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29篇 您的检索式:作者名="Grogan SP"
    题名 作者 年代 出处 被引量
1被激光损伤软骨释放的凋亡因子诱导软骨细胞凋亡的研究显示文摘目的探讨组织损伤后凋亡信号怎样促进细胞的死亡进程。方法在激光照射后猪软骨块置培液中,在不同时间(3、6、9、12、24 h)收集的培液,即实验条件培养液(TCM),从未经激光照射的软骨块培液取得的为对照条件培养液(CCM)。软骨块继续培养28 d,用聚焦显微镜评价其受损区的进展。分离的软骨细胞单层放于 TCM、CCM 或正常培养液(NM)培养,阳性对照组单层细胞经紫外线照射10 min 后继续用正常培养液培养,培养24 h 后,收集细胞并用荧光标记物染色,经流式细胞仪分析。结果所有经 TCM 培养的细胞显现半胱氨酸蛋白水解酶(caspase)-3阳性、CMXRos 和一氧化氮信号减少或失去;经 CCM 或 NM 培养的细胞显现 caspase-3阴性、CMXRos 和一氧化氮信号完好;阳性对照组细胞显现 Caspase-3和 CMXRos 均阳性、一氧化氮信号减少或失去,代表处于凋亡早期的细胞。不同 TCM 浓度(100%、50%、25%、12.5%)和时间(0.5、1、3、9、12 h)对细胞作用后,所有细胞均呈现 caspase-3阳性、CMXRos 和一氧化氮信号减少或失去。结论激光照射受损软骨释放凋亡因子,可诱导单层细胞死亡。郑敏 Grogan SP Schaffner T Mainil-Varlet P 2007中华医学杂志2007,87,21:3
2Chondromyxoid fibro- ma resembles in vitro chondrogenesis,but differs in expres- sion of signalling molecules显示文摘Romeo S Bov6e JV Grogan SP 2005J Pathol2005,206,2:1
3A study of recurrence and death from papillary thyroid cancer with 27 years of median follow-up显示文摘Grogan RH Kaplan SP Cao H 2013Surgery2013,154,6:1
4Tissue neogenesis and STRO-1 expression in immature and mature articular cartilage显示文摘Otsuki S Grogan SP Miyaki S 0,,1:1
5Repression of chondrogenesis through binding of notch signaling proteins HES-1 and HEY-1 to N-box domains in the COL2A1 enhancer site显示文摘Grogan SP Olee T Hiraoka K 0,,09:1
6Repression of chondrogenesis through binding of notch signaling proteins HES-1 and HEY-1 to N-box domains in the COL2A1 enhancer site 显示文摘Grogan SP Olee T Himoka K Arthritis Rheum0,58,9:1
7Repression of chondrogenesis through binding of notch signaling proteins HES-1 and HEY-1 to N-box domains in the COL2A1 en- hancer site显示文摘Grogan SP Olee T Hiraoka K Lotz MK 2008Arthritis Rheum2008,58,:1
8Repression of chondrogen- esis through binding of notch signaling proteins HES-1 and HEY- 1 to N-box domains in the COL2A1 enhancer site 显示文摘Grogan SP Olee T Hiraoka K 2008Arthritis Rheum2008,58,9:1
9Repression of chon- drogenesis through binding of notch signaling proteins HES1 and HEY1 to N-box domains in the COL2A1 enhancer site 显示文摘Grogan SP Olee T Hiraoka K 2008Arthritis Rheum2008,58,9:1
10Immunophenotypic analysis of human articular chondrocytes:changes in surface markers associated with cel expansion in monolayer culture显示文摘Diaz-Romero J Gail ard JP Grogan SP 0,,03:1
11Expansionon specific substrates regulates the phenotype and differ-entiation capacity of human articular chondrocytes 显示文摘Barbero A Grogan SP Mainil-Varlet P 2006JCell Bioc2006,98,5:1
12Osteoarthritis: detection, pathophysiotogy, and current/future treatment strategies 显示文摘Sovani S Grogan SP 2013Orthop Nurs2013,32,1:1
13Tissue engineering ofbiphasic cartilage constructs using various biodegradable scaffolds: an in vitro study显示文摘Wang X Grogan SP Rieser F 2004Biomaterials2004,25,17:1
14Immunophenotypic changes of human articular chondrocytes during monolayer culture reflect bona fide dedifferentiation rather than amplification of progenitor cel s显示文摘Diaz-Romero J Nesic D Grogan SP 0,,01:1
15Visual histological grading system for the evalua-tion of in vitro-generated neocartilage显示文摘Grogan SP Brabero A 2006Tissue Eng2006,8,:1
16Repression of chondrogenesis through binding of notch signaling proteins hes-1 and hey-1 to n-box domains in the COL2A1 enhancer site显示文摘Grogan SP Olee T Hiraoka K 2008Arthritis Rheum2008,58,9:1
17Mesenchymal progenitor cell markers in human articular cartilage: normal distribution and changes in osteoarthritis 显示文摘Grogan SP Miyaki S Asahara H 2009Arthritis Res Ther2009,11,3:1
18Digital micromir- ror device projection printing system for meniscus tissue engineering 显示文摘Grogan SP Chung PH Soman P 2013Aeta Biomater2013,9,7:1
19Immunophenotypic analysis of human articular chondrocytes:changes in surface markers associated with cel expansion in monolayer culture显示文摘Diaz-Romero J Gail ard JP Grogan SP 0,,03:1
20Immunophenotypic changes of human articular chondrocytes during monolayer culture reflect bona fide dedifferentiation rather than amplification of progenitor cel s显示文摘Diaz-Romero J Nesic D Grogan SP 0,,01:1
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