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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… 
2018
2018
SNX10 mediates alcohol-induced liver injury and steatosis by regulating the activation of chaperone-mediated autophagy.
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.
2018
2018
Sorting nexin 10 controls mTOR activation through regulating amino-acid metabolism in colorectal cancer
Amino-acid metabolism plays a vital role in mammalian target of rapamycin (mTOR) signaling, which is the pivot in colorectal… 
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… 
2017
2017
SNX10 promotes phagosome maturation in macrophages and protects mice against Listeria monocytogenes infection
Listeria monocytogenes (L. monocytogenes), which is a facultative intracellular bacterial pathogen that causes listeriosis, is… 
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… 
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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