نتایج جستجو برای: ret proto

تعداد نتایج: 37432  

احیائی, سمیرا, امینی, سید اسدالله, شیخ‌الاسلامی, سارا, ظریف یگانه, مرجان, هدایتی, مهدی,

Background: Thyroid carcinoma is the most common endocrine malignancy and approximately accounts 2% of all cancer cases. Medullary thyroid cancer (MTC) is an endocrine tumor with differentiation of Parafollicular or C-cells and is categorized into hereditary or sporadic types. Medullary thyroid carcinoma approximately accounts for 5-10% of all thyroid carcinoma. Germ-line and somatic mutations ...

دهقانی اشکذری, محمود , هدایتی, مهدی , گلاب قدکساز, هدی ,

Background: Medullary thyroid cancer (MTC), includes 5-10% of all the thyroid cancers. RET proto-oncogene mutations have been found in association with MTC development. Therefore, identification of the mutations in RET can allow early diagnosis of the families who are at the risk of the disease. The goal of this study was to investigate existence and association between mutations in exon 19 of ...

Safura Pakizehkar, Samaneh Hosseinzadeh,

Medullary thyroid cancer accounts for 5-10% of thyroid carcinomas. RET proto-oncogene mutations occur in all of the hereditary MTCs and about 66% of the sporadic MTCs. So, the detection of the RET mutations is necessary for rapid and proper diagnosis and treatment. This systematic review seeks to find a comprehensive list of RET gene mutations in the diagnosis of medullary thyroid cancer. The ...

حسان منش, حسنا, شیخ‌الاسلامی, سارا, ظریف یگانه, مرجان, هدایتی, مهدی, کبیری, سمیرا,

Background: Thyroid carcinoma is the most common endocrine malignancy. Medullary thyroid carcinoma (MTC) approximately accounts for 5-10% of all thyroid carcinoma. Nowadays, it is obviously, the mutations in REarranged during transfection (RET) proto-oncogene, especially, mutations in exons 10, 11 and 16 are associated with MTC pathogenesis and occurrence. Thus, early diagnosis of MTC by mutati...

Journal: :Cancer research 2000
G Bunone M Uggeri P Mondellini M A Pierotti I Bongarzone

The RET proto-oncogene encodes a receptor tyrosine kinase for transforming growth factor-beta-related neurotrophic factors, which include GDNF and neurturin. The expression of RET proto-oncogene was detected in several tissues, such as spleen, thymus, lymph nodes, salivary gland, and spinal cord, and in several neural crest-derived cell lines. RET expression in the thyroid gland was reported to...

FATEMEH HAJI-GHASEMI, FEREIDOUN AZIZI, IRAJ NABIPOUR, REZA BARADAR-JALILI, SHAHRIAR KIAI,

MeduIIary thyroid carcinoma (MTC) occurs both sporadically and in the autosomal dominantly inherited multiple endocrine neoplasia (MEN) type 2 syndromes. The distinction between true sporadic MTC and a new mutation familial case is important for future clinical management of both the patient and family. The susceptibility gene for hereditary MTC is the RET proto-oncogene. DNA analysis for g...

Journal: :iranian journal of public health 0
sara sheikholeslami cellular and molecular research center, research institute for endocrine sciences, obesity research center, shahid beheshti university of medical sciences , tehran, iran. marjan zarif yeganeh cellular and molecular research center, research institute for endocrine sciences, obesity research center, shahid beheshti university of medical sciences , tehran, iran. laleh hoghooghi rad cellular and molecular research center, research institute for endocrine sciences, obesity research center, shahid beheshti university of medical sciences , tehran, iran. hoda golab ghadaksaz cellular and molecular research center, research institute for endocrine sciences, obesity research center, shahid beheshti university of medical sciences , tehran, iran. mehdi hedayati cellular and molecular research center, research institute for endocrine sciences, obesity research center, shahid beheshti university of medical sciences , tehran, iran.

medullary thyroid carcinoma (mtc) occurs in both sporadic (75%) and hereditary (25%) forms. the missense mutations of the rearranged during transfection (ret) proto-oncogene in mtc development have been well demonstrated. the aim of this study was to investigate frequency of g691s/s904s haplotype in mtc patients and their relatives.in this research 293 participants were studied, including 181 p...

2013
Young Sik Choi Hye Jung Kwon Bu Kyung Kim Su Kyoung Kwon Yo Han Park Jeong Hoon Kim Sang Bong Jung Chang Hoon Lee Seong Keun Lee Shinya Uchino

Many cases of RET proto-oncogene mutations of hereditary medullary thyroid carcinoma (MTC) have been reported in Korea. However, MTC with V804M RET proto-oncogene germline mutations have not been reported in Korea. A 33-yr-old man was diagnosed with a 0.7-cm sized thyroid nodule. Laboratory testing revealed serum calcitonin was elevated. The patient underwent total thyroidectomy with central co...

Journal: :Journal of the National Cancer Institute 1998
D M Dawson E G Lawrence G T MacLennan S B Amini H J Kung D Robinson M I Resnick E D Kursh T P Pretlow T G Pretlow

BACKGROUND The RET proto-oncogene encodes a protein that belongs to the tyrosine kinase growth factor receptor family. Germline point mutations in RET are found in individuals with multiple endocrine neoplasia (MEN) syndromes, and gene rearrangements have been reported in papillary thyroid cancers. We recently identified transcripts of the RET proto-oncogene in human prostate cancer xenografts ...

2012
Giuseppe Martucciello Margherita Lerone Lara Bricco Gian Paolo Tonini Laura Lombardi Carmine G Del Rossi Sergio Bernasconi

Multiple Endocrine Neoplasia type 2B (MEN 2B) is an autosomal dominant complex oncologic neurocristopathy including medullary thyroid carcinoma, pheochromocytoma, gastrointestinal disorders, marphanoid face, and mucosal multiple ganglioneuromas. Medullary thyroid carcinoma is the major cause of mortality in MEN 2B syndrome, and it often appears during the first years of life. RET proto-oncogene...

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