Proliferation & Neurodevelopmental Disorders

To form the complex network of the CNS, there is a synchronous flow of proliferation, migration and differentiation of neuronal cells. When errors in these processes occur, it is thought to be a contributing factor to cognitive deficits and neurodevelopmental disorders. Here is the latest research on proliferation and neurodevelopmental disorders.

July 30, 2020

Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum

American Journal of Human Genetics
Marialetizia MottaMarco Tartaglia
August 8, 2020
Review

In vitro modeling for inherited neurological diseases using induced pluripotent stem cells: from 2D to organoid

Archives of Pharmacal Research
Ki Hong NamJaecheol Lee
July 3, 2020
Case Report
Open Access

Onset of valganciclovir resistance in two infants with congenital cytomegalovirus infection

International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases
Francesca GarofoliFausto Baldanti
June 27, 2020

Single-cell genomic analysis of human cerebral organoids

Methods in Cell Biology
Sabina KantonJ Gray Camp
July 15, 2020
Open Access

Targeting VGLUT Machinery: Implications on mGluR5 Signaling and Behavior

Molecular Pharmacology
Karim S IbrahimStephen Sg Ferguson
June 26, 2020
Open Access

Maternal Immune Activation Alters Fetal Brain Development and Enhances Proliferation of Neural Precursor Cells in Rats

Frontiers in Immunology
Kelly J BainesStephen J Renaud
June 26, 2020

Multiple doses of umbilical cord blood cells improve long-term brain injury in the neonatal rat

Brain Research
Tayla R PennyCourtney A McDonald
August 8, 2020
Open Access

Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature

European Journal of Medical Genetics
Anna LengyelIrén Haltrich
July 12, 2020
Preprint
Open Access

Wide phenotypic spectrum of human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations

BioRxiv : the Preprint Server for Biology
June 26, 2020
Case Report
Open Access

Inherited duplication of the pseudoautosomal region Xq28 in a subject with Gilles de la Tourette syndrome and intellectual disability: a case report

Molecular Cytogenetics
Stefania MaccariniEleonora Marchina
July 8, 2020

Postnatal di-2-ethylhexyl phthalate exposure affects hippocampal dentate gyrus morphogenesis

Journal of Applied Toxicology : JAT
Munekazu KomadaNao Kagawa
August 2, 2020

The neocortical progenitor specification program is established through combined modulation of SHH and FGF signaling

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
Odessa R YabutSamuel J Pleasure
August 2, 2020
Open Access

Symmetric neural progenitor divisions require chromatin-mediated homologous recombination DNA repair by Ino80

Nature Communications
Jason M KeilKenneth Y Kwan
July 28, 2020

In vitro models for ASD-patient-derived iPSCs and cerebral organoids

Progress in Molecular Biology and Translational Science
Sonja Simone HohmannTanja Maria Michel
July 8, 2020

The EJC component Magoh in non-vertebrate chordates

Development Genes and Evolution
Rosa Maria SepePaolo Sordino
June 27, 2020

Germline PTEN mutations are associated with a skewed peripheral immune repertoire in humans and mice

Human Molecular Genetics
Ritika JainiCharis Eng
July 22, 2020
Review

ODLURO syndrome: personal experience and review of the literature

La Radiologia medica
Renata ConfortiFerdinando Caranci

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