Results 71 to 80 of about 14,919 (139)

Proteomic profiling identifies candidate biomarkers for small intestinal neuroendocrine tumours G1 and G2

open access: yesJournal of Neuroendocrinology, Volume 38, Issue 10, October 2026.
Abstract Although small intestinal neuroendocrine tumours (SI‐NET) Grade 1 (G1) and 2 (G2) are often studied together, clinical course and response to treatment may differ. We hypothesized that these tumour groups express different markers in blood that may inform future treatment strategies. Blood from 107 SI‐NET patients (G1 n = 64, G2 n = 43) and 50
Malin Grönberg   +2 more
wiley   +1 more source

RET is a sex-biased regulator of intestinal tumorigenesis

open access: yesFrontiers in Gastroenterology
Ret is implicated in colorectal cancer (CRC) as both a proto-oncogene and a tumor suppressor. We asked whether RET signaling regulates tumorigenesis in an Apc-deficient preclinical model of CRC.
Sean T. Koester   +5 more
doaj   +1 more source

Surgical Remission of Diabetes in a Patient With Mutation of RET Proto-Oncogene. [PDF]

open access: yesAACE Clin Case Rep, 2021
Concepción Zavaleta MJ   +7 more
europepmc   +1 more source

RET Proto-Oncogene Mutational Analysis in 45 Iranian Patients Affected with Medullary Thyroid Carcinoma: Report of a New Variant. [PDF]

open access: yesJ Thyroid Res, 2021
Damavandi E   +6 more
europepmc   +1 more source

Dual targeting of RET and SRC synergizes in RET fusion‐positive cancer cells

open access: yesMolecular Oncology
Rearranged during transfection (RET) fusions drive subsets of non‐small cell lung cancer (NSCLC) and papillary thyroid carcinoma (PTC). Despite new selective RET tyrosine kinase inhibitors (TKIs), resistance usually occurs and is often driven by RET ...
Juhyeon Son   +13 more
doaj   +1 more source

Advanced medullary thyroid cancer: pathophysiology and management

open access: yesCancer Management and Research, 2013
Carla Vaz Ferreira, Débora Rodrigues Siqueira, Lucieli Ceolin, Ana Luiza MaiaThyroid Section, Endocrine Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, BrazilAbstract: Medullary thyroid carcinoma (MTC) is a rare malignant ...
Ferreira CV   +3 more
doaj  

Total colonic aganglionosis and cleft palate in a newborn with Janus-cysteine 618 mutation of RET proto-oncogene: a case report. [PDF]

open access: yesItal J Pediatr, 2020
Schierz IAM   +6 more
europepmc   +1 more source

MEN2 phenotype in a family with germline heterozygous rare RET K666N variant

open access: yesEndocrinology, Diabetes & Metabolism Case Reports
Multiple endocrine neoplasia type 2 (MEN2) is a hereditary cancer syndrome caused by germline-activating pathogenic variants in the RET proto-oncogene.
A La Greca   +8 more
doaj   +1 more source

A Brief Review on The Molecular Basis of Medullary Thyroid Carcinoma

open access: yesCell Journal, 2016
Approximately 5-10% of all thyroid cancers are medullary thyroid carcinomas (MTC). MTC is mainly sporadic in nature, but 20-30% of cases are hereditary. Genetic testing for hereditary MTC is very important for the patient and his family, but the patients
Mohammadi Masoumeh, Mehdi Hedayati
doaj  

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