Baihui Ma

State Key Laboratory Of Cardiovascular Disease, Beijing Key Laboratory For Molecular Diagnostics Of Cardiovascular Diseases, Chinese Academy Of Medical Sciences And Peking Union Medical College
Beijing, China

Last Updated: 09/26/2026

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Found 15 publications

Human iPSC-Derived Vascularised Lung Organoids for Modelling COPD and Pulmonary Hypertension.

Human iPSC-Derived Vascularised Lung Organoids for Modelling COPD and Pulmonary Hypertension.

Journal: Cell proliferation

Published: December 26, 2025

Corrigendum to "MMP19 in vascular smooth muscle cells protects against thoracic aortic aneurysm and dissection via the MMP19/Aggrecan/Wnt/β-catenin axis"[J Mol Cell Cardiol. 202 (2025) 35-49].

Corrigendum to "MMP19 in vascular smooth muscle cells protects against thoracic aortic aneurysm and dissection via the MMP19/Aggrecan/Wnt/β-catenin axis"[J Mol Cell Cardiol. 202 (2025) 35-49].

Journal: Journal of molecular and cellular cardiology

Published: August 21, 2025

Patient-specific and gene-corrected induced pluripotent stem cell-derived endothelial cells elucidate single-cell phenotype of pulmonary veno-occlusive disease.

Patient-specific and gene-corrected induced pluripotent stem cell-derived endothelial cells elucidate single-cell phenotype of pulmonary veno-occlusive disease.

Journal: Stem cell reports

Published: May 29, 2025

MMP19 in vascular smooth muscle cells protects against thoracic aortic aneurysm and dissection via the MMP19/Aggrecan/Wnt/β-catenin axis.

MMP19 in vascular smooth muscle cells protects against thoracic aortic aneurysm and dissection via the MMP19/Aggrecan/Wnt/β-catenin axis.

Journal: Journal of molecular and cellular cardiology

Published: August 11, 2024

Matrix metalloproteinases in aortic dissection.

Matrix metalloproteinases in aortic dissection.

Journal: Vascular pharmacology

Published: June 14, 2024

Patient-specific and gene-corrected induced pluripotent stem cell-derived endothelial cells elucidate single-cell phenotype of pulmonary veno-occlusive disease.

Patient-specific and gene-corrected induced pluripotent stem cell-derived endothelial cells elucidate single-cell phenotype of pulmonary veno-occlusive disease.

Journal: Stem cell reports

Published: April 15, 2022

Association of PLXND1 with a novel subtype of anomalous pulmonary venous return.

Association of PLXND1 with a novel subtype of anomalous pulmonary venous return.

Journal: Human molecular genetics

Published: September 28, 2021

Nidogen-2 Maintains the Contractile Phenotype of Vascular Smooth Muscle Cells and Prevents Neointima Formation via Bridging Jagged1-Notch3 Signaling.

Nidogen-2 Maintains the Contractile Phenotype of Vascular Smooth Muscle Cells and Prevents Neointima Formation via Bridging Jagged1-Notch3 Signaling.

Journal: Circulation

Published: July 28, 2021

Generation of a CRISPR/Cas9-corrected-hiPSC (NCCDFWi001-A-1) from a Marfan syndrome patient hiPSC with a heterozygous c.2613A>C variant in the fibrillin 1 (FBN1) gene.

Generation of a CRISPR/Cas9-corrected-hiPSC (NCCDFWi001-A-1) from a Marfan syndrome patient hiPSC with a heterozygous c.2613A>C variant in the fibrillin 1 (FBN1) gene.

Journal: Stem cell research

Published: June 16, 2021

Single-Cell RNA-Sequencing Reveals Lineage-Specific Regulatory Changes of Fibroblasts and Vascular Endothelial Cells in Keloids.

Single-Cell RNA-Sequencing Reveals Lineage-Specific Regulatory Changes of Fibroblasts and Vascular Endothelial Cells in Keloids.

Journal: The Journal of investigative dermatology

Published: January 06, 2021

Exome-Based Case-Control Analysis Highlights the Pathogenic Role of Ciliary Genes in Transposition of the Great Arteries.

Exome-Based Case-Control Analysis Highlights the Pathogenic Role of Ciliary Genes in Transposition of the Great Arteries.

Journal: Circulation research

Published: February 21, 2020

Generation of a human induced pluripotent stem cell line (NCCDFWi001-A) from a Marfan syndrome patient carrying two FBN1 variants (c.2613A > C and c.684_736 + 4del).

Generation of a human induced pluripotent stem cell line (NCCDFWi001-A) from a Marfan syndrome patient carrying two FBN1 variants (c.2613A > C and c.684_736 + 4del).

Journal: Stem cell research

Published: November 28, 2019

Showing 1-12 of 15

Last Updated: 09/26/2026