نتایج جستجو برای: adenomatous polyposis coli apc

تعداد نتایج: 167846  

2017
Luca Roncucci Monica Pedroni Francesco Mariani

Attenuated adenomatous polyposis (AAP) is a poorly understood syndrome, that can be defined as the presence of 10-99 synchronous adenomas in the large bowel, and it is considered a phenotypic variant of familial adenomatous polyposis (FAP). This definition has the advantage of simplicity, but it may include sporadic multiple adenomas of the large bowel at an extreme, or FAP cases on the other s...

Journal: :Cancer genomics & proteomics 2011
Sarah E Gray Elaine W Kay Mary Leader Mohamed Mabruk

BACKGROUND The adenomatous polyposis coli (APC) gene is a tumor suppressor gene which is mutated in the hereditary disease, familial adenomatous polyposis (FAP). Somatic mutations of the APC gene have also been identified in the majority of sporadic colorectal carcinomas, and mutation of the APC gene appears to be an early step in the initiation of colon cancer. Loss of heterozygosity (LOH) of ...

2014
Seyed Mohammad Hossein Kashfi Faeghe Behboudi Farahbakhsh Mina Golmohammadi Ehsan Nazemalhosseini Mojarad Pedram Azimzadeh Hamid Asadzadeh Aghdaie

Familial adenomatous polyposis (FAP) is responsible for <1% of colorectal cancer (CRC) cases and is inherited an autosomal dominant trait. Patients generally present hundreds to thousands of adenomas and develop colorectal cancer by age 35- 40 if left untreated. Here we report four patients with germline frameshift mutation (small deletion) at exon 15 of adenomatous polyposis coli (APC) tumor s...

2017

Colorectal cancer is undoubtedly one of the most genetically studied malignancies. In the past 20 years, substantial progress has been made in understanding the genetic and molecular pathogenesis of this cancer. It is instructive that the genes involved in the inherited colon cancer syndromes are the same genes involved in the etiology of most colorectal cancers. Familial adenomatous polyposis ...

Journal: :Gut 2004
N J H Sturt M C Gallagher P Bassett C R Philp K F Neale I P M Tomlinson A R J Silver R K S Phillips

BACKGROUND Many patients with familial adenomatous polyposis (FAP) die from desmoid tumours which can arise spontaneously but often appear to be surgically induced by prophylactic colectomy. FAP results from germline adenomatous polyposis coli (APC) gene mutations and desmoids arise following biallelic APC mutation, with one change usually occurring distal to the second beta-catenin binding/deg...

Journal: :Journal of medical genetics 2016
Isabel Spier Dmitriy Drichel Martin Kerick Jutta Kirfel Sukanya Horpaopan Andreas Laner Stefanie Holzapfel Sophia Peters Ronja Adam Bixiao Zhao Tim Becker Richard P Lifton Sven Perner Per Hoffmann Glen Kristiansen Bernd Timmermann Markus M Nöthen Elke Holinski-Feder Michal R Schweiger Stefan Aretz

BACKGROUND In 30-50% of patients with colorectal adenomatous polyposis, no germline mutation in the known genes APC, causing familial adenomatous polyposis, MUTYH, causing MUTYH-associated polyposis, or POLE or POLD1, causing polymerase-proofreading-associated polyposis can be identified, although a hereditary aetiology is likely. This study aimed to explore the impact of APC mutational mosaici...

2016
Taina T. Nieminen Walter Pavicic Noora Porkka Matti Kankainen Heikki J. Järvinen Anna Lepistö Päivi Peltomäki

Allele-specific expression (ASE) of the Adenomatous Polyposis Coli (APC) gene occurs in up to one-third of families with adenomatous polyposis (FAP) that have screened mutation-negative by conventional techniques. To advance our understanding of the genomic basis of this phenomenon, 54 APC mutation-negative families (21 with classical FAP and 33 with attenuated FAP, AFAP) were investigated. We ...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2010
Kan Wang Shuchen Gu Omaima Nasir Michael Föller Teresa F Ackermann Karin Klingel Reinhard Kandolf Dietmar Kuhl Christos Stournaras Florian Lang

Adenomatous polyposis coli (APC) is inactivated in familial adenomatous polyposis and sporadic colorectal cancer. Mice carrying defective APC (apc(Min/+)) spontaneously develop gastrointestinal tumors. APC binds GSK3beta, which phosphorylates beta-catenin thus fostering its degradation. beta-catenin upregulates the serum- and glucocorticoid-inducible kinase Sgk1, which inhibits GSK3beta. The pr...

2015
Luisa Gonzalez Jose Alvarez Erica Weinstein Panagiota Korenis

Schizophrenia is associated with high mortality and morbidity. The etiology of schizophrenia remains unclear, studies implicate a multifactorial origin with genetic and environmental factors. The adenomatous polyposis coli (APC) gene has been associated with FAP (familial adenomatous polyposis), and studies have linked it to schizophrenia. However, there are few studies which examine the associ...

2004
N J H Sturt P M Tomlinson A R J Silver R K S Phillips

Background: Many patients with familial adenomatous polyposis (FAP) die from desmoid tumours which can arise spontaneously but often appear to be surgically induced by prophylactic colectomy. FAP results from germline adenomatous polyposis coli (APC) gene mutations and desmoids arise following biallelic APC mutation, with one change usually occurring distal to the second b-catenin binding/degra...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید