Yafang Hu-Yafang

253 Middle Industrial Avenue
Guangzhou, 510282, China

Last Updated: 09/26/2026

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Found 10 publications

APTX deficiency is associated with altered neuronal differentiation and alternative splicing in patient-derived neurons.

APTX deficiency is associated with altered neuronal differentiation and alternative splicing in patient-derived neurons.

Journal: Neurobiology of disease

Published: July 18, 2026

Knockdown of OPTN modulates miRNA-125b-5p expression via NF-κB pathways in amyotrophic lateral sclerosis.

Knockdown of OPTN modulates miRNA-125b-5p expression via NF-κB pathways in amyotrophic lateral sclerosis.

Journal: Archives of biochemistry and biophysics

Published: December 24, 2024

Induced pluripotent stem cells carrying novel APTX mutations presented defective neural differentiation with the accumulation of DNA single-strand breaks.

Induced pluripotent stem cells carrying novel APTX mutations presented defective neural differentiation with the accumulation of DNA single-strand breaks.

Journal: Cell death discovery

Published: December 17, 2024

Prenatal p25-activated Cdk5 induces pituitary tumorigenesis through MCM2 phosphorylation-mediated cell proliferation.

Prenatal p25-activated Cdk5 induces pituitary tumorigenesis through MCM2 phosphorylation-mediated cell proliferation.

Journal: Neoplasia (New York, N.Y.)

Published: June 24, 2024

CHCHD2 rescues the mitochondrial dysfunction in iPSC-derived neurons from patient with Mohr-Tranebjaerg syndrome.

CHCHD2 rescues the mitochondrial dysfunction in iPSC-derived neurons from patient with Mohr-Tranebjaerg syndrome.

Journal: Cell death & disease

Published: May 29, 2024

Vessel flow void sign and hyperintense vessel sign on FLAIR images distinguish between MELAS and AIS.

Vessel flow void sign and hyperintense vessel sign on FLAIR images distinguish between MELAS and AIS.

Journal: Mitochondrion

Published: September 23, 2020

Frameshift mutation of Timm8a1 gene in mouse leads to an abnormal mitochondrial structure in the brain, correlating with hearing and memory impairment.

Frameshift mutation of Timm8a1 gene in mouse leads to an abnormal mitochondrial structure in the brain, correlating with hearing and memory impairment.

Journal: Journal of medical genetics

Published: March 05, 2020

Vibrio vulnificus meningoencephalitis in a patient with thalassemia and a splenectomy.

Vibrio vulnificus meningoencephalitis in a patient with thalassemia and a splenectomy.

Journal: Journal of neurovirology

Published: April 09, 2018

Interaction of Cdk5 and cAMP/PKA Signaling in the Mediation of Neuropsychiatric and Neurodegenerative Diseases.

Interaction of Cdk5 and cAMP/PKA Signaling in the Mediation of Neuropsychiatric and Neurodegenerative Diseases.

Journal: Advances in neurobiology

Published: September 29, 2017

Disruption of AT-hook 1 domain in MeCP2 protein caused behavioral abnormality in mice.

Disruption of AT-hook 1 domain in MeCP2 protein caused behavioral abnormality in mice.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: June 17, 2017

Showing 1-10 of 10

Last Updated: 09/26/2026