Cilia in cell signaling and human disorders.
10.1007/s13238-010-0098-7
- Author:
Neil A DULDULAO
1
;
Jade LI
;
Zhaoxia SUN
Author Information
1. Department of Genetics, Yale University School of Medicine, 333 Cedar St., SHM I-329A, New Haven, CT 06520, USA.
- Publication Type:Journal Article
- MeSH:
Abnormalities, Multiple;
pathology;
Animals;
Cerebellar Diseases;
genetics;
pathology;
Cilia;
physiology;
ultrastructure;
Flagella;
physiology;
Hedgehog Proteins;
metabolism;
Humans;
Models, Animal;
Polycystic Kidney Diseases;
pathology;
Protein Transport;
Signal Transduction;
Wnt Proteins;
metabolism
- From:
Protein & Cell
2010;1(8):726-736
- CountryChina
- Language:English
-
Abstract:
One of the most widespread cellular organelles in nature is cilium, which is found in many unicellular and multicellular organisms. Formerly thought to be a mostly vestigial organelle, the cilium has been discovered in the past several decades to play critical motile and sensory roles involved in normal organogenesis during development. The role of cilia has also been implicated in an ever increasing array of seemingly unrelated human diseases, including blindness, kidney cysts, neural tube defects and obesity. In this article we review some of the recent developments in research on cilia, and how defects in ciliogenesis and function can give rise to developmental disorders and disease.
