Han-yi Lin
No. 7, Chung Shan South Road, 100
TPQ, Taiwan
TPQ, Taiwan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 16 publications
Reply to: Mild Chronic Colitis Triggers Parkinsonism in LRRK2 Mutant Mice through Activating TNF-α Pathway.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 13, 2022
Neuroinflammation Upregulated Neuronal Toll-Like Receptors 2 and 4 to Drive Synucleinopathy in Neurodegeneration.
Journal: Frontiers in pharmacology
Published: December 30, 2021
Endocrine and Growth Disorders in Taiwanese Children With 22q11.2 Deletion Syndrome.
Journal: Frontiers in endocrinology
Published: September 05, 2021
Mild Chronic Colitis Triggers Parkinsonism in LRRK2 Mutant Mice Through Activating TNF-α Pathway.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 15, 2021
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
Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48).
Journal: Journal of biomedical science
Published: June 12, 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
UQCRC1 engages cytochrome c for neuronal apoptotic cell death.
Journal: Cell reports
Published: November 05, 2020
Reprogramming of a human induced pluripotent stem cell (iPSC) line from a patient with neurodegeneration with brain iron accumulation (NBIA) harboring a novel frameshift mutation in C19orf12 gene.
Journal: Stem cell research
Published: September 05, 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
Last Updated: 09/26/2026