|
rs121913516
|
|
|
0.750 |
GeneticVariation |
BEFREE |
In addition, it could inhibit imatinib resistant cKIT T670I and V654A mutants <i>in vitro</i> and <i>in vivo</i> GIST preclinical models.
|
31205508 |
2019 |
|
rs121913523
|
|
|
0.730 |
GeneticVariation |
BEFREE |
In addition, it could inhibit imatinib resistant cKIT T670I and V654A mutants <i>in vitro</i> and <i>in vivo</i> GIST preclinical models.
|
31205508 |
2019 |
|
rs121913516
|
|
|
0.750 |
GeneticVariation |
BEFREE |
Compound 24 displays good antiproliferative effects against c-KIT T670I mutant-driven GIST cell lines (GIST-T1/T670I and GIST-5R) and also exhibits suitable in vivo pharmacokinetic profiles as well as dose-dependent antitumor efficacy.
|
31046271 |
2019 |
|
rs17084733
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We identified the <i>KIT</i> variant rs17084733 as a possible novel genetic biomarker for risk of developing <i>KIT</i>-WT GIST.
|
30983504 |
2019 |
|
rs121913517
|
|
|
0.850 |
GeneticVariation |
BEFREE |
Its superior selectivity would make it a good pharmacological tool for further dissection of KIT V559D mediated pathology in the GISTs.
|
29340041 |
2017 |
|
rs121913516
|
|
|
0.750 |
GeneticVariation |
BEFREE |
These were PDX models harboring primary and secondary <i>KIT</i> and additional mutations; <i>KIT</i> exon 11 (p.Y570_L576del), <i>KIT</i> exon 17 (p.D816E), and <i>PTEN</i> (p.T321fs) mutations in GIST-RX1 from a patient who was unresponsive to imatinib, sunitinib, and sorafenib, and <i>KIT</i> exon 11 (p.K550_splice) and <i>KIT</i> exon 14 (p.T670I) mutations in GIST-RX2 and <i>KIT</i> exon 9 (p.502_503insYA) and <i>KIT</i> exon 17 (p.D820E) mutations in GIST-RX4 from patients with imatinib and imatinib/sunitinib resistance, respectively.
|
29100343 |
2017 |
|
rs1057519711
|
|
|
0.010 |
GeneticVariation |
BEFREE |
These were PDX models harboring primary and secondary <i>KIT</i> and additional mutations; <i>KIT</i> exon 11 (p.Y570_L576del), <i>KIT</i> exon 17 (p.D816E), and <i>PTEN</i> (p.T321fs) mutations in GIST-RX1 from a patient who was unresponsive to imatinib, sunitinib, and sorafenib, and <i>KIT</i> exon 11 (p.K550_splice) and <i>KIT</i> exon 14 (p.T670I) mutations in GIST-RX2 and <i>KIT</i> exon 9 (p.502_503insYA) and <i>KIT</i> exon 17 (p.D820E) mutations in GIST-RX4 from patients with imatinib and imatinib/sunitinib resistance, respectively.
|
29100343 |
2017 |
|
rs121913235
|
|
|
0.730 |
GeneticVariation |
BEFREE |
This paper describes a 52-year old patient with a de novo germline p.Trp557Arg mutation with multiple GISTs throughout the gastrointestinal tract and cutaneous hyperpigmentation.
|
28710566 |
2018 |
|
rs121913513
|
|
|
0.730 |
GeneticVariation |
BEFREE |
A case of multiple gastrointestinal stromal tumors caused by a germline KIT gene mutation (p.Leu576Pro).
|
27771813 |
2017 |
|
rs121913516
|
|
|
0.750 |
GeneticVariation |
BEFREE |
Compound 35 displayed strong antiproliferative effect against GISTs cancer cell lines GIST-T1 (cKIT wt, GI50 = 4 nM) and GIST-5R (cKIT T670I, GI50 = 26 nM).
|
27545040 |
2016 |
|
rs121913521
|
|
|
0.740 |
GeneticVariation |
BEFREE |
Although targeted therapy involving tyrosine kinase inhibitors (TKIs) such as imatinib mesylate is highly effective for gastrointestinal stromal tumor carrying V560G c-kit mutation, it does not show much potential for targeting wild-type KIT (WT-KIT).
|
26428235 |
2016 |
|
rs121913517
|
|
|
0.850 |
GeneticVariation |
BEFREE |
According to Western blot analysis, in imatinib-resistant GIST with both KIT V559D and BRAF V600E mutations, the inhibition of KIT V559D by imatinib caused a strong decrease of AKT phosphorylation, while ERK1/2 phosphorylation was not affected.
|
25182956 |
2015 |
|
rs121913507
|
|
|
0.020 |
GeneticVariation |
BEFREE |
A KIT mutation was identified in six cases (67%), including three with the D816V mutation typical of adult-onset disease, and another three with an internal tandem duplication (p.A502_Y503dup) in exon 9, previously described in gastrointestinal stromal tumour.
|
24128084 |
2014 |
|
rs121913682
|
|
|
0.020 |
GeneticVariation |
BEFREE |
A KIT mutation was identified in six cases (67%), including three with the D816V mutation typical of adult-onset disease, and another three with an internal tandem duplication (p.A502_Y503dup) in exon 9, previously described in gastrointestinal stromal tumour.
|
24128084 |
2014 |
|
rs121913516
|
|
|
0.750 |
GeneticVariation |
BEFREE |
Herein, by introducing adaptive elements into the inhibitor core structure, we undertake the structure-based development of type II hybrid inhibitors to overcome gatekeeper drug-resistant mutations in cSrc-T338M, as well as clinically relevant tyrosine kinase KIT-T670I and Abl-T315I variants, as essential targets in gastrointestinal stromal tumors (GISTs) and chronic myelogenous leukemia (CML).
|
23773153 |
2013 |
|
rs121913512
|
|
|
0.760 |
GeneticVariation |
BEFREE |
Imatinib was efficient in GISTs with p.K642E mutation with a disease control rate superior to 90% whatever the sporadic or inherited origin of the tumour.
|
23648119 |
2013 |
|
rs121913513
|
|
|
0.730 |
GeneticVariation |
BEFREE |
Sequencing of DNA extracted from tumor tissue of one of his GISTs revealed the KIT mutation in exon 11 (c.1727T>C).
|
23598963 |
2013 |
|
rs121913506
|
|
|
0.710 |
GeneticVariation |
BEFREE |
Imatinib delays GIST xenograft growth despite the presence of the D816H resistance mutation.
|
23480638 |
2013 |
|
rs1057519710
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Imatinib delays GIST xenograft growth despite the presence of the D816H resistance mutation.
|
23480638 |
2013 |
|
rs121913517
|
|
|
0.850 |
GeneticVariation |
BEFREE |
Further comparison of localized GISTs in the MolecGIST cohort with advanced GISTs from previous clinical trials showed that the mutations of PDGFRA exon18 (D842V and others) as well as KIT exon11 substitutions (W557R and V559D) were more likely to be seen in patients with localized GISTs (odds ratio 7.9, 3.1, 2.7 and 2.5, respectively), while KIT exon 9 502_503dup and KIT exon 11 557_559del were more frequent in metastatic GISTs (odds ratio of 0.3 and 0.5, respectively).
|
21953054 |
2012 |
|
rs121913235
|
|
|
0.730 |
GeneticVariation |
BEFREE |
Further comparison of localized GISTs in the MolecGIST cohort with advanced GISTs from previous clinical trials showed that the mutations of PDGFRA exon18 (D842V and others) as well as KIT exon11 substitutions (W557R and V559D) were more likely to be seen in patients with localized GISTs (odds ratio 7.9, 3.1, 2.7 and 2.5, respectively), while KIT exon 9 502_503dup and KIT exon 11 557_559del were more frequent in metastatic GISTs (odds ratio of 0.3 and 0.5, respectively).
|
21953054 |
2012 |
|
rs121913512
|
|
|
0.760 |
GeneticVariation |
BEFREE |
Abnormal elevated PTEN expression in the mouse antrum of a model of GIST Kit(K641E/K641E).
|
21757001 |
2011 |
|
rs121913512
|
|
|
0.760 |
GeneticVariation |
BEFREE |
Here we have investigated Eng expression in the Kit(K641E) mouse GIST model, in human GIST and in the Ba/F3 cell model.
|
21435173 |
2012 |
|
rs121913512
|
|
|
0.760 |
GeneticVariation |
BEFREE |
Here we characterized Ntsr1 mRNA and protein expression in the murine Kit(K641E) GIST model and in tissue microarrays of human GIST.
|
21364741 |
2011 |
|
rs1057519710
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Hereditary gastrointestinal stromal tumors sharing the KIT Exon 17 germline mutation p.Asp820Tyr develop through different cytogenetic progression pathways.
|
19847891 |
2010 |