Results 1 to 10 of about 14,919 (139)

RET Proto-Oncogene Variants in Patients with Medullary Thyroid Carcinoma from the Mediterranean Basin: A Brief Report [PDF]

open access: yesLife, 2023
Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant (AD) condition with very high penetrance and expressivity. It is characterized into three clinical entities recognized as MEN2A, MEN2B, and familial medullary thyroid carcinoma (FMTC ...
Vassos Neocleous   +4 more
doaj   +2 more sources

Distribution of RET proto‐oncogene variants in children with appendicitis [PDF]

open access: yesMolecular Genetics & Genomic Medicine, 2022
Background In addition to patient‐related systemic factors directing the immune response, the pathomechanisms of appendicitis (AP) might also include insufficient drainage leading to inflammation caused by decreased peristalsis.
Jurek Schultz   +7 more
doaj   +2 more sources

A study on genetic polymorphism of RET proto-oncogene in Hirschsprung's disease in children [PDF]

open access: yesAfrican Journal of Paediatric Surgery, 2020
Background: Hirschsprung's disease (HD) is a genetic disorder with a complex pattern of inheritance. Some single-nucleotide polymorphisms (SNPs) are identified to be associated with the risk of Hirschsprung's Disease (HSCR).
Madhu Kumari   +5 more
doaj   +2 more sources

A post-irradiation-induced replication stress promotes RET proto-oncogene breakage [PDF]

open access: yesEuropean Thyroid Journal
Objective: Ionizing radiation generates genomic instability by promoting the accumulation of chromosomal rearrangements. The oncogenic translocation RET/PTC1 is present in more than 70% of radiation-induced thyroid cancers.
Fabio Hecht   +8 more
doaj   +2 more sources

Targeted therapy in the treatment of lung cancer in Iceland 2010–2023 [PDF]

open access: yesActa Oncologica
Background and purpose: Lung cancer is the third most common malignancy in Iceland and remains the leading cause of cancer-related mortality. Lung cancer may harbor driver mutations affecting the function of Epidermal growth factor receptor (EGFR ...
Stefanía Ásta Tryggvadóttir   +8 more
doaj   +2 more sources

RET Proto-oncogene C634Y Mutation-associated Multiple Endocrine Adenomatosis Type 2A: a Case Report and Literature Review [PDF]

open access: yesZhongguo quanke yixue, 2023
Multiple endocrine adenomatosis type 2A (MEN2A) is a subtype of multiple endocrine adenomatosis type 2, which is clinically characterized by medulloid thyroid carcinoma (MTC) , pheochromocytoma (PHEO) , and hyperparathyroidism, and has been reported to ...
DENG Yuxuan, HE Li, SONG Zhiwang, JIANG Yanxia
doaj   +1 more source

Precious Gene: The Application of RET-Altered Inhibitors

open access: yesMolecules, 2022
The well-known proto-oncogene rearrangement during transfection (RET), also known as ret proto-oncogene Homo sapiens (human), is a rare gene that is involved in the physiological development of some organ systems and can activate various cancers, such as
Qitao Gou   +4 more
doaj   +1 more source

Profiling Oncogenic Germline Mutations in Unselected Chinese Lung Cancer Patients

open access: yesFrontiers in Oncology, 2021
IntroductionEmerging evidence has suggested that inherited factors are also involved in lung cancer development. However, most studies focused on well-elucidated cancer predisposition genes, the majority of which are tumor suppressor genes.
Jie Yang   +7 more
doaj   +1 more source

CRISPR/Cas9 RET Gene Knockout in Medullary Thyroid Carcinoma Cell-lines: Optimization and Validation

open access: yesIranian Journal of Public Health, 2022
Background: Medullary Thyroid Cancer (MTC) is a very aggressive type of thyroid carcinoma. Mutation in RET proto-oncogene is demonstrated in MTC development. We aimed to knock-out of RET-oncogene using CRISPR/Cas9 genome editing method in MTC cell-lines.
Marjan Zarif-Yeganeh   +5 more
doaj   +1 more source

Chinese siblings with hereditary medullary thyroid carcinoma caused by RET mutation: implications for RET oncogene detection

open access: yesBMC Endocrine Disorders, 2020
Background Hereditary medullary thyroid carcinoma (MTC) is mainly caused by germline mutations in the RET proto-oncogene, which accounts for 20–30% of all MTC according to foreign studies.
Qin Huang, Aihua Hu, Mingsheng Zhang
doaj   +1 more source

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