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Netrin-G2 dysfunction causes a Rett-like phenotype with areflexia
Gali Heimer
, Geeske M. van Woerden
, Ortal Barel
, Dina Marek-Yagel
, Nitzan Kol
, Johannes B. Munting
, Minoeshka Borghei
, Osama M. Atawneh
, Andreea Nissenkorn
, Gideon Rechavi
, Yair Anikster
, Ype Elgersma
, Steven A. Kushner
, Bruria Ben Zeev
Research output
:
Contribution to journal
›
Article
›
peer-review
9
Scopus citations
Overview
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Keyphrases
Areflexia
100%
Rett-like
100%
Netrin-G2
100%
Rett Syndrome
80%
Knockdown
40%
Netrin
40%
Neuronal Morphology
40%
NTNG1
40%
Family Members
20%
Targeted Gene
20%
Synaptic Transmission
20%
Nonsense-mediated Decay
20%
Sanger Sequencing
20%
Whole Exome Sequencing
20%
Functional Studies
20%
G Protein
20%
Genetic Causes
20%
Short Hairpin RNA (shRNA)
20%
N-methyl-D-aspartate
20%
Gene Knockout
20%
Severe Impairment
20%
Neurodevelopmental Phenotypes
20%
Methyl-CpG-binding Protein 2 (MeCP2)
20%
Homozygous Frameshift mutation
20%
Neuronal Migration
20%
Primary Hippocampal Neurons
20%
Axonal Guidance
20%
Cortical Migration
20%
Neurodevelopmental Defects
20%
In Utero Electroporation
20%
Early Brain Development
20%
G-family
20%
Neuroscience
Netrin
100%
Rett Syndrome
57%
In Vivo
14%
Transfection
14%
Electroporation
14%
Brain Development
14%
Synaptic Transmission
14%
G Protein
14%
Exome Sequencing
14%
Gene Knockdown
14%
Dextro Aspartic Acid
14%
Small Hairpin RNA
14%
Nonsense Mediated mRNA Decay
14%
Frameshift Mutation
14%
Methyl CpG Binding Protein 2
14%
Dideoxynucleotide Sequencing
14%