Related references
Note: Only part of the references are listed.Ultrasonic vocalizations in mouse models for speech and socio-cognitive disorders: insights into the evolution of vocal communication
J. Fischer et al.
GENES BRAIN AND BEHAVIOR (2011)
HUMANIZED Foxp2 SPECIFICALLY AFFECTS CORTICO-BASAL GANGLIA CIRCUITS
S. Reimers-Kipping et al.
NEUROSCIENCE (2011)
Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain
Sonja C. Vernes et al.
PLOS GENETICS (2011)
The structure of innate vocalizations in Foxp2-deficient mouse pups
S. Gaub et al.
GENES BRAIN AND BEHAVIOR (2010)
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex
Patrice Roll et al.
HUMAN MOLECULAR GENETICS (2010)
A Humanized Version of Foxp2 Affects Cortico-Basal Ganglia Circuits in Mice
Wolfgang Enard et al.
CELL (2009)
A secreted complement-control-related protein ensures acetylcholine receptor clustering
Marie Gendrel et al.
NATURE (2009)
LRRTM2 Interacts with Neurexin1 and Regulates Excitatory Synapse Formation
Joris de Wit et al.
NEURON (2009)
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits
Matthias Groszer et al.
CURRENT BIOLOGY (2008)
Activity-dependent regulation of inhibitory synapse development by Npas4
Yingxi Lin et al.
NATURE (2008)
Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells
Eriko Fujita et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
Tom Walsh et al.
SCIENCE (2008)
The classical complement cascade mediates CNS synapse elimination
Beth Stevens et al.
CELL (2007)
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders
Sonja C. Vernes et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Mouse behavioral assays relevant to the symptoms of autism
Jacqueline N. Crawley
BRAIN PATHOLOGY (2007)
Interaction of the N-terminal domain of the AMPA receptor GIuR4 subunit with the neuronal pentraxin NP1 mediates GluR4 synaptic recruitment
Gek-Ming Sia et al.
NEURON (2007)
Generation of mice with a conditional Foxp2 null allele
Catherine A. French et al.
GENESIS (2007)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari et al.
NATURE GENETICS (2007)
Genome-wide atlas of gene expression in the adult mouse brain
Ed S. Lein et al.
NATURE (2007)
Blue fluorescent proteins with enhanced brightness and photostability from a structurally targeted library
Marco A. Mena et al.
NATURE BIOTECHNOLOGY (2006)
SALM synaptic cell adhesion-like molecules regulate the differentiation of excitatory synapses
JW Ko et al.
NEURON (2006)
SRPX2 mutations in disorders of language cortex and cognition
P Roll et al.
HUMAN MOLECULAR GENETICS (2006)
Activity-dependent regulation of MEF2 transcription factors suppresses excitatory synapse number
SW Flavell et al.
SCIENCE (2006)
In vivo electroporation in the embryonic mouse central nervous system
Tetsuichiro Saito
NATURE PROTOCOLS (2006)
Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene
WG Shu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
F Laumonnier et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins
ER Graf et al.
CELL (2004)
SynCAM, a synaptic adhesion molecule that drives synapse assembly
T Biederer et al.
SCIENCE (2002)
Total arrest of spontaneous and evoked synaptic transmission but normal synaptogenesis in the absence of Munc13-mediated vesicle priming
F Varoqueaux et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
A forkhead-domain gene is mutated in a severe speech and language disorder
CSL Lai et al.
NATURE (2001)
Structure and flexibility of the multiple domain proteins that regulate complement activation
MD Kirkitadze et al.
IMMUNOLOGICAL REVIEWS (2001)
Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons
P Scheiffele et al.
CELL (2000)
Synaptic assembly of the brain in the absence of neurotransmitter secretion
M Verhage et al.
SCIENCE (2000)
Share Paper
