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Title
Human-Specific Genes, Cortical Progenitor Cells, and Microcephaly
Authors
Keywords
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Journal
Cells
Volume 10, Issue 5, Pages 1209
Publisher
MDPI AG
Online
2021-05-17
DOI
10.3390/cells10051209
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Note: Only part of the references are listed.- Cortical Malformations: Lessons in Human Brain Development
- (2020) Lakshmi Subramanian et al. Frontiers in Cellular Neuroscience
- Cell Metabolic Alterations due to Mcph1 Mutation in Microcephaly
- (2020) Nathalie Journiac et al. Cell Reports
- Human-specific ARHGAP11B increases size and folding of primate neocortex in the fetal marmoset
- (2020) Michael Heide et al. SCIENCE
- Metabolic Regulation of Neocortical Expansion in Development and Evolution
- (2020) Takashi Namba et al. NEURON
- Establishing Cerebral Organoids as Models of Human-Specific Brain Evolution
- (2019) Alex A. Pollen et al. CELL
- Malformations of Cerebral Cortex Development: Molecules and Mechanisms
- (2019) Gordana Juric-Sekhar et al. Annual Review of Pathology-Mechanisms of Disease
- Paired involvement of human-specific Olduvai domains and NOTCH2NL genes in human brain evolution
- (2019) Ian T. Fiddes et al. HUMAN GENETICS
- Individual brain organoids reproducibly form cell diversity of the human cerebral cortex
- (2019) Silvia Velasco et al. NATURE
- Malformations of Human Neocortex in Development – Their Progenitor Cell Basis and Experimental Model Systems
- (2019) Anneline Pinson et al. Frontiers in Cellular Neuroscience
- Modeling microcephaly with cerebral organoids reveals a WDR62–CEP170–KIF2A pathway promoting cilium disassembly in neural progenitors
- (2019) Wei Zhang et al. Nature Communications
- New insights into the development of the human cerebral cortex
- (2019) Zoltán Molnár et al. JOURNAL OF ANATOMY
- Organoid single-cell genomic atlas uncovers human-specific features of brain development
- (2019) Sabina Kanton et al. NATURE
- Human-Specific ARHGAP11B Acts in Mitochondria to Expand Neocortical Progenitors by Glutaminolysis
- (2019) Takashi Namba et al. NEURON
- Genetic Modification of Brain Organoids
- (2019) Jan Fischer et al. Frontiers in Cellular Neuroscience
- The human-specific paralogs SRGAP2B and SRGAP2C differentially modulate SRGAP2A-dependent synaptic development
- (2019) Ewoud R. E. Schmidt et al. Scientific Reports
- The Genetics of Primary Microcephaly
- (2018) Divya Jayaraman et al. Annual Review of Genomics and Human Genetics
- Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch Regulation
- (2018) Ikuo K. Suzuki et al. CELL
- Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis
- (2018) Ian T. Fiddes et al. CELL
- Brain organoids as models to study human neocortex development and evolution
- (2018) Michael Heide et al. CURRENT OPINION IN CELL BIOLOGY
- Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex
- (2018) Marta Florio et al. eLife
- Transcriptional fates of human-specific segmental duplications in brain
- (2018) Max L. Dougherty et al. GENOME RESEARCH
- Human-specific ARHGAP11B induces hallmarks of neocortical expansion in developing ferret neocortex
- (2018) Nereo Kalebic et al. eLife
- Cell diversity and network dynamics in photosensitive human brain organoids
- (2017) Giorgia Quadrato et al. NATURE
- Diagnostic Approach to Primary Microcephaly
- (2017) Maja von der Hagen NEUROPEDIATRICS
- Recapitulating cortical development with organoid culture in vitro and modeling abnormal spindle-like (ASPM related primary) microcephaly disease
- (2017) Rui Li et al. Protein & Cell
- The evolution and population diversity of human-specific segmental duplications
- (2017) Megan Y. Dennis et al. Nature Ecology & Evolution
- The Molecular Basis of Human Brain Evolution
- (2016) Wolfgang Enard CURRENT BIOLOGY
- CPAP promotes timely cilium disassembly to maintain neural progenitor pool
- (2016) Elke Gabriel et al. EMBO JOURNAL
- SRGAP2 and Its Human-Specific Paralog Co-Regulate the Development of Excitatory and Inhibitory Synapses
- (2016) Matteo Fossati et al. NEURON
- A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
- (2016) M. Florio et al. Science Advances
- Molecular genetics of human primary microcephaly: an overview
- (2015) Muhammad Faheem et al. BMC Medical Genomics
- Molecular Identity of Human Outer Radial Glia during Cortical Development
- (2015) Alex A. Pollen et al. CELL
- All-or-(N)One – an epistemological characterization of the human tumorigenic neuronal paralogous FAM72 gene loci
- (2015) Arne Kutzner et al. GENOMICS
- Single-cell analysis reveals transcriptional heterogeneity of neural progenitors in human cortex
- (2015) Matthew B Johnson et al. NATURE NEUROSCIENCE
- The Outer Subventricular Zone and Primate-Specific Cortical Complexification
- (2015) Colette Dehay et al. NEURON
- Human cerebral organoids recapitulate gene expression programs of fetal neocortex development
- (2015) J. Gray Camp 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
- Further delineation of eye manifestations in homozygous 15q13.3 microdeletions includingTRPM1: A differential diagnosis of ceroid lipofuscinosis
- (2014) Alice Masurel-Paulet et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Genetic disorders associated with postnatal microcephaly
- (2014) Laurie E. Seltzer et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Congenital microcephaly
- (2014) Diana Alcantara et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- DUF1220 protein domains drive proliferation in human neural stem cells and are associated with increased cortical volume in anthropoid primates
- (2014) J. G. Keeney et al. Brain Structure & Function
- H3K4me3 Breadth Is Linked to Cell Identity and Transcriptional Consistency
- (2014) Bérénice A. Benayoun et al. CELL
- Neural progenitors, neurogenesis and the evolution of the neocortex
- (2014) M. Florio et al. DEVELOPMENT
- Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature
- (2014) Chelsea Lowther et al. GENETICS IN MEDICINE
- Transcriptional landscape of the prenatal human brain
- (2014) Jeremy A. Miller et al. NATURE
- Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability
- (2014) Francesca Antonacci et al. NATURE GENETICS
- Molecular and Cellular Basis of Autosomal Recessive Primary Microcephaly
- (2014) Marine Barbelanne et al. Biomed Research International
- Investigating microcephaly
- (2013) C. G. Woods et al. ARCHIVES OF DISEASE IN CHILDHOOD
- A Conserved RhoGAP Limits M Phase Contractility and Coordinates with Microtubule Asters to Confine RhoA during Cytokinesis
- (2013) Esther Zanin et al. DEVELOPMENTAL CELL
- Genome-wide gene expression in a patient with 15q13.3 homozygous microdeletion syndrome
- (2013) Jean-Baptiste Le Pichon et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Cerebral organoids model human brain development and microcephaly
- (2013) Madeline A. Lancaster et al. NATURE
- Precursor Diversity and Complexity of Lineage Relationships in the Outer Subventricular Zone of the Primate
- (2013) Marion Betizeau et al. NEURON
- Cell Cycle-Dependent Rho GTPase Activity Dynamically Regulates Cancer Cell Motility and Invasion In Vivo
- (2013) Yoshinori Kagawa et al. PLoS One
- Self-organization of axial polarity, inside-out layer pattern, and species-specific progenitor dynamics in human ES cell-derived neocortex
- (2013) T. Kadoshima et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Evolutionary History and Genome Organization of DUF1220 Protein Domains
- (2013) Majesta S. O’Bleness et al. G3-Genes Genomes Genetics
- A developmental and genetic classification for malformations of cortical development: update 2012
- (2012) A. James Barkovich et al. BRAIN
- Inhibition of SRGAP2 Function by Its Human-Specific Paralogs Induces Neoteny during Spine Maturation
- (2012) Cécile Charrier et al. CELL
- Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication
- (2012) Megan Y. Dennis et al. CELL
- Identification of single gene deletions at 15q13.3: further evidence thatCHRNA7causes the 15q13.3 microdeletion syndrome phenotype
- (2012) N Hoppman-Chaney et al. CLINICAL GENETICS
- Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal
- (2012) S. A. Fietz et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Development and Evolution of the Human Neocortex
- (2011) Jan H. Lui et al. CELL
- Homozygous deletion of chromosome 15q13.3 including CHRNA7 causes severe mental retardation, seizures, muscular hypotonia, and the loss of KLF13 and TRPM1 potentially cause macrocytosis and congenital retinal dysfunction in siblings
- (2011) Malte Spielmann et al. European Journal of Medical Genetics
- A 15q13.3 homozygous microdeletion associated with a severe neurodevelopmental disorder suggests putative functions of theTRPM1,CHRNA7, and other homozygously deleted genes
- (2010) Jean-Baptiste LePichon et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia
- (2010) Volker Endris et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A Role for Intermediate Radial Glia in the Tangential Expansion of the Mammalian Cerebral Cortex
- (2010) Isabel Reillo et al. CEREBRAL CORTEX
- Neurogenic radial glia in the outer subventricular zone of human neocortex
- (2010) David V. Hansen et al. NATURE
- OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling
- (2010) Simone A Fietz et al. NATURE NEUROSCIENCE
- Diversity of Human Copy Number Variation and Multicopy Genes
- (2010) Peter H. Sudmant et al. SCIENCE
- Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders
- (2009) S Ben-Shachar et al. JOURNAL OF MEDICAL GENETICS
- Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome
- (2009) B W M van Bon et al. JOURNAL OF MEDICAL GENETICS
- Evolution of the neocortex: a perspective from developmental biology
- (2009) Pasko Rakic NATURE REVIEWS NEUROSCIENCE
- Selection of differentiating cells by different levels of delta-like 1 among neural precursor cells in the developing mouse telencephalon
- (2008) D. Kawaguchi et al. DEVELOPMENT
- Brain abnormalities in Williams syndrome: A review of structural and functional magnetic resonance imaging findings
- (2008) Andrea Parolin Jackowski et al. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
- Large recurrent microdeletions associated with schizophrenia
- (2008) Hreinn Stefansson et al. NATURE
- A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
- (2008) Andrew J Sharp et al. NATURE GENETICS
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
- (2008) Nicola Brunetti-Pierri et al. NATURE GENETICS
- Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
- (2008) Heather C. Mefford et al. NEW ENGLAND JOURNAL OF MEDICINE
- Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome
- (2004) Timothy A. Hinsley et al. PROTEIN SCIENCE
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