Emerging major synaptic signaling pathways involved in intellectual disability
Published 2011 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Emerging major synaptic signaling pathways involved in intellectual disability
Authors
Keywords
-
Journal
MOLECULAR PSYCHIATRY
Volume 17, Issue 7, Pages 682-693
Publisher
Springer Nature
Online
2011-10-25
DOI
10.1038/mp.2011.139
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Loss-of-function mutation of collybistin is responsible for X-linked mental retardation associated with epilepsy
- (2011) Keiko Shimojima et al. JOURNAL OF HUMAN GENETICS
- 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
- Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function
- (2011) M. Etherton et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A Focal Epilepsy and Intellectual Disability Syndrome Is Due to a Mutation in TBC1D24
- (2010) Mark A. Corbett et al. AMERICAN JOURNAL OF HUMAN GENETICS
- TBC1D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic Epilepsy
- (2010) Antonio Falace et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly
- (2010) Maila Giannandrea et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Aarskog-Scott syndrome: Clinical update and report of nine novel mutations of theFGD1gene
- (2010) A. Orrico et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Molecular and Cellular Mechanisms of Learning Disabilities: A Focus on NF1
- (2010) C. Shilyansky et al. Annual Review of Neuroscience
- A Postsynaptic Signaling Pathway that May Account for the Cognitive Defect Due to IL1RAPL1 Mutation
- (2010) Alice Pavlowsky et al. CURRENT BIOLOGY
- Rho-kinase inhibition: a novel therapeutic target for the treatment of cardiovascular diseases
- (2010) Ming Dong et al. DRUG DISCOVERY TODAY
- PH-Domain-driven targeting of collybistin but not Cdc42 activation is required for synaptic gephyrin clustering
- (2010) Suneel Reddy-Alla et al. EUROPEAN JOURNAL OF NEUROSCIENCE
- Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome
- (2010) Tahir Mehmood et al. HUMAN GENETICS
- Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model
- (2010) Mélissa Bowerman et al. HUMAN MOLECULAR GENETICS
- Regulation of PIP5K activity by Arf6 and its physiological significance
- (2010) Yuji Funakoshi et al. JOURNAL OF CELLULAR PHYSIOLOGY
- Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability
- (2010) Cheryl Shoubridge et al. NATURE GENETICS
- AMPA Receptor Signaling through BRAG2 and Arf6 Critical for Long-Term Synaptic Depression
- (2010) Ralf Scholz et al. NEURON
- Structural and Functional Deficits in a Neuronal Calcium Sensor-1 Mutant Identified in a Case of Autistic Spectrum Disorder
- (2010) Mark T. W. Handley et al. PLoS One
- The Coffin-Lowry Syndrome-associated Protein RSK2 Controls Neuroendocrine Secretion through the Regulation of Phospholipase D1 at the Exocytotic Sites
- (2009) Maria Zeniou-Meyer et al. Annals of the New York Academy of Sciences
- No Association Between SRGAP3/MEGAP Haploinsufficiency and Mental Retardation
- (2009) Fadi F. Hamdan et al. ARCHIVES OF NEUROLOGY
- Characterization of a Novel Mitogen-Activated Protein Kinase Kinase 1/2 Inhibitor with a Unique Mechanism of Action for Cancer Therapy
- (2009) S. Daouti et al. CANCER RESEARCH
- The Rho-Linked Mental Retardation Protein OPHN1 Controls Synaptic Vesicle Endocytosis via Endophilin A1
- (2009) Akiko Nakano-Kobayashi et al. CURRENT BIOLOGY
- Dendritic spine formation and stabilization
- (2009) Yoshihiro Yoshihara et al. CURRENT OPINION IN NEUROBIOLOGY
- Coffin–Lowry syndrome
- (2009) Patricia Marques Pereira et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- The Rho-linked mental retardation protein oligophrenin-1 controls synapse maturation and plasticity by stabilizing AMPA receptors
- (2009) N. Nadif Kasri et al. GENES & DEVELOPMENT
- Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation
- (2009) Malik Khelfaoui et al. HUMAN MOLECULAR GENETICS
- X-linked mental retardation: focus on synaptic function and plasticity
- (2009) Yann Humeau et al. JOURNAL OF NEUROCHEMISTRY
- 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
- A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation
- (2009) Ginevra Zanni et al. NEUROGENETICS
- Neuroligin 2 Drives Postsynaptic Assembly at Perisomatic Inhibitory Synapses through Gephyrin and Collybistin
- (2009) Alexandros Poulopoulos et al. NEURON
- Mutations inSYNGAP1in Autosomal Nonsyndromic Mental Retardation
- (2009) Fadi F. Hamdan et al. NEW ENGLAND JOURNAL OF MEDICINE
- Association of syndromic mental retardation with an Xq12q13.1 duplication encompassing the oligophrenin 1 gene
- (2008) Maria Francesca Bedeschi et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Novel mutation ofIL1RAPL1gene in a nonspecific X-linked mental retardation (MRX) family
- (2008) Magdalena Nawara et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Genes, plasticity and mental retardation
- (2008) Cyrille Vaillend et al. BEHAVIOURAL BRAIN RESEARCH
- The postsynaptic density protein, IQ-ArfGEF/BRAG1, can interact with IRSp53 through its proline-rich sequence
- (2008) Masashi Sanda et al. BRAIN RESEARCH
- Rapid and bi-directional regulation of AMPA receptor phosphorylation and trafficking by JNK
- (2008) Gareth M Thomas et al. EMBO JOURNAL
- Cognitive impairment in Gdi1-deficient mice is associated with altered synaptic vesicle pools and short-term synaptic plasticity, and can be corrected by appropriate learning training
- (2008) Veronica Bianchi et al. HUMAN MOLECULAR GENETICS
- Mutations in the calcium-related gene IL1RAPL1 are associated with autism
- (2008) A. Piton et al. HUMAN MOLECULAR GENETICS
- SynGAP Regulates Steady-State and Activity-Dependent Phosphorylation of Cofilin
- (2008) H. J. Carlisle et al. JOURNAL OF NEUROSCIENCE
- PIX Rho GTPase Guanine Nucleotide Exchange Factor Regulates Lymphocyte Functions and Antigen Receptor Signaling
- (2008) K. Missy et al. MOLECULAR AND CELLULAR BIOLOGY
- Neuroligins and neurexins link synaptic function to cognitive disease
- (2008) Thomas C. Südhof NATURE
- The Coffin-Lowry syndrome-associated protein RSK2 is implicated in calcium-regulated exocytosis through the regulation of PLD1
- (2008) M. Zeniou-Meyer et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- IQ-ArfGEF/BRAG1 is a guanine nucleotide exchange factor for Arf6 that interacts with PSD-95 at postsynaptic density of excitatory synapses
- (2007) Hiroyuki Sakagami et al. NEUROSCIENCE RESEARCH
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