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。Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5
Andrew Kodani et al.
NEURON (2020)
Artificial intelligence and the future of global health
Nina Schwalbe et al.
LANCET (2020)
Definitions and classification of malformations of cortical development: practical guidelines
Mariasavina Severino et al.
BRAIN (2020)
In vivo Perturb-Seq reveals neuronal and glial abnormalities associated with autism risk genes
Xin Jin et al.
SCIENCE (2020)
Establishing Cerebral Organoids as Models of Human-Specific Brain Evolution
Alex A. Pollen et al.
CELL (2019)
Altered neuronal migratory trajectories in human cerebral organoids derived from individuals with neuronal heterotopia
Johannes Klaus et al.
NATURE MEDICINE (2019)
Cell migration promotes dynamic cellular interactions to control cerebral cortex morphogenesis
Carla G. Silva et al.
NATURE REVIEWS NEUROSCIENCE (2019)
Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice
Milka Pringsheim et al.
ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY (2019)
Temporal patterning of apical progenitors and their daughter neurons in the developing neocortex
L. Telley et al.
SCIENCE (2019)
Single-cell genomics identifies cell type-specific molecular changes in autism
Dmitry Velmeshev et al.
SCIENCE (2019)
The Integrative Function of Silent Synapses on Subplate Neurons in Cortical Development and Dysfunction
Patrick O. Kanold et al.
FRONTIERS IN NEUROANATOMY (2019)
Individual brain organoids reproducibly form cell diversity of the human cerebral cortex
Silvia Velasco et al.
NATURE (2019)
Beyond the Exome: The Non-coding Genome and Enhancers in Neurodevelopmental Disorders and Malformations of Cortical Development
Elena Perenthaler et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2019)
Development and Arealization of the Cerebral Cortex
Cathryn R. Cadwell et al.
NEURON (2019)
Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia
Ana Uzquiano et al.
CELL REPORTS (2019)
Reduced White Matter Fiber Density in Autism Spectrum Disorder
Dennis Dimond et al.
CEREBRAL CORTEX (2019)
Direct and Collateral Alterations of Functional Cortical Circuits in a Rat Model of Subcortical Band Heterotopia
Vanessa Plantier et al.
CEREBRAL CORTEX (2019)
A Translaminar Genetic Logic for the Circuit Identity of Intracortically Projecting Neurons
Esther Klingler et al.
CURRENT BIOLOGY (2019)
Spontaneous epileptiform activity in a rat model of bilateral subcortical band heterotopia
Surajit Sahu et al.
EPILEPSIA (2019)
Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly
Nataliya Di Donato et al.
GENETICS IN MEDICINE (2018)
A mixed model of neuronal diversity
Ludovic Telley et al.
NATURE (2018)
Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration
Ashleigh E. Schaffer et al.
NATURE GENETICS (2018)
Synaptic transmission from subplate neurons controls radial migration of neocortical neurons
Chiaki Ohtaka-Maruyama et al.
SCIENCE (2018)
Single-cell reconstruction of developmental trajectories during zebrafish embryogenesis
Jeffrey A. Farrell et al.
SCIENCE (2018)
Genetics and mechanisms leading to human cortical malformations
Delfina M. Romero et al.
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2018)
De novo and inherited private variants in MAP1B in periventricular nodular heterotopia
Erin L. Heinzen et al.
PLOS GENETICS (2018)
Progenitor Hyperpolarization Regulates the Sequential Generation of Neuronal Subtypes in the Developing Neocortex
Ilaria Vitali et al.
CELL (2018)
Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development
Richard S. Smith et al.
NEURON (2018)
The roles of dystroglycan in the nervous system: insights from animal models of muscular dystrophy
Alec R. Nickolls et al.
DISEASE MODELS & MECHANISMS (2018)
Somatic mosaicism and neurodevelopmental disease
Alissa M. D'Gama et al.
NATURE NEUROSCIENCE (2018)
Development and Functional Diversification of Cortical Interneurons
Lynette Lim et al.
NEURON (2018)
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
Mingfeng Li et al.
SCIENCE (2018)
The rise of three-dimensional human brain cultures
Sergiu P. Pasca
NATURE (2018)
Dermatologist-level classification of skin cancer with deep neural networks
Andre Esteva et al.
NATURE (2017)
The use of brain organoids to investigate neural development and disease
Elizabeth Di Lullo et al.
NATURE REVIEWS NEUROSCIENCE (2017)
SHANK proteins: roles at the synapse and in autism spectrum disorder
Patricia Monteiro et al.
NATURE REVIEWS NEUROSCIENCE (2017)
Spatiotemporal gene expression trajectories reveal developmental hierarchies of the human cortex
Tomasz J. Nowakowski et al.
SCIENCE (2017)
Fate and freedom in developing neocortical circuits
Denis Jabaudon
NATURE COMMUNICATIONS (2017)
Folding of the Cerebral Cortex Requires Cdk5 in Upper-Layer Neurons in Gyrencephalic Mammals
Yohei Shinmyo et al.
CELL REPORTS (2017)
The Primate-Specific Gene TMEM14B Marks Outer Radial Glia Cells and Promotes Cortical Expansion and Folding
Jing Liu et al.
CELL STEM CELL (2017)
Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy
Elisabetta Flex et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and intellectual disability: a case report
Anna Winczewska-Wiktor et al.
BMC NEUROLOGY (2016)
Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex
Xiaochang Zhang et al.
CELL (2016)
Prolonged Mitosis of Neural Progenitors Alters Cell Fate in the Developing Brain
Louis-Jan Pilaz et al.
NEURON (2016)
The Cellular and Molecular Landscapes of the Developing Human Central Nervous System
John C. Silbereis et al.
NEURON (2016)
Review: Roles for astrocytes in epilepsy: insights from malformations of cortical development
M. Kielbinski et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2016)
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia
Laura A. Jansen et al.
BRAIN (2015)
Discrete domains of gene expression in germinal layers distinguish the development of gyrencephaly
Camino de Juan Romero et al.
EMBO JOURNAL (2015)
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5
Daniella Magen et al.
HUMAN GENETICS (2015)
Radial Glial Cell-Neuron Interaction Directs Axon Formation at the Opposite Side of the Neuron from the Contact Site
Chundi Xu et al.
JOURNAL OF NEUROSCIENCE (2015)
Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study
Ghayda M. Mirzaa et al.
LANCET NEUROLOGY (2015)
Development, evolution and pathology of neocortical subplate neurons
Anna Hoerder-Suabedissen et al.
NATURE REVIEWS NEUROSCIENCE (2015)
Cerebrospinal fluid-derived Semaphorin3B orients neuroepithelial cell divisions in the apicobasal axis
Elise Arbeille et al.
NATURE COMMUNICATIONS (2015)
Developmental disruptions underlying brain abnormalities in ciliopathies
Jiami Guo et al.
NATURE COMMUNICATIONS (2015)
Ectopic clustering of Cajal-Retzius and subplate cells is an initial pathological feature in Pomgnt2-knockout mice, a model of dystroglycanopathy
Naoki Nakagawa et al.
SCIENTIFIC REPORTS (2015)
The Cell Biology of Neurogenesis: Toward an Understanding of the Development and Evolution of the Neocortex
Elena Taverna et al.
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 30 (2014)
Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes
Timothy J. Edwards et al.
BRAIN (2014)
The multifaceted roles of Slits and Robos in cortical circuits: from proliferation to axon guidance and neurological diseases
Heike Blockus et al.
CURRENT OPINION IN NEUROBIOLOGY (2014)
Malformations of cortical development: clinical features and genetic causes
Renzo Guerrini et al.
LANCET NEUROLOGY (2014)
Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human
Michel Kielar et al.
NATURE NEUROSCIENCE (2014)
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
Shafali S. Jeste et al.
NATURE REVIEWS NEUROLOGY (2014)
Patches of Disorganization in the Neocortex of Children with Autism
Rich Stoner et al.
NEW ENGLAND JOURNAL OF MEDICINE (2014)
Evolutionarily Dynamic Alternative Splicing of GPR56 Regulates Regional Cerebral Cortical Patterning
Byoung-Il Bae et al.
SCIENCE (2014)
Integration of gray matter nodules into functional cortical circuits in periventricular heterotopia
Joanna A. Christodoulou et al.
EPILEPSY & BEHAVIOR (2013)
Cerebral organoids model human brain development and microcephaly
Madeline A. Lancaster et al.
NATURE (2013)
In vivo reprogramming of circuit connectivity in postmitotic neocortical neurons
Andres De la Rossa et al.
NATURE NEUROSCIENCE (2013)
A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-A
Aurelie Carabalona et al.
HUMAN MOLECULAR GENETICS (2012)
Development and Evolution of the Human Neocortex
Jan H. Lui et al.
CELL (2011)
Excitatory Projection Neuron Subtypes Control the Distribution of Local Inhibitory Interneurons in the Cerebral Cortex
Simona Lodato et al.
NEURON (2011)
The Somatosensory Cortex of reeler Mutant Mice Shows Absent Layering But Intact Formation and Behavioral Activation of Columnar Somatotopic Maps
Robin J. Wagener et al.
JOURNAL OF NEUROSCIENCE (2010)
Diffusion imaging and tractography of congenital brain malformations
Michael Wahl et al.
PEDIATRIC RADIOLOGY (2010)
Characterization of the HeCo Mutant Mouse: A New Model of Subcortical Band Heterotopia Associated with Seizures and Behavioral Deficits
Alexandre Croquelois et al.
CEREBRAL CORTEX (2009)
Pax6 3′ deletion results in aniridia, autism and mental retardation
L. K. Davis et al.
HUMAN GENETICS (2008)
EphB receptors couple dendritic filopodia motility to synapse formation
Matthew S. Kayser et al.
NEURON (2008)
Role of intermediate progenitor cells in cerebral cortex development
Adria Pontious et al.
DEVELOPMENTAL NEUROSCIENCE (2008)
Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue
Jin-Wu Tsai et al.
NATURE NEUROSCIENCE (2007)
Slit-Robo interactions during cortical development
William D. Andrews et al.
JOURNAL OF ANATOMY (2007)
Cyclin-dependent kinase 5 governs learning and synaptic plasticity via control of NMDAR degradation
Ammar H. Hawasli et al.
NATURE NEUROSCIENCE (2007)
Cell-cycle control and cortical development
Colette Dehay et al.
NATURE REVIEWS NEUROSCIENCE (2007)
Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis
Lekbir Baala et al.
NATURE GENETICS (2007)
N-cadherin mediates cortical organization in the mouse brain
Masakazu Kadowaki et al.
DEVELOPMENTAL BIOLOGY (2007)
Periventricular heterotopia:: phenotypic heterogeneity and correlation with Filamin A mutations
E. Parrini et al.
BRAIN (2006)
αE-catenin controls cerebral cortical size by regulating the hedgehog signaling pathway
WH Lien et al.
SCIENCE (2006)
Comparative aspects of cerebral cortical development
Z Molnár et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2006)
Neuronal migration disorders, genetics, and epileptogenesis
R Guerrini et al.
JOURNAL OF CHILD NEUROLOGY (2005)
G protein-coupled receptor-dependent development of human frontal cortex
XH Piao et al.
SCIENCE (2004)
Distribution of cortical interneurons in grey matter heterotopia in patients with epilepsy
M Thom et al.
EPILEPSIA (2004)
Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation
M Kato et al.
HUMAN MUTATION (2004)
A neuropathological, stereo-EEG, and MRI study of subcortical band heterotopia
R Mai et al.
NEUROLOGY (2003)
EphB receptors interact with NMDA receptors and regulate excitatory synapse formation
MB Dalva et al.
CELL (2000)
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
SE Hong et al.
NATURE GENETICS (2000)