Member database | CDD |
CDD type | domain |
Short name | KH-I_BICC1_rpt1 |
Set | KH-I |
Description
References
1.A single KH domain in Bicaudal-C links mRNA binding and translational repression functions to maternal development. Dowdle ME, Park S, Blaser Imboden S, Fox CA, Houston DW, Sheets MD. Development 146, dev172486, (2019). PMID: 31023875
2.Analysis of the effects of depression associated polymorphisms on the activity of the BICC1 promoter in amygdala neurones. Davidson S, Shanley L, Cowie P, Lear M, McGuffin P, Quinn JP, Barrett P, MacKenzie A. Pharmacogenomics J 16, 366-74, (2016). PMID: 26440730
3.BICC1 expression is elevated in depressed subjects and contributes to depressive behavior in rodents. Ota KT, Andres W, Lewis DA, Stockmeier CA, Duman RS. Neuropsychopharmacology 40, 711-8, (2015). PMID: 25178406
4.Two mutations in human BICC1 resulting in Wnt pathway hyperactivity associated with cystic renal dysplasia. Kraus MR, Clauin S, Pfister Y, Di Maio M, Ulinski T, Constam D, Bellanne-Chantelot C, Grapin-Botton A. Hum Mutat 33, 86-90, (2012). PMID: 21922595
5.BICC1 as a novel prognostic biomarker in gastric cancer correlating with immune infiltrates. Zhao R, Peng C, Song C, Zhao Q, Rong J, Wang H, Ding W, Wang F, Xie Y. Int Immunopharmacol 87, 106828, (2020). PMID: 32736193
6.Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation. Lee H, Lin MC, Kornblum HI, Papazian DM, Nelson SF. Hum Mol Genet 23, 3481-9, (2014). PMID: 24501278