Baojin Ding

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Assistant Professor

United States

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About

Dr. Baojin Ding is an Assistant Professor at the Louisiana State University Health Sciences Center Shreveport Health Sciences Library in the United States. His research focuses on the generation and modeling of human induced pluripotent stem cells, particularly in relation to motor neuron diseases and neurodevelopmental disorders. Recent publications include studies on photobiomodulation effects on brain endothelial cells and the generation of isogenic control cell lines for dystonia research.

Recent Grants

Grant: Close

Determining the Pathogenesis of DYT1 Dystonia in Reprogrammed Human Neurons

Open Date: 2020-04-01

Close Date: 2022-09-01

Grant: Close

Determining the Pathogenesis of Dystonia in Reprogrammed Human Neurons

Open Date: 2020-03-01

Close Date: 2023-03-01

Grant: Close

Nucleocytoplasmic Transport Defect in Alzheimer's Disease

Open Date: 2017-05-01

Close Date: 2018-05-01

Articles (14)

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2025

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2024

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2024

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2021

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2021

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2021

Collaborators (1)

Vesna Tesic

Assistant Professor - Research

UNITED STATES

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Baojin Ding

Research Interests

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About

Recent Grants

Articles (14)

Comparative analysis of chemical and lentiviral approaches in the generation of human induced pluripotent stem cell–derived motor neurons

Correction: Feng et al. Photobiomodulation Inhibits Ischemia-Induced Brain Endothelial Senescence via Endothelial Nitric Oxide Synthase. Antioxidants 2024, 13, 633

Photobiomodulation Inhibits Ischemia-Induced Brain Endothelial Senescence via Endothelial Nitric Oxide Synthase

RANBP17 Overexpression Restores Nucleocytoplasmic Transport and Ameliorates Neurodevelopment in Induced DYT1 Dystonia Motor Neurons

Generation of two induced pluripotent stem cell lines with heterozygous and homozygous amyotrophic lateral sclerosis-causing mutation P525L (c.1574C > T) in FUS gene

Generation of two induced pluripotent stem cell lines with heterozygous and homozygous amyotrophic lateral sclerosis-causing mutation R521G (c.1561C > G) in FUS gene

Protocol to image and quantify nucleocytoplasmic transport in cultured cells using fluorescent in situ hybridization and a dual reporter system

Modeling Movement Disorders via Generation of hiPSC-Derived Motor Neurons

Generation of gene-corrected isogenic control cell lines from a DYT1 dystonia patient iPSC line carrying a heterozygous GAG mutation in TOR1A gene.

Generation of highly pure motor neurons from human induced pluripotent stem cells.

Novel insights into the pathogenesis of DYT1 dystonia from induced patient-derived neurons.

Direct conversion of adult fibroblasts into motor neurons

Generation of two induced pluripotent stem cell lines with heterozygous and homozygous GAG deletion in TOR1A gene from a healthy hiPSC line

Generation of patient-specific motor neurons in modeling movement diseases.

Collaborators (1)

Vesna Tesic

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