Literature DB >> 25635582

Nephronophthisis and related syndromes.

Matthias T F Wolf1.   

Abstract

PURPOSE OF REVIEW: Nephronophthisis (NPHP) is an autosomal recessive cystic kidney disease and is one of the most common genetic disorders causing end-stage renal disease (ESRD) in children and adolescents. NPHP is a genetically heterogenous disorder with 20 identified genes. NPHP occurs as an isolated kidney disease, but approximately 15% of NPHP patients have additional extrarenal symptoms affecting other organs [e.g. eyes, liver, bones and central nervous system (CNS)]. The pleiotropy in NPHP is explained by the finding that almost all NPHP gene products share expression in primary cilia, a sensory organelle present in most mammalian cells. If extrarenal symptoms are present in addition to NPHP, these disorders are classified as NPHP-related ciliopathies (NPHP-RC). This review provides an update about recent advances in the field of NPHP-RC. RECENT
FINDINGS: The identification of novel disease-causing genes has improved our understanding of the pathomechanisms contributing to NPHP-RC. Multiple interactions between different NPHP-RC gene products have been published and outline the interconnectivity of the affected proteins and shared pathways.
SUMMARY: The significance of recently identified genes for NPHP-RC is discussed and the complex role and interaction of NPHP proteins in ciliary function and cellular signalling pathways is highlighted.

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Year:  2015        PMID: 25635582      PMCID: PMC4422489          DOI: 10.1097/MOP.0000000000000194

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  90 in total

Review 1.  Clinical spectrum and pathogenesis of nephronophthisis.

Authors:  Thomas Benzing; Bernhard Schermer
Journal:  Curr Opin Nephrol Hypertens       Date:  2012-05       Impact factor: 2.894

2.  A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1.

Authors:  F Hildebrandt; E Otto; C Rensing; H G Nothwang; M Vollmer; J Adolphs; H Hanusch; M Brandis
Journal:  Nat Genet       Date:  1997-10       Impact factor: 38.330

3.  Intraflagellar transport proteins cycle between the flagellum and its base.

Authors:  Johanna Buisson; Nicolas Chenouard; Thibault Lagache; Thierry Blisnick; Jean-Christophe Olivo-Marin; Philippe Bastin
Journal:  J Cell Sci       Date:  2012-09-19       Impact factor: 5.285

4.  Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling.

Authors:  Moumita Chaki; Rannar Airik; Amiya K Ghosh; Rachel H Giles; Rui Chen; Gisela G Slaats; Hui Wang; Toby W Hurd; Weibin Zhou; Andrew Cluckey; Heon Yung Gee; Gokul Ramaswami; Chen-Jei Hong; Bruce A Hamilton; Igor Cervenka; Ranjani Sri Ganji; Vitezslav Bryja; Heleen H Arts; Jeroen van Reeuwijk; Machteld M Oud; Stef J F Letteboer; Ronald Roepman; Hervé Husson; Oxana Ibraghimov-Beskrovnaya; Takayuki Yasunaga; Gerd Walz; Lorraine Eley; John A Sayer; Bernhard Schermer; Max C Liebau; Thomas Benzing; Stephanie Le Corre; Iain Drummond; Sabine Janssen; Susan J Allen; Sivakumar Natarajan; John F O'Toole; Massimo Attanasio; Sophie Saunier; Corinne Antignac; Robert K Koenekoop; Huanan Ren; Irma Lopez; Ahmet Nayir; Corinne Stoetzel; Helene Dollfus; Rustin Massoudi; Joseph G Gleeson; Sharon P Andreoli; Dan G Doherty; Anna Lindstrad; Christelle Golzio; Nicholas Katsanis; Lars Pape; Emad B Abboud; Ali A Al-Rajhi; Richard A Lewis; Heymut Omran; Eva Y-H P Lee; Shaohui Wang; Joann M Sekiguchi; Rudel Saunders; Colin A Johnson; Elizabeth Garner; Katja Vanselow; Jens S Andersen; Joseph Shlomai; Gudrun Nurnberg; Peter Nurnberg; Shawn Levy; Agata Smogorzewska; Edgar A Otto; Friedhelm Hildebrandt
Journal:  Cell       Date:  2012-08-03       Impact factor: 41.582

Review 5.  Joubert syndrome: congenital cerebellar ataxia with the molar tooth.

Authors:  Marta Romani; Alessia Micalizzi; Enza Maria Valente
Journal:  Lancet Neurol       Date:  2013-07-17       Impact factor: 44.182

6.  Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome.

Authors:  Valeska Frank; Anneke I den Hollander; Nadina Ortiz Brüchle; Marijke N Zonneveld; Gudrun Nürnberg; Christian Becker; Gabriele Du Bois; Heide Kendziorra; Susanne Roosing; Jan Senderek; Peter Nürnberg; Frans P M Cremers; Klaus Zerres; Carsten Bergmann
Journal:  Hum Mutat       Date:  2008-01       Impact factor: 4.878

7.  Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis.

Authors:  Massimo Attanasio; N Henriette Uhlenhaut; Vitor H Sousa; John F O'Toole; Edgar Otto; Katrin Anlag; Claudia Klugmann; Anna-Corina Treier; Juliana Helou; John A Sayer; Dominik Seelow; Gudrun Nürnberg; Christian Becker; Albert E Chudley; Peter Nürnberg; Friedhelm Hildebrandt; Mathias Treier
Journal:  Nat Genet       Date:  2007-07-08       Impact factor: 38.330

8.  Mutations of CEP83 cause infantile nephronophthisis and intellectual disability.

Authors:  Marion Failler; Heon Yung Gee; Pauline Krug; Kwangsic Joo; Jan Halbritter; Lilya Belkacem; Emilie Filhol; Jonathan D Porath; Daniela A Braun; Markus Schueler; Amandine Frigo; Olivier Alibeu; Cécile Masson; Karine Brochard; Bruno Hurault de Ligny; Robert Novo; Christine Pietrement; Hulya Kayserili; Rémi Salomon; Marie-Claire Gubler; Edgar A Otto; Corinne Antignac; Joon Kim; Alexandre Benmerah; Friedhelm Hildebrandt; Sophie Saunier
Journal:  Am J Hum Genet       Date:  2014-05-29       Impact factor: 11.025

9.  ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3.

Authors:  Sylvia Hoff; Jan Halbritter; Daniel Epting; Valeska Frank; Thanh-Minh T Nguyen; Jeroen van Reeuwijk; Christopher Boehlke; Christoph Schell; Takayuki Yasunaga; Martin Helmstädter; Miriam Mergen; Emilie Filhol; Karsten Boldt; Nicola Horn; Marius Ueffing; Edgar A Otto; Tobias Eisenberger; Mariet W Elting; Joanna A E van Wijk; Detlef Bockenhauer; Neil J Sebire; Søren Rittig; Mogens Vyberg; Troels Ring; Martin Pohl; Lars Pape; Thomas J Neuhaus; Neveen A Soliman Elshakhs; Sarah J Koon; Peter C Harris; Florian Grahammer; Tobias B Huber; E Wolfgang Kuehn; Albrecht Kramer-Zucker; Hanno J Bolz; Ronald Roepman; Sophie Saunier; Gerd Walz; Friedhelm Hildebrandt; Carsten Bergmann; Soeren S Lienkamp
Journal:  Nat Genet       Date:  2013-06-23       Impact factor: 38.330

Review 10.  Nephronophthisis.

Authors:  Rémi Salomon; Sophie Saunier; Patrick Niaudet
Journal:  Pediatr Nephrol       Date:  2008-07-08       Impact factor: 3.714

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  45 in total

1.  Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis.

Authors:  Maxence S Macia; Jan Halbritter; Marion Delous; Cecilie Bredrup; Arthur Gutter; Emilie Filhol; Anne E C Mellgren; Sabine Leh; Albane Bizet; Daniela A Braun; Heon Y Gee; Flora Silbermann; Charline Henry; Pauline Krug; Christine Bole-Feysot; Patrick Nitschké; Dominique Joly; Philippe Nicoud; André Paget; Heidi Haugland; Damien Brackmann; Nayir Ahmet; Richard Sandford; Nurcan Cengiz; Per M Knappskog; Helge Boman; Bolan Linghu; Fan Yang; Edward J Oakeley; Pierre Saint Mézard; Andreas W Sailer; Stefan Johansson; Eyvind Rødahl; Sophie Saunier; Friedhelm Hildebrandt; Alexandre Benmerah
Journal:  Am J Hum Genet       Date:  2017-01-12       Impact factor: 11.025

2.  A Compound Heterozygous Mutation in the Ciliary Gene TTC21B Causes Nephronophthisis Type 12.

Authors:  Wafaa Moustafa M Abo El Fotoh; Amira Fathy Al-Fiky
Journal:  J Pediatr Genet       Date:  2019-11-04

3.  NPHP1 (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRD.

Authors:  Rozemarijn Snoek; Jessica van Setten; Brendan J Keating; Ajay K Israni; Pamala A Jacobson; William S Oetting; Arthur J Matas; Roslyn B Mannon; Zhongyang Zhang; Weijia Zhang; Ke Hao; Barbara Murphy; Roman Reindl-Schwaighofer; Andreas Heinzl; Rainer Oberbauer; Ondrej Viklicky; Peter J Conlon; Caragh P Stapleton; Stephan J L Bakker; Harold Snieder; Edith D J Peters; Bert van der Zwaag; Nine V A M Knoers; Martin H de Borst; Albertien M van Eerde
Journal:  J Am Soc Nephrol       Date:  2018-04-13       Impact factor: 10.121

Review 4.  Little fish, big catch: zebrafish as a model for kidney disease.

Authors:  Shahram Jevin Poureetezadi; Rebecca A Wingert
Journal:  Kidney Int       Date:  2016-04-16       Impact factor: 10.612

Review 5.  The small members of the JMJD protein family: Enzymatic jewels or jinxes?

Authors:  Sangphil Oh; Sook Shin; Ralf Janknecht
Journal:  Biochim Biophys Acta Rev Cancer       Date:  2019-04-26       Impact factor: 10.680

Review 6.  Ciliopathies: Genetics in Pediatric Medicine.

Authors:  Machteld M Oud; Ideke J C Lamers; Heleen H Arts
Journal:  J Pediatr Genet       Date:  2016-11-10

7.  Juvenile nephronophthisis and dysthyroidism: a rare association.

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

8.  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

9.  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

10.  Metabolic perturbations caused by depletion of nephronophthisis factor Anks6 in mIMCD3 cells.

Authors:  Manuel Schlimpert; Simon Lagies; Barbara Müller; Vadym Budnyk; Kelly Daryll Blanz; Gerd Walz; Bernd Kammerer
Journal:  Metabolomics       Date:  2019-04-30       Impact factor: 4.290

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