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Mostrando ítems 61-70 de 1885
Evaluation of Lateral Lymph Node Metastases in Advanced Distal Rectal Cancer
(H G E Update Medical Publishing S AAthensGrécia, 2010)
Elevated serum levels of proinflammatory cytokines potentially correlate with depression and anxiety in colorectal cancer patients in different stages of the antitumor therapy
(Elsevier B.V., 2018-04-01)
Depression and anxiety, the most important psychological disorders in cancer patients, have now been considered as psychoneuroimmunological disorders, in which peripheral immune activation, through the release of proinflammatory ...
KRAS insertions in colorectal cancer: What do we know about unusual KRAS mutations?
(Elsevier B.V., 2014-04-01)
Introduction: KRAS mutations are negative predictors of the response to anti-EGFR therapy in colorectal carcinomas (CRCs). Point mutations in codons 12,13, and 61 are the most common KRAS mutations in CRC There are few ...
A new therapeutic approach for bone metastasis in colorectal cancer: intratumoral melittin
(Cevap-sao Paulo State Univ-unesp, 2022-03-14)
Background: Melittin has shown antiproliferative effects on tumor cells. Therefore, it comprises a valuable compound for studies on cancer treatment. To the best of our knowledge, no studies have reported melittin effects ...
The rectosigmoid junction: Are limits important?
(ARAN Ediciones, 2019)
The rectosigmoid junction (RSJ) is the limit between the sigmoid colon and the rectum. The limits of this transition zone have been a source of controversy. There are multiple definitions that aim to establish the beginning ...
Valor del antígeno carcinoembrionario pre-operatorio como factor pronóstico independiente en cáncer de colón y recto
(Sociedad de Gastroenterología del Perú, 2002)
HMSH2 and HMSH6 gene expression profiles in colorectal adenocarcinoma in patients up to 50 years of age
(Elsevier France-Editions Scientifiques Medicales Elsevier, 2016)
Lynch syndrome, previously called hereditary non-polyposis colorectal cancer (HNPCC), is a major mortality threat. It is an autosomal dominant disease which is caused by a germline mutation in the DNA mismatch repair (MMR), ...