نتایج جستجو برای: rb1

تعداد نتایج: 1799  

2016
Thomas Naert Robin Colpaert Tom Van Nieuwenhuysen Dionysia Dimitrakopoulou Jannick Leoen Jurgen Haustraete Annekatrien Boel Wouter Steyaert Trees Lepez Dieter Deforce Andy Willaert David Creytens Kris Vleminckx

Retinoblastoma is a pediatric eye tumor in which bi-allelic inactivation of the Retinoblastoma 1 (RB1) gene is the initiating genetic lesion. Although recently curative rates of retinoblastoma have increased, there are at this time no molecular targeted therapies available. This is, in part, due to the lack of highly penetrant and rapid retinoblastoma animal models that facilitate rapid identif...

2013
Hersharan Nischal Hua Sun Yuchun Wang David A Ford Ying Cao Peng Wei Ba-Bie Teng

Target substrate-specific hammerhead ribozyme cleaves the specific mRNA efficiently and results in the inhibition of gene expression. In humans, overproduction of apolipoprotein B (apoB) is positively associated with premature coronary artery diseases. The goal of this study is to demonstrate that long-term reduction of apoB gene expression using hammerhead ribozyme would result in inhibition o...

Journal: :Onco 2021

The status of RB1 in cancer may help us determine the optimal therapeutic approach to patients [...]

Journal: :Cancer Investigation 2021

Tumor suppressor genes RB1 and TP53 are altered frequently in prostate cancer (PC), whether inactivation promotes radioresistance remains unclear. Herein, we demonstrated that loss enhanced ionizing radiation (IR)-induced DNA damage to inhibit cell proliferation promote cellular senescence through a TP53-dependent pathway LNCaP cells. Furthermore, the stabilization of was regulated by ATM-media...

Journal: :Neuro-oncology 2022

Abstract PURPOSE There is evidence that molecular heterogeneity of glioblastoma associated with MR imaging signatures. Modern machine learning models, such as deep neural networks, provide a tool for capturing complex relationships in high-dimensional datasets. This study leverages recent advances visualizing networks to construct radiogenomics coordinate system whose axes reflect the expressio...

Journal: :Brain pathology 2011
Young-Ho Kim Joel Lachuer Michel Mittelbronn Werner Paulus Benjamin Brokinkel Kathy Keyvani Ulrich Sure Karsten Wrede Sumihito Nobusawa Yoichi Nakazato Yuko Tanaka Anne Vital Luigi Mariani Hiroko Ohgaki

We recently reported that the vast majority (>90%) of low-grade diffuse gliomas (diffuse astrocytoma, oligoastrocytoma and oligodendroglioma) carry at least one of the following genetic alterations: IDH1/2 mutation, TP53 mutation or 1p/19q loss. Only 7% of cases were triple-negative (ie, lacking any of these alterations). In the present study, array comparative genomic hybridization (CGH) in 15...

2011
Zhizhen Zhang Xiao-Yuan Lian

A ginseng Rb extract (GRbE) containing three major ingredients of ginsenoside Rb1 (G-Rb1), ginsenoside Rb3 (G-Rb3) and ginsenoside Rd (G-Rd) has been shown to have anticonvulsant and neuroprotective activity. As such, sufficient characterization and standardization of this active GRbE are demanded to facilitate an ongoing preclinical investigation on its potential for the treatment of epilepsy....

2014
Hideaki Toki Maki Inoue Osamu Minowa Hiromi Motegi Yuriko Saiki Shigeharu Wakana Hiroshi Masuya Yoichi Gondo Toshihiko Shiroishi Ryoji Yao Tetsuo Noda

Mutant mouse models are indispensable tools for clarifying gene functions and elucidating the pathogenic mechanisms of human diseases. Here, we describe novel cancer models bearing point mutations in the retinoblastoma gene (Rb1) generated by N-ethyl-N-nitrosourea mutagenesis. Two mutations in splice sites reduced Rb1 expression and led to a tumor spectrum and incidence similar to those observe...

Journal: :Cancer research 2000
H Primdahl H von der Maase M Christensen H Wolf T F Orntoft

Cell growth regulators include proteins of the p53 pathway encoded by the genes CDKN2A (p16, p14arf), MDM2, TP53, and CDKN1A (p21) as well as proteins encoded by genes like RB1, E2F, and MYCL. In the present study we investigated allelic deletions of all these genes in each recurrent bladder tumor from well-defined clinical material with more than 3 years of follow-up. We followed three groups ...

2010
Sumit Gupta Salman Siddiqui Pranab Haldar James J Entwisle Dean Mawby Andrew J Wardlaw Peter Bradding Ian D Pavord Ruth H Green Christopher E Brightling

BACKGROUND Severe asthma is a heterogeneous condition. Airway remodelling is a feature of severe asthma and can be determined by the assessment of high-resolution computed tomography (HRCT) scans. The aim of this study was to assess whether airway remodelling is restricted to specific subphenotypes of severe asthma. METHODS A retrospective analysis was performed of HRCT scans from subjects wh...

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