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12篇 您的检索式:作者名="Less C A"
    题名 作者 年代 出处 被引量
1Problematic internet use: Proposed classification and diagnostic criteria 显示文摘Shapira N A Lessing M C 2003Depression and Anxiety2003,,17:1
2Construction of a mutant and characterization of the role of the vaccine antigen P6 in outer membrane integrity of nontypeable Haemophilus influenzae 显示文摘Murphy T F Kirkham C Lesse A J 2006Infect Immun2006,74,9:1
3A strategic contingencies theory of intrao- rganizational power 显示文摘Hiekson D J Hinings C R Less C A Schneck R E Pennings J M 1971Administrative Science Quar- terly1971,16,2:1
4Low-temperature hydrogen transport using a palladium/copper membrane显示文摘Lessing P A Wood H C Zunk L D 0,,11:1
5Electrophoretic deposition applied to reaction joining of silicon carbide and silicon nitride ceramics 显示文摘Lessing P A Erickson A W Kunerth D C 2000J Mater Sci2000,,35:1
6Construction of a mutant and characterization of the role of the vaccine antigen P6 in outer membrane integrity of nontypeable Haemophilus influ- enzae 显示文摘Murphy T F Kirkham C Lesse A J 2006Infection Immunity2006,74,:1
7Inkjet printing of conductive inks with high lateral resolution on omniphob ic 'RF Paper' for paper-based electronics and MEMS显示文摘Lessing J Glavan A C Walker S B 2014Advanced Materials2014,26,27:1
8When sould healthcare workers be screened for methicillin- resistant Staphlococcus aureus 显示文摘Lessing M P A Jordem J Z Bowler I C J 1996J Hosp Infect1996,34,:1
9Con-struction of a mutant and characterization of the role of the vaccine antigen P6in outer membrane integrity of nontypeable Haemophilus influenzae显示文摘MURPHY T F KIRKHAM C LESSE A J 2006Infect Immun2006,74,:1
10Thermal cycling of siliconized-SiC at hightemperatures显示文摘Lessing P A Erickson A W Kunerth D C 2001Journal of Materials Science2001,36,:1
11Thermal cycling of siliconized-SiC at high temperature显示文摘LESSING P A ERICKSON A W KUNERTH D C 2001Journal of Materials Science2001,36,6:1
12Investigational growth factors utilized in animal models of spinal fusion: Systematic review显示文摘BACKGROUND Over 400000 Americans annually undergo spinal fusion surgeries, yet up to 40%of these procedures result in pseudoarthrosis even with iliac crest autograft, the current 'gold standard' treatment. Tissue engineering has the potential to solve this problem via the creation of bone grafts involving bone-promoting growth factors(e.g., bone morphogenetic protein 2). A broad assessment of experimental growth factors is important to inform future work and clinical potential in this area. To date, however, no study has systematically reviewed the investigational growth factors utilized in preclinical animal models of spinal fusion.AIM To review all published studies assessing investigational growth factors for spinal fusion in animal models and identify promising agents for translation.METHODS We conducted a systematic review of the literature using PubMed, Embase,Cochrane Library, and Web of Science databases with searches run on May 29 th,2018. The search query was designed to include all non-human, preclinical animal models of spinal fusion reported in the literature without a timespan limit. Extracted data for each model included surgical approach, level of fusion,animal species and breed, animal age and sex, and any other relevant characteristics. The dosages/sizes of all implant materials, spinal fusion rates,and follow-up time points were recorded. The data were analyzed and the results reported in tables and text. PRISMA guidelines were followed for this systematic review.RESULTS Twenty-six articles were included in this study, comprising 14 experimental growth factors: AB204(n = 1); angiopoietin 1(n = 1); calcitonin(n = 3);erythropoietin(n = 1); basic fibroblast growth factor(n = 1); growth differentiation factor 5(n = 4), combined insulin-like growth factor 1 +transforming growth factor beta(n = 4); insulin(n = 1); NELL-1(n = 5); noggin(n= 1); P-15(n = 1); peptide B2 A(n = 2); and secreted phosphoprotein 24(n = 1).The fusion rates of the current gold standard treatment(autologous iliac crest bone graft, ICBG) and the leading clinically used growth factor(BMP-2) ranged widely in the included studies, from 0-100% for ICBG and from 13%-100% for BMP-2. Among the identified growth factors, calcitonin, GDF-5, NELL-1, and P-15 resulted in fusion rates of 100% in some cases. In addition, six growth factors-AB204, angiopoietin 1, GDF-5, insulin, NELL-1, and peptide B2 A-resulted in significantly enhanced fusion rates compared to ICBG, BMP-2, or other internal control in some studies. Large heterogeneity in animal species, fusion method,and experimental groups and time points was observed across the included studies, limiting the direct comparison of the growth factors identified herein.CONCLUSION Several promising investigational growth factors for spinal fusion have been identified herein; directly comparing the fusion efficacy and safety of these agents may inform clinical translation.Ethan Cottrill A Karim Ahmed Noah Lessing Zachary Pennington Wataru Ishida Alexander Perdomo-Pantoja Sheng-fu Lo Elizabeth Howell Christina Holmes C Rory Goodwin Nicholas Theodore Daniel M Sciubba Timothy F Witham 2019World Journal of Orthopedics2019,10,4:0
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