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SEMA3C gene

Known as: SEMAE, SEMA3C, SEMAPHORIN E 
National Institutes of Health

Related topics

Related topics

2 relations
SEMA3B geneSEMA6A gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Distinctive genetic variation of long‐segment Hirschsprung's disease in Taiwan
Hirschsprung's disease (HSCR) is a congenital disorder with the absence of myenteric and submucosal ganglion cells within distal… 
2019
2019
Correlation of Peritumoral Edema and Microvessel Density with Tissue Expression of VEGF, Semaphorins 3A and 3C in Patients with Meningioma
Background: Several angiogenic factors correlate with angiogenesis in meningioma while their exact role is yet to be identified… 
2016
2016
Expression of Semaphorin 3C in Breast Cancer and its Impact on Adhesion and Invasion of Breast Cancer Cells.
BACKGROUND The aim of the current study was to examine the role of semaphorin 3C (SEMA3C) in breast cancer. MATERIALS AND… 
2016
2016
Down‐regulation of semaphorin 3F in rat retinal ganglion cells in response to optic nerve crush
Glaucoma is characterized by degeneration of optic nerve axons and death of retinal ganglion cells (RGCs). Nerve crush and… 
2016
2016
A Sema3C Mutant Resistant to Cleavage by Furin (FR-Sema3C) Inhibits Choroidal Neovascularization
In age-related macular degeneration (AMD), abnormal sub retinal choroidal neovascularization (CNV) is a major cause of blindness… 
2015
2015
Genome wide identification and expression profile in epithelial cells exposed to TiO2 particles
Environmental particles are believed to provoke airway inflammation in susceptible individuals by stimulating epithelial cells to… 
2012
2012
Rapid and efficient human mutation detection using a bench‐top next‐generation DNA sequencer
Next‐generation sequencing (NGS) technologies can be a boon to human mutation detection given their high throughput: consequently… 
2012
2012
The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy
Background Reading disability (RD) is a common neurodevelopmental disorder with genetic basis established in families segregating… 
2007
2007
Semaphorin signaling facilitates cleft formation in the developing salivary gland
Semaphorin signaling plays integral roles in multiple developmental processes. Branching morphogenesis is one such role that has… 
Highly Cited
2005
Highly Cited
2005
Null and conditional semaphorin 3B alleles using a flexible puroΔtk loxP/FRT vector
In neural development, Semaphorin 3B (SEMA3B) is thought to play a role in guiding axons by repulsion. In nonneuronal tissue… 
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