WOS: 000307518400001PubMed ID: 22767446It has been shown that BRAF(V600E) mutation in papillary thyroid carcinomas (PTC) is associated both with pathogenesis and poor prognosis. In this study, we aimed to investigate the relationship of the BRAF(V600E) mutation and the established prognostic factors in a cohort of Turkish patients with PTC. Forty-six cases of papillary thyroid carcinoma have been evaluated for the presence of BRAF(V600E) mutation. BRAF(V600E) has been examined by restriction fragment length polymorphism. BRAF(V600E) mutation status has been compared with well-known histopathological and clinical prognostic parameters such as invasion of thyroid capsule, extrathyroidal extension, and the presence of lymph node and/or distant...
An association between the BRAFV600E mutation and the clinicopathological progression of papillary t...
Background. Over the past ten years, the incidence rate of papillary thyroid carcinoma (PTC) worldwi...
BACKGROUND: BRAF(V600E) mutation, which represents the most frequent genetic mutation in papillary t...
Background: The BRAF(V600E) mutation is the most frequent genetic alteration in papillary thyroid ca...
SummaryObjectivesBRAF pV600E mutation is the most common oncogenic event and the most specific mutat...
Abstract CONTEXT: Because very few studies have examined the correlation between BRAF mutations an...
Papillary thyroid cancer (PTC) offers excellent prognosis, however relapse risk or persistent diseas...
Introduction: BRAF(V600E) activating mutation is the most frequent genetic abnormality in the pathog...
Purpose To investigate the prognostic value of BRAF V600E mutation for the recurrence of papillary t...
Papillary thyroid cancer (PTC) constitutes more than 90 % of the thyroid cancers. MAP kinase/ERK pat...
In this study, BRAF mutation was found in 219 of 500 cases (43.8%). In particular, we found the most...
The aim of this study was to investigate the association between the BRAF V600E mutation incidence a...
BACKGROUND: The BRAF(V600E) mutation, the most frequent genetic alteration in papillary thyroid c...
Papillary thyroid cancer (PTC) is the most common endocrine malignancy, accounting for 85–90% of all...
Background: The BRAF mutation has been shown to be associated with aggressive clinicopathologic char...
An association between the BRAFV600E mutation and the clinicopathological progression of papillary t...
Background. Over the past ten years, the incidence rate of papillary thyroid carcinoma (PTC) worldwi...
BACKGROUND: BRAF(V600E) mutation, which represents the most frequent genetic mutation in papillary t...
Background: The BRAF(V600E) mutation is the most frequent genetic alteration in papillary thyroid ca...
SummaryObjectivesBRAF pV600E mutation is the most common oncogenic event and the most specific mutat...
Abstract CONTEXT: Because very few studies have examined the correlation between BRAF mutations an...
Papillary thyroid cancer (PTC) offers excellent prognosis, however relapse risk or persistent diseas...
Introduction: BRAF(V600E) activating mutation is the most frequent genetic abnormality in the pathog...
Purpose To investigate the prognostic value of BRAF V600E mutation for the recurrence of papillary t...
Papillary thyroid cancer (PTC) constitutes more than 90 % of the thyroid cancers. MAP kinase/ERK pat...
In this study, BRAF mutation was found in 219 of 500 cases (43.8%). In particular, we found the most...
The aim of this study was to investigate the association between the BRAF V600E mutation incidence a...
BACKGROUND: The BRAF(V600E) mutation, the most frequent genetic alteration in papillary thyroid c...
Papillary thyroid cancer (PTC) is the most common endocrine malignancy, accounting for 85–90% of all...
Background: The BRAF mutation has been shown to be associated with aggressive clinicopathologic char...
An association between the BRAFV600E mutation and the clinicopathological progression of papillary t...
Background. Over the past ten years, the incidence rate of papillary thyroid carcinoma (PTC) worldwi...
BACKGROUND: BRAF(V600E) mutation, which represents the most frequent genetic mutation in papillary t...