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14篇 您的检索式:作者名="Maris BA"
    题名 作者 年代 出处 被引量
1Microsatellite analysis of Toxoplasma gondii shows considerable polymorphism structured into two main clonal groups显示文摘Daniel Ajzenberg Anne-Laure Ba?uls Michel Tibayrenc Marie Laure Dardé 2002International Journal for Parasitology2002,,1:1
2Fractures of the femur after hip replacement显示文摘Duncan CP Maris BA 1995Instr Course Lect1995,44,:1
3Psychosocial intervention for rural women with breast cancer显示文摘Dr. Karyn L. Angell PhD Mary Anne Kreshka MA Rebecca McCoy MSW Patricia Donnelly RN Julie M. Turner-Cobb PhD Kathy Graddy BA Helena C. Kraemer PhD Cheryl Koopman PhD 2003Journal of General Internal Medicine2003,,7:1
4Determination of Clinically Relevant Cutoffs for HIV-1 Phenotypic Resistance Estimates Through a Combined Analysis of Clinical Trial and Cohort Data显示文摘Bart Winters Julio Montaner P Richard Harrigan Brian Gazzard Anton Pozniak Michael D Miller Sean Emery Frank van Leth Patrick Robinson John D Baxter Marie Perez-Elias Delivette Castor Scott Hammer Alex Rinehart Hans Vermeiren Elke Van Craenenbroeck Lee Ba 2008JAIDS Journal of Acquired Immune Deficiency Syndromes2008,,1:1
5Sequence analysis of Toll- like receptor genes 1-10 of goat (Capra hircus)显示文摘Raja A Vignesh AR Mary BA 2011Vet Immunol Im- munopathol2011,140,34:1
6应用UW液储存待植皮片的改良储皮法——皮片的储存显示文摘目的 营养液可延长移植物的存储时间。本文将探讨应用Wisconsin大学保存液(UW液)灌注组织(皮瓣),使其耐受缺血,以延长皮片保存时间和提高延期移植的成活率。方法设计小鼠模型,评估待植断层皮片及全厚皮片在普通生理盐水、UW液和Roswell Park Memorial Institute(RPMI)-1640培养基中的活力。将取下的皮片在4℃下分别储存1,2,4,7,10d,然后回植并分别测定其成活百分率。结果在储存期内,保存在UW液中的断层皮片与在生理盐水和RPMI—1640中的相比,植皮效果明显改善;而3种液体保存的全厚皮片无明显差异。结论选用UW液储存断层皮片进行异体植皮或延期植皮可延长储皮时间,并可在保质期内明显改善植皮效果。本研究发现,更厚的皮片厚度会限制保存液的渗透力,从而限制储存全厚皮片的能力。Mark W Kiehn rryler Staelin Mary Nutt BA David Robinson Michael L Bentz 王娜(译者) 张晨(译) 2010中国美容整形外科杂志2010,21,3:1
7Hybrids of gold nanoparticles and oligo(p-phenyleneethynylene)s end-functionalized with alkynylruthenium groups:Outstanding two-photon absorption in the second biological window显示文摘Oligo(p-phenyleneethynylene)s(OPEs)end-capped with(alkynyl)bis(diphosphine)ruthenium and thiol/thiolate groups stabilize ca.2 nm diameter gold nanoparticles(AuNPs).The morphology,elemental composition and stability of the resultant organometallic OPE/AuNP hybrid materials have been defined using a combination of molecular-and nano-material chacterization techniques.The hybrids display long-term stability in solution(more than a month),good solubility in organic solvents,reversible rutheniumcentered oxidation,and transparency beyond 800 nm,and possess very strong nonlinear absorption activity at the first biological window,and unprecedented two-photon absorption activity in the second biological window(σ2 up to 38,000 GM at 1,050 nm).Cristóbal Quintana Mahbod Morshedi Jun Du Joseph P.L.Morrall Jan K.Zaręba Marek Samoc Marie P.Cifuentes Mark G.Humphrey 2020Nano Research2020,13,10:1
8The pathology of cervical cancer显示文摘Caitriona BA Elainc WK Mary BL 1995Clin Obstert Gynecol1995,38,:1
9Allergic contact dermatitis from a natural deodorant: A report of 4 cases associated with lichen acid mix allergy显示文摘Mary Sheu MD Eric L Simpson MD Sandra V Law BA 2006JAm Acad Dermatol2006,55,2:1
10Absorption of clindamycin after intravaginnal administration of clindamycin phosphate ovule or cream显示文摘Marie T Borin KK Ryan BA 2003J Clin Pharmacol2003,43,4:1
11Saccharomyces cerevisiae prevents postoperative recurrence of Crohn's disease modeled by ileocecal resection in HLA-B27 transgenic rats显示文摘BACKGROUND Postoperative recurrence(POR)after ileocecal resection(ICR)affects most Crohn's disease patients within 3-5 years after surgery.Adherent-invasive Escherichia coli(AIEC)typified by the LF82 strain are pathobionts that are frequently detected in POR of Crohn's disease and have a potential role in the early stages of the disease pathogenesis.Saccharomyces cerevisiae CNCM I-3856 is a probiotic yeast reported to inhibit AIEC adhesion to intestinal epithelial cells and to favor their elimination from the gut.AIM To evaluate the efficacy of CNCM I-3856 in preventing POR induced by LF82 in an HLA-B27 transgenic(TgB27)rat model.METHODS Sixty-four rats[strain F344,38 TgB27,26 control non-Tg(nTg)]underwent an ICR at the 12th wk(W12)of life and were sacrificed at the 18th wk(W18)of life.TgB27 rats were challenged daily with oral administration of LF82(109 colony forming units(CFUs)/day(d),n=8),PBS(n=5),CNCM I-3856(109 CFUs/d,n=7)or a combination of LF82 and CNCM I-3856(n=18).nTg rats receiving LF82(n=5),PBS(n=5),CNCM I-3856(n=7)or CNCM I-3856 and LF82(n=9)under the same conditions were used as controls.POR was analyzed using macroscopic(from 0 to 4)and histologic(from 0 to 6)scores.Luminal LF82 quantifications were performed weekly for each animal.Adherent LF82 and inflammatory/regulatory cytokines were quantified in biopsies at W12 and W18.Data are expressed as the median with the interquartile range.RESULTS nTg animals did not develop POR.A total of 7/8(87%)of the TgB27 rats receiving LF82 alone had POR(macroscopic score≥2),which was significantly prevented by CNCM I-3856 administration[6/18(33%)TgB27 rats,P=0.01].Macroscopic lesions were located 2 cm above the anastomosis in the TgB27 rats receiving LF82 alone and consisted of ulcerations with a score of 3.5(2-4).Seven out of 18 TgB27 rats(39%)receiving CNCM I-3856 and LF82 had no macroscopic lesions.Compared to untreated TgB27 animals receiving LF82 alone,coadministration of CNCM I-3856 and LF82 significantly reduced the macroscopic[3.5(2-4)vs 1(0-3),P=0.002]and histological lesions by more than 50%[4.5(3.3-5.8)vs 2(1.3-3),P=0.003].The levels of adherent LF82 were correlated with anastomotic macroscopic scores in TgB27 rats(r=0.49,P=0.006),with a higher risk of POR in animals having high levels of luminal LF82(71.4%vs 25%,P=0.02).Administration of CNCM I-3856 significantly reduced the levels of luminal and adherent LF82,increased the production of interleukin(IL)-10 and decreased the production of IL-23 and IL-17 in TgB27 rats.CONCLUSION In a reliable model of POR induced by LF82 in TgB27 rats,CNCM I-3856 prevents macroscopic POR by decreasing LF82 infection and gut inflammation.Caroline Valibouze Silvia Speca Caroline Dubuquoy Florian Mourey Lena M'Ba Lucil Schneider Marie Titecat Benoît Foligné Michaël Genin Christel Neut Philippe Zerbib Pierre Desreumaux 2023World Journal of Gastroenterology2023,29,5:1
12Microsatellite analysis of Toxoplasma gondii shows considerable polymorphism structured into two main clonal groups显示文摘Daniel Ajzenberg Anne-Laure Ba?uls Michel Tibayrenc Marie Laure Dardé 2002International Journal for Parasitology2002,,1:1
13International variation in the prevalence of COPD (the BOLD Study): a population-based prevalence study显示文摘Sonia BA Mary Ann M Vollmer WM Suzanne G 2007Lancet2007,370,9589:1
14Approaches to staging sleep in polysom-nographic studies with epileptic activity 显示文摘Mary L Marzec BA Sleep medicine0,,:1
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