GJB4 抗体
(Gap Junction Protein, beta 4, 30.3kDa (GJB4))
This gene encodes a transmembrane connexin protein that is a component of gap junctions. Mutations in this gene have been associated with erythrokeratodermia variabilis, progressive symmetric erythrokeratoderma and hearing impairment. [provided by RefSeq, Dec 2009].
Recommended next Filters:
您想试用我们的人工智能搜索吗？
32 results
Latest Publications for our GJB4 抗体
: "Expression pattern of connexins in the corneal and limbal epithelium of a primate." in: Cornea, Vol. 28, Issue 2, pp. 194-9, (2009) (PubMed).: "Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlations." in: The Journal of investigative dermatology, Vol. 120, Issue 4, pp. 601-9, (2003) (PubMed).
: "Complete sequencing and characterization of 21,243 full-length human cDNAs. ..." in: Nature genetics, Vol. 36, Issue 1, pp. 40-5, (2003) (PubMed).
: "Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis." in: American journal of human genetics, Vol. 67, Issue 5, pp. 1296-301, (2000) (PubMed).
Aliases for GJB4 抗体
gap junction protein beta 4 (GJB4) 抗体gap junction protein, beta 4 (Gjb4) 抗体
Cnx30.3 抗体
Cx30.3 抗体
CX30.3 抗体
EKV 抗体
Gjb-4 抗体
GJB4 抗体
您还需要查找其他产品吗？
You are here:
