Literature DB >> 27070443

The evolving spectrum of ciliopathies and respiratory disease.

Carlos E Milla1.   

Abstract

PURPOSE OF REVIEW: Research on the biology of cilia, complex hair-like cellular organelles, has greatly informed our understanding of its crucial role in respiratory health and the pathogenesis of primary ciliary dyskinesia (PCD), including the genetics behind this condition. This review will summarize the current state of the art in the field highlighting its clinical implications. RECENT
FINDINGS: The genetics of PCD have exploded over the past few years as knowledge acquired from model systems has permitted the identification of genes that are key components of the ciliary apparatus and its function. In addition, clinical criteria and diagnostic tools have emerged that permit more clear identification of affected individuals.
SUMMARY: The rate of progress in the field continues to accelerate through international collaborative efforts and standardization of methods. Although the genetics behind PCD are complex, given the large number of genes associated with disease, as well as the large number of possible mutations even at the individual gene level, this knowledge is rapidly translating in improved diagnostics and hopefully in the near future in the identification of potential therapeutics.

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Year:  2016        PMID: 27070443      PMCID: PMC4904788          DOI: 10.1097/MOP.0000000000000358

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


  82 in total

1.  Mechanisms of cilia-driven transport in the airways in the absence of mucus.

Authors:  Saskia Bermbach; Karina Weinhold; Thomas Roeder; Frank Petersen; Christian Kugler; Torsten Goldmann; Jan Rupp; Peter König
Journal:  Am J Respir Cell Mol Biol       Date:  2014-07       Impact factor: 6.914

2.  Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.

Authors:  Heike Olbrich; Miriam Schmidts; Claudius Werner; Alexandros Onoufriadis; Niki T Loges; Johanna Raidt; Nora Fanni Banki; Amelia Shoemark; Tom Burgoyne; Saeed Al Turki; Matthew E Hurles; Gabriele Köhler; Josef Schroeder; Gudrun Nürnberg; Peter Nürnberg; Eddie M K Chung; Richard Reinhardt; June K Marthin; Kim G Nielsen; Hannah M Mitchison; Heymut Omran
Journal:  Am J Hum Genet       Date:  2012-09-27       Impact factor: 11.025

3.  CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs.

Authors:  Anne-Christine Merveille; Erica E Davis; Anita Becker-Heck; Marie Legendre; Israel Amirav; Géraldine Bataille; John Belmont; Nicole Beydon; Frédéric Billen; Annick Clément; Cécile Clercx; André Coste; Rachelle Crosbie; Jacques de Blic; Stephane Deleuze; Philippe Duquesnoy; Denise Escalier; Estelle Escudier; Manfred Fliegauf; Judith Horvath; Kent Hill; Mark Jorissen; Jocelyne Just; Andreas Kispert; Mark Lathrop; Niki Tomas Loges; June K Marthin; Yukihide Momozawa; Guy Montantin; Kim G Nielsen; Heike Olbrich; Jean-François Papon; Isabelle Rayet; Gilles Roger; Miriam Schmidts; Henrique Tenreiro; Jeffrey A Towbin; Diana Zelenika; Hanswalter Zentgraf; Michel Georges; Anne-Sophie Lequarré; Nicholas Katsanis; Heymut Omran; Serge Amselem
Journal:  Nat Genet       Date:  2010-12-05       Impact factor: 38.330

4.  Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.

Authors:  Christina Austin-Tse; Jan Halbritter; Maimoona A Zariwala; Renée M Gilberti; Heon Yung Gee; Nathan Hellman; Narendra Pathak; Yan Liu; Jennifer R Panizzi; Ramila S Patel-King; Douglas Tritschler; Raqual Bower; Eileen O'Toole; Jonathan D Porath; Toby W Hurd; Moumita Chaki; Katrina A Diaz; Stefan Kohl; Svjetlana Lovric; Daw-Yang Hwang; Daniela A Braun; Markus Schueler; Rannar Airik; Edgar A Otto; Margaret W Leigh; Peadar G Noone; Johnny L Carson; Stephanie D Davis; Jessica E Pittman; Thomas W Ferkol; Jeffry J Atkinson; Kenneth N Olivier; Scott D Sagel; Sharon D Dell; Margaret Rosenfeld; Carlos E Milla; Niki T Loges; Heymut Omran; Mary E Porter; Stephen M King; Michael R Knowles; Iain A Drummond; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2013-10-03       Impact factor: 11.025

5.  Early lung disease in young children with primary ciliary dyskinesia.

Authors:  David E Brown; Jessica E Pittman; Margaret W Leigh; Lynn Fordham; Stephanie D Davis
Journal:  Pediatr Pulmonol       Date:  2008-05

6.  Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations.

Authors:  Georg C Schwabe; Katrin Hoffmann; Niki Tomas Loges; Daniel Birker; Colette Rossier; Margherita M de Santi; Heike Olbrich; Manfred Fliegauf; Mike Failly; Uta Liebers; Mirella Collura; Gerhard Gaedicke; Stefan Mundlos; Ulrich Wahn; Jean-Louis Blouin; Bodo Niggemann; Heymut Omran; Stylianos E Antonarakis; Lucia Bartoloni
Journal:  Hum Mutat       Date:  2008-02       Impact factor: 4.878

Review 7.  Zebrafish as a Model for Human Ciliopathies.

Authors:  Zhu Song; Xiaoli Zhang; Shuo Jia; Pamela C Yelick; Chengtian Zhao
Journal:  J Genet Genomics       Date:  2016-02-12       Impact factor: 4.275

8.  Establishing normative nasal nitric oxide values in infants.

Authors:  Phillip S Adams; Xin Tian; Maliha Zahid; Omar Khalifa; Linda Leatherbury; Cecilia W Lo
Journal:  Respir Med       Date:  2015-07-15       Impact factor: 3.415

9.  Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia.

Authors:  Michael R Knowles; Margaret W Leigh; Lawrence E Ostrowski; Lu Huang; Johnny L Carson; Milan J Hazucha; Weining Yin; Jonathan S Berg; Stephanie D Davis; Sharon D Dell; Thomas W Ferkol; Margaret Rosenfeld; Scott D Sagel; Carlos E Milla; Kenneth N Olivier; Emily H Turner; Alexandra P Lewis; Michael J Bamshad; Deborah A Nickerson; Jay Shendure; Maimoona A Zariwala
Journal:  Am J Hum Genet       Date:  2012-12-20       Impact factor: 11.025

10.  Accuracy of diagnostic testing in primary ciliary dyskinesia.

Authors:  Claire L Jackson; Laura Behan; Samuel A Collins; Patricia M Goggin; Elizabeth C Adam; Janice L Coles; Hazel J Evans; Amanda Harris; Peter Lackie; Samantha Packham; Anton Page; James Thompson; Woolf T Walker; Claudia Kuehni; Jane S Lucas
Journal:  Eur Respir J       Date:  2015-12-02       Impact factor: 16.671

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  5 in total

1.  C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia.

Authors:  Mahmoud R Fassad; Amelia Shoemark; Pierrick le Borgne; France Koll; Mitali Patel; Mellisa Dixon; Jane Hayward; Charlotte Richardson; Emily Frost; Lucy Jenkins; Thomas Cullup; Eddie M K Chung; Michel Lemullois; Anne Aubusson-Fleury; Claire Hogg; David R Mitchell; Anne-Marie Tassin; Hannah M Mitchison
Journal:  Am J Hum Genet       Date:  2018-05-03       Impact factor: 11.025

Review 2.  Aquatic models of human ciliary diseases.

Authors:  Mark E Corkins; Vanja Krneta-Stankic; Malgorzata Kloc; Rachel K Miller
Journal:  Genesis       Date:  2021-01-26       Impact factor: 2.487

Review 3.  Airway Epithelial Cell Cilia and Obstructive Lung Disease.

Authors:  Asma Yaghi; Myrna B Dolovich
Journal:  Cells       Date:  2016-11-11       Impact factor: 6.600

Review 4.  Primary ciliary dyskinesia: a major player in a bigger game.

Authors:  Reena Bhatt; Claire Hogg
Journal:  Breathe (Sheff)       Date:  2020-06

5.  CEP97 phosphorylation by Dyrk1a is critical for centriole separation during multiciliogenesis.

Authors:  Moonsup Lee; Kunio Nagashima; Jaeho Yoon; Jian Sun; Ziqiu Wang; Christina Carpenter; Hyun-Kyung Lee; Yoo-Seok Hwang; Christopher J Westlake; Ira O Daar
Journal:  J Cell Biol       Date:  2021-11-17       Impact factor: 10.539

  5 in total

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