نتایج جستجو برای: foxc1

تعداد نتایج: 321  

2012
Zhi-Yuan Xu Song-Ming Ding Lin Zhou Hai-Yang Xie Kang-Jie Chen Wu Zhang Chun-Yan Xing Hai-Jun Guo Shu-Sen Zheng

The existence of microvascular invasion (MVI) formation is one of the most important risk factors predicting poor outcome in hepatocellular carcinoma (HCC) and its mechanism remains largely unknown. Epithelial-Mesenchymal Transition (EMT) has been suggested to be involved in many steps of the invasion-metastasis cascade. To elucidate the possible contribution of EMT to MVI, we initially evaluat...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2013
Iacopo Petrini Yisong Wang Paolo A Zucali Hye Seung Lee Trung Pham Donna Voeller Paul S Meltzer Giuseppe Giaccone

PURPOSES To determine whether the deregulation of genes relevant for normal thymus development can contribute to the biology of thymic epithelial tumors (TET). EXPERIMENTAL DESIGN Using array comparative genomic hybridization, we evaluated the copy number aberrations of genes regulating thymus development. The expression of genes most commonly involved in copy number aberrations was evaluated...

2017
Zhi Yang Shuai Jiang Yicheng Cheng Tian Li Wei Hu Zhiqiang Ma Fulin Chen Yang Yang

Forkhead box C1 (FOXC1) is an essential member of the forkhead box transcription factors and has been highlighted as an important transcriptional regulator of crucial proteins associated with a wide variety of carcinomas. FOXC1 regulates tumor-associated genes and is regulated by multiple pathways that control its mRNA expression and protein activity. Aberrant FOXC1 expression is involved in di...

Journal: :American journal of cancer research 2017
Xiaoming Zhu Li Wei Yangqiu Bai Sen Wu Shuangyin Han

Esophageal cancer (EC) was one of the most lethal malignancies worldwide with intricate mechanisms. Here we reported that Forkhead box C1 (FoxC1), a member of the forkhead family transcription factors, was up-regulated in EC tissues and cell lines in comparison with controls. FoxC1 levels were negatively correlated with tumor stage, lymph node metastasis and survival status of EC patients. Knoc...

2015
LEI OU-YANG SHENG-JUN XIAO PENG LIU SHI-JANG YI XIAO-LING ZHANG SHI OU-YANG SHENG-KUI TAN XUN LEI

Nasopharyngeal carcinoma (NPC) is a highly invasive malignancy with cervical lymphopathy as the initial presentation. Epithelial‑mesenchymal transition (EMT), a process by which epithelial cells lose cell‑cell adhesion and gain migratory and invasive properties, has a pivotal role in metastasis. Forkhead box C1 (FoxC1), a member of the forkhead family of transcription factors, induces EMT and h...

2013
Susan J. Harrison-Uy Julie A. Siegenthaler Andrea Faedo John L. R. Rubenstein Samuel J. Pleasure

We examined the role of the orphan nuclear hormone receptor CoupTFI in mediating cortical development downstream of meningeal retinoic acid signaling. CoupTFI is a regulator of cortical development known to collaborate with retinoic acid (RA) signaling in other systems. To examine the interaction of CoupTFI and cortical RA signaling we utilized Foxc1-mutant mice in which defects in meningeal de...

Journal: :Cell 2009
Julie A. Siegenthaler Amir M. Ashique Konstantinos Zarbalis Katelin P. Patterson Jonathan H. Hecht Maureen A. Kane Alexandra E. Folias Youngshik Choe Scott R. May Tsutomu Kume Joseph L. Napoli Andrew S. Peterson Samuel J. Pleasure

Extrinsic signals controlling generation of neocortical neurons during embryonic life have been difficult to identify. In this study we demonstrate that the dorsal forebrain meninges communicate with the adjacent radial glial endfeet and influence cortical development. We took advantage of Foxc1 mutant mice with defects in forebrain meningeal formation. Foxc1 dosage and loss of meninges correla...

Journal: :Journal of Experimental & Clinical Cancer Research 2021

Abstract Background Forkhead box C1 (FOXC1), as a member of the FOX family, is important for promote HCC invasion and metastasis. family protein lays pivotal role in metabolism. ROS involved tumor progression associated with expression lots transcription factors. We next explored mechanism underlying FOXC1 modulating metabolism hemostasis HCC. Methods used amino acids arrays to verify which FOX...

Journal: :Investigative ophthalmology & visual science 2006
Wener Cella José Paulo Cabral de Vasconcellos Mônica Barbosa de Melo Bianca Kneipp Fernando Ferreira Costa Carlos Alberto Longui Vital Paulino Costa

PURPOSE Axenfeld-Rieger (AR) is an autosomal dominant disorder with phenotypic heterogeneity characterized by anterior segment dysgenesis, facial bone defects, and redundant periumbilical skin. The PITX2 gene, on chromosome 4q25, and the FOXC1 gene, on chromosome 6p25, have been implicated in the different phenotypes of the syndrome through mutational events. Recently, the CYP1B1 gene was found...

Journal: :The Journal of clinical investigation 2014
Curtis R French Sudha Seshadri Anita L Destefano Myriam Fornage Corey R Arnold Philip J Gage Jonathan M Skarie William B Dobyns Kathleen J Millen Ting Liu William Dietz Tsutomu Kume Marten Hofker Derek J Emery Sarah J Childs Andrew J Waskiewicz Ordan J Lehmann

Patients with cerebral small-vessel disease (CSVD) exhibit perturbed end-artery function and have an increased risk for stroke and age-related cognitive decline. Here, we used targeted genome-wide association (GWA) analysis and defined a CSVD locus adjacent to the forkhead transcription factor FOXC1. Moreover, we determined that the linked SNPs influence FOXC1 transcript levels and demonstrated...

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