Cheng-yen Huang
TPQ 10023, Taiwan
Last Updated: 09/26/2026
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Found 10 publications
Low Efficiency of Homology-Independent Targeted Integration for CRISPR/Cas9 Correction in the Vicinity of the SLC26A4 c.919-2A>G Variant.
Journal: International journal of molecular sciences
Published: March 31, 2025
A novel C19orf12 frameshift mutation in a MPAN pedigree impairs mitochondrial function and connectivity leading to neurodegeneration.
Journal: Parkinsonism & related disorders
Published: November 24, 2022
Generation of induced pluripotent stem cells (IBMSi027-A) from a patient with hearing loss carrying WFS1 c.2051C > T (p.Ala684Val) variant.
Journal: Stem cell research
Published: August 09, 2022
In vitro genome editing rescues parkinsonism phenotypes in induced pluripotent stem cells-derived dopaminergic neurons carrying LRRK2 p.G2019S mutation.
Journal: Stem cell research & therapy
Published: June 18, 2021
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-070-02) from a patient with neurodegeneration with brain iron accumulation (NBIA) having compound heterozygous mutations in PANK2 gene.
Journal: Stem cell research
Published: December 14, 2020
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-057-05) from a patient with familial parkinsonism and polyneuropathy having a heterozygous p.Y314S mutation in UQCRC1 gene.
Journal: Stem cell research
Published: September 02, 2020
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy.
Journal: Brain : a journal of neurology
Published: February 24, 2020
R26R-GR: a Cre-activable dual fluorescent protein reporter mouse.
Journal: PloS one
Published: February 20, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026