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CHODL gene

Known as: FLJ12627, CHODL, MT75 
 
National Institutes of Health

Papers overview

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2018
2018
Aims: This study aimed to develop a valuable nomogram by integrating molecular markers and tumor-node-metastasis (TNM) staging… Expand
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2017
2017
Hepatocellular carcinoma (HCC) is the third leading cause of cancer-associated death. Due to rapid progression and metastasis… Expand
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2016
2016
Spinal muscular atrophy (SMA) is an autosomal-recessive pediatric neurodegenerative disease characterized by selective loss of… Expand
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Highly Cited
2014
Highly Cited
2014
Spinal muscular atrophy (SMA) is characterized by the selective loss of spinal motor neurons owing to reduced levels of survival… Expand
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2012
2012
The C-type lectin chondrolectin (chodl) represents one of the major gene products dysregulated in spinal muscular atrophy models… Expand
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2011
2011
Purpose: This study aims to identify molecules that might be useful as diagnostic/prognostic biomarkers and as targets for the… Expand
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Highly Cited
2010
Highly Cited
2010
Spinal cholinergic neurons are critical for motor function in both the autonomic and somatic nervous systems and are affected in… Expand
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2003
2003
In this study, we identified and characterized the mouse orthologue of the human chondrolectin gene, Chodl. Chodl is located at… Expand
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2003
2003
Chondrolectin (CHODL) is a novel type I transmembrane protein containing one carbohydrate recognition domain (CRD) of C-type… Expand
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2002
2002
CHODL, a novel human gene encoding chondrolectin, was isolated by PCR screening. It is localized at chromosome 21q21 and consists… Expand
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