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2009 SEP 21 ... Current study results from the report, 'Impact of connexin32 deletion on E7 or RET/PTC3 oncogene-driven growth and neoplastic transformation of the ...
2007 DEC 4 ... system (UPS)-mediated degradation of the wild-type (WT) gap junction protein connexin32 (Cx32) is inhibited by mild forms of cytosolic stress at a step before its dislocation ...
2005 APR 18 ... Scientists found that liver tumorigenesis was modulated in connexin32 (Cx32)-deficient mice.
According to recent research from the United ...
2008 JAN 7 ... Investigators publish new data in the report 'Connexin36 vs. connexin32, "miniature" neuronal gap junctions, and limited electrotonic coupling in rodent ...
2007 OCT 8 ... contaminant mixture to influence mRNA stability and length of the 3'-end poly(A)tail of Connexin32, Connexin-43, and heat shock protein-70. Consistent with this observation, ...
2007 DEC 27 ... from Oslo, Norway, "X- linked Charcot- Marie Tooth ( CMT) is caused by mutations in the connexin32 gene that encodes a polypeptide which is arranged in hexameric array and form gap ...
2008 DEC 29 ... rna research are presented in the report 'A quantitative inverse relationship between connexin32 expression and cell proliferation in a rat hepatoma cell line.' According to a study ...
2006 DEC 20 ... CMT disease with late onset. Molecular genetic analysis excluded mutations in PMP22, connexin32, MPZ, LITAF and MFNZ genes, as well as duplication and deletion of PMP22. The twins were ...
2007 OCT 2 ... that these neurons are linked by extraordinarily abundant gap junctions consisting of connexin32 (Cx32) and connexin26 (Cx26), and that those same connexins abundantly link neurons to ...
2007 APR 24 ... New investigation results, "The gap junction protein connexin32 interacts with the Src homology 3/Hook domain of discs large homolog 1," are detailed ...
2007 AUG 6 ... Research findings, "Cytoplasmic accumulation of connexin32 protein enhances motility and metastatic ability of human hepatoma cells in vitro and in ...
2008 AUG 4 ... "Murine oligodendrocytes express the gap junction (GJ) proteins connexin32 (Cx32), Cx47, and Cx29. CNS phenotypes in patients with X-linked Charcot-Marie-Tooth ...
2008 NOV 17 ... "X-linked Charcot-Marie-Tooth disease (CMTX), caused by mutations in the gene encoding connexin32, is the second most common form of inherited demyelinating neuropathy, next to CMT 1A, ...
2005 APR 18 ... According to a study from the United States, transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in...
