نتایج جستجو برای: ژن magi2‎

تعداد نتایج: 15852  

Journal: :Human molecular genetics 2014
Katharina Bauß Barbara Knapp Pia Jores Ronald Roepman Hannie Kremer Erwin V Wijk Tina Märker Uwe Wolfrum

The human Usher syndrome (USH) is a complex ciliopathy with at least 12 chromosomal loci assigned to three clinical subtypes, USH1-3. The heterogeneous USH proteins are organized into protein networks. Here, we identified Magi2 (membrane-associated guanylate kinase inverted-2) as a new component of the USH protein interactome, binding to the multifunctional scaffold protein SANS (USH1G). We sho...

2012
Takayoshi Koide Masahiro Banno Branko Aleksic Saori Yamashita Tsutomu Kikuchi Kunihiro Kohmura Yasunori Adachi Naoko Kawano Itaru Kushima Yukako Nakamura Takashi Okada Masashi Ikeda Kazutaka Ohi Yuka Yasuda Ryota Hashimoto Toshiya Inada Hiroshi Ujike Tetsuya Iidaka Michio Suzuki Masatoshi Takeda Nakao Iwata Norio Ozaki

Schizophrenia is a complex psychiatric disorder characterized by positive symptoms, negative symptoms, and cognitive impairment. MAGI2, a relatively large gene (∼1.5 Mbps) that maps to chromosome 7q21, is involved in recruitment of neurotransmitter receptors such as AMPA- and NMDA-type glutamate receptors. A genetic association study designed to evaluate the association between MAGI2 and cognit...

2013
Rian M. Nijmeijer Hjalmar C. van Santvoort Alexandra Zhernakova Steffen Teller Jonas A. Scheiber Carolien G. de Kovel Marc G. H. Besselink Jeroen T. J. Visser Femke Lutgendorff Thomas L. Bollen Marja A. Boermeester Ger T. Rijkers Frank U. Weiss Julia Mayerle Markus M. Lerch Hein G. Gooszen Louis M. A. Akkermans Cisca Wijmenga

INTRODUCTION Impairment of the mucosal barrier plays an important role in the pathophysiology of acute pancreatitis. The myosin IXB (MYO9B) gene and the two tight-junction adaptor genes, PARD3 and MAGI2, have been linked to gastrointestinal permeability. Common variants of these genes are associated with celiac disease and inflammatory bowel disease, two other conditions in which intestinal per...

Introduction: Defects in PTEN gene play an important role in the initiation of the prostate cancer. MAGI2 is recognized as a frame which assists in stabilizing PTEN protein and enhances its tumor suppressor function. As miR-101 down-regulates MAGI2 expression, it can indirectly cause to reduce the PTEN activity. Methods:LnCap, PC3 and DU-145 prostate cancer cell lines were studied in order to ...

2018
Cheng Chang Chang Hui Chen Wang Yu Ping Liao Yu Chih Chen Yu Chun Weng Mu Hsien Yu Hung Cheng Lai

OBJECTIVE We hypothesized that DNA methylation of development-related genes may occur in endometrial cancer (EC)/ovarian cancer (OC) and may be detected in cervical scrapings. METHODS We tested methylation status by quantitative methylation-specific polymerase chain reaction for 14 genes in DNA pools of endometrial and OC tissues. Tissues of EC/normal endometrium, OC/normal ovary, were verifi...

2016
Mengtao Ma Miao He Qian Jiang Yuanyuan Yan Shu Guan Jing Zhang Zhaojin Yu Qiuchen Chen Mingli Sun Weifan Yao Haishan Zhao Feng Jin Minjie Wei

Tumor metastasis is a complex and multistep process and its exact molecular mechanisms remain unclear. We attempted to find novel microRNAs (miRNAs) contributing to the migration and invasion of breast cancer cells. In this study, we found that the expression of miR-487a was higher in MDA-MB-231breast cancer cells with high metastasis ability than MCF-7 breast cancer cells with low metastasis a...

Journal: :Journal of biochemistry 2015
Shunta Nagashima Manami Kodaka Hiroaki Iwasa Yutaka Hata

Membrane-associated guanylate kinase with an inverted arrangement of protein-protein interaction domains (MAGI)2 (also called synaptic scaffolding molecule (S-SCAM), atrophin-1-interacting protein 1, activin receptor-interacting protein 1) is a scaffold protein that binds a wide variety of receptors, cell adhesion molecules and signalling molecules. It also interacts with other scaffold protein...

Journal: :American journal of human genetics 2008
Christian R Marshall Edwin J Young Ariel M Pani Mary-Louise Freckmann Yves Lacassie Cédric Howald Kristi K Fitzgerald Maarit Peippo Colleen A Morris Kate Shane Manuela Priolo Masafumi Morimoto Ikuko Kondo Esra Manguoglu Sibel Berker-Karauzum Patrick Edery Holly H Hobart Carolyn B Mervis Orsetta Zuffardi Alexandre Reymond Paige Kaplan May Tassabehji Ronald G Gregg Stephen W Scherer Lucy R Osborne

Infantile spasms (IS) is the most severe and common form of epilepsy occurring in the first year of life. At least half of IS cases are idiopathic in origin, with others presumed to arise because of brain insult or malformation. Here, we identify a locus for IS by high-resolution mapping of 7q11.23-q21.1 interstitial deletions in patients. The breakpoints delineate a 500 kb interval within the ...

Journal: :Journal of the American Society of Nephrology 2016

Journal: :Indian Journal of Pharmaceutical Sciences 2022

To investigate the effect of long non coding RNA MAGI2-antisense 3 on proliferation, invasion and migration cervical cancer cells underlying mechanism. SiHa were divided into plasmid cloning DNA group, DNA-MAGI2-antisense anti-microRNA-negative control anti-microRNA-31-5p 3+microRNAnegative group 3+microRNA-31-5p group; quantitative reverse transcription polymerase chain reaction was used to de...

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