 10 (ARHGEF10)
- (2011) Taro Chaya et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- WRP/srGAP3 Facilitates the Initiation of Spine Development by an Inverse F-BAR Domain, and Its Loss Impairs Long-Term Memory
- (2011) B. R. Carlson et al. JOURNAL OF NEUROSCIENCE
- Functional PAK-2 knockout and replacement with a caspase cleavage-deficient mutant in mice reveals differential requirements of full-length PAK-2 and caspase-activated PAK-2p34
- (2011) Jerry W. Marlin et al. MAMMALIAN GENOME
- Control of synapse development and plasticity by Rho GTPase regulatory proteins
- (2011) Kimberley F. Tolias et al. PROGRESS IN NEUROBIOLOGY
- Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review
- (2010) Fabiola Quintero-Rivera et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia
- (2010) Alistair T. Pagnamenta et al. BIOLOGICAL PSYCHIATRY
- SFARI Gene: an evolving database for the autism research community
- (2010) S. Banerjee-Basu et al. Disease Models & Mechanisms
- Trio Is a Key Guanine Nucleotide Exchange Factor Coordinating Regulation of the Migration and Morphogenesis of Granule Cells in the Developing Cerebellum
- (2010) Ya-Jing Peng et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Rac1 Regulates Neuronal Polarization through the WAVE Complex
- (2010) S. Tahirovic et al. JOURNAL OF NEUROSCIENCE
- Mouse Model for Lowe Syndrome/Dent Disease 2 Renal Tubulopathy
- (2010) S. P. Bothwell et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia
- (2010) A Piton et al. MOLECULAR PSYCHIATRY
- Motorized RhoGAP myosin IXb (Myo9b) controls cell shape and motility
- (2010) P. J. Hanley et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees
- (2010) Hilary Coon et al. Molecular Autism
- 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
- Prevalence of autism-spectrum conditions: UK school-based population study
- (2009) Simon Baron-Cohen et al. BRITISH JOURNAL OF PSYCHIATRY
- DOG 1.0: illustrator of protein domain structures
- (2009) Jian Ren et al. CELL RESEARCH
- A PH domain within OCRL bridges clathrin-mediated membrane trafficking to phosphoinositide metabolism
- (2009) Yuxin Mao et al. EMBO JOURNAL
- Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances
- (2009) Marianne Doornbos et al. European Journal of Medical Genetics
- Dynamic expression of the Slit-Robo GTPase activating protein genes during development of the murine nervous system
- (2009) Claire Bacon et al. JOURNAL OF COMPARATIVE NEUROLOGY
- A central role for the small GTPase Rac1 in hippocampal plasticity and spatial learning and memory
- (2009) Ursula Haditsch et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- Increased network excitability and impaired induction of long-term potentiation in the dentate gyrus of collybistin-deficient mice in vivo
- (2009) Peter Jedlicka et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility
- (2009) E Maestrini et al. MOLECULAR PSYCHIATRY
- A tale of two Paks
- (2008) Luis E. Arias-Romero et al. BIOLOGY OF THE CELL
- PAK signalling in neuronal physiology
- (2008) Patricia Kreis et al. CELLULAR SIGNALLING
- Coordination of Rho and Rac GTPase Function via p190B RhoGAP
- (2008) Rodrigo I. Bustos et al. CURRENT BIOLOGY
- Rac1 deficiency in the forebrain results in neural progenitor reduction and microcephaly
- (2008) Lei Chen et al. DEVELOPMENTAL BIOLOGY
- Expression of MEGAP mRNA during embryonic development
- (2008) Robert Waltereit et al. GENE EXPRESSION PATTERNS
- PX-RICS mediates ER-to-Golgi transport of the N-cadherin/ -catenin complex
- (2008) T. Nakamura et al. GENES & DEVELOPMENT
- A high-density SNP genome-wide linkage scan in a large autism extended pedigree
- (2008) K Allen-Brady et al. MOLECULAR PSYCHIATRY
- Mammalian Rho GTPases: new insights into their functions from in vivo studies
- (2008) Sarah J. Heasman et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- AutDB: a gene reference resource for autism research
- (2008) Saumyendra N. Basu et al. NUCLEIC ACIDS RESEARCH
- Structural Basis of Protein Kinase C Isoform Function
- (2008) Susan F. Steinberg PHYSIOLOGICAL REVIEWS
- The atypical Rac activator Dock180 (Dock1) regulates myoblast fusion in vivo
- (2008) M. Laurin et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- P-Rex2 regulates Purkinje cell dendrite morphology and motor coordination
- (2008) S. Donald et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationPublish 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 More