Medullary thyroid carcinoma (MTC) originates from the parafollicular C cells of the thyroid gland. Mutations of the RET proto-oncogene are implicated in the pathogenesis of MTC. Germline activating mutations of this gene have been reported in about 88-98% of familial MTCs, while somatic mutations of RET gene have been detected in about 23-70% of sporadic forms. Although these genetic events are well characterized, much less is known about the role of epigenetic abnormalities in MTC
WOS: 000233729900006PubMed ID: 16370559Objective: Medullary thyroid carcinoma (MTC) frequently occur...
Abstract: Medullary thyroid carcinoma (MTC) is a rare calcitonin producing neuroendocrine tumour tha...
Activating germ-line point mutations in the RET receptor are responsible for multiple endocrine neop...
Medullary thyroid carcinoma (MTC) originates from the parafollicular C cells of the thyroid gland. M...
Background: Medullary thyroid carcinoma (MTC) originates from the parafollicular C cells of the thyr...
Medullary thyroid carcinoma (MTC) is a rare tumour arising from neural crest-derived parafollicular ...
Medullary thyroid carcinoma (MTC) originates from the parafollicular C cells of the thyroid gland. M...
Medullary thyroid carcinoma (MTC) is a rare neoplasm supported by a strong genetic determinism. This...
Abstract Medullary thyroid carcinoma (MTC) is a rare calcitonin producing neuroendocrine tumour tha...
Background: The molecular pathogenesis of hereditary medullary thyroid carcinoma is well known to be...
Medullary thyroid carcinoma (MTC) may occur either as a sporadic or familial (FMTC) disease. Multipl...
The rearranged during transfection (RET) proto-oncogene was identified in 1985 and, very soon therea...
in patients. Medullary thyroid cancer (MTC) derives from paraf- of 100, 93, 71, and 21 % for stages ...
Medullary thyroid carcinoma (MTC) occurs as a sporadic form (75%) or as an autosomal dominant inheri...
Background & Aims: Thyroid cancer is the most common endocrine malignancy. Medullary thyroid carcino...
WOS: 000233729900006PubMed ID: 16370559Objective: Medullary thyroid carcinoma (MTC) frequently occur...
Abstract: Medullary thyroid carcinoma (MTC) is a rare calcitonin producing neuroendocrine tumour tha...
Activating germ-line point mutations in the RET receptor are responsible for multiple endocrine neop...
Medullary thyroid carcinoma (MTC) originates from the parafollicular C cells of the thyroid gland. M...
Background: Medullary thyroid carcinoma (MTC) originates from the parafollicular C cells of the thyr...
Medullary thyroid carcinoma (MTC) is a rare tumour arising from neural crest-derived parafollicular ...
Medullary thyroid carcinoma (MTC) originates from the parafollicular C cells of the thyroid gland. M...
Medullary thyroid carcinoma (MTC) is a rare neoplasm supported by a strong genetic determinism. This...
Abstract Medullary thyroid carcinoma (MTC) is a rare calcitonin producing neuroendocrine tumour tha...
Background: The molecular pathogenesis of hereditary medullary thyroid carcinoma is well known to be...
Medullary thyroid carcinoma (MTC) may occur either as a sporadic or familial (FMTC) disease. Multipl...
The rearranged during transfection (RET) proto-oncogene was identified in 1985 and, very soon therea...
in patients. Medullary thyroid cancer (MTC) derives from paraf- of 100, 93, 71, and 21 % for stages ...
Medullary thyroid carcinoma (MTC) occurs as a sporadic form (75%) or as an autosomal dominant inheri...
Background & Aims: Thyroid cancer is the most common endocrine malignancy. Medullary thyroid carcino...
WOS: 000233729900006PubMed ID: 16370559Objective: Medullary thyroid carcinoma (MTC) frequently occur...
Abstract: Medullary thyroid carcinoma (MTC) is a rare calcitonin producing neuroendocrine tumour tha...
Activating germ-line point mutations in the RET receptor are responsible for multiple endocrine neop...