Abnormal Rab11-Rab8-vesicles cluster in enterocytes of patients with microvillus inclusion disease-Reference-Cited by-同舟云学术

Abnormal Rab11-Rab8-vesicles cluster in enterocytes of patients with microvillus inclusion disease

Published:2017-05-17 Issue:7 Volume:18 Page:453-464
ISSN:1398-9219
Container-title:Traffic
language:en
Short-container-title:Traffic

Author:

Vogel Georg F.¹²³,Janecke Andreas R.³,Krainer Iris M.²³,Gutleben Karin¹,Witting Barbara¹,Mitton Sally G.⁴,Mansour Sahar⁵,Ballauff Antje⁶,Roland Joseph T.⁷⁸⁹,Engevik Amy C.⁷⁸⁹,Cutz Ernest¹⁰,Müller Thomas³,Goldenring James R.⁷⁸⁹,Huber Lukas A.²,Hess Michael W.¹

Affiliation:

1. Division of Histology and Embryology; Medical University of Innsbruck; Innsbruck Austria

2. Division of Cell Biology; Medical University of Innsbruck; Innsbruck Austria

3. Department of Paediatrics I; Medical University of Innsbruck; Innsbruck Austria

4. St. George's University Hospitals; London UK

5. Human Genetics Research Center; St. George's University of London; London UK

6. Helios Klinikum Krefeld; Krefeld Germany

7. Section of Surgical Sciences; Vanderbilt University School of Medicine; Nashville Tennessee

8. Epithelial Biology Center; Vanderbilt University School of Medicine; Nashville Tennessee

9. Departments of Cell and Developmental Biology; Vanderbilt University School of Medicine; Nashville Tennessee

10. Division of Pathology, Department of Paediatric Laboratory Medicine; The Hospital for Sick Children; Toronto Canada

Funder

Austrian Science Fund

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/tra.12486/fullpdf

Reference78 articles.

1. Familial enteropathy: a syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy;Davidson;Gastroenterology,1978

2. Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation;Cutz;N Engl J Med,1989

3. Familial microvillous atrophy: a clinicopathological survey of 23 cases;Phillips;J Pediatr Gastroenterol Nutr,1992

4. Towards understanding microvillus inclusion disease;Vogel;Mol Cell Pediatr,2016

5. MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity;Muller;Nat Genet,2008

Cited by 45 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Altered cellular metabolic pathway and epithelial cell maturation induced by MYO5B defects are partially reversible by LPAR5 activation;2024-09-08

2. Intracellular Trafficking Defects in Congenital Intestinal and Hepatic Diseases;Traffic;2024-08

3. Downregulation of V-ATPase V0 Sector Induces Microvillus Atrophy Independently of Apical Trafficking in the Mammalian Intestine;Cellular and Molecular Gastroenterology and Hepatology;2024

4. Uncovering the Relationship Between Genes and Phenotypes Beyond the Gut in Microvillus Inclusion Disease;Cellular and Molecular Gastroenterology and Hepatology;2024

5. ALS-linked C9orf72–SMCR8 complex is a negative regulator of primary ciliogenesis;Proceedings of the National Academy of Sciences;2023-12-08