نتایج جستجو برای: runx2 gene

تعداد نتایج: 1142462  

Journal: :Journal of endodontics 2014
Fan Yang Na Xu Dongmei Li Lina Guan Ying He Yaqing Zhang Qun Lu Xudong Zhang

INTRODUCTION Runt-related transcription factor 2 (RUNX2) is a transcription factor that is indispensable for bone and tooth development. Smad ubiquitylation regulatory factor-1 (SMURF1) promotes RUNX2 degradation and negatively regulates osteoblast differentiation, whereas RUNX2 activates SMURF1 transcription in osteoblasts. However, the relationship between RUNX2 and SMURF1 in tooth developmen...

Journal: :Human molecular genetics 2009
Bekim Sadikovic Maisa Yoshimoto Susan Chilton-MacNeill Paul Thorner Jeremy A Squire Maria Zielenska

Altered gene expression in tumors can be caused by copy number alterations to DNA or mutation affecting coding or regulatory regions of genes. However, epigenetic events may also influence gene expression. Malignant cells can show major disruptions in DNA methylation profiles, which are manifested as aberrant hypermethylation or as hypomethylation of gene promoters, as well as global genomic hy...

ژورنال: :مجله علمی دانشگاه علوم پزشکی رفسنجان 0
مجید فرش‏دوستی‏حق m. farshdousti hagh دکتری گروه آموزشی هماتولوژی، دانشکده علوم پزشکی، دانشگاه تربیت مدرسسازمان اصلی تایید شده: دانشگاه تربیت مدرس (tarbiat modares university)سازمان های دیگر: ستادیار مرکز تحقیقات هماتولوژی و انکولوژی، دانشگاه علوم پزشکی تبریز مهرداد نوروزی‏نیا m. noruzinia استادیار گروه آموزشی هماتولوژی، دانشکده علوم پزشکی، دانشگاه تربیت مدرسسازمان اصلی تایید شده: دانشگاه تربیت مدرس (tarbiat modares university) یوسف مرتضوی y. mortazavi دانشیار گروه آموزشی هماتولوژی، دانشکده علوم پزشکی، دانشگاه علوم پزشکی زنجانسازمان اصلی تایید شده: دانشگاه علوم پزشکی زنجان (zanjan university of medical sciences) مسعود سلیمانی m. soleimani استادیار گروه آموزشی هماتولوژی، دانشکده علوم پزشکی، دانشگاه تربیت مدرسسازمان اصلی تایید شده: دانشگاه تربیت مدرس (tarbiat modares university) سعید کاویانی s. kaviani استادیار گروه آموزشی هماتولوژی، دانشکده علوم پزشکی، دانشگاه تربیت مدرسسازمان اصلی تایید شده: دانشگاه تربیت مدرس (tarbiat modares university) مریم محمودی‏نیا میمند m. mahmoodinia maymand کارشناس ارشد مرکز تحقیقات سلولی مولکولی و سلولهای بنیادی صارم، تهران

چکیده   زمینه و هدف: runx2 اختصاصی ترین فاکتور نسخه برداری در تمایز سلول های بنیادی مزانشیمی به استئوبلاست می باشد. در این تحقیق، میزان بیان کمّی این فاکتور در طول تمایز سلول های بنیادی مزانشیمی به استئوبلاست با استفاده از محیط تمایزی استئوبلاستی و داروی زولدرونیک اسید مورد ارزیابی قرار گرفت.   مواد و روش ها: در این مطالعه تجربی، سلول‏های بنیادی مزانشیمی انسانی تحت تیمار با محیط تمایزی استئوبلاس...

Background & Aim: Extremely low-frequency electromagnetic field (ELF-EMF) and betaine are safe factors in bone fracture repair. This study aimed to compare the effects of these two stimuli on osteogenic differentiation of human adipose stem cells (hADSCs). Methods: After obtaining written informed consent, cells were extracted from abdominal adipose tissue and then cultured in vitro until the ...

2016
M Nakamura H Sugimoto T Ogata K Hiraoka H Yoda M Sang M Sang Y Zhu M Yu O Shimozato T Ozaki

Pancreatic cancer exhibits the worst prognostic outcome among human cancers. Recently, we have described that depletion of RUNX2 enhances gemcitabine (GEM) sensitivity of p53-deficient pancreatic cancer AsPC-1 cells through the activation of TAp63-mediated cell death pathway. These findings raised a question whether RUNX2 silencing could also improve GEM efficacy on pancreatic cancer cells bear...

Journal: :Journal of immunology 2002
François Vaillant Karen Blyth Linda Andrew James C Neil Ewan R Cameron

The development of T cells in the thymus is regulated by a series of stage-specific transcription factors. Deregulated expression of these factors can lead to alterations in thymocyte development with the production of aberrant cell subsets and predispose to tumor formation. The three genes of the Runx family are multilineage regulators of differentiation that have been reported to be expressed...

2012
Nigel A. Morrison Alexandre A. Stephens Motomi Osato Patsie Polly Timothy C. Tan Namiko Yamashita James D. Doecke Julie Pasco Nicolette Fozzard Graeme Jones Stuart H. Ralston Philip N. Sambrook Richard L. Prince Geoff C. Nicholson

RUNX2 is an essential transcription factor required for skeletal development and cartilage formation. Haploinsufficiency of RUNX2 leads to cleidocranial displaysia (CCD) a skeletal disorder characterised by gross dysgenesis of bones particularly those derived from intramembranous bone formation. A notable feature of the RUNX2 protein is the polyglutamine and polyalanine (23Q/17A) domain coded b...

Journal: :Cells, tissues, organs 2011
Mitra Adhami Farah Y Ghori-Javed Haiyan Chen Soraya E Gutierrez Amjad Javed

Glucose intolerance seen in metabolic disorders, such as type II diabetes, is commonly associated with improper execution of the insulin signaling pathway, as well as an imbalance of bone and fat tissues, such that a gain in adipose tissue occurs at the expense of bone loss. Fat-producing adipocytes and bone-forming osteoblasts stem from a common mesenchymal progenitor cell. Runx2 positively re...

2004
Eames A. J. Kaplan R. A. Schneider

Introduction: Many inherited or trauma-induced conditions, such as cleidocranial dysplasia or non-union fractures, result from inadequate bone formation [1]. Perhaps providing insight into such clinical maladies, bone formation was lost during evolution. Chondrichthyes, fish whose internal skeleton is entirely cartilaginous, evolved from an ancestral vertebrate population that possessed bone. W...

Journal: :Journal of pharmacological sciences 2011
Kyosuke Uno Takeshi Takarada Yukari Nakamura Hiroyuki Fujita Eiichi Hinoi Yukio Yoneda

We have previously demonstrated that glutamate (Glu) suppresses cellular proliferation toward self-renewal through a mechanism associated with the depletion of intracellular GSH after promoting the retrograde operation of the bidirectional cystine/Glu antiporter in undifferentiated osteoblastic MC3T3-E1 cells. In this study, we investigated the expression profile of the xCT subunit of the antip...

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