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Evidence that S‐phase kinase associated protein 2 (SKP2) is ubiquitinated and degraded via a Rho‐related BTB domain containing 1 (RhoBTB1) and Cullin‐3 mechanism in placenta

open access: yesPhysiological Reports, Volume 14, Issue 15, August 2026.
Graphical representation of mechanism by which RhoBTB1 regulates SKP2. Abstract Rho related BTB domain containing 1 (RhoBTB1) is highly expressed in placenta and functions to deliver protein targets to the Cullin‐3 (CUL3) E3 ubiquitin ligase where they are targeted for ubiquitination and degradation.
Alina L. Tvina   +11 more
wiley   +1 more source

Rho GTPases [PDF]

open access: yesSmall GTPases, 2014
Since their discovery in the late eighties, the role of Rho GTPases in the regulation of cell migration has been extensively studied and has mainly focused on the hallmark family members Rho, Rac, and Cdc42. Recent technological advances in cell biology, such as Rho-family GTPase activity biosensors, studies in 3D, and unbiased RNAi-based screens, have
Sadok, Amine, Marshall, Chris J
exaly   +3 more sources
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Rho GTPases and cancer

BioFactors, 2013
AbstractRho GTPases are a family of small GTPases, which play an important role in the regulation of the actin cytoskeleton. Not surprisingly, Rho GTPases are crucial for cell migration and therefore highly important for cancer cell invasion and the formation of metastases. In addition, Rho GTPases are involved in growth and survival of tumor cells, in
Li, Hui   +3 more
openaire   +3 more sources

Signaling to Rho GTPases

Experimental Cell Research, 1999
Rho GTPases regulate many important processes in all eukaryotic cells, including the organization of the actin cytoskeleton, gene transcription, cell cycle progression, and membrane trafficking. Their activity is regulated by signals originating from different classes of surface receptors including G-protein-coupled receptors, tyrosine kinase receptors,
L, Kjoller, A, Hall
exaly   +3 more sources

RHO–GTPases and cancer

Nature Reviews Cancer, 2002
The RAS oncogenes were identified almost 20 years ago. Since then, we have learnt that they are members of a large family of small GTPases that bind GTP and hydrolyse it to GDP. This is then exchanged for GTP and the cycle is repeated. The switching between these two states regulates a wide range of cellular processes.
Erik, Sahai, Christopher J, Marshall
openaire   +2 more sources

Deregulation of Rho GTPases in cancer [PDF]

open access: yesSmall GTPases, 2016
In vitro and in vivo studies and evidence from human tumors have long implicated Rho GTPase signaling in the formation and dissemination of a range of cancers. Recently next generation sequencing has identified direct mutations of Rho GTPases in human cancers.
Angeliki Malliri   +2 more
exaly   +4 more sources

Rho GTPases and Cancer

2005
The Rho (Ras-homologous) family of proteins constitutes a major branch of the Ras superfamily of small GTPases, and is evolutionarily conserved across several phyla. Thus far, 25 members have been identified, and these may be divided into 6 subfamilies based on amino acid sequence identity, structural motifs, and biological function.
Pinella, Buongiorno, Bharati, Bapat
openaire   +2 more sources

Effectors for the Rho GTPases

Current Opinion in Cell Biology, 1999
The Rho GTPases are simple enzymes with complex roles in regulating cell morphology, gene transcription, cell cycle progression, apoptosis and tumour progression. The picture has been further complicated by the steady rise in the number of known Rho GTPases as well as in the number of known regulators and target proteins of these GTPases.
openaire   +2 more sources

Rho family GTPases

Biochemical Society Transactions, 2012
Rho GTPases comprise a family of molecular switches that control signal transduction pathways in eukaryotic cells. A conformational change induced upon binding GTP promotes an interaction with target (effector) proteins to generate a cellular response. A highly conserved function of Rho GTPases from yeast to humans is to control the actin cytoskeleton,
openaire   +2 more sources

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