huCaV2.2 (pSAD442-1) Citations (2)
Originally described in: CACNA1B mutation is linked to unique myoclonus-dystonia syndrome.Groen JL, Andrade A, Ritz K, Jalalzadeh H, Haagmans M, Bradley TE, Jongejan A, Verbeek DS, Nurnberg P, Denome S, Hennekam RC, Lipscombe D, Baas F, Tijssen MA Hum Mol Genet. 2015 Feb 15;24(4):987-993. Epub 2014 Oct 8. PubMed Journal
Articles Citing huCaV2.2 (pSAD442-1)
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Ca(v)2.2-NFAT2-USP43 axis promotes invadopodia formation and breast cancer metastasis through cortactin stabilization. Xue Y, Li M, Hu J, Song Y, Guo W, Miao C, Ge D, Hou Y, Wang X, Huang X, Liu T, Zhang X, Huang Q. Cell Death Dis. 2022 Sep 22;13(9):812. doi: 10.1038/s41419-022-05174-0. PubMed |
The Interplay Between Splicing of Two Exon Combinations Differentially Affects Membrane Targeting and Function of Human Ca(V)2.2. Dahimene S, Page KM, Nieto-Rostro M, Pratt WS, Dolphin AC. Function (Oxf). 2023 Oct 19;5(1):zqad060. doi: 10.1093/function/zqad060. eCollection 2024. PubMed |
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