نتایج جستجو برای: ژن fol six1

تعداد نتایج: 17237  

Journal: :Molecular microbiology 2004
Martijn Rep H Charlotte van der Does Michiel Meijer Ringo van Wijk Petra M Houterman Henk L Dekker Chris G de Koster Ben J C Cornelissen

A 12 kDa cysteine-rich protein is secreted by Fusarium oxysporum f. sp. lycopersici during colonization of tomato xylem vessels. Peptide sequences obtained with mass spectrometry allowed identification of the coding sequence. The gene encodes a 32 kDa protein, designated Six1 for secreted in xylem 1. The central part of Six1 corresponds to the 12 kDa protein found in xylem sap of infected plant...

2016
Shu-Hua Sun Dan Liu Yun-Te Deng Xiao-Xue Zhang Dong-Yi Wan Bi-Xin Xi Wei Huang Qian Chen Meng-Chen Li Ming-Wei Wang Fei Yang Ping Shu Ke-Zhi Wu Qing-Lei Gao

Epithelial-mesenchymal transition (EMT) plays a critical role in promoting tumor invasion and metastasis. However, the key cofactors that modulate the signal transduction to induce EMT have note been fully explored to date. The present study reports that sine oculis homeobox homolog 1 (SIX1) is able to promote EMT of cervical cancer by coordinating with transforming growth factor (TGF)β-SMAD si...

Journal: :Development 2003
Christine Laclef Ghislaine Hamard Josiane Demignon Evelyne Souil Christophe Houbron Pascal Maire

Six homeoproteins are expressed in several tissues, including muscle, during vertebrate embryogenesis, suggesting that they may be involved in diverse differentiation processes. To determine the functions of the Six1 gene during myogenesis, we constructed Six1-deficient mice by replacing its first exon with the lacZ gene. Mice lacking Six1 die at birth because of severe rib malformations and sh...

Journal: :The Journal of clinical investigation 2011
Chaoshe Guo Ye Sun Bin Zhou Rosalyn M Adam XiaoKun Li William T Pu Bernice E Morrow Anne Moon Xue Li

Shared molecular programs govern the formation of heart and head during mammalian embryogenesis. Development of both structures is disrupted in human chromosomal microdeletion of 22q11.2 (del22q11), which causes DiGeorge syndrome (DGS) and velo-cardio-facial syndrome (VCFS). Here, we have identified a genetic pathway involving the Six1/Eya1 transcription complex that regulates cardiovascular an...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2004
Rainer G Ruf Pin-Xian Xu Derek Silvius Edgar A Otto Frank Beekmann Ulla T Muerb Shrawan Kumar Thomas J Neuhaus Markus J Kemper Richard M Raymond Patrick D Brophy Jennifer Berkman Michael Gattas Valentine Hyland Eva-Maria Ruf Charles Schwartz Eugene H Chang Richard J H Smith Constantine A Stratakis Dominique Weil Christine Petit Friedhelm Hildebrandt

Urinary tract malformations constitute the most frequent cause of chronic renal failure in the first two decades of life. Branchio-otic (BO) syndrome is an autosomal dominant developmental disorder characterized by hearing loss. In branchio-oto-renal (BOR) syndrome, malformations of the kidney or urinary tract are associated. Haploinsufficiency for the human gene EYA1, a homologue of the Drosop...

Journal: :Applied Biological Chemistry 2022

Abstract Fibronectin 1-derived circular RNA hsa_circ_0058092 is a novel potential oncogene in gastric cancer (GC). Yet, previous studies have not determined the role of GC progression and underlying mechanism. Herein, we investigated its competing endogenous (ceRNA) pathway development GC. The results showed that was substantially upregulated patients’ tissues cells, allied with SIX1 downregula...

2015
Shigeru Sato Hiroshi Yajima Yasuhide Furuta Keiko Ikeda Kiyoshi Kawakami Berta Alsina

SIX1 homeodomain protein is one of the essential key regulators of sensory organ development. Six1-deficient mice lack the olfactory epithelium, vomeronasal organs, cochlea, vestibule and vestibuloacoustic ganglion, and also show poor neural differentiation in the distal part of the cranial ganglia. Simultaneous loss of both Six1 and Six4 leads to additional abnormalities such as small trigemin...

2017
Zhuo Yang ZiYi Feng JiaHui Gu XinHui Li QianZhe Dong KuiRan Liu Yan Li Ling OuYang

Dysregulation of miR-488 has been implicated in several human cancers. In this study, we aim to explore its expression and biological function in ovarian cancers. We found miR-488 expression was downregulated in ovarian cancer tissues. Using CCK8 and colony formation assay showed that miR-488 inhibited SKOV3 cell proliferation and colony formation, with downregulation of cyclin D1 and cyclin E ...

Journal: :The International journal of developmental biology 2010
Keiko Ikeda Ryoichiro Kageyama Yuko Suzuki Kiyoshi Kawakami

The rodent olfactory epithelium (OE) is a good model system for studying the principles of stem and progenitor cell biology, because of its capacity for continuous neurogenesis throughout life and relatively well-characterized neuronal lineage. The development of mouse OE is divided into two stages, early and established neurogenesis. In established neurogenesis, which starts at embryonic day (...

2018
Dawei Wei Anning Li Chunping Zhao Hongbao Wang Chugang Mei Rajwali Khan Linsen Zan

DNA methylation is a major epigenetic modification of the genome and has an essential role in muscle development. The SIX1 gene is thought to play a principal role in mediating skeletal muscle development. In the present study, we determined that bovine SIX1 expression levels were significantly higher in the fetal bovine group (FB) and in undifferentiated Qinchuan cattle muscle cells (QCMCs) th...

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