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SMPD3 gene

Known as: SMPD3, sphingomyelin phosphodiesterase 3, NSMASE2 
This gene plays a role in phospholipid metabolism.
National Institutes of Health

Related topics

Related topics

7 relations
HydrolysisPhospholipid MetabolismSMPD1 geneSMPD2 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Neutral Sphingomyelinase 2 (SMPD3)-Deficiency in Mice Causes Chondrodysplasia with Unimpaired Skeletal Mineralization.
2018
2018
Genome-Wide DNA Methylation Profiles of Phlegm-Dampness Constitution
Background/Aims: Metabolic diseases are leading health concerns in today’s global society. In traditional Chinese medicine (TCM… 
2018
2018
Abstract 3316: Hypermethylation at the SMPD3 promoter is frequently detected in hepatocellular carcinoma tumor tissue and corresponding plasma circulating DNA, and potentially differs by tumor…
2017
2017
TLR‐Induced SMPD3 Defects Enhance Inflammatory Response of B Cell and Macrophage in the Pathogenesis of SLE
B lymphocyte and macrophages may contribute to SLE pathogenesis through cytokine production after TLR stimulation. Emerging… 
2014
2014
162 Regulated Exosome Secretion by Vascular Smooth Muscle Cells Mediates Vascular Calcification
Arterial stiffening caused by deposition of calcium phosphate salts in the vessel wall is common in patients with atherosclerosis… 
2014
2014
Osteoblast-Specific Krm2 Overexpression and Lrp5 Deficiency Have Different Effects on Fracture Healing in Mice
The canonical Wnt/β-catenin pathway plays a key role in the regulation of bone remodeling in mice and humans. Two transmembrane… 
2013
2013
Local Regulation of Tooth Mineralization by Sphingomyelin Phosphodiesterase 3
Sphingomyelin phosphodiesterase 3 (Smpd3) encodes a membrane-bound enzyme that cleaves sphingomyelin to generate several… 
2011
2011
DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2
DFNB89 is a novel autosomal recessive nonsyndromic hearing impairment (ARNSHI) locus that was mapped to 16q21-q23.2. Linkage to… 
Highly Cited
2005
Highly Cited
2005
A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse
The mouse mutation fragilitas ossium (fro) leads to a syndrome of severe osteogenesis and dentinogenesis imperfecta with no… 
1978
1978
Resistivity minimum in Pd : Pr dilute alloys
2014 The electrical resistivity of some Pd1 _xPrx (x = 0.02 and 0.03) alloys has been measured between 1.5 and 300 K. Resistivity… 
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