Proteomic Identification Reveals the Role of Ciliary Extracellular‐Like Vesicle in Cardiovascular Function-Reference-Cited by-同舟云学术

Proteomic Identification Reveals the Role of Ciliary Extracellular‐Like Vesicle in Cardiovascular Function

Published:2020-06-16 Issue:16 Volume:7 Page:1903140
ISSN:2198-3844
Container-title:Advanced Science
language:en
Short-container-title:Adv. Sci.

Author:

Mohieldin Ashraf M.¹,Pala Rajasekharreddy¹,Sherpa Rinzhin T.¹,Alanazi Madhawi¹,Alanazi Ashwaq¹,Shamloo Kiumars¹,Ahsan Amir²,AbouAlaiwi Wissam A.³,Moresco James J.⁴,Yates John R.⁴,Nauli Surya M.¹⁵^ORCID

Affiliation:

1. Department of Biomedical and Pharmaceutical SciencesChapman University Irvine CA 92618 USA

2. Department of Physics, Computer Science and EngineeringChapman University Orange CA 92866 USA

3. Department of Pharmacology and Experimental TherapeuticsUniversity of Toledo Toledo OH 43614 USA

4. Department of Molecular MedicineThe Scripps Research Institute La Jolla CA 92037 USA

5. Department of MedicineUniversity of California Irvine Irvine CA 92868 USA

Funder

National Institutes of Health

American Heart Association

Chapman University

National Institute of General Medical Sciences

Congressionally Directed Medical Research Programs

U.S. Department of Defense

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/advs.201903140

Reference61 articles.

1. Vertebrate Smoothened functions at the primary cilium

2. Removal of the MDCK Cell Primary Cilium Abolishes Flow Sensing

3. TMEM237 Is Mutated in Individuals with a Joubert Syndrome Related Disorder and Expands the Role of the TMEM Family at the Ciliary Transition Zone

4. A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition

5. Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes

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