|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Microsatellite 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 | 2002 | International Journal for Parasitology2002,,1: | 1 |
| 2 | Fractures of the femur after hip replacement显示文摘 | Duncan CP Maris BA | 1995 | Instr Course Lect1995,44,: | 1 |
| 3 | Psychosocial 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 | 2003 | Journal of General Internal Medicine2003,,7: | 1 |
| 4 | Determination 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 | 2008 | JAIDS Journal of Acquired Immune Deficiency Syndromes2008,,1: | 1 |
| 5 | Sequence analysis of Toll- like receptor genes 1-10 of goat (Capra hircus)显示文摘 | Raja A Vignesh AR Mary BA | 2011 | Vet 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 |
| 7 | Hybrids 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 | 2020 | Nano Research2020,13,10: | 1 |
| 8 | The pathology of cervical cancer显示文摘 | Caitriona BA Elainc WK Mary BL | 1995 | Clin Obstert Gynecol1995,38,: | 1 |
| 9 | Allergic 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 | 2006 | JAm Acad Dermatol2006,55,2: | 1 |
| 10 | Absorption of clindamycin after intravaginnal administration of clindamycin phosphate ovule or cream显示文摘 | Marie T Borin KK Ryan BA | 2003 | J Clin Pharmacol2003,43,4: | 1 |
| 11 | Saccharomyces 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 | 2023 | World Journal of Gastroenterology2023,29,5: | 1 |
| 12 | Microsatellite 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 | 2002 | International Journal for Parasitology2002,,1: | 1 |
| 13 | International 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 | 2007 | Lancet2007,370,9589: | 1 |
| 14 | Approaches to staging sleep in polysom-nographic studies with epileptic activity 显示文摘 | Mary L Marzec BA | | Sleep medicine0,,: | 1 |