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ROBO3 gene

Known as: RIG1, HGPS, RBIG1 
This gene is involved in neuronal cell shape.
National Institutes of Health

Related topics

Related topics

8 relations
LMNA geneLigand BindingMigration, CellNeurogenesis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Corrigendum: GnRH-1 Neural Migration From the Nose to the Brain Is Independent From Slit2, Robo3 and NELL2 Signaling
[This corrects the article DOI: 10.3389/fncel.2019.00070.]. 
Review
2018
Review
2018
IN SILICO ANALYSIS OF PROTEIN-PROTEIN INTERACTION NETWORK OF HUTCHINSON GILFORD PROGERIA SYNDROME
HGPS is a rare genetic disorder, caused by mutations in genes, encoding proteins of the nuclear lamina. Analysis of protein… 
2017
2017
CRISPR-based gene replacement reveals evolutionarily conserved axon guidance functions of Drosophila Robo3 and Tribolium Robo2/3
Axon guidance receptors of the Roundabout (Robo) family regulate a number of axon guidance outcomes in bilaterian animals in… 
2017
2017
A novel mutation of ROBO3 in horizontal gaze palsy with progressive scoliosis
A novel mutation of ROBO3 in horizontal gaze palsy with progressive scoliosis Sevcan Tuğ Bozdoğan, Erdem Dinç, A. Ayça Sarı, Anıl… 
2016
2016
Human placental multipotent mesenchymal stromal cells modulate placenta angiogenesis through Slit2-Robo signaling
abstract The objective of this study was to investigate whether human placental multipotent mesenchymal stromal cell (hPMSC… 
2012
2012
Midline crossing is not required for subsequent pathfinding decisions in commissural neurons
Growth cone navigation across the vertebrate midline is critical in the establishment of nervous system connectivity. While… 
2009
2009
Sequential bilateral central retinal artery occlusions in a female carrier of Fabry disease
table or a sporadic defect in somatic cells during embryogenesis, with a possible combination of environmental and genetic… 
2008
2008
Association study between gilles de la tourette syndrome and two genes in the robo‐slit pathway located in the chromosome 11q24 linked/associated region
Gilles de la Tourette Syndrome (GTS) is an inherited neuropsychiatric disorder characterized by the presence of motor and phonic… 
Review
2005
Review
2005
LMNA mutations in progeroid syndromes.
Segmental progeroid syndromes are disorders in which affected individuals. present various features that suggest accelerated… 
2000
2000
The Come-Hither, Don't-Touch-Me Proteins
Two newly discovered receptors, Slit and Roundabout (Robo), help determine how far axons in developing fruit flies travel after… 
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