Tze-tze Liu
TPQ, Taiwan
Last Updated: 09/26/2026
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Found 20 publications
SUMO Modification of Histone Demethylase KDM4A in Kaposi's Sarcoma-Associated Herpesvirus-Induced Primary Effusion Lymphoma.
Journal: Journal of virology
Published: August 01, 2022
Deletion of intestinal SIRT1 exacerbated muscle wasting in cirrhotic mice by decreasing the intestinal concentration of short-chain fatty acids and inflammation.
Journal: Journal of pharmacological sciences
Published: May 17, 2021
Intestinal SIRT1 Deficiency-Related Intestinal Inflammation and Dysbiosis Aggravate TNFα-Mediated Renal Dysfunction in Cirrhotic Ascitic Mice.
Journal: International journal of molecular sciences
Published: January 06, 2021
Prediction of functional consequences of the five newly discovered G6PD variations in Taiwan.
Journal: Data in brief
Published: April 25, 2019
Applying a multiplexed primer extension method on dried blood spots increased the detection of carriers at risk of glucose-6-phosphate dehydrogenase deficiency in newborn screening program.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: January 17, 2019
Role of protein structure in variant annotation: structural insight of mutations causing 6-pyruvoyl-tetrahydropterin synthase deficiency.
Journal: Pathology
Published: September 14, 2018
Somatic mutations of PREX2 gene in patients with hepatocellular carcinoma.
Journal: Scientific reports
Published: May 23, 2018
The roles of alcohol dehydrogenase in patients with atrial fibrillation.
Journal: Pacing and clinical electrophysiology : PACE
Published: August 29, 2017
Transcriptome analysis and prognosis of ALDH isoforms in human cancer.
Journal: Scientific reports
Published: May 25, 2017
Early measurement of IL-10 predicts the outcomes of patients with acute respiratory distress syndrome receiving extracorporeal membrane oxygenation.
Journal: Scientific reports
Published: December 16, 2016
A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy.
A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy.
Journal: Brain : a journal of neurology
Published: September 08, 2016
Last Updated: 09/26/2026