An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutations-Reference-Cited by-同舟云学术

An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutations

Published:2017-05-09 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Stayner C.,Poole C. A.,McGlashan S. R.,Pilanthananond M.,Brauning R.,Markie D.,Lett B.,Slobbe L.,Chae A.,Johnstone A. C.,Jensen C. G.,McEwan J. C.^ORCID,Dittmer K.,Parker K.,Wiles A.,Blackburne W.,Leichter A.,Leask M.,Pinnapureddy A.,Jennings M.,Horsfield J. A.^ORCID,Walker R. J.,Eccles M. R.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-01519-4.pdf

Reference51 articles.

1. Wilson, P. D. Polycystic kidney disease. N Engl J Med. 350, 151–64 (2004).

2. Guay-Woodford, L. M. Murine models of polycystic kidney disease: molecular and therapeutic insights. Am J Physiol Renal Physiol. 285, F1034–49 (2003).

3. Igarashi, P. & Somlo, S. Genetics and pathogenesis of polycystic kidney disease. J Am Soc Nephrol. 13, 2384–98 (2002).

4. Guay-Woodford, L. M. Renal cystic diseases: diverse phenotypes converge on the cilium/centrosome complex. Pediatr Nephrol. 21, 1369–76 (2006).

5. Zerres, K. et al. Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology. American Journal of Medical Genetics 76, 137–44 (1998).

Cited by 15 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. XIAP-mediated degradation of IFT88 disrupts HSC cilia to stimulate HSC activation and liver fibrosis;EMBO Reports;2024-02-13

2. Insights Gained From Zebrafish Models for the Ciliopathy Joubert Syndrome;Frontiers in Genetics;2022-06-30

3. Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis;Molecular Neurobiology;2022-05-31

4. Association of novel TMEM67 variants with mild phenotypes of high gamma‐glutamyl transpeptidase cholestasis and congenital hepatic fibrosis;Journal of Cellular Physiology;2022-05-27

5. Transmission Electron Microscopy Tilt-Series Data from In-Situ Chondrocyte Primary Cilia;Data;2021-11-15