نتایج جستجو برای: cdk

تعداد نتایج: 3845  

2013
Katherine Louise Tibbles Sourav Sarkar Bela Novak Prakash Arumugam

Cyclin-dependent kinases (CDK) are master regulators of the cell cycle in eukaryotes. CDK activity is regulated by the presence, post-translational modification and spatial localization of its regulatory subunit cyclin. In budding yeast, the B-cyclin Clb1 is phosphorylated and localizes to the nucleus during meiosis I. However the functional significance of Clb1's phosphorylation and nuclear lo...

Journal: :Molecular and cellular biology 1995
D Desai H C Wessling R P Fisher D O Morgan

The cyclin-dependent protein kinases (CDKs) are activated by association with cyclins and by phosphorylation at a conserved threonine residue by the CDK-activating kinase (CAK). We have studied the binding of various human CDK and cyclin subunits in vitro, using purified proteins derived from baculovirus-infected insect cells. We find that most CDK-cyclin complexes known to exist in human cells...

Journal: :American journal of physiology. Heart and circulatory physiology 1998
Mimi Tamamori Hiroshi Ito Michiaki Hiroe Yoshio Terada Fumiaki Marumo Masa-Aki Ikeda

Although cardiomyocytes undergo terminal differentiation soon after birth, irreversibly withdrawing from the cell cycle, growth stimulation induces cell hypertrophy. Such growth stimulation is also responsible for the upregulation of G1 cyclins and cyclin-dependent kinase (CDK) activity in proliferating cells. We sought to determine whether G1 CDK activity is involved in the hypertrophy of rat ...

2011
Yuefeng Wang John C. Fisher Rose Mathew Li Ou Steve Otieno Jack Sublett Limin Xiao Jianhan Chen Martine F. Roussel Richard W. Kriwacki

Traditionally, well-defined three-dimensional structure has been thought to be essential for protein function. However, myriad biological functions are performed by highly dynamic, intrinsically disordered proteins (IDPs). IDPs often fold upon binding their biological targets and frequently show 'binding diversity' by targeting multiple ligands. We sought to understand the physical basis of IDP...

2015
Gloria Palou Roger Palou Fanli Zeng Ajay A. Vashisht James A. Wohlschlegel David G. Quintana Peter McKinnon

A surveillance mechanism, the S phase checkpoint, blocks progression into mitosis in response to DNA damage and replication stress. Segregation of damaged or incompletely replicated chromosomes results in genomic instability. In humans, the S phase checkpoint has been shown to constitute an anti-cancer barrier. Inhibition of mitotic cyclin dependent kinase (M-CDK) activity by Wee1 kinases is cr...

2017
Jingwen Bai Yaochen Li Guojun Zhang

Cellular growth, development, and differentiation are tightly controlled by a conserved biological mechanism: the cell cycle. This cycle is primarily regulated by cyclin-dependent kinase (CDK)-cyclin complexes, checkpoint kinases, and CDK inhibitors. Deregulation of the cell cycle is a hallmark of the transformation of normal cells into tumor cells. Given its importance in tumorigenesis, severa...

2015
Thomas Kuilman Alessio Maiolica Molly Godfrey Noémie Scheidel Ruedi Aebersold Frank Uhlmann

The final event of the eukaryotic cell cycle is cytokinesis, when two new daughter cells are born. How the timing and execution of cytokinesis is controlled is poorly understood. Here, we show that downregulation of cyclin-dependent kinase (Cdk) activity, together with upregulation of its counteracting phosphatase Cdc14, controls each of the sequential steps of cytokinesis, including furrow ing...

Journal: :EMBO reports 2010
Anja M Duursma Karlene A Cimprich

The cyclin-dependent kinases (CDKs) must be inhibited when DNA damage occurs to prevent cell-cycle progression and to allow for repair. A paper in the June issue of EMBO reports from Rene Medema’s group now suggests that some CDK activity must actually be retained during arrest for efficient checkpoint recovery to occur (Alvarez-Fernández et al, 2010). Cells have evolved several mechanisms to e...

Journal: :Current Biology 2007
Mignon A. Keaton Elaine S.G. Bardes Aron R. Marquitz Christopher D. Freel Trevin R. Zyla Johannes Rudolph Daniel J. Lew

BACKGROUND Several checkpoint pathways employ Wee1-mediated inhibitory tyrosine phosphorylation of cyclin-dependent kinases (CDKs) to restrain cell-cycle progression. Whereas in vertebrates this strategy can delay both DNA replication and mitosis, in yeast cells only mitosis is delayed. This is particularly surprising because yeasts, unlike vertebrates, employ a single family of cyclins (B type...

2009
Nathalie Fiaschi-Taesch Todd A. Bigatel Brian Sicari Karen K. Takane Fatima Salim Silvia Velazquez-Garcia George Harb Karen Selk Irene Cozar-Castellano Andrew F. Stewart

OBJECTIVES To comprehensively inventory the proteins that control the G1/S cell cycle checkpoint in the human islet and compare them with those in the murine islet, to determine whether these might therapeutically enhance human beta-cell replication, to determine whether human beta-cell replication can be demonstrated in an in vivo model, and to enhance human beta-cell function in vivo. RESEA...

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