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Making sense of cilia in disease: the human ciliopathies.
- Source :
-
American journal of medical genetics. Part C, Seminars in medical genetics [Am J Med Genet C Semin Med Genet] 2009 Nov 15; Vol. 151C (4), pp. 281-95. - Publication Year :
- 2009
-
Abstract
- Ubiquitous in nature, cilia and flagella comprise nearly identical structures with similar functions. The most obvious example of the latter is motility: driving movement of the organism or particle flow across the epithelial surface in fixed structures. In vertebrates, such motile cilia are evident in the respiratory epithelia, ependyma, and oviducts. For over a century, non-motile cilia have been observed on the surface of most vertebrate cells but until recently their function has eluded us. Gathering evidence now points to critical roles for the mono-cilium in sensing the extracellular environment, and perturbation of this function gives rise to a predictable panoply of clinical problems. We review the common clinical phenotypes associated with ciliopathies and interrogate Online Mendelian Inheritance in Man (OMIM) to compile a comprehensive list of putative disorders in which ciliary dysfunction may play a role.<br /> (Copyright 2009 Wiley-Liss, Inc.)
- Subjects :
- Animals
Bardet-Biedl Syndrome physiopathology
Biological Transport
Female
Genetic Diseases, Inborn genetics
Genetic Diseases, Inborn physiopathology
Humans
Male
Mice
Models, Biological
Phenotype
Signal Transduction
Syndrome
Bardet-Biedl Syndrome diagnosis
Cilia pathology
Ciliary Motility Disorders physiopathology
Congenital Abnormalities physiopathology
Genetic Diseases, Inborn diagnosis
Subjects
Details
- Language :
- English
- ISSN :
- 1552-4876
- Volume :
- 151C
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- American journal of medical genetics. Part C, Seminars in medical genetics
- Publication Type :
- Academic Journal
- Accession number :
- 19876933
- Full Text :
- https://doi.org/10.1002/ajmg.c.30231