Chien-yi Tung

No. 155, Sec. 2, Linong St
Beitou, TPQ 11221, Taiwan

Last Updated: 09/26/2026

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Found 29 publications

Hierarchical analysis of metabolic phenotype reveals distinct microbiota and circulatory transcriptome in metabolic dysfunction-associated steatotic liver disease.

Hierarchical analysis of metabolic phenotype reveals distinct microbiota and circulatory transcriptome in metabolic dysfunction-associated steatotic liver disease.

Journal: Gene

Published: March 21, 2026

Activation of CISD2 as a protective strategy against doxorubicin-induced cardiotoxicity.

Activation of CISD2 as a protective strategy against doxorubicin-induced cardiotoxicity.

Journal: Redox biology

Published: July 14, 2025

Cisd2 delays atrial aging via a modulation of calcium homeostasis that mitigates atrial myopathy.

Cisd2 delays atrial aging via a modulation of calcium homeostasis that mitigates atrial myopathy.

Journal: Cell communication and signaling : CCS

Published: May 01, 2025

Epilepsy-associated FOXJ3 variants link a transcriptional program of the PTEN-mTOR pathway to neuronal specification and cortical lamination.

Epilepsy-associated FOXJ3 variants link a transcriptional program of the PTEN-mTOR pathway to neuronal specification and cortical lamination.

Journal: Nature communications

Published: January 24, 2025

Wolfram syndrome 2 gene (CISD2) deficiency disrupts Ca2+-mediated insulin secretion in β-cells.

Wolfram syndrome 2 gene (CISD2) deficiency disrupts Ca2+-mediated insulin secretion in β-cells.

Journal: Molecular metabolism

Published: November 10, 2024

Transcriptomic predictors of rapid progression from mild cognitive impairment to Alzheimer's disease.

Transcriptomic predictors of rapid progression from mild cognitive impairment to Alzheimer's disease.

Journal: Alzheimer's research & therapy

Published: September 27, 2024

Functional defects in FOXG1 variants predict the severity of brain anomalies in FOXG1 syndrome.

Functional defects in FOXG1 variants predict the severity of brain anomalies in FOXG1 syndrome.

Journal: Molecular psychiatry

Published: March 13, 2024

Regulation of primary cilia disassembly through HUWE1-mediated TTBK2 degradation plays a crucial role in cerebellar development and medulloblastoma growth.

Regulation of primary cilia disassembly through HUWE1-mediated TTBK2 degradation plays a crucial role in cerebellar development and medulloblastoma growth.

Journal: Cell death and differentiation

Published: February 21, 2024

Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations.

Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations.

Journal: Acta neuropathologica

Published: October 23, 2023

Single-cell analysis of castration-resistant prostate cancers to identify potential biomarkers for diagnosis and prognosis of neuroendocrine prostate cancer.

Single-cell analysis of castration-resistant prostate cancers to identify potential biomarkers for diagnosis and prognosis of neuroendocrine prostate cancer.

Journal: American journal of cancer research

Published: August 04, 2023

Hesperetin activates CISD2 to attenuate senescence in human keratinocytes from an older person and rejuvenates naturally aged skin in mice.

Hesperetin activates CISD2 to attenuate senescence in human keratinocytes from an older person and rejuvenates naturally aged skin in mice.

Journal: Journal of biomedical science

Published: July 10, 2023

A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development.

A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development.

Journal: Development (Cambridge, England)

Published: April 26, 2023

Showing 1-12 of 29

Last Updated: 09/26/2026