The cerebral cavernous malformation disease causing gene KRIT1 participates in intestinal epithelial barrier maintenance and regulation-Reference-Cited by-同舟云学术

The cerebral cavernous malformation disease causing gene KRIT1 participates in intestinal epithelial barrier maintenance and regulation

Published:2018-09-25 Issue:2 Volume:33 Page:2132-2143
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Wang Yitang¹²,Li Ye¹²,Zou Jinjing²³,Polster Sean P.¹,Lightle Rhonda¹,Moore Thomas¹,Dimaano Matthew⁴,He Tong-Chuan⁵,Weber Christopher R.²,Awad Issam A.¹,Shen Le¹²

Affiliation:

1. Section of NeurosurgeryDepartment of SurgeryThe University of ChicagoChicagoIllinoisUSA

2. Department of PathologyThe University of ChicagoChicagoIllinoisUSA

3. Department of Pulmonary and Critical Care MedicineRenmin Hospital of Wuhan UniversityWuhanChina

4. Department of MedicineThe University of ChicagoChicagoIllinoisUSA

5. Department of Orthopaedic Surgery and Rehabilitation MedicineThe University of ChicagoChicagoIllinoisUSA

Funder

National Institutes of Health

National Institute of Diabetes and Digestive and Kidney Diseases

University of Chicago

National Natural Science Foundation of China

American Association of Neurological Surgeons

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.201800343R

Reference65 articles.

1. Tight junctions as regulators of tissue remodelling

2. The Molecular Constituents of the Blood–Brain Barrier

3. Regulation of Endothelial Permeability via Paracellular and Transcellular Transport Pathways

4. Cell Biology of Tight Junction Barrier Regulation and Mucosal Disease

5. Celiac Disease: Role of the Epithelial Barrier

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