Increased signalling by the small G protein Ras is found in many human cancers and is often caused by direct mutation of this protein. Hence, small-molecule attenuation of pathological Ras activity is of utmost interest in oncology. However, despite nearly three decades of intense drug discovery efforts, no clinically viable option for Ras inhibition has been developed. Very recently, reports of a number of new approaches of addressing Ras activity have led to the revival of this molecular target with the prospect of finally fulfilling the therapy promises associated with this important protein
Abstract RAS mutations (HRAS, NRAS, and KRAS) are among the most common oncogenes, and around 19% of...
The Ras superfamily of small GTPases is composed of more than 150 members, which share a conserved s...
SummaryOncogenic mutations in the small GTPase Ras are highly prevalent in cancer, but an understand...
Increased signalling by the small G protein Ras is found in many human cancers and is often caused b...
Ras proteins are key elements in the regulation of cellular proliferation, differentiation and survi...
RAS drug development has made enormous strides in the past ten years, with the first direct KRAS inh...
Despite more than three decades of intensive effort, no effective pharmacologic inhibitors of the Ra...
AbstractThree decades after identification of the Ras oncogene, no effective treatments for Ras muta...
Somatic mutations in the RAS genes are frequent in human tumors, especially in pancreatic, colorecta...
Mutations of RAS oncogenes are responsible for about 30% of all human cancer types, including pancre...
The H- and N-Ras GTPases are prominent examples of proteins, whose localizations and signalling capa...
© 2021 by the authors.It has been over forty years since the isolation of the first human oncogene (...
Abnormal expression or mutations in Ras proteins has been found in up to 30 % of cancer cell types, ...
Rat sarcoma (RAS) family members are small GTPases that control a number of signaling pathways impor...
RAS proteins (KRAS4A, KRAS4B, NRAS and HRAS) function as GDP–GTP-regulated binary on-off switches, w...
Abstract RAS mutations (HRAS, NRAS, and KRAS) are among the most common oncogenes, and around 19% of...
The Ras superfamily of small GTPases is composed of more than 150 members, which share a conserved s...
SummaryOncogenic mutations in the small GTPase Ras are highly prevalent in cancer, but an understand...
Increased signalling by the small G protein Ras is found in many human cancers and is often caused b...
Ras proteins are key elements in the regulation of cellular proliferation, differentiation and survi...
RAS drug development has made enormous strides in the past ten years, with the first direct KRAS inh...
Despite more than three decades of intensive effort, no effective pharmacologic inhibitors of the Ra...
AbstractThree decades after identification of the Ras oncogene, no effective treatments for Ras muta...
Somatic mutations in the RAS genes are frequent in human tumors, especially in pancreatic, colorecta...
Mutations of RAS oncogenes are responsible for about 30% of all human cancer types, including pancre...
The H- and N-Ras GTPases are prominent examples of proteins, whose localizations and signalling capa...
© 2021 by the authors.It has been over forty years since the isolation of the first human oncogene (...
Abnormal expression or mutations in Ras proteins has been found in up to 30 % of cancer cell types, ...
Rat sarcoma (RAS) family members are small GTPases that control a number of signaling pathways impor...
RAS proteins (KRAS4A, KRAS4B, NRAS and HRAS) function as GDP–GTP-regulated binary on-off switches, w...
Abstract RAS mutations (HRAS, NRAS, and KRAS) are among the most common oncogenes, and around 19% of...
The Ras superfamily of small GTPases is composed of more than 150 members, which share a conserved s...
SummaryOncogenic mutations in the small GTPase Ras are highly prevalent in cancer, but an understand...