INTRODUCTION: BRAFV600E activating mutation is the most frequent genetic abnormality in the pathogenesis of papillary thyroid carcinoma. We aimed to evaluate the association between BRAFV600E mutation and well-established prognostic clinicopathological characteristics as well as iodine exposure. MATERIAL AND METHODS: From 2000 to 2012, the data of PTC patients admitted to Dr. Lutfi Kirdar Kartal Education and Research Hospital in Turkey were reviewed retrospectively. Clinicopathological parameters were collected. BRAFV600E mutation was analysed by DNA sequencing method in tumour specimens. We hypothesised thatBRAFV600E mutation prevalence is positively correlated with prolonged iodine exposure and expected to be higher in the second half of...
Papillary thyroid cancer (PTC) is the most common endocrine malignancy, accounting for 85–90% of all...
Papillary thyroid cancer (PTC) is the most common endocrine malignancy, accounting for 85–90% of all...
BACKGROUND: The BRAF(V600E) mutation, the most frequent genetic alteration in papillary thyroid c...
Introduction: BRAF(V600E) activating mutation is the most frequent genetic abnormality in the pathog...
SummaryObjectivesBRAF pV600E mutation is the most common oncogenic event and the most specific mutat...
BACKGROUND: Although several studies undoubtedly demonstrated that BRAF mutation is an important gen...
Background: The BRAF mutation has been shown to be associated with aggressive clinicopathologic char...
Abstract CONTEXT: Because very few studies have examined the correlation between BRAF mutations an...
ABSTRACT Objectives: We aimed to investigate the prevalence of the BRAF (V600E) mutation in consecu...
Background: The BRAF(V600E) mutation is the most frequent genetic alteration in papillary thyroid ca...
Background. Over the past ten years, the incidence rate of papillary thyroid carcinoma (PTC) worldwi...
Importance: BRAF V600E is a prominent oncogene in papillary thyroid cancer (PTC), but its role in PT...
Introduction: Papillary thyroid carcinoma is the most frequent endocrine neoplasia and its incidence...
BRAF((V600E)) mutation is the most frequent genetic alteration in papillary thyroid carcinomas (PTCs...
The mutation BRAF V600E is thought to be a putative prognostic marker of the aggressiveness of sever...
Papillary thyroid cancer (PTC) is the most common endocrine malignancy, accounting for 85–90% of all...
Papillary thyroid cancer (PTC) is the most common endocrine malignancy, accounting for 85–90% of all...
BACKGROUND: The BRAF(V600E) mutation, the most frequent genetic alteration in papillary thyroid c...
Introduction: BRAF(V600E) activating mutation is the most frequent genetic abnormality in the pathog...
SummaryObjectivesBRAF pV600E mutation is the most common oncogenic event and the most specific mutat...
BACKGROUND: Although several studies undoubtedly demonstrated that BRAF mutation is an important gen...
Background: The BRAF mutation has been shown to be associated with aggressive clinicopathologic char...
Abstract CONTEXT: Because very few studies have examined the correlation between BRAF mutations an...
ABSTRACT Objectives: We aimed to investigate the prevalence of the BRAF (V600E) mutation in consecu...
Background: The BRAF(V600E) mutation is the most frequent genetic alteration in papillary thyroid ca...
Background. Over the past ten years, the incidence rate of papillary thyroid carcinoma (PTC) worldwi...
Importance: BRAF V600E is a prominent oncogene in papillary thyroid cancer (PTC), but its role in PT...
Introduction: Papillary thyroid carcinoma is the most frequent endocrine neoplasia and its incidence...
BRAF((V600E)) mutation is the most frequent genetic alteration in papillary thyroid carcinomas (PTCs...
The mutation BRAF V600E is thought to be a putative prognostic marker of the aggressiveness of sever...
Papillary thyroid cancer (PTC) is the most common endocrine malignancy, accounting for 85–90% of all...
Papillary thyroid cancer (PTC) is the most common endocrine malignancy, accounting for 85–90% of all...
BACKGROUND: The BRAF(V600E) mutation, the most frequent genetic alteration in papillary thyroid c...