期刊文献+
共找到5篇文章
< 1 >
每页显示 20 50 100
随机定位模拟微重力促进人前破骨细胞增殖和分化 被引量:7
1
作者 狄升蒙 田宗成 +3 位作者 高翔 骞爱荣 maria luisa brandi 商澎 《航天医学与医学工程》 CAS CSCD 北大核心 2012年第1期13-17,共5页
目的观察随机定位模拟微重力对人前破骨细胞FLG29.1增殖和分化的影响。方法 FLG29.1细胞分为正常对照组与随机定位处理组,分别培养72 h后收集细胞。采用细胞计数法检测细胞总数和活细胞数;流式细胞术检测细胞周期;Griess法检测培养基中N... 目的观察随机定位模拟微重力对人前破骨细胞FLG29.1增殖和分化的影响。方法 FLG29.1细胞分为正常对照组与随机定位处理组,分别培养72 h后收集细胞。采用细胞计数法检测细胞总数和活细胞数;流式细胞术检测细胞周期;Griess法检测培养基中NO(nitric oxide,NO)浓度;抗酒石酸盐酸性磷酸酶(TRAP)染色计算TRAP阳性细胞比例;对硝基苯磷酸(pNPP)法检测胞内TRAP活性。结果随机定位处理后,FLG29.1细胞增殖能力与活细胞比例均较对照组明显增加;细胞周期分布发生变化,处于G1期的细胞比例增加;培养基中NO浓度有增加趋势;在回转处理的同时添加诱导剂12-氧-十四烷酰佛波醋酸酯-13乙酸酯(TPA),发现TRAP阳性细胞数量增多;胞内TRAP活性较对照组明显增加。结论随机定位模拟微重力提高了FLG29.1细胞活力并促进其向破骨细胞分化。 展开更多
关键词 模拟微重力 破骨细胞 随机定位仪
下载PDF
WJSC 6^(th) Anniversary Special Issues(2):Mesenchymal stem cellsAdipose mesenchymal stem cells in the field of bone tissue engineering 被引量:5
2
作者 Cecilia Romagnoli maria luisa brandi 《World Journal of Stem Cells》 SCIE CAS 2014年第2期144-152,共9页
Bone tissue engineering represents one of the most challenging emergent fields for scientists and clinicians.Current failures of autografts and allografts in many pathological conditions have prompted researchers to f... Bone tissue engineering represents one of the most challenging emergent fields for scientists and clinicians.Current failures of autografts and allografts in many pathological conditions have prompted researchers to find new biomaterials able to promote bone repair or regeneration with specific characteristics of biocompatibility,biodegradability and osteoinductivity.Recent advancements for tissue regeneration in bone defects have occurred by following the diamond concept and combining the use of growth factors and mesenchymal stem cells(MSCs).In particular,a more abundant and easily accessible source of MSCs was recently discovered in adipose tissue.These adipose stem cells(ASCs)can be obtained in large quantities with little donor site morbidity or patient discomfort,in contrast to the invasive and painful isolation of bone marrow MSCs.The osteogenic potential of ASCs on scaffolds has been examined in cell cultures and animal models,with only a few cases reporting the use of ASCs for successful reconstruction or accelerated healing of defects of the skull and jaw in patients.Although these reports extend our limited knowledge concerning the use of ASCs for osseous tissue repair and regeneration,the lack of standardization in applied techniques makes the comparison between studies difficult.Additional clinical trials are needed to assess ASC therapy and address potential ethical and safety concerns,which must be resolved to permit application in regenerative medicine. 展开更多
关键词 Adipose-derived stem cells Bone tissue engineering OSTEOGENIC DIFFERENTIATION SCAFFOLD REGENERATIVE medicine
下载PDF
Biliary tree gastrinomas in multiple endocrine neoplasia type 1 syndrome 被引量:3
3
作者 Francesco Tonelli Francesco Giudici +2 位作者 Gabriella Nesi Giacomo Batignani maria luisa brandi 《World Journal of Gastroenterology》 SCIE CAS 2013年第45期8312-8320,共9页
AIM:To describe our patients affected with ectopic biliary tree gastrinoma and review the literature on this topic.METHODS:Between January 1992 and June 2012,28 patients affected by duodenopancreatic endocrine tumors ... AIM:To describe our patients affected with ectopic biliary tree gastrinoma and review the literature on this topic.METHODS:Between January 1992 and June 2012,28 patients affected by duodenopancreatic endocrine tumors in multiple endocrine neoplasia type 1(MEN1)syndrome underwent surgery at our institution.This retrospective review article analyzes our experience regarding seventeen of these patients subjected to duodenopancreatic surgery for Zollinger-Ellison syndrome(ZES).Surgical treatment consisted of duodenopancreatectomy(DP)or total pancreatectomy(TP).Regional lymphadenectomy was always performed.Any hepatic tumoral lesions found were removed during surgery.In MEN1 patients,removal of duodenal lesions can sometimes lead to persistence or recurrence of hypergastrinemia.One possible explanation for this unfavorable outcome could be unrecognized ectopic localization of gastrin-secreting tumors.This study described three cases among the seventeen patients who were found to have an ectopic gastrinoma located in the biliary tree.RESULTS:Seventeen MEN1 patients affected with ZES were analyzed.The mean age was 40 years.Fifteen patients underwent DP and two TP.On histopathological examination,duodeno pancreatic endocrine tumors were found in all 17 patients.Eighty-one gastrinomas were detected in the first three portions of the duodenum.Only one gastrinoma was found in the pancreas.The mean number of gastrinomas per patient was 5(range 1-16).Malignancy was established in 12 patients(70.5%)after lymph node,liver and omental metastases were found.Three patients exhibited biliary tree gastrinomas as well as duodenal gastrinoma(s).In two cases,the ectopic gastrinoma was removed at the same time as pancreatic surgery,while in the third case,the biliary tree gastrinoma was resected one year after DP because of recurrence of ZES.CONCLUSION:These findings suggest the importance of checking for the presence of ectopic gastrinomas in the biliary tree in MEN1 patients undergoing ZES surgery. 展开更多
关键词 GASTRINOMA Multiple endocrine NEOPLASIA TYPE 1 Zollinger-Ellison SYNDROME Ectopic GASTRINOMA Biliary tree DUODENOPANCREATECTOMY
下载PDF
Ten years of hip fractures in Italy: For the first time a decreasing trend in elderly women 被引量:2
4
作者 Prisco Piscitelli Maurizio Feola +10 位作者 Cecilia Rao Monica Celi Elena Gasbarra Cosimo Neglia Giuseppe Quarta Federico maria Liuni Simone Parri Giovanni Iolascon maria luisa brandi Alessandro Distante Umberto Tarantino 《World Journal of Orthopedics》 2014年第3期386-391,共6页
AIM:To evaluate the hospitalization rate of femoralneck fractures in the elderly Italian population over ten years.METHODS:We analyzed national hospitalizations records collected at central level by the Ministry of He... AIM:To evaluate the hospitalization rate of femoralneck fractures in the elderly Italian population over ten years.METHODS:We analyzed national hospitalizations records collected at central level by the Ministry of Health from 2000 to 2009.Age-and sex-specific rates of fractures occurred at femoral neck in people≥65 years old.We performed a sub-analysis over a three-year period(2007-2009),presenting data per five-year age groups,in order to evaluate the incidence of the hip fracture in the oldest population.RESULTS:We estimated a total of 839008 hospitalizations due to femoral neck fractures between 2000 and2009 in people≥65,with an overall increase of 29.8%over 10 years.The incidence per 10000 inhabitants remarkably increased in people≥75,passing from158.5 to 166.8(+5.2%)and from 72.6 to 77.5(+6.8%)over the ten-year period in women and men,respectively.The oldest age group(people>85 years old)accounted for more than 42%of total hospital admissions in 2009(n=39000),despite representing only 2.5%of the Italian population.Particularly,women aged>85accounted for 30.8%of total fractures,although they represented just 1.8%of the general population.The results of this analysis indicate that the incidence of hip fractures progressively increased from 2000 to 2009,but a reduction can be observed for the first time in women≤75(-7.9%between 2004 and 2009).CONCLUSION:Incidence of hip fractures in Italy are continuously increasing,although women aged 65-74years old started showing a decreasing trend. 展开更多
关键词 FEMORAL FRACTURES Hip FRAGILITY FRACTURES Osteoporosis HOSPITALIZATIONS Incidence
下载PDF
Genetic test in multiple endocrine neoplasia type 1 syndrome: An evolving story 被引量:2
5
作者 Francesca Marini Francesca Giusti maria luisa brandi 《World Journal of Experimental Medicine》 2015年第2期124-129,共6页
Multiple endocrine neoplasia type 1(MEN1) is an autosomal dominant inherited tumour syndrome expressing various endocrine and non-endocrine lesions and tumours. Since the identification of the causative gene, the onco... Multiple endocrine neoplasia type 1(MEN1) is an autosomal dominant inherited tumour syndrome expressing various endocrine and non-endocrine lesions and tumours. Since the identification of the causative gene, the oncosuppressor gene MEN1, in 1997, genetic testing has revealed an important approach for the early and differential diagnosis of the disease. The finding of a MEN1 mutation in a patient has important clinical implications for relatives since it allows very early disease diagnosis and identification of carriers, even before biochemical and/or clinical manifestation, permitting their inclusion in a specific program of surveillance and subsequent praecox therapy. Currently, genetic testing for MEN1 consists principally of the sequencing of coding regions and intron-exon junctions of the MEN1 gene. However, the recent acquisition of novel high throughput technologies will allow the design of innovative, accurate, complete and rapid genetic diagnosis. These new tools are able to increase the strength of the analysis and almost completely eliminate the possibility of false negative results. This review aims to give an overview on genetic testing of MEN1 syndrome, reporting the positive aspects of performing the analysis and the future perspectives for improving the performance of the test, as well as its application in clinical practice. 展开更多
关键词 Multiple ENDOCRINE NEOPLASIA TYPE 1 Genetic test Clinical practice Next-generation SEQUENCING
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部