BBS9 抗体
(Bardet-Biedl Syndrome 9 (BBS9))
This gene is downregulated by parathyroid hormone in osteoblastic cells, and therefore, is thought to be involved in parathyroid hormone action in bones. The exact function of this gene has not yet been determined. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008].
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Latest Publications for our BBS9 抗体
: "The centriolar satellite protein AZI1 interacts with BBS4 and regulates ciliary trafficking of the BBSome." in: PLoS genetics, Vol. 10, Issue 2, pp. e1004083, (2014) (PubMed).: "BBS mutations modify phenotypic expression of CEP290-related ciliopathies." in: Human molecular genetics, Vol. 23, Issue 1, pp. 40-51, (2013) (PubMed).
: "ARL13B, PDE6D, and CEP164 form a functional network for INPP5E ciliary targeting." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 109, Issue 48, pp. 19691-6, (2012) (PubMed).
Aliases for BBS9 抗体
Bardet-Biedl syndrome 9 (BBS9) 抗体Bardet-Biedl syndrome 9 (bbs9) 抗体
bardet-biedl syndrome 9 (BBS9) 抗体
Bardet-Biedl syndrome 9 (Bbs9) 抗体
Bardet-Biedl syndrome 9 (human) (Bbs9) 抗体
b1 抗体
B1 抗体
C18 抗体
D1 抗体
E130103I17Rik 抗体
PTHB1 抗体
RGD1308472 抗体
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