ⓘ BBS10

                                     

ⓘ BBS10

The Bardet-Biedl syndrome 10 protein has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this proteins expression impairs ciliogenesis in preadipocytes.

                                     
  • shown to be mediated by a complex containing a further three BBS proteins: BBS 6, BBS10 and BBS 12. In addition chaperonins of the CCT TRiC family are involved
  • BBS Kraftfahrzeugtechnik AG English: BBS Automotive Technology AG is a high - performance automobile wheel design company headquartered in Schiltach
  • BBS The Documentary commonly referred to as BBS Documentary is a 3 - disc, 8 - episode documentary about the subculture born from the creation of the bulletin
  • Formosa BBS or NYSYU Formosa BBS was one of the earliest, if not the first, telnet - based Bulletin board systems BBS to have Chinese language capability
  • A door in a bulletin board system BBS is an interface between the BBS software and an external application. The term is also used to refer to the external
  • Bardet Biedl syndrome protein, BBS 7, that shares structural features with BBS 1 and BBS 2 Am J Hum Genet. 72 3 650 8. doi: 10 1086 368204. PMC 1180240. PMID 12567324
  • causing Bardet Biedl syndrome BBS 2 Hum Mol Genet. 10 8 865 74. doi: 10 1093 hmg 10 8.865. PMID 11285252. Entrez Gene: BBS 2 Bardet - Biedl syndrome 2
  • Bardet - Biedl syndrome protein, BBS 7, that shares structural features with BBS 1 and BBS 2 Am. J. Hum. Genet. 72 3 650 8. doi: 10 1086 368204. PMC 1180240
  • Bardet Biedl syndrome 4 is a protein that in humans is encoded by the BBS 4 gene. This gene encodes a protein which contains tetratricopeptide repeats
  • Bardet Biedl syndrome 9 is a protein that in humans is encoded by the BBS 9 gene. The expression of the Bardet Biedl syndrome 9 protein is downregulated
  • Bardet Biedl syndrome 12 is a protein that in humans is encoded by the BBS 12 gene. Mutations in this gene are associated with the Bardet Biedl syndrome