نتایج جستجو برای: adenomatous polyposis coli apc

تعداد نتایج: 167846  

Journal: :Journal of pediatric genetics 2016
Alexia Waller Sarah Findeis Michael J Lee

Familial adenomatous polyposis (FAP), caused by a germline mutation in the adenomatous polyposis coli (APC) gene on chromosome 5q21, is an autosomal dominant disorder characterized by hundreds to thousands of adenomas throughout the gastrointestinal tract. A variety of extraintestinal manifestations, including thyroid, soft tissue, and brain tumors, may also be present. These patients inevitabl...

2017
Kei Miyakawa Mayuko Nishi Satoko Matsunaga Akiko Okayama Masaki Anraku Ayumi Kudoh Hisashi Hirano Hirokazu Kimura Yuko Morikawa Naoki Yamamoto Akira Ono Akihide Ryo

Diverse cellular proteins and RNAs are tightly regulated in their subcellular localization to exert their local function. Here we report that the tumour suppressor adenomatous polyposis coli protein (APC) directs the localization and assembly of human immunodeficiency virus (HIV)-1 Gag polyprotein at distinct membrane components to enable the efficient production and spread of infectious viral ...

ژورنال: پیاورد سلامت 2016
آزاد, مهدی, الحذیفی, رجاء, دهقانی فرد, علی, رضایی, سمیرا, سلالی, سعید, مشهدی خان, مائده, نوروزی نیا, مهرداد, کاویانی, سعید,

Background and Aim: Different regulation processes have an effect on osteoblastic differentiation of mesenchymal stem cells (MSCs), and among them Wnt signaling pathway is particularly desirable. In Wnt signaling pathway, Adenomatous Polyposis Coli (APC) bind to β-catenin and induce its degradation, thereby acting as a negative regulator of canonical Wnt pathway. In this study, gene expression ...

Journal: :Cancer research 2001
K Heinimann A Thompson A Locher T Furlanetto E Bader A Wolf R Meier K Walter P Bauerfeind G Marra H Müller D Foernzler Z Dobbie

Familial adenomatous polyposis, an autosomal-dominantly inherited colorectal cancer predisposition syndrome, is caused by germ-line mutations in the adenomatous polyposis coli (APC) gene. Despite the use of different screening methods, studies worldwide fail to identify APC mutations in 20-50% of all familial adenomatous polyposis patients (APC mutation-negatives). In this study, missense mutat...

2017

The evidence for genetic testing for the adenomatous polyposis coli (APC) mutation in individuals with a clinical differential diagnosis of attenuated familial adenomatous polyposis (aFAP), MUTYHassociated polyposis and Lynch syndrome, or individuals who are at-risk relatives of patients with FAP, includes a TEC Assessment. Outcomes of interest are overall survival, disease-specific survival, t...

2014
Bin Li Colin A. Flaveny Camilla Giambelli Dennis Liang Fei Lu Han Brian I. Hang Feng Bai Xin-Hai Pei Vania Nose Oname Burlingame Anthony J. Capobianco Darren Orton Ethan Lee David J. Robbins

Mutations in the WNT-pathway regulator ADENOMATOUS POLYPOSIS COLI (APC) promote aberrant activation of the WNT pathway that is responsible for APC-associated diseases such as Familial Adenomatous Polyposis (FAP) and 85% of spontaneous colorectal cancers (CRC). FAP is characterized by multiple intestinal adenomas, which inexorably result in CRC. Surprisingly, given their common occurrence, there...

2015
Shan-Shan Jiang Jian-Jun Li Yin Li Long-Jun He Qi-Jing Wang De-Sheng Weng Ke Pan Qing Liu Jing-Jing Zhao Qiu-Zhong Pan Xiao-Fei Zhang Yan Tang Chang-Long Chen Hong-Xia Zhang Guo-Liang Xu Yi-Xin Zeng Jian-Chuan Xia

Familial adenomatous polyposis (FAP) is an autosomal dominant disease manifesting as colorectal cancer in middle-aged patients. Mutations of the adenomatous polyposis coli (APC) gene contribute to both FAP and sporadic or familial colorectal carcinogenesis. Here we describe the identification of the causative APC gene defects associated with FAP in a Chinese pedigree. All patients with FAP were...

Journal: :Cancer research 1992
A Horii S Nakatsuru Y Miyoshi S Ichii H Nagase H Ando A Yanagisawa E Tsuchiya Y Kato Y Nakamura

The APC (adenomatous polyposis coli) gene is responsible for familial adenomatous polyposis and is also associated with the development of sporadic tumors of the colon and stomach. To investigate whether or not mutations of APC play any role in tumors arising in other organs, we examined somatic mutations of this gene in sporadic (nonfamilial) renal cell carcinomas, hepatocellular carcinomas, a...

Journal: :Cancer research 2002
Yasuhiro Yamada Kazuya Hata Yoshinobu Hirose Akira Hara Shigeyuki Sugie Toshiya Kuno Naoki Yoshimi Takuji Tanaka Hideki Mori

Mutations in the human adenomatous polyposis coli (APC) gene are causative for familial adenomatous polyposis (FAP), a rare condition in which numerous colonic polyps arise during puberty and, if left untreated, lead to colon cancer. Mouse model for human FAP, Apc(Min/+) mouse, contains a truncating mutation in the Apc gene and spontaneously develops intestinal adenomas. However, the distributi...

Ashraf Mohamadkhani, Maliheh Moradzadeh, Mehrdad Aghaei, Mohammad Hassan Jokar, Sima Sedighi,

Familial adenomatous polyposis is characterized by over 100 colorectal adenomas in the colorectum. The disease equally affects both sexes, with an incidence estimated at 1.14025-1.8300. The disease is premature in people with familial adenomatous polyposis. Patients suffering from familial adenomatous polyposis have a range of extra-intestinal diseases such as papillae, gastric, small intestine...

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