SUMMARY In this paper, we propose a new modulation named parallel combinatory/high compaction multi-carrier modulation (PC/HC-MCM) using the techniques of parallel combinatory orthogonal frequency division multiplexing (PC-OFDM) and high compaction multi-carrier modulation (HC-MCM). Two types of PC/HC-MCM systems, which are named as modulated PC/HC-MCM system and (unmodulated) PC/HC-MCM system ...

The minichromosome maintenance (MCM) proteins are highly conserved proteins essential for initiating and regulating eukaryotic DNA replication. Recent studies have demonstrated the potential use of MCM proteins as markers of proliferation. We characterized the pattern of Mcm 2 staining in benign and malignant prostate tissues and examined the role of Mcm 2 expression in disease-free survival af...

Silica was extracted from agriculture waste rice husk ash (RHA) and was used as the silica source for synthesis of RMCM-48 and RSBA-16. An alkali fusion process was utilized to separate silicate supernatant and the sediment effectively. The CTAB/Si and F127/Si molar ratio was employed to control the structure properties of the obtained RMCM-48 and RSBA-16 materials. The N2 adsorption-desorption...

The minichromosome maintenance (MCM) proteins MCM2-MCM7 are conserved eukaryotic replication factors that assemble in a heterohexameric complex. In fission yeast, these proteins are nuclear throughout the cell cycle. In studying the mechanism that regulates assembly of the MCM complex, we analyzed the cis and trans elements required for nuclear localization of a single subunit, Mcm2p. Mutation ...

We studied equilibrium adsorption and uptake kinetics and identified molecular species that formed during sorption of carbon dioxide on amine-modified silica. Bicontinuous silicas (AMS-6 and MCM-48) were postsynthetically modified with (3-aminopropyl)triethoxysilane or (3-aminopropyl)methyldiethoxysilane, and amine-modified AMS-6 adsorbed more CO(2) than did amine-modified MCM-48. By in situ FT...

5. Regulation of MCM proteins during the cell cycle . . . . . . . . . . . . . . . . . . . . . . . . . . . . 125 5.1. MCM protein levels in proliferating and non-proliferating cells . . . . . . . . . . . . . . . . . 125 5.2. Involvement of ORC and Cdc6rcdc18 in binding of MCM proteins to chromatin . . . . . . 126 5.3. Role of phosphorylation in regulating MCM function . . . . . . . . . . . . . ....

Origins of DNA replication are licensed by recruiting MCM2-7 to assemble the prereplicative complex (pre-RC). How MCM2-7 is inactivated or removed from chromatin at the end of S phase is still unclear. Here, we show that MCM-BP can disassemble the MCM2-7 complex and might function as an unloader of MCM2-7 from chromatin. In Xenopus egg extracts, MCM-BP exists in a stable complex with MCM7, but ...