CLDN14 抗体
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Latest Publications for our CLDN14 抗体
: "Identification of transcription factor E3 (TFE3) as a receptor-independent activator of Gα16: gene regulation by nuclear Gα subunit and its activator." in: The Journal of biological chemistry, Vol. 286, Issue 20, pp. 17766-76, (2011) (PubMed).: "Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density." in: Nature genetics, Vol. 41, Issue 8, pp. 926-30, (2009) (PubMed).
: "Mutation in gap and tight junctions in patients with non-syndromic hearing loss." in: Biochemical and biophysical research communications, Vol. 385, Issue 1, pp. 1-5, (2009) (PubMed).
: "Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29." in: Cell, Vol. 104, Issue 1, pp. 165-72, (2001) (PubMed).
: "Role of macrophage oxidative burst in the action of anthrax lethal toxin." in: Molecular medicine (Cambridge, Mass.), Vol. 1, Issue 1, pp. 7-18, (1996) (PubMed).
Aliases for CLDN14 抗体
claudin 14 L homeolog (cldn14.L) 抗体claudin 14 (CLDN14) 抗体
claudin 14 (Cldn14) 抗体
AI851731 抗体
claudin-14 抗体
CLDN14 抗体
DFNB29 抗体