Results 1 to 10 of about 110,630 (313)

Evaluation of mutations in KRAS and BRAF genes in Iranian population with diffuse gastric cancer [PDF]

open access: yesWorld Cancer Research Journal, 2019
OBJECTIVE: RAS proteins control signaling pathways which are the main regulators of the normal cell growth and malignant transformation cells. The point mutations in the KRAS gene are current event in numerous human cancers including pancreatic, lung ...
M. Saneipour, A. Moridnia
doaj   +3 more sources

Younger Than 55 Years Old and BRAF V600E Mutation are Risk Factors for Lymph Node Metastasis in Papillary Thyroid Carcinomas ≤1.0 cm but Not in >1.0 cm [PDF]

open access: yesInternational Journal of General Medicine, 2023
Yeqian Lai,1,2 Yihua Gu,1,2 Ming Yu,1,2 Jiaqin Deng1,2 1Department of Thyroid Surgery, Meizhou People’s Hospital, Meizhou Academy of Medical Sciences, Meizhou, People’s Republic of China; 2Guangdong Provincial Key Laboratory of Precision Medicine and ...
Lai Y, Gu Y, Yu M, Deng J
doaj   +1 more source

Prevalence of BRAF, NRAS and c-KIT mutations in Slovenian patients with advanced melanoma

open access: yesRadiology and Oncology, 2018
BRAF, NRAS and c-KIT mutations are characteristics of tumour tissues that influence on treatment decisions in metastatic melanoma patients. Mutation frequency and their correlation with histological characteristics in Slovenian population have not been ...
Moltara Maja Ebert   +6 more
doaj   +1 more source

Somatic mutations in colorectal cancer: regional experience

open access: yesConsilium Medicum, 2022
Introduction. Colorectal cancer is one of the most common malignant neoplasms in economically developed countries, ranking 3rd and 2nd in the structure of morbidity and mortality, respectively. Current knowledge about the molecular features of colorectal
Nikolai A. Ognerubov, Elena N. Ezhova
doaj   +1 more source

The frequency of mutations in advanced thyroid cancer in Japan: a single-center study

open access: yesEndocrine Journal
We analyzed the outcomes of genetic testing to study the frequency of mutations in advanced thyroid cancer in Japan. Patients (n = 96) with unresectable or metastatic thyroid carcinoma were included for retrospective chart review.
Soji Toda   +8 more
doaj   +1 more source

Prognostic value of somatic mutation testing and different methods of treatment of low-risk differentiated thyroid cancer [PDF]

open access: yesЭндокринная хирургия, 2019
Background: Using molecular testing for prediction the course of the disease could possibly help doctors in making therapeutic decisions about the management of patients, because it remains controversial issues in low-risk differentiated thyroid cancer ...
Vera A. Kachko   +2 more
doaj   +1 more source

REQUIREMENTS FOR EFFICIENT PCR CLAMPING BY LOCKED NUCLEIC ACID OLIGONUCLEOTIES FOR SIMPLE AND SENSITIVE DETECTION OF SOMATIC MUTATIONS

open access: yesСибирский онкологический журнал, 2018
PCR clamping/wild-type blocking PCR with non-extendable locked nucleic acid (LNA) oligonucleotides is used for sensitive detection of somatic mutations in tumors.
V. A. Shamanin   +4 more
doaj   +1 more source

Current Advance in Targeted Treatment and Immunotherapy for BRAF-mutant 
Advanced Non-small Cell Lung Cancer

open access: yesChinese Journal of Lung Cancer, 2021
With the development of precision medicine, therapies of targeting driver genes have significantly prolonged survival in advanced non-small cell lung cancer (NSCLC) patients.
Na LI, Yanjun XU, Yun FAN
doaj   +1 more source

Hyperplastic Polyposis Syndrome Identified with a BRAF Mutation

open access: yesGut and Liver, 2012
Background/AimsHydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors (statins) and peroxisome proliferator-activated receptor gamma (PPARγ) ligands can modulate cellular differentiation, proliferation, and apoptosis through various pathways.
doaj   +1 more source

Real-world data analysis of next-generation sequencing and corresponding clinical characteristics in thyroid tumor

open access: yesEndocrine Connections
Next-generation sequencing (NGS) is of great benefit to clinical practice in terms of identifying genetic alterations. This study aims to clarify the gene background and its influence on thyroid tumors in the Chinese population.
Xu-Feng Chen   +6 more
doaj   +1 more source

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