نتایج جستجو برای: prp gene

تعداد نتایج: 1146211  

Journal: :Clinical and experimental rheumatology 2009
M Saito K A Takahashi Y Arai A Inoue K Sakao H Tonomura K Honjo S Nakagawa H Inoue Y Tabata T Kubo

OBJECTIVE To investigate the therapeutic potential of administration of gelatin hydrogel microspheres containing platelet-rich plasma (PRP), by examining its effects on progression of osteoarthritis (OA) in a rabbit model. METHODS PRP and platelet-poor plasma (PPP) were prepared from rabbit blood. Adult rabbit chondrocytes were cultured in the alginate beads with the presence of 3% PRP or 3% ...

2006
Louay Fallouh Koichi Nakagawa Takahisa Sasho Momoko Arai Shuhei Ogino Sota Kitahara Hideshige Moriya

INTRODUCTION: Activated platelets are known to release many kinds of growth factors such as Platelet Derived Growth Factor (PDGF) and Transforming Growth Factor-β (TGF-β). Platelet-rich plasma (PRP) is a fraction of plasma in which platelets are concentrated and is reported to be utilized as a source of multiple growth factors that promote tissue repair. Recent studies has shown that platelet r...

Journal: :Nucleic acids research 1986
D Westaway S B Prusiner

The major protein, PrP 27-30, in purified preparations of hamster scrapie prions is encoded within the genome of the experimental host. DNA sequences related to a PrP cDNA clone can be detected in a wide variety of organisms under relatively stringent conditions where the only signal generated by hamster or mouse DNA corresponds to the PrP gene. Three hosts for scrapie, goat, sheep and rat gave...

2009
Jie Liang Jingbo Wang Guanhong Luo Yanglin Pan Xin Wang Changcun Guo Dexin Zhang Fang Yin Xiaoyin Zhang Jie Liu Jianhong Wang Xuegang Guo Kaichun Wu Daiming Fan

Approximately 10-15% of the human prion disease is inherited and one of the important genetic mutations occurs in the octapeptide repeat region of prion protein gene. One of the variants, one octapeptide repeat deletion (1-OPRD), existed in several gastric cancer cell lines and its mutation frequency was higher in gastric cancer cases. However, the biological functions of it remain unknown. Wil...

2014
Lisa Gasperini Giuseppe Legname

The cellular prion protein (PrP(C)) has been widely investigated ever since its conformational isoform, the prion (or PrP(Sc)), was identified as the etiological agent of prion disorders. The high homology shared by the PrP(C)-encoding gene among mammals, its high turnover rate and expression in every tissue strongly suggest that PrP(C) may possess key physiological functions. Therefore, defini...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شیراز - دانشکده دامپزشکی 1392

یکی از مسائل مهم طب امروز، بیماری های درگیرکننده ی تاندون ها می باشد. بنابراین هدف از این مطالعه بررسی تاثیر prpخودی در ترمیم نقص تاندونی تجربی در خوکچه هندی می باشد. تعداد40 سر خوکچه ی هندی بالغ، از هر دو جنس تهیه گردید. بعد از بیهوش شدن حیوانات، در سطح خلفی اندام عقبی راست، برشی به طول 3سانتی متر در پوست ایجاد شد. تاندون خم کننده ی عمقی انگشتان مجزا و نقیصه ی تاندونی به طول 7/0 سانتی متر در آ...

2015
Hao-Che Tang Wei-Chuan Chen Chih-Wei Chiang Lei-Yen Chen Yu-Ching Chang Chih-Hwa Chen Mohamed N. Rahaman

This article studied the effects of platelet-rich plasma (PRP) on the potential of synovial fluid mesenchymal stem cells (SF-MSCs) to differentiate. The PRP and SF-MSCs were obtained from the blood and knees of pigs, respectively. The identification of SF-MSCs and their ability to differentiate were studied by histological and surface epitopes, respectively. The SF-MSCs can undergo trilineage m...

Journal: :Oncology reports 2013
Miao He Limin Wang Jun Pu Qiaozhen Yang Gang Li Jie Hao

As reported in the literature, the worldwide 5-year overall survival rate for patients with gastric cancer receiving surgical treatment in the progressive stage is less than 25%. Therefore, there is an urgent need for the development of novel therapeutic strategies. Our preliminary studies demonstrated that proliferin-related protein (PRP) inhibits the proliferation of TM3 Leydig testicular cel...

Journal: :The EMBO journal 2007
Aimin Li Pedro Piccardo Sami J Barmada Bernardino Ghetti David A Harris

Familial prion diseases are due to dominantly inherited, germline mutations in the PRNP gene that encodes the prion protein (PrP). The cellular mechanism underlying the pathogenic effect of these mutations remains uncertain. To investigate whether pathogenic mutations impair a normal, physiological activity of PrP, we have crossed Tg(PG14) mice, which express PrP with an octapeptide insertion a...

2016
Juan C. González Catalina López María E. Álvarez Jorge E. Pérez Jorge U. Carmona

Leukocyte-reduced platelet-rich plasma (LR-PRP) is a therapy for tendinopathy of the Achilles tendon (TAT); however, there is scarce information regarding LR-PRP effects in rabbit models of TAT. We compared, at 4 and 12 weeks (w), the LR-PRP and placebo (PBS) effects on ultrasonography, histology and relative gene expression of collagen types I (COL1A1) and III (COL3A1) and vascular endothelial...

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