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Updated: May 29, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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HSPB7 Deficiency Drives Aortic Aneurysm Progression in Marfan Syndrome Through Vascular Smooth Muscle Cell Phenotypic

Zining An1, Tao Yan2, Yang Ming2

  • 1Department of Cardiovascular Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Clinical and Experimental Pharmacology & Physiology
|May 27, 2026
PubMed
Abstract

Keywords:
HSPB7Marfan syndromehiPSC‐derived modelsorgan‐on‐a‐chipsingle‐cell transcriptomicssmooth muscle cellsthoracic aortic aneurysm

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