An unexpected new role of mutant Ras: perturbation of human embryonic development
about
Function, regulation and pathological roles of the Gab/DOS docking proteinsCurrent management of juvenile myelomonocytic leukemia and the impact of RAS mutationsMultiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndromeMek1/2 gene dosage determines tissue response to oncogenic Ras signaling in the skin.Differential Regulation of RasGAPs in Cancer.Dysregulation of astrocyte extracellular signaling in Costello syndrome.Peripheral blood cells from children with RASopathies show enhanced spontaneous colonies growth in vitro and hyperactive RAS signaling.BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas.Ras proteins: paradigms for compartmentalised and isoform-specific signalling.Negative regulation of Stat3 by activating PTPN11 mutants contributes to the pathogenesis of Noonan syndrome and juvenile myelomonocytic leukemia.The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration.Impaired synaptic plasticity in RASopathies: a mini-review.C4ST-1/CHST11-controlled chondroitin sulfation interferes with oncogenic HRAS signaling in Costello syndrome.Segregation of negatively charged phospholipids by the polycationic and farnesylated membrane anchor of Kras.Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders.A novel KRAS gene mutation report in sporadic colorectal cancer, from Northwest of Iran.Behavioral phenotype in Costello syndrome with atypical mutation: a case report.Does Harvey-Ras gene expression lead to oral squamous cell carcinoma? A clinicopathological aspect.Retinal dystrophy in two boys with Costello syndrome due to the HRAS p.Gly13Cys mutation.Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13CMultiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship?
P2860
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P2860
An unexpected new role of mutant Ras: perturbation of human embryonic development
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
An unexpected new role of mutant Ras: perturbation of human embryonic development
@ast
An unexpected new role of mutant Ras: perturbation of human embryonic development
@en
type
label
An unexpected new role of mutant Ras: perturbation of human embryonic development
@ast
An unexpected new role of mutant Ras: perturbation of human embryonic development
@en
prefLabel
An unexpected new role of mutant Ras: perturbation of human embryonic development
@ast
An unexpected new role of mutant Ras: perturbation of human embryonic development
@en
P2860
P921
P1476
An unexpected new role of mutant Ras: perturbation of human embryonic development
@en
P2093
Charlotte M Niemeyer
Christian P Kratz
P2860
P2888
P304
P356
10.1007/S00109-006-0135-4
P577
2007-01-09T00:00:00Z
2007-03-01T00:00:00Z