Laboratory of Hong Chen, Ph.D.

Vascular Biology Program, Boston Children's Hospital
Department of Surgery, Harvard Medical School

Primary menu

Kui Cui

A neuro-lymphatic communication guides lymphatic development by CXCL12/CXCR4 signaling.
Novel Role of Endothelial CD45 in Regulating Endothelial-to-Mesenchymal Transition in Atherosclerosis
Machine Learning Uncovers Vascular Endothelial Cell Identity Genes by Expression Regulation Features in Single Cells
Targeting Liver Epsins Ameliorates Dyslipidemia in Atherosclerosis
Oxidative Stress, Endothelial Dysfunction, and N-Acetylcysteine in Type 2 Diabetes Mellitus
Molecular insights and clinical implications for the tumor suppressor role of SCFFBXW7 E3 ubiquitin ligase
The long noncoding RNA CARDINAL attenuates cardiac hypertrophy by modulating protein translation
Elucidating the crosstalk between endothelial-to-mesenchymal transition (EndoMT) and endothelial autophagy in the pathogenesis of atherosclerosis
Interplay Between FoxM1 and Dab2 Promotes Endothelial Cell Responses in Diabetic Wound Healing
Two sides of the same coin: Non-alcoholic fatty liver disease and atherosclerosis
Epsins oversee smooth muscle cell reprograming by influencing master regulators KLF4 and OCT4
Targeting endothelial FOXO1 protects diabetic β-cells and improves wound healing
Epsin Endocytic Adaptor Proteins in Angiogenic and Lymphangiogenic Signaling
Reduced Mitochondrial Protein Translation Promotes Cardiomyocyte Proliferation and Heart Regeneration
Epsin Nanotherapy Regulates Cholesterol Transport to Fortify Atheroma Regression

Secondary menu