ALMS1 抗体
(Alstrom Syndrome 1 (ALMS1))
This gene encodes a protein containing a large tandem-repeat domain. The mouse ortholog of this gene has been shown to function in ciliogenesis in inner medullary collecting duct cells. Mutations in this gene have been associated with Alstrom syndrome. Alternative splice variants have been described but their full length sequences have not been determined.[provided by RefSeq, Mar 2009].
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Latest Publications for our ALMS1 抗体
: "Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome." in: Nature genetics, Vol. 31, Issue 1, pp. 74-8, (2002) (PubMed).: "An immunochemical analysis of the human nuclear phosphoprotein p53. New monoclonal antibodies and epitope mapping using recombinant p53." in: Journal of immunological methods, Vol. 151, Issue 1-2, pp. 237-44, (1992) (PubMed).
Aliases for ALMS1 抗体
ALMS1, centrosome and basal body associated protein (ALMS1) 抗体Alstrom syndrome 1 (alms1) 抗体
putative ALMS1-like protein (LOC459325) 抗体
ALMS1, centrosome and basal body associated (Alms1) 抗体
ALMS1, centrosome and basal body associated protein (Alms1) 抗体
ALMS1 抗体
ALSS 抗体
bbb 抗体
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