Neuropilin-1 deficiency in vascular smooth muscle cells is associated with hereditary hemorrhagic telangiectasia arteriovenous malformations-Reference-Cited by-同舟云学术

Neuropilin-1 deficiency in vascular smooth muscle cells is associated with hereditary hemorrhagic telangiectasia arteriovenous malformations

Published:2022-05-09 Issue:9 Volume:7 Page:
ISSN:2379-3708
Container-title:JCI Insight
language:en
Short-container-title:

Author:

Kilari Sreenivasulu^ORCID,Wang Ying^ORCID,Singh Avishek,Graham Rondell P.^ORCID,Iyer Vivek^ORCID,Thompson Scott M.,Torbenson Michael S.^ORCID,Mukhopadhyay Debabrata,Misra Sanjay^ORCID

Funder

NIH Clinical Center

Armstrong McDonald Foundation

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://insight.jci.org/articles/view/155565/files/pdf

Reference65 articles.

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3. Somatic PIK3CA Mutations in Sporadic Cerebral Cavernous Malformations

4. Developmental vascular malformations in EPAS1 gain-of-function syndrome

5. Cerebrovascular Manifestations of Hereditary Hemorrhagic Telangiectasia

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