甘油磷酸

结果发现：微弧氧化方法适合于Ti在甘油磷酸钠和醋酸钙电解液中形成富含有Ca和P的氧化膜。

It was found that the MAO method is suitable for Ti to form oxide film containing Ca and P in the electrolyte of β - GP and CA.

方法取4-8代间质细胞单独或与内皮细胞共种植于Ⅰ型胶原凝胶支架内，以含有p-甘油磷酸、维生素C、地塞米松的钙化培养基进行钙化诱导培养2周。

VIC at 4-8 passages were cultured with or without VEC in collagen I gel scaffolds , and osteogenic media was used to induce calcification of interstitial cells for up to 2 weeks .

结论：体外培养的MSCs具有一定的成骨能力，使用含有地塞米松、β-甘油磷酸钠和维生素C的条件培养基可以大大提高其成骨能力。

CONCLUSION : Cultured MSCs in vitro have osteogenic potential , which can be improved greatly with conditional culture medium containing dexamethasone ,β sodium glycerophosphate and vitamin C.

方法：使用密度梯度法分离成年大鼠骨髓MSCs，以地塞米松、β-甘油磷酸钠、维生素C为成骨诱导剂。

Methods : MSCs were isolated from adult rat by using density gradient separation method . The osteo-genic inducers were compounds of Dexone , β - glycerophosphate sodium and vitamin C.

丙酮酸与三羧循环各中间产物等分别组合进行同时氧化时，可使线粒体的呼吸率接近或达到α-甘油磷酸的Q（O2）水平。

Combinations of pyruvate with some of the citric acid cycle intermediates individually also significantly enchanted the respiratory rate of mitochondrial preparations , which may approach or reach the level of α - glycerophosphate oxidation .

方法：对细胞使用钙化培养基（含p甘油磷酸钠，地塞米松和维生素C）促进主动脉瓣膜间质细胞向成骨细胞分化。

Objective : To establish the osteoblastic differentiation model of aortic valve interstitial cells by pro-calcific medium . Methods : Pro-calcific medium ( containing β - glycerophosphate disodium , dexamethasone and ascorbic acid ) was used to promote the osteoblastic differentiation of cultured cells .

采用β-甘油磷酸钠、维生素C、地塞米松联合诱导，使胎盘贴壁细胞分化为成骨细胞，诱导后10d行茜素红染色；

Cells of 3 passages were induced to differentiate into osteoblasts with vitamin C , dexamethasone and sodium β - glycerophosphate , and the induced cells were observed in the change of matrix mineralization with alizarin red staining ;

结果6个蛋白分别为海藻糖磷酸磷酸酶、铁钼蛋白A、莽草酸5脱氢酶、葡萄糖胺果糖6磷酸氨基转移酶、吲哚3甘油磷酸合成酶、TetR家族转录调控因子。

Results Six spots of proteins in gel were identified as trehalose-6-phosphate phosphatase , moaA , shikimate 5-dehydrogenase , glucosamine-fructose-6-phosphate aminotransferase , indole-3-glycerol phosphate synthase and TetR-family transcriptional regulator .

目的探讨可注射性温固化凝胶壳聚糖-甘油磷酸钠（C-GP）复合同种异体软骨细胞在体内形成透明软骨和注入关节腔后修复关节软骨缺损的可行性和有效性。

Objective To investigate the feasibility and the effectiveness of allograft chondrocytes mixed in the injectable thermosetting chitosan and glycerophosphate ( C-GP ) gel forming hyaline cartilage in vivo and repairing the whole layer defects of femur trochlea of rabbit keen joint .

植物磷酸脂是含有两个长链脂肪酸的甘油磷酸脂。

Plant phosphatides containing two long-chain fatty acids .

尾加压素Ⅱ加重β-甘油磷酸诱导的大鼠血管平滑肌细胞钙化

Urotensin ⅱ aggravated β - glycerophosphate-stimulated calcification in cultured rat vascular smooth muscle cells

采用β-甘油磷酸缓冲液提取食管上皮组织中糖原或含糖物质。

Glycogen from the esophageal mucous epithelium was extracted with β - glycerophosphate buffer .

根据磷酸盐与甘油磷酸钠的化学关系求得甘油磷酸钠的含量。

The content of sodium glycerophosphate was calculated according to chemical relationship of phosphorus and sodium glycerophosphate .

抗坏血酸、β-甘油磷酸钠和地塞米松联合诱导大鼠骨髓间充质干细胞向成骨细胞的分化

Differentiation of rat bone marrow mesenchymal stem cells into osteoblasts following induction of ascorbic acid , beta-sodium glycerophosphate and dexamethasone

有机磷（β-甘油磷酸二钠）存在时磷和镉的去除特点与磷酸盐存在时不同。

The removal characters of phosphorus and cadmium were different under organophosphorus ( disodium β - glycerophosphate ) and phosphate .

本实验制备了温敏性壳聚糖／β-甘油磷酸盐水凝胶，并探讨了这些关键因素对体系凝胶化过程的影响。

In this study we prepare thermo-sensitive chitosan / p-glycerol-phosphate and discuss the influence of these key factors on gelation .

结论：骨髓基质细胞作为构建组织工程骨的种子细胞在地塞米松、β-甘油磷酸、L-坏血酸诱导下成骨具有可靠的重复性。

Conclusion : The induced BMSCs with Dex 、β - Gp and AA is a reliable tool for the bone tissue engineer .

在细胞贴壁后，加入地塞米松、β-甘油磷酸和抗坏血酸，向成骨细胞定向诱导。

The adherent cells were treated with dexamethasone ( Dex ), ? - glycerophosphate ( GP ) and ascorbic acid to induce osteogenic differentiation .

部分在培养基中添加成骨诱导剂地塞米松，β-甘油磷酸钠及抗坏血酸向成骨细胞诱导分化。

The osteogenic inducer desamethasone ,β - sodium glycerophosphate and ascorbic acid were added in part of the culture medium , which were used to induce differentiation into osteoblast .

目前可注射壳聚糖生物水凝胶主要是通过加入多元醇或多元醛，如甘油磷酸钠溶液，在体温下，通过氢键等相互作用形成凝胶。

Most recent research showed that injectable chitosan hydrogels can form in suit at the body temperature by hydrogen bond interactions with multiple aldehydes or hydroxyl , such as glycerophosphate solution .

考查了细胞各部分镉和磷的积累，磷对细菌积累镉的影响，胞外聚合物的作用，并与以β-甘油磷酸二钠形式有机磷存在时镉的去除特点进行了对比。

Phosphorus and cadmium accumulation on cell , effects of phosphorus on cadmium accumulation , function of extracellular polymeric substances ( EPS ), and comparison with organophosphorus present as disodium β - glycerophosphate also included .

制备了壳聚糖/β-甘油磷酸钠/纳米磷酸钙（CS/GP/nCP）水凝胶，对水凝胶的凝胶时间、形貌、低温下的储存性能进行了表征。

Chitosan / β - glycerophosphate / nCP ( CS / GP / nCP ) hydrogel was prepared . Several properties of the hydrogel , such as gelation time , morphology and storage property at low temperature et al , were characterized as well .

七种不同抗冷性植物甘油-3-磷酸转酰酶mRNA二级结构研究

Study on the Predicted mRNA Secondary Structures of Plant Glycerol-3-Phosphate Acyltransferases

简并引物在PCR扩增甘油-3-磷酸转酰酶基因中的应用

Application of Degenerate Primers for Amplification of the Gene Encoding Glycerol-3-Phosphate Acyltransferase by Polymerase Chain Reaction

大鼠附睾精子膜甘油-3-磷酸胆碱含量变化的研究

Study of the glycerol-3-phosphorylcholine content on rat sperm membrane during epididymal transit

本研究从番茄叶片中分离到叶绿体甘油-3-磷酸酰基转移酶基因，并对该基因的表达和功能进行了分析。

In this study , we isolated and characterized chloroplast glycerol-3-phosphate acyltransferase gene from tomato .

从节点磷酸二羟丙酮和三磷酸甘油醛流向三磷酸甘油合成甘油的碳流量增加了67.2%，而流向三梭酸（TCA）循环的流量减少了26.9%。

At the same time , the carbon flux flowed toward glycerol-3-phosphate ( G3P ) to form glycerol from dihydroxyacetone phosphate ( DHAP ) and glyceraldehydes-3-phosphate ( GAP ) node increases 67.2 % , while the carbon flux flowed toward TCA cycle decreases 26.9 % .

国产染料配基层析介质分离纯化甘油激酶α-磷酸甘油脱氢酶和心肌黄酶

Purification of glycerokinase ,α - glycerophosphate dehydrogenase and diaphorase by dye-ligand chromatography