Chasing the cilium

Scientist

Volumn 18, Issue 19, 2004, Pages 14-16

  Stephan, Megan M ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CELL DIVISION; CELL FUNCTION; CILIARY MOTILITY; CYTOLOGY; DEVELOPMENTAL DISORDER; DIABETES MELLITUS; DISEASE ASSOCIATION; GENETIC DISORDER; HUMAN; MOLECULAR DYNAMICS; NERVE CELL DIFFERENTIATION; NONHUMAN; OBESITY; ORGANOGENESIS; SCHIZOPHRENIA; SIGNAL TRANSDUCTION;

EID: 7744246066     PISSN: 08903670     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. G.J. Pazour et al., "Chlamydomonas IFT88 and its mouse homologue polycystic kidney disease gene Tg737, are required for assembly of cilia and flagella,", J Cell Biol, 151:709-18, 2000.
2. G.J. Pazour et al., "Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease," Curr Biol, 12:3778-80, 2002.
3. S.M. Nauli et al., "Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells," Nat Gen, 33:129-37, 2003.
4. T. Avidor-Reiss et al., "Decoding cilia function: Defining specialized genes required for compartmentalized cilia biogenesis," Cell, 117:527-39, May 14, 2004.
5. J.B. Li et al., "Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene," Cell, 117:541-52, May 14, 2004.