Calmodulin-binding transcription activator 1
Appearance
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Calmodulin-binding transcription activator 1 is a protein that in humans is encoded by the CAMTA1 gene.[4][5]
References
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000014592 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Bouche N, Scharlat A, Snedden W, Bouchez D, Fromm H (Jun 2002). "A novel family of calmodulin-binding transcription activators in multicellular organisms". J Biol Chem. 277 (24): 21851–61. doi:10.1074/jbc.M200268200. PMID 11925432.
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: CS1 maint: unflagged free DOI (link) - ^ "Entrez Gene: CAMTA1 calmodulin binding transcription activator 1".
Further reading
- Katoh M, Katoh M (2004). "Identification and characterization of FLJ10737 and CAMTA1 genes on the commonly deleted region of neuroblastoma at human chromosome 1p36.31-p36.23". Int. J. Oncol. 23 (4): 1219–24. doi:10.3892/ijo.23.4.1219. PMID 12964007.
- Nakatani K, Nishioka J, Itakura T, et al. (2004). "Cell cycle-dependent transcriptional regulation of calmodulin-binding transcription activator 1 in neuroblastoma cells". Int. J. Oncol. 24 (6): 1407–12. doi:10.3892/ijo.24.6.1407. PMID 15138581.
- Barbashina V, Salazar P, Holland EC, et al. (2005). "Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor suppressor gene". Clin. Cancer Res. 11 (3): 1119–28. PMID 15709179.
- Henrich KO, Claas A, Praml C, et al. (2007). "Allelic variants of CAMTA1 and FLJ10737 within a commonly deleted region at 1p36 in neuroblastoma". Eur. J. Cancer. 43 (3): 607–16. doi:10.1016/j.ejca.2006.09.023. PMID 17222547.
- Huentelman MJ, Papassotiropoulos A, Craig DW, et al. (2007). "Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance". Hum. Mol. Genet. 16 (12): 1469–77. doi:10.1093/hmg/ddm097. PMID 17470457.