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GPD1L gene

Known as: GLYCEROL-3-PHOSPHATE DEHYDROGENASE 1-LIKE, GPD1L, KIAA0089 
National Institutes of Health

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GPD1 gene

Papers overview

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2020
2020
A novel mutation in GPD1‑L associated with early repolarization syndrome via modulation of cardiomyocyte fast sodium currents.
Early repolarization syndrome (ERS) is associated with genetic mutations, but the role of the glycerol‑3‑phosphate dehydrogenase… 
2019
2019
Long Noncoding RNA Nuclear Enriched Abundant Transcript 1 (NEAT1) Regulates Proliferation, Apoptosis, and Inflammation of Chondrocytes via the miR-181a/Glycerol-3-Phosphate Dehydrogenase 1-Like…
Background Osteoarthritis (OA) is one of the most common chronic musculoskeletal diseases, yet to date it lacks effective… 
2018
2018
miR-210 and GPD1L regulate EDN2 in primary and immortalized human granulosa-lutein cells.
Endothelin-2 (EDN2), expressed at a narrow window during the periovulatory period, critically affects ovulation and corpus luteum… 
2017
2017
A Systems Genetics Approach Identified GPD1L and its Molecular Mechanism for Obesity in Human Adipose Tissue
To explore novel molecular mechanisms underlying obesity, we applied a systems genetics framework to integrate risk genetic loci… 
2017
2017
GPD1L is down-regulated by a three-microRNA signature in pancreatic cancer
Background: The prognosis of pancreatic ductal adenocarcinoma (PDAC) is very poor and its underlying mechanism is far from clear… 
Highly Cited
2011
Highly Cited
2011
A Hypoxia-Induced Positive Feedback Loop Promotes Hypoxia-Inducible Factor 1α Stability through miR-210 Suppression of Glycerol-3-Phosphate Dehydrogenase 1-Like
ABSTRACT Oxygen-dependent regulation of the transcription factor HIF-1α relies on a family of prolyl hydroxylases (PHDs) that… 
Highly Cited
2009
Highly Cited
2009
Exercise-Induced ECG Changes in Brugada Syndrome
Background—Ventricular arrhythmia occurrence during exercise is reported in Brugada syndrome (BrS). Accordingly, experimental… 
2009
2009
Cardiac metabolic state and Brugada syndrome: a link revealed.
See related article, pages 737–745 Brugada syndrome (BrS) is an inherited cardiac disorder with variable ECG features… 
Highly Cited
2007
Highly Cited
2007
Genetic basis of Brugada syndrome.
2006
2006
AB16-1: A mutation in the glycerol-3-phosphate dehydrogenase 1-like gene (GPD1L) causes Brugada syndrome
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