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SNX10 gene

Known as: SNX10, SORTING NEXIN 10 
National Institutes of Health

Related topics

Related topics

1 relation
SNX16 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Sorting Nexin 10 Mediates Metabolic Reprogramming of Macrophages in Atherosclerosis Through the Lyn-Dependent TFEB Signaling Pathway
Supplemental Digital Content is available in the text. Rationale: SNX10 (sorting nexin 10) has been reported to play a critical… 
2020
2020
Snx10 and PIKfyve are required for lysosome formation in osteoclasts
Bone resorption and organelle homeostasis in osteoclasts require specialized intracellular trafficking. Sorting nexin 10 (Snx10… 
2019
2019
FKBP12: A partner of Snx10 required for vesicular trafficking in osteoclasts
Osteoclasts employ highly specialized intracellular trafficking controls for bone resorption and organelle homeostasis. The… 
2018
2018
Sorting nexin 10 acts as a tumor suppressor in tumorigenesis and progression of colorectal cancer through regulating chaperone mediated autophagy degradation of p21Cip1/WAF1.
2017
2017
SNX10 Plays a Critical Role in MMP9 Secretion via JNK‐p38‐ERK Signaling Pathway
Matrix metalloproteinases (MMPs) plays a critical role in the degradation of extracellular matrix (ECM). Sorting nexin (SNX) 10… 
2016
2016
Sorting nexin 10 acting as a novel regulator of macrophage polarization mediates inflammatory response in experimental mouse colitis
In response to changes in microenvironment, macrophages polarize into functionally distinct phenotypes, playing a crucial role in… 
2015
2015
Osteopetrorickets due to Snx10 Deficiency in Mice Results from Both Failed Osteoclast Activity and Loss of Gastric Acid-Dependent Calcium Absorption
Mutations in sorting nexin 10 (Snx10) have recently been found to account for roughly 4% of all human malignant osteopetrosis… 
2014
2014
Structure of human SNX10 reveals insights into its role in human autosomal recessive osteopetrosis
Sorting nexin 10 (SNX10), the unique member of the SNX family having vacuolation activity in cells, was shown to be involved in… 
Highly Cited
2013
Highly Cited
2013
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity
Human Autosomal Recessive Osteopetrosis (ARO) is a genetically heterogeneous disorder caused by reduced bone resorption by… 
2012
2012
SNX10 is required for osteoclast formation and resorption activity
RANKL‐stimulation of osteoclast precursors results in up‐regulation of genes involved in the process of differentiation and… 
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