Literature DB >> 3907978

The immotile-cilia syndrome: a microtubule-associated defect.

B A Afzelius.   

Abstract

The immotile-cilia syndrome is a congenital disorder characterized by all the cilia in the body being either immotile or showing an abnormal and inefficient beating pattern. Most symptoms come from the ciliated airways (nose, paranasal sinuses, and bronchs) and from the middle ear. Two further symptoms are situs inversus and male sterility. Situs inversus occurs in 50% of the cases and this subgroup is termed the Kartagener's syndrome; it might be due to an inability of the embryonic cilia to shift the heart to the left side and situs laterality seems to be a random process in the immotile-cilia syndrome. Male sterility is caused by the spermatozoa being unable to swim progressively; the sperm tail has the same structure as a cilium. In a few cases only the sperm tail or only the cilia of the body are affected. Female patients have a decreased fertility; most are involuntarily childless. The immotile-cilia syndrome is a heterogeneous disorder in that one out of many different genes may be involved. The different subtypes can be distinguished by an electron microscopic examination which will show defects in either one of a number of the ciliary components.

Entities:  

Mesh:

Year:  1985        PMID: 3907978     DOI: 10.3109/10409238509086788

Source DB:  PubMed          Journal:  CRC Crit Rev Biochem        ISSN: 0045-6411


  29 in total

1.  Situs inversus and embryonic ciliary morphogenesis defects in mouse mutants lacking the KIF3A subunit of kinesin-II.

Authors:  J R Marszalek; P Ruiz-Lozano; E Roberts; K R Chien; L S Goldstein
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-27       Impact factor: 11.205

Review 2.  The radial spokes and central apparatus: mechano-chemical transducers that regulate flagellar motility.

Authors:  Elizabeth F Smith; Pinfen Yang
Journal:  Cell Motil Cytoskeleton       Date:  2004-01

Review 3.  Axonemal positioning and orientation in three-dimensional space for primary cilia: what is known, what is assumed, and what needs clarification.

Authors:  Cornelia E Farnum; Norman J Wilsman
Journal:  Dev Dyn       Date:  2011-11       Impact factor: 3.780

4.  Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.

Authors:  Esther Kott; Marie Legendre; Bruno Copin; Jean-François Papon; Florence Dastot-Le Moal; Guy Montantin; Philippe Duquesnoy; William Piterboth; Daniel Amram; Laurence Bassinet; Julie Beucher; Nicole Beydon; Eric Deneuville; Véronique Houdouin; Hubert Journel; Jocelyne Just; Nadia Nathan; Aline Tamalet; Nathalie Collot; Ludovic Jeanson; Morgane Le Gouez; Benoit Vallette; Anne-Marie Vojtek; Ralph Epaud; André Coste; Annick Clement; Bruno Housset; Bruno Louis; Estelle Escudier; Serge Amselem
Journal:  Am J Hum Genet       Date:  2013-08-29       Impact factor: 11.025

5.  Mutation analysis in patients with total sperm immotility.

Authors:  Rute Pereira; Jorge Oliveira; Luis Ferraz; Alberto Barros; Rosário Santos; Mário Sousa
Journal:  J Assist Reprod Genet       Date:  2015-04-16       Impact factor: 3.412

6.  Ciliary ultrastructure in two sisters with Kartagener's syndrome.

Authors:  Kayoko Tanaka; Akihisa Sutani; Yuka Uchida; Yoshihiko Shimizu; Michio Shimizu; Masumi Akita
Journal:  Med Mol Morphol       Date:  2007-03-29       Impact factor: 2.309

Review 7.  Gene mutations in primary ciliary dyskinesia related to otitis media.

Authors:  Manuel Mata; Lara Milian; Miguel Armengot; Carmen Carda
Journal:  Curr Allergy Asthma Rep       Date:  2014-03       Impact factor: 4.806

8.  Rotation of the central pair microtubules in eukaryotic flagella.

Authors:  C K Omoto; I R Gibbons; R Kamiya; C Shingyoji; K Takahashi; G B Witman
Journal:  Mol Biol Cell       Date:  1999-01       Impact factor: 4.138

9.  The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia.

Authors:  G Pennarun; C Chapelin; E Escudier; A M Bridoux; F Dastot; V Cacheux; M Goossens; S Amselem; B Duriez
Journal:  Hum Genet       Date:  2000-12       Impact factor: 4.132

10.  Hydrocephalus, bronchiectasis, and ciliary aplasia.

Authors:  M M De Santi; A Magni; E A Valletta; C Gardi; G Lungarella
Journal:  Arch Dis Child       Date:  1990-05       Impact factor: 3.791

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