Cilia and disease
- 1 June 2005
- journal article
- review article
- Published by Elsevier in Current Opinion in Genetics & Development
- Vol. 15 (3) , 308-314
- https://doi.org/10.1016/j.gde.2005.04.008
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- Targeted deletion of the novel cytoplasmic dynein mD2LIC disrupts the embryonic organiser, formation of the body axes and specification of ventral cell fatesDevelopment, 2004
- Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasmKidney International, 2004
- Hedgehog signalling in the mouse requires intraflagellar transport proteinsNature, 2003
- Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationNature Genetics, 2003
- Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31Nature Genetics, 2003
- Intraflagellar transportNature Reviews Molecular Cell Biology, 2002
- Planar cell polarity in the inner ear: How do hair cells acquire their oriented structure?Journal of Neurobiology, 2002
- A healthy understanding of intraflagellar transportCell Motility, 2002
- Myosin VIIa, the product of the Usher 1B syndrome gene, is concentrated in the connecting cilia of photoreceptor cellsCell Motility, 1997
- The kinocilium of auditory hair cells and evidence for its morphogenetic role during the regeneration of stereocilia and cuticular platesJournal of Neurocytology, 1995