Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Human cutaneous melanoma; a review of NRAS and BRAF mutation frequencies in relation to histogenetic subclass and body site.
|
19383313 |
2008 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Absence of BRAF gene mutation in non-melanoma skin tumors.
|
16687919 |
2006 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
We sought to further evaluate the prognostic value of BRAF mutations in localized cutaneous melanoma.
|
24388723 |
2014 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Correction to: Dynamic and unpredictable changes in mutant allele fractions of BRAF and NRAS during visceral progression of cutaneous malignant melanoma.
|
31464610 |
2019 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
BRAF mutations in cutaneous melanoma are independently associated with age, anatomic site of the primary tumor, and the degree of solar elastosis at the primary tumor site.
|
21324100 |
2011 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The present study investigated the BRAF V600E mutation frequency and its clinical implications in a group of 77 primary cutaneous melanoma patients treated in a cancer reference center in Brazil.
|
24535907 |
2014 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The purpose of this study is to describe a case of concurrent medullary and papillary thyroid carcinoma (MTC and PTC) and cutaneous melanoma and to analyze BRAF(V600E) mutation in plasma and tissues.
|
24858900 |
2014 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Herein, we report the case of a 65-year-old man with papillary TC and cutaneous malignant melanoma metastatic to masseter muscle, both characterized by BRAF mutation.
|
24574369 |
2014 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
We obtained blood and tissue samples from a patient diagnosed with a BRAF(V600E)-mutant cutaneous melanoma that was treated with vemurafenib and achieved a near-complete response.
|
23948972 |
2013 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
As the current knowledge about pathogenesis, clinical and genetic features of cutaneous melanoma is not very clear, we aim to use bioinformatics to identify the potential key genes involved in the expression and mutation status of BRAF.
|
30925905 |
2019 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
BRAF inhibitors target the BRAF-V600E/K mutated kinase, the driver mutation found in 50% of cutaneous melanoma.
|
30429474 |
2018 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Frequencies of BRAF and NRAS mutations are different in histological types and sites of origin of cutaneous melanoma: a meta-analysis.
|
21166657 |
2011 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Recently, a high incidence of activating mutations in the kinase domain of the BRAF gene has been reported in malignant melanoma of the skin.
|
15588860 |
2005 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
NRAS and BRAF mutations in cutaneous melanoma and the association with MC1R genotype: findings from Spanish and Austrian populations.
|
23096702 |
2013 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The purpose of this study was to determine whether the T1799A BRAF mutation found in cutaneous melanoma is also present in conjunctival melanoma.
|
15277467 |
2004 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The most common recurring mutation in cutaneous melanoma is the prooncogenic BRAF V600E mutation that drives melanoma cell proliferation.
|
23174497 |
2012 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Ocular toxicity in BRAF mutant cutaneous melanoma patients treated with vemurafenib.
|
25036880 |
2014 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
BRAF is the most frequently mutated gene in skin melanoma.
|
30347273 |
2018 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Recent molecular studies have identified recurrent BRAF mutations in both cutaneous melanoma and thyroid malignancies.
|
16049985 |
2006 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The classical V600E BRAF mutation was not found; instead a novel V600L was observed suggesting that the oncogenic event in OMM is different from that in skin melanoma.
|
21750866 |
2011 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
A set of 250 probes representing 209 genes that were significantly (raw P< or =0.001) associated with BRAF mutation status was identified and 17 of these were previously shown to be implicated in cutaneous melanoma progression or pigmentation pathway-associated genes driven by the microphthalmia transcription factor (MITF).
|
19383316 |
2008 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The significance of BRAF V600E mutation status discordance between primary cutaneous melanoma and brain metastases: The implications for BRAF inhibitor therapy.
|
29310328 |
2017 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
In contrast to cutaneous melanoma, there is no evidence that BRAF mutations are involved in the activation of the mitogen-activated protein kinase (MAPK) pathway in uveal melanoma, although there is increasing evidence that this pathway is activated frequently in the latter tumours.
|
15928660 |
2005 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
We investigated 132 cases of primary cutaneous melanoma in patients aged between 18 and 30 years with emphasis on clinical characteristics, pathologic features, and molecular evaluation of mutation in the BRAF gene (BRAF(V600E)).
|
24471189 |
2014 |
Cutaneous Melanoma
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
To identify the dermoscopic features associated with BRAF mutation in cutaneous melanoma and to evaluate a model capable of predicting BRAF mutations on the basis of dermoscopic and clinicopathologic features that are easily accessible in normal clinical practice.
|
29307636 |
2018 |