Literature DB >> 22388554

Clinical spectrum and pathogenesis of nephronophthisis.

Thomas Benzing1, Bernhard Schermer.   

Abstract

PURPOSE OF REVIEW: Nephronophthisis (NPH) comprises a group of autosomal recessive cystic kidney diseases and is the most frequent genetic cause of end-stage renal disease in children and adolescents. Causative mutations in more than a dozen genes have been identified that encode for the NPH protein family. Almost all of these proteins localize to primary cilia leading to the classification of NPH as a ciliopathy. The purpose of this review is to highlight the latest research on the molecular pathogenesis of the ciliopathy NPH. RECENT
FINDINGS: Recent identification of novel disease causing genes and research on the localization and signaling function of nephrocystins have paved the way to a more detailed understanding of the molecular and cellular pathology of NPH and associated ciliopathies.
SUMMARY: Here we discuss the most recently identified NPH related genes, the role of the NPH protein complex in ciliary biology and recently discovered functions of NPH proteins in cellular signaling.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22388554     DOI: 10.1097/MNH.0b013e3283520f17

Source DB:  PubMed          Journal:  Curr Opin Nephrol Hypertens        ISSN: 1062-4821            Impact factor:   2.894


  22 in total

Review 1.  New frontiers: discovering cilia-independent functions of cilia proteins.

Authors:  Anastassiia Vertii; Alison Bright; Benedicte Delaval; Heidi Hehnly; Stephen Doxsey
Journal:  EMBO Rep       Date:  2015-09-09       Impact factor: 8.807

Review 2.  The primary cilium: Its role as a tumor suppressor organelle.

Authors:  Estanislao Peixoto; Seth Richard; Kishor Pant; Aalekhya Biswas; Sergio A Gradilone
Journal:  Biochem Pharmacol       Date:  2020-03-10       Impact factor: 5.858

3.  Juvenile nephronophthisis and dysthyroidism: a rare association.

Authors:  Fateme Shamekhi Amiri; Ariana Kariminejad
Journal:  CEN Case Rep       Date:  2017-03-13

Review 4.  Nephronophthisis and related syndromes.

Authors:  Matthias T F Wolf
Journal:  Curr Opin Pediatr       Date:  2015-04       Impact factor: 2.856

5.  Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies.

Authors:  Jens König; Birgitta Kranz; Sabine König; Karl Peter Schlingmann; Andrea Titieni; Burkhard Tönshoff; Sandra Habbig; Lars Pape; Karsten Häffner; Matthias Hansen; Anja Büscher; Martin Bald; Heiko Billing; Raphael Schild; Ulrike Walden; Tobias Hampel; Hagen Staude; Magdalena Riedl; Norbert Gretz; Martin Lablans; Carsten Bergmann; Friedhelm Hildebrandt; Heymut Omran; Martin Konrad
Journal:  Clin J Am Soc Nephrol       Date:  2017-11-16       Impact factor: 8.237

6.  Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD.

Authors:  Ekim Z Taskiran; Emine Korkmaz; Safak Gucer; Can Kosukcu; Figen Kaymaz; Cansu Koyunlar; Elizabeth C Bryda; Moumita Chaki; Dongmei Lu; Komal Vadnagara; Cengiz Candan; Rezan Topaloglu; Franz Schaefer; Massimo Attanasio; Carsten Bergmann; Fatih Ozaltin
Journal:  J Am Soc Nephrol       Date:  2014-03-07       Impact factor: 10.121

7.  Renal-Hepatic-Pancreatic Dysplasia: An Ultra-Rare Ciliopathy with a Novel NPHP3 Genotype.

Authors:  Yeliz Cagan Appak; Masallah Baran; Burcu Ozturk Hismi; Berk Ozyilmaz; Kader Vardi; Ozge Ozer Kaya; Betul Aksoy; Belde Kasap Demir
Journal:  J Pediatr Genet       Date:  2019-09-12

8.  Loss of the ciliary kinase Nek8 causes left-right asymmetry defects.

Authors:  Danielle K Manning; Mikhail Sergeev; Roy G van Heesbeen; Michael D Wong; Jin-Hee Oh; Yan Liu; R Mark Henkelman; Iain Drummond; Jagesh V Shah; David R Beier
Journal:  J Am Soc Nephrol       Date:  2013-01       Impact factor: 10.121

9.  The ratio of urinary α1-microglobulin to microalbumin can be used as a diagnostic criterion for tubuloproteinuria.

Authors:  Hongwen Zhang; Fang Wang; Huijie Xiao; Yong Yao
Journal:  Intractable Rare Dis Res       Date:  2018-02

Review 10.  Actualizing the Benefits of Genomic Discovery in Pediatric Nephrology.

Authors:  Matthew G Sampson
Journal:  J Pediatr Genet       Date:  2015-08-13
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.