نتایج جستجو برای: ژن col11a2

تعداد نتایج: 15855  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2007
Riku Sakimura Kazuhiro Tanaka Syunsaku Yamamoto Tomoya Matsunobu Xu Li Masuo Hanada Takamitsu Okada Tomoyuki Nakamura Yang Li Yukihide Iwamoto

PURPOSE Histologically, chondrosarcomas represent the degree of chondrogenic differentiation, which is associated with the prognosis of the disease. Histone acetylation and deacetylation play key roles in the regulation of chondrocytic differentiation. Here, we describe the antitumor effects of histone deacetylase (HDAC) inhibitors as differentiating reagents on chondrosarcomas. EXPERIMENTAL ...

2017
Camilla A. M. Glad Johanna C. Andersson-Assarsson Peter Berglund Ragnhildur Bergthorsdottir Oskar Ragnarsson Gudmundur Johannsson

Patients with Cushing's Syndrome (CS) in remission were used as a model to test the hypothesis that long-standing excessive cortisol exposure induces changes in DNA methylation that are associated with persisting neuropsychological consequences. Genome-wide DNA methylation was assessed in 48 women with CS in long-term remission (cases) and 16 controls matched for age, gender and education. The ...

2016
S.L. Dunn J. Soul S. Anand J.-M. Schwartz R.P. Boot-Handford T.E. Hardingham

OBJECTIVES Joint degeneration in osteoarthritis (OA) is characterised by damage and loss of articular cartilage. The pattern of loss is consistent with damage occurring only where the mechanical loading is high. We have investigated using RNA-sequencing (RNA-seq) and systems analyses the changes that occur in damaged OA cartilage by comparing it with intact cartilage from the same joint. METH...

2016
Colleen J. Saunders Mahjoubeh Jalali Sefid Dashti Junaid Gamieldien

Tendinopathy is a multifactorial syndrome characterised by tendon pain and thickening, and impaired performance during activity. Candidate gene association studies have identified genetic factors that contribute to intrinsic risk of developing tendinopathy upon exposure to extrinsic factors. Bioinformatics approaches that data-mine existing knowledge for biological relationships may assist with...

2017
Hiroki Tsuji Yukio Taniguchi Shintaro Ishizuka Hirokazu Matsuda Takahisa Yamada Kazuaki Naito Hiroaki Iwaisaki

The major histocompatibility complex (MHC) is highly polymorphic and plays a central role in the vertebrate immune system. Despite its functional consistency, the MHC genomic structure differs substantially among organisms. In birds, the MHCs of Galliformes and the Japanese crested ibis (Pelecaniformes) are well-characterized, but information about other avian MHCs remains scarce. The Oriental ...

Journal: : 2023

زمینه و هدف: کم‌تحرکی در مقابل آن تمرین جزء عوامل مرتبط با شاخص‌های آسیب کبدی به‌شمار می‌روند. وجود این هنوز نقش بسیاری از تمرین‌های ورزشی به‌ویژه تمرینات تناوبی مقاومتی مصرف برخی مکمل‌های غذایی جمله اسپیرولینا بر ایمنی التهابی کاملاٌ شناخته نشده است؛ بنابراین هدف پژوهش تعیین اثر هشت هفته مکمل‌دهی هوازی فعالیت بافت کبد بیان ژن CXCL1 عضلة موش‌های صحرایی نر بود.مواد روش‌ها: نیمه‌تجربی، 60 سر موش ن...

Journal: :Journal of cell science 2010
Yoko Takigawa Kenji Hata Shuji Muramatsu Katsuhiko Amano Koichiro Ono Makoto Wakabayashi Akio Matsuda Kenji Takada Riko Nishimura Toshiyuki Yoneda

Sox9 is an essential transcription factor for chondrogenesis by regulating the expression of chondrogenic genes. However, its regulatory mechanism is not fully understood. To address this, we attempted to identify the transcriptional partners of Sox9 by screening the cDNA library of the chondrogenic cell line ATDC5 using the collagen 2α1 (Col2α1) gene promoter fused to a luciferase reporter gen...

2016
Xin Chen Jun Guo Tao Cai Fengshan Zhang Shengfa Pan Li Zhang Shaobo Wang Feifei Zhou Yinze Diao Yanbin Zhao Zhen Chen Xiaoguang Liu Zhongqiang Chen Zhongjun Liu Yu Sun Jie Du

Ossification of the posterior longitudinal ligament of the spine (OPLL), which is characterized by ectopic bone formation in the spinal ligaments, can cause spinal-cord compression. To date, at least 11 susceptibility genes have been genetically linked to OPLL. In order to identify potential deleterious alleles in these OPLL-associated genes, we designed a capture array encompassing all coding ...

2016
Liao Chang Shiyang He Danqing Mao Yuanhong Liu Zijun Xiong Dongke Fu Bo Li Shuguang Wei Xun Xu Shengbin Li Hui Yuan

Whole-genome shotgun (WGS) sequencing has become a routine method in genome research over the past decade. However, the assembly of highly polymorphic regions in WGS projects remains a challenge, especially for large genomes. Employing BAC library constructing, PCR screening and Sanger sequencing, traditional strategy is laborious and expensive, which hampers research on polymorphic genomic reg...

2012
Kohji Miura Noriyuki Namba Keiko Yamamoto Makoto Fujiwara Yasuhisa Ohata Taichi Kitaoka Takuo Kubota Toshimi Michigami Keiichi Ozono

We describe a three-generation family with tall stature, scoliosis and macrodactyly of the great toes and a heterozygous p.Val883Met mutation in Npr2, the gene that encodes the CNP receptor NPR2 (natriuretic peptide receptor 2). When expressed in HEK293A cells, the mutant Npr2 cDNA generated intracellular cGMP (cyclic guanosine monophosphate) in the absence of CNP ligand. In the presence of CNP...

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