Keiichi Asano
Tsukuba, 3058577, Japan
Last Updated: 09/26/2026
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Found 8 publications
Novel Aortic Dissection Model Links Endothelial Dysfunction and Immune Infiltration.
Journal: Circulation research
Published: May 14, 2025
Fibrillin-1 G234D mutation in the hybrid1 domain causes tight skin associated with dysregulated elastogenesis and increased collagen cross-linking in mice.
Journal: Matrix biology : journal of the International Society for Matrix Biology
Published: June 04, 2024
Fibrillin-1 Deficiency Perturbs Aortic Cholinergic Relaxation and Adrenergic Contraction in a Mouse Model of Early Onset Progressively Severe Marfan Syndrome.
Journal: Journal of vascular research
Published: May 28, 2024
Fibrillin-1 deficiency in the outer perichondrium causes longitudinal bone overgrowth in mice with Marfan syndrome.
Journal: Human molecular genetics
Published: March 10, 2022
The Multiple Functions of Fibrillin-1 Microfibrils in Organismal Physiology.
Journal: International journal of molecular sciences
Published: December 17, 2021
Pathophysiology and Therapeutics of Thoracic Aortic Aneurysm in Marfan Syndrome.
Journal: Biomolecules
Published: November 30, 2021
Showing 1-8 of 8
Last Updated: 09/26/2026