Papers using
Aurora-C
antibodies
Papers on
Aurora-C
Male infertility and its genetic causes.Sengoku et al., Asahikawa, Japan. In J Obstet Gynaecol Res, Oct 2015
We discuss here the contribution to male factor infertility of a number of genes identified in the azoospermia factor (AZF) region on the Y chromosome, as well as the autosomally located genes: SYKP3, KLHL10, AURKC and SPATA16.
Transcriptome analysis of the cancer/testis genes, DAZ1, AURKC, and TEX101, in breast tumors and six breast cancer cell lines.Modarressi et al., Tehrān, Iran. In Tumour Biol, Sep 2015
In this context, we investigated the expression of two known cancer testis genes, Aurora kinase C (AURKC) and testis expressed 101 (TEX101), and one new candidate, deleted in azoospermia 1 (DAZ1), in six breast cancer cell lines including two ductal carcinomas, T47D and BT-474, and four adenocarcinomas, MDA-MB-231, MDA-MB-468, MCF7, and SKBR3 as well as 50 breast cancer tumors in comparison to normal mammary epithelial cells using quantitative real-time reverse transcription PCR (RT-PCR).
Functions of Aurora kinase C in meiosis and cancer.Schindler et al., United States. In Front Cell Dev Biol, 2014
The mammalian genome encodes three Aurora kinase protein family members: A, B, and C. While Aurora kinase A (AURKA) and B (AURKB) are found in cells throughout the body, significant protein levels of Aurora kinase C (AURKC) are limited to cells that undergo meiosis (sperm and oocyte).
Possible Role of Aurora-C in Meiosis.Tang et al., Taipei, Taiwan. In Front Oncol, 2014
The Aurora kinases, which include Aurora-A, Aurora-B, and Aurora-C, are highly conserved serine-threonine kinases that play essential roles in centrosome function, chromosome segregation, and cytokinesis during mitosis and meiosis.
Aurora Kinase Inhibitors: Current Status and Outlook.Linardopoulos et al., London, United Kingdom. In Front Oncol, 2014
In humans, the Aurora kinase family consists of three members; Aurora-A, Aurora-B, and Aurora-C, which each share a conserved C-terminal catalytic domain but differ in their sub-cellular localization, substrate specificity, and function during mitosis.