نتایج جستجو برای: fap p

تعداد نتایج: 1271291  

Journal: :Molecular cancer therapeutics 2016
Peter Brünker Katharina Wartha Thomas Friess Sandra Grau-Richards Inja Waldhauer Claudia Ferrara Koller Barbara Weiser Meher Majety Valeria Runza Huifeng Niu Kathryn Packman Ningping Feng Sherif Daouti Ralf J Hosse Ekkehard Mössner Thomas G Weber Frank Herting Werner Scheuer Hadassah Sade Cuiying Shao Bin Liu Peng Wang Gary Xu Suzana Vega-Harring Christian Klein Klaus Bosslet Pablo Umaña

Dysregulated cellular apoptosis and resistance to cell death are hallmarks of neoplastic initiation and disease progression. Therefore, the development of agents that overcome apoptosis dysregulation in tumor cells is an attractive therapeutic approach. Activation of the extrinsic apoptotic pathway is strongly dependent on death receptor (DR) hyperclustering on the cell surface. However, strate...

2013
Andrzej Plawski Tomasz Banasiewicz Pawel Borun Lukasz Kubaszewski Piotr Krokowicz Marzena Skrzypczak-Zielinska Jan Lubinski

Familial adenomatous polyposis (FAP) is a well-defined autosomal dominant predisposition to the development of polyposis in the colon and rectum at unusually early ages. The first symptoms of FAP are diarrhea and blood in the stool. Weight loss and weaknesses occur after the development of advanced tumour. The incidence of the FAP disorder is one per 10000 newborns. There are high levels of het...

2009
Osamu Dohi Haruo Ohtani Masahito Hatori Elichi Sato Masami Hosaka Hiroshi Nagura Eiji Itoi Shoichi Kokubun

AIMS Fibroblast activation protein (FAP)/seprase and dipeptidylpeptidase-IV (DPP-IV)/CD26 are serine integral membrane proteases. They are involved in tissue remodelling, cancer invasion and metastases, mechanisms that are controversial. The aim was to identify cell types that express FAP and DPP-IV in human bone and soft tissue tumours, and to determine whether there are any correlations betwe...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2014
Seyed Reza Fatemi Azadeh Safaee Sara Pasha Mohamad Amin Pourhoseingholi Rasool Bahrainei Mahsa Molaei

BACKGROUND Familial adenomatous polyposis (FAP) is a disease inherited in an autosomal dominant fashion. Most FAP patients develop upper gastrointestinal polyps; especially those in the antrum and duodenum are usually neoplastic. The aim of this study was to evaluate the prevalence of gastroduodenal polyps in Iranian FAP patients. MATERIALS AND METHODS 28 patients affected by FAP underwent fr...

Journal: :International journal of pharmaceutics 2011
Z Mohammadi F A Dorkoosh S Hosseinkhani K Gilani T Amini A Rouholamini Najafabadi M Rafiee Tehrani

Gene therapy targeted at the respiratory epithelium holds therapeutic potential for diseases such as cystic fibrosis and lung cancer. We recently reported that Chitosan-DNA-FAP-B nanoparticles are good candidates for targeted gene delivery to fibronectin molecules (FAP-B receptors) of lung epithelial cell membrane. In this study Chitosan-DNA-FAP-B nanoparticles were nebulized to mice using air ...

Journal: :Physical chemistry chemical physics : PCCP 2016
Iuliia V Voroshylova Filipe Teixeira Renata Costa Carlos M Pereira M Natália D S Cordeiro

Gas-phase electronic and structural properties of the room temperature ionic liquid 1-ethyl-3-methylimidazolium tris(perfluoroethyl)trifluorophosphate ([EMIM][FAP]) were studied using density functional theory, and confirmed with results from infrared spectroscopy. A conformational analysis allowed the identification of several plausible conformers of the ion pairs. For the detected conformers,...

2010
Shukuro ARAKI Yukio ANDO

The authors reviewed contribution of Kumamoto University group to the progress of the studies on transthyretin (TTR)-related familial amyloidotic polyneuropathy (TTR-related FAP) for 42 years (from 1967 to 2009). Andrade (1952) first described a large group of patients with FAP in Portugal and Araki et al. (1967) in second discovered similar FAP patients in Arao, Kumamoto, Japan. Owing to progr...

2015
Nádia Pereira Gonçalves Paula Gonçalves Miguel Ventosa Ana Varela Coelho Maria João Saraiva

Background Transthyretin (TTR) deposition in the peripheral nervous system (PNS) is the hallmark of Familial Amyloidotic Polyneuropathy (FAP). Mice expressing human TTR with the V30M mutation in a heterozygous heat shock factor 1 (Hsf-1) background show extensive TTR deposits in PNS and gastrointestinal tract, as well as extracellular matrix (ECM) remodeling, similar to those seen in human FAP ...

2014
Kyu Young Kim Seong Woo Jeon Jung Gil Park Chung Hoon Yu Se Young Jang Jae Kwang Lee Hee Young Hwang

Familial adenomatous polyposis (FAP) is an autosomal dominant disorder characterized by hundreds of colorectal adenomatous polyps that progress to colorectal cancer. Management of patients with FAP is with a total colectomy. Chemopreventive strategies have been studied in FAP patients in an effort to delay the development of adenomas in the upper and the lower gastrointestinal tract and to prev...

2005
D. S. HARPER W. J. LOESCHE

The inhibitory effect offluorapatite (FAP)-derivedfluoride upon resting cell suspensions of Streptococcus mutans incubated at pH 4.5 and 6.5 was studied using lactic acid production from 0.1% sucrose as an indicator offermentation activity. Cells incubated with FAP produced significantly less lactic acid than did cells incubated with hydroxyapatite (HAP). Addition of HAP to cell suspensions con...

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