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Neuropilin-1 deficiency in vascular smooth muscle cells is associated with hereditary hemorrhagic telangiectasia arteriovenous malformations.
Kilari, Sreenivasulu; Wang, Ying; Singh, Avishek; Graham, Rondell P; Iyer, Vivek; Thompson, Scott M; Torbenson, Michael S; Mukhopadhyay, Debabrata; Misra, Sanjay.
Affiliation
  • Kilari S; Vascular and Interventional Radiology Translational laboratory, Division of Vascular and Interventional Radiology, Department of Radiology.
  • Wang Y; Department of Cardiovascular Medicine.
  • Singh A; Department of Biochemistry and Molecular Biology.
  • Graham RP; Vascular and Interventional Radiology Translational laboratory, Division of Vascular and Interventional Radiology, Department of Radiology.
  • Iyer V; Department of Laboratory Medicine and Pathology, and.
  • Thompson SM; Mayo Clinic Hereditary Hemorrhagic Telangiectasia Center of Excellence, Mayo Clinic, Rochester, Minnesota, USA.
  • Torbenson MS; Vascular and Interventional Radiology Translational laboratory, Division of Vascular and Interventional Radiology, Department of Radiology.
  • Mukhopadhyay D; Department of Laboratory Medicine and Pathology, and.
  • Misra S; Department of Biochemistry and Molecular Biology, College of Medicine and Science, Mayo Clinic, Jacksonville, Florida, USA.
JCI Insight ; 7(9)2022 05 09.
Article in En | MEDLINE | ID: mdl-35380991
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arteriovenous Malformations / Telangiectasia, Hereditary Hemorrhagic Type of study: Risk_factors_studies Limits: Animals / Humans Language: En Journal: JCI Insight Year: 2022 Document type: Article Country of publication: United States
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arteriovenous Malformations / Telangiectasia, Hereditary Hemorrhagic Type of study: Risk_factors_studies Limits: Animals / Humans Language: En Journal: JCI Insight Year: 2022 Document type: Article Country of publication: United States