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Saunders, Philadelphia.",{},{"id":24,"text":417,"url":24,"identifiers":418},"Potts, J. T. Jr., and Roberts, B. (1958). Amer. J. med. Sci., 235, 206.",{"doi":419},"10.1097\u002F00000441-195802000-00014",{"id":24,"text":421,"url":24,"identifiers":422},"Randall, R. E. Jr., Rossmeisl, E. C., and Bleifer, K. H. (1959). Ann.",{},{"id":24,"text":424,"url":24,"identifiers":425},"Schachter, D. (1959). J. Lab. Clin. Med., 54, 763.",{},{"id":24,"text":427,"url":24,"identifiers":428},"Silverman, S. H., and Gardner, L. I. (1954). NewEngl.J. Med., 250.938.",{},{"id":24,"text":430,"url":24,"identifiers":431},"Simonsen, D. G., Westover, L. M., and Wertman, M. (1947). J. biol. Chem., 169, 39.",{"doi":432},"10.1016\u002FS0021-9258(17)35058-5",{"id":24,"text":434,"url":24,"identifiers":435},"Smith, W. O., and Eliel, L. P. (1956). Clin. Res. Proc., 4, 245.",{},{"id":24,"text":437,"url":24,"identifiers":438},"Vallee, B. L., Wacker, W. E. C., and Ulmer, D. D. (1960). New Engl. J. Med., 262, 155.",{"doi":439},"10.1056\u002FNEJM196001282620401",{"id":24,"text":441,"url":24,"identifiers":442},"Van Fossan, D. D., Baird, E. E., and Tekell, G. S. (1959). Amer. J. clin. Path., 31, 368.",{"doi":443},"10.1093\u002Fajcp\u002F31.4_ts.368",{"id":24,"text":445,"url":24,"identifiers":446},"Wacker, W. E. C., and Vallee, B. L. (1957). New Engl. J. Med., 257, 1254.",{"doi":447},"10.1056\u002FNEJM195712262572602",{"id":24,"text":449,"url":24,"identifiers":450},"Walker, B. S., and Walker, E. W. (1936). J. Lab. clin. Med., 21, 713.",{},{"id":24,"text":452,"url":24,"identifiers":453},"Watchorn, E., and McCance, R. A. (1932). Biochem. J., 26, 54.",{"doi":454},"10.1042\u002Fbj0260054",{"id":24,"text":456,"url":24,"identifiers":457},"Watchorn, E., and McCance, R. A. (1937). Ibid., 31, 1379.",{},{"id":459,"createTime":460,"updateTime":461,"relativeEntities":462,"slug":463,"properties":464,"entityType":109,"verifyStatus":110,"verifyTime":460,"verifyNote":111,"languages":485,"translateLanguages":486,"viewCount":25,"primaryUrl":488,"fullTextUrl":24,"authors":489,"publicationType":133,"publisherRelationship":507,"citationCount":550,"citationInfo":551,"publishDate":279,"publishYear":277,"citationAnalyzeStatus":23,"lastCitationAnalyze":461,"indexDatabases":569,"openAccess":24,"references":570,"isForceReanalyzing":187},"acab8de1-6d79-47dc-8077-700835871f0b","2025-01-07T20:20:44.102+00:00","2026-03-29T15:09:29.279+00:00",[],"Methicillin-resistant-staphylococci",{"mag":465,"gsPaper":467,"keywords":469,"pmc":471,"openalex":473,"abstract":475,"title":478,"pm":481,"doi":483},{"VOID":466},"2123689798",{"VOID":468},"[\"13170130993465289031\"]",{"VI":470},"Staphylococcus, kháng methicillin, kháng thuốc, penicillin, nghiên cứu vi sinh",{"VOID":472},"480239",{"VOID":474},"W2123689798",{"VI":476,"EN":477},"\u003Cjats:p>Hai mươi bốn dòng vi khuẩn \u003Cjats:italic>Staph. pyogenes\u003C\u002Fjats:italic> (chín dòng nhạy cảm với penicillin và chín dòng có khả năng phá hủy penicillin) đã được nuôi cấy qua 40 đến 50 lần trên bề mặt đĩa Celbenin\u003Cjats:sup>1\u003C\u002Fjats:sup>.\u003C\u002Fjats:p>\u003Cjats:p>Tất cả các dòng vi khuẩn đều phát triển khả năng kháng lại Celbenin và tám dòng (bốn dòng nhạy cảm với penicillin và bốn dòng có khả năng phá hủy penicillin) có thể phát triển trong môi trường chứa 100 μg\u002Fml Celbenin hoặc cao hơn. Sự kháng thuốc này thuộc kiểu kháng thuốc có khả năng chịu đựng và không có văn hóa nào làm bất hoạt Celbenin. Có sự gia tăng liên quan trong khả năng chịu đựng với benzyl penicillin.\u003C\u002Fjats:p>\u003Cjats:p>Các dòng vi khuẩn có khả năng kháng Celbenin cao được tách ra từ các chủng staphylococci phá hủy penicillin hoàn toàn khác biệt với những dòng từ các chủng nhạy cảm với penicillin, cũng như với các staphylococci có khả năng chịu đựng penicillin G được tách ra \u003Cjats:italic>in vitro\u003C\u002Fjats:italic>, bởi vì chúng vẫn giữ được các đặc điểm văn hóa, hoạt tính đông tụ và hoạt tính hủy huyết, cùng với độ độc lực trên chuột của các dòng mẹ, và mức độ kháng thuốc vẫn ổn định sau nhiều lần nuôi cấy trong môi trường không có Celbenin.\u003C\u002Fjats:p>\u003Cjats:p>Ba dòng vi khuẩn kháng Celbenin xảy ra tự nhiên của \u003Cjats:italic>Staph. pyogenes\u003C\u002Fjats:italic> tách ra từ các quá trình nhiễm trùng cũng đã được nghiên cứu. Cả ba dòng đều phát triển mạnh mẽ trong nồng độ Celbenin lên đến 12,5 μg\u002Fml nhưng rất kém trong các nồng độ cao hơn.\u003C\u002Fjats:p>\u003Cjats:p>Ý nghĩa khả thi của những phát hiện này sẽ được thảo luận.\u003C\u002Fjats:p>","\u003Cjats:p>Eighteen strains of\u003Cjats:italic>Staph. pyogenes\u003C\u002Fjats:italic>(nine penicillin-sensitive and nine penicillin-destroying) were passaged 40 to 50 times on Celbenin\u003Cjats:sup>1\u003C\u002Fjats:sup>ditch plates.\u003C\u002Fjats:p>\u003Cjats:p>All strains developed an increase in resistance to Celbenin and eight strains (four penicillin-sensitive and four penicillin-destroying) were able to grow in 100 μg\u002Fml. or more Celbenin. Resistance was of the drug-tolerant type and none of the cultures inactivated Celbenin. There was an associated increase in tolerance to benzyl penicillin.\u003C\u002Fjats:p>\u003Cjats:p>The highly Celbenin-resistant cultures isolated from penicillin-destroying staphylococci were in sharp contrast to those from penicillin-sensitive strains, as well as to penicillin G-tolerant staphylococci isolated\u003Cjats:italic>in vitro\u003C\u002Fjats:italic>, because they retained the cultural characteristics, coagulase and haemolytic activity, and mouse virulence of the parent strains, and the degree of resistance remained stable after repeated passage in the absence of Celbenin.\u003C\u002Fjats:p>\u003Cjats:p>Three naturally occurring Celbenin-resistant strains of\u003Cjats:italic>Staph. pyogenes\u003C\u002Fjats:italic>isolated from infective processes were also studied. All three strains grew luxuriantly in concentrations of Celbenin up to 12·5 μg\u002Fml. but very poorly in higher concentrations.\u003C\u002Fjats:p>\u003Cjats:p>The possible significance of these findings is discussed.\u003C\u002Fjats:p>",{"EN":479,"VI":480},"Methicillin-resistant staphylococci","Staphylococcus kháng methicillin",{"VOID":482},"13686776",{"VOID":484},"10.1136\u002Fjcp.14.4.385",[113],[487],"VI","https:\u002F\u002Fjcp.bmj.com\u002Flookup\u002Fdoi\u002F10.1136\u002Fjcp.14.4.385",[490],{"id":491,"sortIndex":25,"researcher":24,"roles":492,"affiliations":493,"properties":502},"b2831354-e38c-4cd1-bd68-617eea252917",[],[494],{"id":495,"sortIndex":25,"affiliation":496,"properties":24},"8c4f25b2-edcf-4f23-8d10-c86b90df54da",{"id":495,"createTime":24,"updateTime":24,"relativeEntities":497,"slug":24,"properties":498,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":501,"statistic":24},[],{"title":499},{"EN":500},"Department of Bacteriology, Postgraduate Medical School of London",[],{"title":503,"openalex":505},{"EN":504},"Mary Barber",{"VOID":506},"A5109128044",{"url":24,"publisher":508,"properties":545},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":509,"slug":10,"properties":510,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":515,"manageAffiliations":524,"indexDatabases":530,"url":83,"thumbnailPath":24,"statistic":24,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":511,"eissn":512,"issn":513,"title":514},{"VOID":13},{"VOID":15},{"VOID":17},{"EN":19},[516,520],{"id":28,"createTime":24,"updateTime":24,"relativeEntities":517,"label":518,"description":519,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":31},{},{"id":34,"createTime":24,"updateTime":24,"relativeEntities":521,"label":522,"description":523,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":37},{},[525],{"id":41,"createTime":24,"updateTime":24,"relativeEntities":526,"slug":24,"properties":527,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":529,"statistic":24},[],{"title":528},{"EN":45},[],[531,538],{"id":49,"indexDatabase":532,"url":60,"indexYears":61,"academicFieldIds":537,"indexDatabaseRanking":65},{"id":51,"createTime":24,"updateTime":24,"relativeEntities":533,"label":534,"description":535,"key":57,"publicationTags":536,"standard":24},[],{"EN":54,"VI":54},{"EN":54,"VI":56},[59],[63,64],{"id":67,"indexDatabase":539,"url":80,"indexYears":24,"academicFieldIds":544,"indexDatabaseRanking":24},{"id":69,"createTime":24,"updateTime":24,"relativeEntities":540,"label":541,"description":542,"key":76,"publicationTags":543,"standard":24},[],{"EN":72,"VI":72},{"EN":74,"VI":75},[78,79],[82],{"issue":546,"pages":547,"volume":549},{"VOID":271},{"VOID":548},"385-393",{"VOID":275},425,{"total":550,"publishYear":277,"statisticByYear":552},{"1989":553,"1990":554,"1991":554,"1992":555,"1993":556,"1994":557,"1995":558,"1996":559,"1997":560,"1998":559,"1999":561,"2000":562,"2001":554,"2002":563,"2003":553,"2004":553,"2005":564,"2006":559,"2007":554,"2008":554,"2009":558,"2010":558,"2011":559,"2012":554,"2013":565,"2014":564,"2015":560,"2016":565,"2017":559,"2018":562,"2019":553,"2020":566,"2021":567,"2022":560,"2023":566,"2024":568,"2025":563},9,14,22,19,20,15,10,12,11,13,3,8,17,4,1,6,[78,65],[571,574,578,582,586,589,593,596,600,604,608,611,614],{"id":24,"text":572,"url":24,"identifiers":573},"Barber, M. (1953). J. gen. Microbiol., 8, 1 1 1.",{},{"id":24,"text":575,"url":24,"identifiers":576},"Blair, J. E., Carr, M., and Buchman, J. (1946). J. Immunol., 52, 281",{"doi":577},"10.4049\u002Fjimmunol.52.3.281",{"id":24,"text":579,"url":24,"identifiers":580},"Fairbrother, R. W., and Taylor, G. (1961). Lancet, 1, 473.",{"doi":581},"10.1016\u002FS0140-6736(61)90058-7",{"id":24,"text":583,"url":24,"identifiers":584},"Finland, M., Collins, H. S., and Paine, T. F. Jr. (1948). J. Amer. med. Ass., 138, 946.",{"doi":585},"10.1001\u002Fjama.1948.02900130010004",{"id":24,"text":587,"url":24,"identifiers":588},"Hayes, W. (1957). In Ciba Foundation Symposium on Drug Resistance in Micro-organisms, p. 275. Churchill, London.",{},{"id":24,"text":590,"url":24,"identifiers":591},"Jevons, M. P. (1961). Brit. med. J., 1, 124.",{"doi":592},"10.1136\u002Fbmj.1.5219.124-a",{"id":24,"text":594,"url":24,"identifiers":595},"Knox, R. (1961). Ibid., 1, 126.",{},{"id":24,"text":597,"url":24,"identifiers":598},"Paine, T. F. Jr., Collins, H. S., and Finland, M. (1948). J. Bact., 56, 489.",{"doi":599},"10.1128\u002FJB.56.4.489-497.1948",{"id":24,"text":601,"url":24,"identifiers":602},"Rake, G., McKee, C. M., Hamre, D. M., and Houck, C. L. (1944). J. Immunol., 48, 271.",{"doi":603},"10.4049\u002Fjimmunol.48.5.271",{"id":24,"text":605,"url":24,"identifiers":606},"Rolinson, G. N. (1961). Brit. med. J., 1, 125.",{"doi":607},"10.1136\u002Fbmj.1.5219.125",{"id":24,"text":609,"url":24,"identifiers":610},"Stevens, S., Batchelor, F. R., Wood, J. C., and Chain, E. B. (1961). Lancet, 1, 562.",{},{"id":24,"text":612,"url":24,"identifiers":613},"Selbie, F. R., and Simon, R. D. (1952). Brit. J. exp. Path., 33, 315.",{},{"id":24,"text":615,"url":24,"identifiers":616},"Spink, W. W., Ferris, V., and Vivino, J. J. (1944). Proc. Soc. exp. Biol. (N. Y.), 55, 210.",{"doi":617},"10.3181\u002F00379727-55-14523",{"id":619,"createTime":620,"updateTime":621,"relativeEntities":622,"slug":623,"properties":624,"entityType":109,"verifyStatus":110,"verifyTime":620,"verifyNote":111,"languages":639,"translateLanguages":24,"viewCount":25,"primaryUrl":640,"fullTextUrl":24,"authors":641,"publicationType":133,"publisherRelationship":819,"citationCount":864,"citationInfo":865,"publishDate":868,"publishYear":866,"citationAnalyzeStatus":869,"lastCitationAnalyze":870,"indexDatabases":871,"openAccess":24,"references":872,"isForceReanalyzing":187},"b75f057e-c428-4fa6-8077-e1fc80b6ff61","2024-09-29T02:06:06.269+00:00","2025-08-27T13:58:11.290+00:00",[],"p16-sup-INK4a-sup-immunostaining-as-an-alternative-to-histology-review-for-reliable-grading-of-cervical-intraepithelial-lesions",{"mag":625,"gsPaper":627,"openalex":629,"abstract":631,"title":633,"pm":635,"doi":637},{"VOID":626},"2100273422",{"VOID":628},"[]",{"VOID":630},"W2100273422",{"EN":632},"\u003Cjats:sec>\u003Cjats:title>Background\u003C\u002Fjats:title>\u003Cjats:p>Histomorphological grading of cervical intraepithelial neoplasia (CIN) is crucial for clinical management. CIN grading is however subjective and affected by substantial rates of discordance among pathologists, which may lead to overtreatment. To minimise this problem, a histology review of CIN lesions by a consensus panel of pathologists is often used. Diffuse strong p16\u003Cjats:sup>INK4a\u003C\u002Fjats:sup>immunostaining has been proposed to aid the identification of true high-grade cervical lesions (ie, CIN2\u002F3).\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Aim\u003C\u002Fjats:title>\u003Cjats:p>To assess the value of additional interpretation of p16\u003Cjats:sup>INK4a\u003C\u002Fjats:sup>immunostains for making a more reproducible diagnosis of CIN2\u002F3 lesions.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Methods\u003C\u002Fjats:title>\u003Cjats:p>The authors used a series of 406 biopsies of cervical lesions, with known HPV status, stained for both H&E- and p16\u003Cjats:sup>INK4a\u003C\u002Fjats:sup>. First, in a randomly selected set of 49 biopsies, we examined the effect of additional interpretation of p16\u003Cjats:sup>INK4a\u003C\u002Fjats:sup>immunostained slides, on the agreement of CIN diagnosis among three pathologists. Second, the full series of samples was used to assess the accuracy of p16\u003Cjats:sup>INK4a\u003C\u002Fjats:sup>-supported lesion grading by a single pathologist, by evaluating the degree of diagnostic agreement with the consensus diagnosis of expert pathologists based on H&E-stained sections only.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Results\u003C\u002Fjats:title>\u003Cjats:p>The study shows that the interobserver agreement between three pathologists for the routine H&E-based diagnosis ranged from fair (weighted kappa 0.44 (95% CI 0.19 to 0.64)) to moderate (weighted kappa 0.66 (95% CI 0.47 to 0.79)). The concordance increased substantially for p16\u003Cjats:sup>INK4a\u003C\u002Fjats:sup>-supported grading (mean weighted kappa 0.80 (95% CI 0.66 to 0.89)). Furthermore, an almost perfect agreement was found between the p16\u003Cjats:sup>INK4a\u003C\u002Fjats:sup>-supported diagnosis of a single pathologist and the consensus diagnosis of an expert pathology panel (kappa 0.88 (95% CI 0.85 to 0.89)).\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Conclusions\u003C\u002Fjats:title>\u003Cjats:p>These data demonstrate that additive use of p16\u003Cjats:sup>INK4a\u003C\u002Fjats:sup>immunohistochemistry significantly improves the accuracy of grading CIN lesions by a single pathologist, equalling an expert consensus diagnosis. Hence, the authors advocate the combined use of p16\u003Cjats:sup>INK4a\u003C\u002Fjats:sup>-stained slides and conventional H&E sections in routine histopathology to improve accuracy of diagnosis.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>",{"EN":634},"p16\u003Csup>INK4a\u003C\u002Fsup>immunostaining as an alternative to histology review for reliable grading of cervical intraepithelial lesions",{"VOID":636},"20924035",{"VOID":638},"10.1136\u002Fjcp.2010.078634",[113],"https:\u002F\u002Fjcp.bmj.com\u002Flookup\u002Fdoi\u002F10.1136\u002Fjcp.2010.078634",[642,659,676,694,711,730,748,765,783,802],{"id":643,"sortIndex":25,"researcher":24,"roles":644,"affiliations":645,"properties":654},"11f019df-6a29-49e2-b4cc-829d57ca8117",[],[646],{"id":647,"sortIndex":25,"affiliation":648,"properties":24},"18c24d9b-b29c-4449-8d43-69185aff94e1",{"id":647,"createTime":24,"updateTime":24,"relativeEntities":649,"slug":24,"properties":650,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":653,"statistic":24},[],{"title":651},{"EN":652},"Department of Pathology, VU University Medical Center, Amsterdam, The Netherlands",[],{"title":655,"openalex":657},{"EN":656},"Maaike G. 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Endodermal sinus tumors arising in the endometrium. Obstet Gynecol 1980;56:391-6.",{},{"id":24,"text":1180,"url":24,"identifiers":1181},"Ohta M, Sakakibara K, Mizuno K, Kano T, Matsuzawa K, Tomoda Y, et al. Successful treatment of primary endodermal sinus tumor of the endometrium. Gynecol Oncol 1988;31:357-64.",{"doi":1182},"10.1016\u002FS0090-8258(88)80015-5",{"id":24,"text":1184,"url":24,"identifiers":1185},"Clement P, Young R, Scully R. Extraovarian pelvic yolk sac tumors. Cancer 1988;62:620-6.",{"doi":1186},"10.1002\u002F1097-0142(19880801)62:3\u003C620::AID-CNCR2820620330>3.0.CO;2-P",{"id":24,"text":1188,"url":24,"identifiers":1189},"Joseph M, Fellows F, Heam S. Primary endodermal sinus tumor of the endometrium. A clinicopathologic, immunocytochemical, and ultrastructural study. Cancer 1990;65: 297-302.",{"doi":1190},"10.1002\u002F1097-0142(19900115)65:2\u003C297::AID-CNCR2820650219>3.0.CO;2-E",{"id":24,"text":1192,"url":24,"identifiers":1193},"Kawagoe K. A case of mixed mesodermal tumor of the uterus with alpha-fetoprotein production. Jpn J7 Clin Oncol 1985;15:577-83.",{},{"id":24,"text":1195,"url":24,"identifiers":1196},"Matsukuma K, Tsukamoto N. Alpha-fetoprotein producing endometrial adenocarcinoma: Report of a case. Gynecol Oncol 1988;29:370-7.",{"doi":1197},"10.1016\u002F0090-8258(88)90238-7",{"id":24,"text":1199,"url":24,"identifiers":1200},"Kubo K, Lee G-H, Yamauchi K, Kitagawa T. Alpha-fetoprotein-producing papillary adenocarcinoma originating from a uterine body: A case report. Acta PatholJpn 1991; 41:399-403.",{},{"id":24,"text":1202,"url":24,"identifiers":1203},"Ma CK, Zarbo RJ, Frierson HF, Lee MW. Comparative immunohistochemical study of primary and metastatic carcinomas of the liver. Am GClin Pathol 1993;99:551-7.",{"doi":1204},"10.1093\u002Fajcp\u002F99.5.551",{"id":24,"text":1206,"url":24,"identifiers":1207},"Sinard J, Macleay L, Melamed J. Hepatoid adenocarcinoma in the urinary bladder. Cancer 1994;73:1919-25.",{"doi":1208},"10.1002\u002F1097-0142(19940401)73:7\u003C1919::AID-CNCR2820730724>3.0.CO;2-L",{"id":24,"text":1210,"url":24,"identifiers":1211},"Yamashita K, Taketa K, Nishi S, Fukushima K, Ohkura T. Sugar chains of human cord serum ca-fetoprotein: characteristics of N-linked sugar chains of glycoproteins produced in human liver and hepatocellular carcinomas. Cancer Res 1993;53:2970-5. J Clin Pathol 1996;49:422-425",{},{"id":1213,"createTime":1214,"updateTime":1214,"relativeEntities":1215,"slug":1216,"properties":1217,"entityType":109,"verifyStatus":110,"verifyTime":1214,"verifyNote":111,"languages":1232,"translateLanguages":24,"viewCount":25,"primaryUrl":1233,"fullTextUrl":24,"authors":1234,"publicationType":133,"publisherRelationship":1269,"citationCount":767,"citationInfo":1313,"publishDate":1316,"publishYear":1314,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":1317,"openAccess":24,"references":1318,"isForceReanalyzing":187},"ec9ce386-e66a-4098-bb63-867f6ad0de8d","2025-02-10T08:37:55.078+00:00",[],"Coexistence-of-pernicious-anaemia-and-acute-erythraemic-myelosis",{"mag":1218,"pmc":1220,"openalex":1222,"abstract":1224,"title":1226,"pm":1228,"doi":1230},{"VOID":1219},"2032749011",{"VOID":1221},"473869",{"VOID":1223},"W2032749011",{"EN":1225},"\u003Cjats:p>A patient with the apparently unique combination of pernicious anaemia and acute erythraemic myelosis is described. The implications of some of the unusual features together with the difficulties encountered in diagnosis and treatment are discussed.\u003C\u002Fjats:p>",{"EN":1227},"Coexistence of pernicious anaemia and acute erythraemic myelosis",{"VOID":1229},"5246763",{"VOID":1231},"10.1136\u002Fjcp.21.5.590",[113],"https:\u002F\u002Fjcp.bmj.com\u002Flookup\u002Fdoi\u002F10.1136\u002Fjcp.21.5.590",[1235,1252],{"id":1236,"sortIndex":25,"researcher":24,"roles":1237,"affiliations":1238,"properties":1247},"70c1ff9a-3e4b-4c37-b305-9ae13cc80467",[],[1239],{"id":1240,"sortIndex":25,"affiliation":1241,"properties":24},"442c00e1-dbca-4117-9324-c327fbc64458",{"id":1240,"createTime":24,"updateTime":24,"relativeEntities":1242,"slug":24,"properties":1243,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1246,"statistic":24},[],{"title":1244},{"EN":1245},"Laboratory, City Hospital, Aberdeen",[],{"title":1248,"openalex":1250},{"EN":1249},"E. 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F., and Seaton, D. A. (1960). Scot. mned. J., 5, 145.",{"doi":1322},"10.1177\u002F003693306000500401",{"id":24,"text":1324,"url":24,"identifiers":1325},"Ardeman, S., and Chanarin, I. (1963). Lancet, 2, 1350.",{"doi":1326},"10.1016\u002FS0140-6736(63)90736-0",{"id":24,"text":1328,"url":24,"identifiers":1329},"Baldini, M., Fudenberg, H. H., Fukutake, K., and Dameshek, W. (1959). Blood, 14, 334.",{"doi":1330},"10.1182\u002Fblood.V14.4.334.334",{"id":24,"text":1332,"url":24,"identifiers":1333},"Dameshek, W., and Baldini, M. (1958). Ibid., 13, 192.",{},{"id":24,"text":1335,"url":24,"identifiers":1336},"Dammert, K., and Kaipainen, W. J. (1960). Acta path. microbiol.",{},{"id":24,"text":1338,"url":24,"identifiers":1339},"Delamore, 1. W. (1961). Clin. Sci., 20, 177.",{},{"id":24,"text":1341,"url":24,"identifiers":1342},"Di Guglielmo, G. (1923). Atti Congr. ital. Med. int., Roma.",{},{"id":24,"text":1344,"url":24,"identifiers":1345},"Di Guglielmo, G. and Quattrin, N. (1942). Haematologica, 24, 1.",{},{"id":24,"text":1347,"url":24,"identifiers":1348},"Douglas, A. S., and Rifkind, B. M. (1964). Scot. med. J., 9, 469.",{"doi":1349},"10.1177\u002F003693306400901102",{"id":24,"text":1351,"url":24,"identifiers":1352},"Engel, A. G., and Stickney, J. M. (1962). Arch. intern. Med., 109, 168.",{"doi":1353},"10.1001\u002Farchinte.1962.03620140040007",{"id":24,"text":1355,"url":24,"identifiers":1356},"Gibson, I. I. J. M., Pollock, A., and Stankler, I. (1963). Postgrad.",{},{"id":24,"text":1358,"url":24,"identifiers":1359},"Glass, G. B. J., Boyd, L. J., Gellin, G. A., and Stephanson, L. (1954). Arch. Biochem., 51, 251.",{"doi":1360},"10.1016\u002F0003-9861(54)90472-5",{"id":24,"text":1362,"url":24,"identifiers":1363},"Goodall, H. B., Guthrie, W., and Buist, N. R. M. (1965). Scot. med. J., 10, 425.",{"doi":1364},"10.1177\u002F003693306501001104",{"id":24,"text":1366,"url":24,"identifiers":1367},"Hayhoe, F. G. J., Quaglino, D., and Flemans, R. J. (1960). Brit. J. Haemat., 6, 23.",{"doi":1368},"10.1111\u002Fj.1365-2141.1960.tb06212.x",{"id":24,"text":1370,"url":24,"identifiers":1371},"Hindmarsh, J. R., and Wickham, T. A. J. (1955). Brit. med. J., 1, 1124",{"doi":1372},"10.1136\u002Fbmj.1.4922.1124",{"id":24,"text":1374,"url":24,"identifiers":1375},"Isaacs, R. (1954). J. Amer. med. Ass., 156, 1491.",{"doi":1376},"10.1001\u002Fjama.1954.02950160021006",{"id":24,"text":1378,"url":24,"identifiers":1379},"Israels, M. C. G. (1963). Diagnosis and Treatment of Blood Diseases, p. 110. Heinemann, London.",{},{"id":24,"text":1381,"url":24,"identifiers":1382},"Martin, W. J., and Bayrd, E. D. (1954). Blood, 9, 321.",{"doi":1383},"10.1182\u002Fblood.V9.4.321.321",{"id":24,"text":1385,"url":24,"identifiers":1386},"Metz, J., and Klein, H. R. (1960). Ann. intern. Med., 53, 207.",{"doi":1387},"10.7326\u002F0003-4819-53-1-207",{"id":24,"text":1389,"url":24,"identifiers":1390},"Pegg, D. E., and Ford, H. T. (1961). Brit. med. J., 2, 617.",{"doi":1391},"10.1136\u002Fbmj.2.5252.617",{"id":24,"text":1393,"url":24,"identifiers":1394},"Pengelly, C. D. R. (1966). Lancet, 2, 1381.",{"doi":1395},"10.1016\u002FS0140-6736(66)90421-1",{"id":24,"text":1397,"url":24,"identifiers":1398},"Perkins, J., Israels, M. C. G., and Wilkinson, J. F. (1964). Quart. J. Med., 33, 499.",{},{"id":24,"text":1400,"url":24,"identifiers":1401},"Quaglino, D., and Hayhoe, F. G. J. (1960). Brit. J. Haemat., 6, 26.",{"doi":1402},"10.1111\u002Fj.1365-2141.1960.tb06213.x",{"id":24,"text":1404,"url":24,"identifiers":1405},"Rose, D. P. (1965). J. clin. Path., 18, 486.",{"doi":1406},"10.1136\u002Fjcp.18.4.486",{"id":24,"text":1408,"url":24,"identifiers":1409},"Schwartz, S. O., and Critchlow, J. (1952). Blood, 7, 765.",{"doi":1410},"10.1182\u002Fblood.V7.8.765.765",{"id":24,"text":1412,"url":24,"identifiers":1413},"Scott, R. B., Ellison, R. R., and Ley, A. B. (1964). Amer. J. Med., 37, 162.",{"doi":1414},"10.1016\u002F0002-9343(64)90002-6",{"id":24,"text":1416,"url":24,"identifiers":1417},"Sheets, R. F., Drevets, C. C., and Hamilton, H. E. (1963). Arch.",{},{"id":24,"text":1419,"url":24,"identifiers":1420},"Spray, G. H., and Witts, L. J. (1958). Brit. med. J., 1, 295.",{"doi":1421},"10.1136\u002Fbmj.1.5066.295",{"id":24,"text":1423,"url":24,"identifiers":1424},"Watkins, P. J., Fairley, G. H., and Scott, R. B. (1967). Ibid., 2, 664.",{},{"id":24,"text":1426,"url":24,"identifiers":1427},"Zarafonetis, C. J. D., Overman, R. L., and Molthan, L. (1957).",{},{"id":1429,"createTime":1430,"updateTime":1430,"relativeEntities":1431,"slug":1432,"properties":1433,"entityType":109,"verifyStatus":110,"verifyTime":1430,"verifyNote":111,"languages":1448,"translateLanguages":24,"viewCount":25,"primaryUrl":1449,"fullTextUrl":24,"authors":1450,"publicationType":133,"publisherRelationship":1502,"citationCount":1547,"citationInfo":1548,"publishDate":1551,"publishYear":1549,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":1552,"openAccess":24,"references":1553,"isForceReanalyzing":187},"4bd6eec0-6dfb-4a7d-a768-bb98b11d7a1a","2025-02-10T05:33:09.820+00:00",[],"A-comparison-of-an-effect-of-different-anti-inflammatory-drugs-on-human-platelets",{"mag":1434,"pmc":1436,"openalex":1438,"abstract":1440,"title":1442,"pm":1444,"doi":1446},{"VOID":1435},"2117981903",{"VOID":1437},"476822",{"VOID":1439},"W2117981903",{"EN":1441},"\u003Cjats:p>Different doses of aspirin, indomethacin, paracetamol, benorylate, and sodium salicylate were taken by four volunteers. The minimal dose that altered a platelet function test and the persistence of this alteration at different dose levels were studied. Minute doses of indomethacin (0·035 mg\u002Fkg) were effective but the effect of even a large single dose did not persist. A tenth of the therapeutic dose of aspirin (1 mg\u002Fkg) was effective, and higher doses altered the platelets' function for several days. Benorylate in a high therapeutic dose gave aspirin-like results. Paracetamol and sodium salicylate were relatively inactive. The persistence of the aspirin effect may be related to the acetyl group. These findings are surveyed in relation to a general theory of the action of anti-inflammatory drugs.\u003C\u002Fjats:p>",{"EN":1443},"A comparison of an effect of different anti-inflammatory drugs on human platelets",{"VOID":1445},"5476879",{"VOID":1447},"10.1136\u002Fjcp.23.6.522",[113],"https:\u002F\u002Fjcp.bmj.com\u002Flookup\u002Fdoi\u002F10.1136\u002Fjcp.23.6.522",[1451,1470,1485],{"id":1452,"sortIndex":25,"researcher":24,"roles":1453,"affiliations":1454,"properties":1463},"32bcc35f-8bd4-4483-ada6-b2e835f5f319",[],[1455],{"id":1456,"sortIndex":25,"affiliation":1457,"properties":24},"2b2b3c38-6fa0-4b3c-ae0e-e625a133368c",{"id":1456,"createTime":24,"updateTime":24,"relativeEntities":1458,"slug":24,"properties":1459,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1462,"statistic":24},[],{"title":1460},{"EN":1461},"Portsmouth and Isle of Wight Area Pathological Service, Milton Road, Portsmouth",[],{"orcid":1464,"title":1466,"openalex":1468},{"VOID":1465},"https:\u002F\u002Forcid.org\u002F0000-0002-5468-4466",{"EN":1467},"John O’Brien",{"VOID":1469},"A5033947736",{"id":1471,"sortIndex":567,"researcher":24,"roles":1472,"affiliations":1473,"properties":1480},"29f7faaf-0d97-4f26-a78d-b26cb81a5313",[],[1474],{"id":1456,"sortIndex":25,"affiliation":1475,"properties":24},{"id":1456,"createTime":24,"updateTime":24,"relativeEntities":1476,"slug":24,"properties":1477,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1479,"statistic":24},[],{"title":1478},{"EN":1461},[],{"title":1481,"openalex":1483},{"EN":1482},"Wendy Finch",{"VOID":1484},"A5023855536",{"id":1486,"sortIndex":678,"researcher":24,"roles":1487,"affiliations":1488,"properties":1495},"d847fc99-1a05-45ee-9914-bed7ed0797dc",[],[1489],{"id":1456,"sortIndex":25,"affiliation":1490,"properties":24},{"id":1456,"createTime":24,"updateTime":24,"relativeEntities":1491,"slug":24,"properties":1492,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1494,"statistic":24},[],{"title":1493},{"EN":1461},[],{"orcid":1496,"title":1498,"openalex":1500},{"VOID":1497},"https:\u002F\u002Forcid.org\u002F0000-0003-4289-6370",{"EN":1499},"Elizabeth G. Clark",{"VOID":1501},"A5071721191",{"url":24,"publisher":1503,"properties":1540},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":1504,"slug":10,"properties":1505,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":1510,"manageAffiliations":1519,"indexDatabases":1525,"url":83,"thumbnailPath":24,"statistic":24,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":1506,"eissn":1507,"issn":1508,"title":1509},{"VOID":13},{"VOID":15},{"VOID":17},{"EN":19},[1511,1515],{"id":28,"createTime":24,"updateTime":24,"relativeEntities":1512,"label":1513,"description":1514,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":31},{},{"id":34,"createTime":24,"updateTime":24,"relativeEntities":1516,"label":1517,"description":1518,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":37},{},[1520],{"id":41,"createTime":24,"updateTime":24,"relativeEntities":1521,"slug":24,"properties":1522,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1524,"statistic":24},[],{"title":1523},{"EN":45},[],[1526,1533],{"id":49,"indexDatabase":1527,"url":60,"indexYears":61,"academicFieldIds":1532,"indexDatabaseRanking":65},{"id":51,"createTime":24,"updateTime":24,"relativeEntities":1528,"label":1529,"description":1530,"key":57,"publicationTags":1531,"standard":24},[],{"EN":54,"VI":54},{"EN":54,"VI":56},[59],[63,64],{"id":67,"indexDatabase":1534,"url":80,"indexYears":24,"academicFieldIds":1539,"indexDatabaseRanking":24},{"id":69,"createTime":24,"updateTime":24,"relativeEntities":1535,"label":1536,"description":1537,"key":76,"publicationTags":1538,"standard":24},[],{"EN":72,"VI":72},{"EN":74,"VI":75},[78,79],[82],{"issue":1541,"pages":1543,"volume":1545},{"VOID":1542},"6",{"VOID":1544},"522-525",{"VOID":1546},"23",77,{"total":1547,"publishYear":1549,"statisticByYear":1550},1970,{"2012":567},"1970-09-01",[78,65],[1554,1557,1560,1564,1568,1571,1575,1579,1583,1587,1590,1594,1598,1602,1606],{"id":24,"text":1555,"url":24,"identifiers":1556},"Adams, S. S., and Cobb, R. (1963). In Salicylates: An International Symposium, edited by A. St. J. Dixon, B. K. Martin, M. J. H. Smith, and P. H. N. Wood, p. 127. Churchill, London.",{},{"id":24,"text":1558,"url":24,"identifiers":1559},"Berry, P. A., and Collier, H. 0. J. (1964). Bronchoconstrictor action and antagonism of a slow-reacting substance from anaphylaxis of guinea-pig isolated lung. Brit. J. Pharmacol., 23, 201-216.",{},{"id":24,"text":1561,"url":24,"identifiers":1562},"Brown, J. H., and Mackey. H. K. (1968). Further studies on the erythrocyte anti-inflammatory assay. Proc. Soc. exp. Biol. (N. Y.), 128, 504-509.",{"doi":1563},"10.3181\u002F00379727-128-33051",{"id":24,"text":1565,"url":24,"identifiers":1566},"Collier, H. 0. J. (1969). New light on how aspirin works. Nature (Lond.), 223, 35-37.",{"doi":1567},"10.1038\u002F223035a0",{"id":24,"text":1569,"url":24,"identifiers":1570},"Inglot, A. D., and Wolna, E. (1968). Reactions of non-steroidal anti-inflammatory drugs with the erythrocyte membrane. Biochem. Pharmacol., 17, 269-279.",{},{"id":24,"text":1572,"url":24,"identifiers":1573},"O'Brien, J. R. (1964). Variability in the aggregation of human platelets by adrenaline. Nature (Lond.), 202, 1188-1190.",{"doi":1574},"10.1038\u002F2021188a0",{"id":24,"text":1576,"url":24,"identifiers":1577},"O'Brien, J. R. (1968a). Effects of salicylates on human platelets. Lancet, 1, 779-783.",{"doi":1578},"10.1016\u002FS0140-6736(68)92228-9",{"id":24,"text":1580,"url":24,"identifiers":1581},"O'Brien, J. R. (1968b). Effect of anti-inflammatory agents on platelets. Lancet, 1, 894-895.",{"doi":1582},"10.1016\u002FS0140-6736(68)90242-0",{"id":24,"text":1584,"url":24,"identifiers":1585},"O'Brien, J. R., Finch, W., and Clark, E. (1970). Platelet bound and soluble platelet factor 4: effects of aggregating agents, of aggregation and of aspirin. Proc. Soc. exp. Biol. (N. Y.) (In the press.)",{"doi":1586},"10.3181\u002F00379727-134-34958",{"id":24,"text":1588,"url":24,"identifiers":1589},"O'Brien, J. R., Heywood, J. B., and Heady, J. A. (1966). The quantitation of platelet aggregation induced by four compounds: a study in relation to myocardial infarction. Thrombos. Diathes. haemorrh. (Stuttg.), 16, 752-767.",{},{"id":24,"text":1591,"url":24,"identifiers":1592},"Piper, P. J., and Vane, J. R. (1969). Release of additional factors in anaphylaxis and its antagonism by anti-inflammatory drugs. Nature (Lond.), 223, 29-35.",{"doi":1593},"10.1038\u002F223029a0",{"id":24,"text":1595,"url":24,"identifiers":1596},"Seeman, P. (1966). Erythrocyte membrane stabilization by local anaesthetics and tranquilizers. Biochem. Pharmacol., 15, 1753-1766.",{"doi":1597},"10.1016\u002F0006-2952(66)90082-7",{"id":24,"text":1599,"url":24,"identifiers":1600},"Weiss, H. J., Aledort, L. M., and Kochwa, S. (1968). The effect of salicylates on the hemostatic properties of platelets in man. J. clin. Invest., 47, 2169-2180.",{"doi":1601},"10.1172\u002FJCI105903",{"id":24,"text":1603,"url":24,"identifiers":1604},"Youssef, A. H., and Barkhan, P. (1969). Inhibition by aspirin of release of antiheparin activity from human platelets. Brit. med. J., 3, 394-396.",{"doi":1605},"10.1136\u002Fbmj.3.5667.394",{"id":24,"text":1607,"url":24,"identifiers":1608},"Zucker, M. B., and Peterson, J. (1968). Inhibition of adenosine diphosphate-induced secondary aggregation and other platelet functions by acetylsalicylic acid ingestion. Proc. Soc. exp. Biol. (N. Y), 127, 547-551.",{"doi":1609},"10.3181\u002F00379727-127-32737",{"id":1611,"createTime":1612,"updateTime":1612,"relativeEntities":1613,"slug":1614,"properties":1615,"entityType":109,"verifyStatus":110,"verifyTime":1612,"verifyNote":111,"languages":1628,"translateLanguages":24,"viewCount":25,"primaryUrl":1629,"fullTextUrl":24,"authors":1630,"publicationType":133,"publisherRelationship":1693,"citationCount":1737,"citationInfo":1738,"publishDate":1741,"publishYear":1739,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":1742,"openAccess":24,"references":1743,"isForceReanalyzing":187},"a0baf5bc-1d52-4e72-a667-b65472d73f08","2025-02-10T02:39:21.466+00:00",[],"Immunoturbidimetric-assays-for-serum-apolipoproteins-A1-and-B-using-Cobas-Bio-centrifugal-analyser-",{"openalex":1616,"mag":1618,"title":1620,"pm":1622,"doi":1624,"pmc":1626},{"VOID":1617},"W1969658832",{"VOID":1619},"1969658832",{"EN":1621},"Immunoturbidimetric assays for serum apolipoproteins A1 and B using Cobas Bio centrifugal analyser.",{"VOID":1623},"3366936",{"VOID":1625},"10.1136\u002Fjcp.41.4.471",{"VOID":1627},"1141480",[113],"http:\u002F\u002Fjcp.bmj.com\u002Fcgi\u002Fdoi\u002F10.1136\u002Fjcp.41.4.471",[1631,1648,1663,1678],{"id":1632,"sortIndex":25,"researcher":24,"roles":1633,"affiliations":1634,"properties":1643},"8345b777-001b-404a-8d8c-c611697622ca",[],[1635],{"id":1636,"sortIndex":25,"affiliation":1637,"properties":24},"0d5ab752-99e9-47be-a825-9e1d16a8dfec",{"id":1636,"createTime":24,"updateTime":24,"relativeEntities":1638,"slug":24,"properties":1639,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1642,"statistic":24},[],{"title":1640},{"EN":1641},"Chemical Pathology and Metabolic Disorders, St Thomas's Hospital, London.",[],{"title":1644,"openalex":1646},{"EN":1645},"J N Mount",{"VOID":1647},"A5064804825",{"id":1649,"sortIndex":567,"researcher":24,"roles":1650,"affiliations":1651,"properties":1658},"a876d643-6019-4574-99cc-22a4fb88603f",[],[1652],{"id":1636,"sortIndex":25,"affiliation":1653,"properties":24},{"id":1636,"createTime":24,"updateTime":24,"relativeEntities":1654,"slug":24,"properties":1655,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1657,"statistic":24},[],{"title":1656},{"EN":1641},[],{"title":1659,"openalex":1661},{"EN":1660},"E. 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Plasma lipids and apolipoproteins as discriminators for presence and severity of angiographically defined coronary artery disease. Atherosclerosis 1983;49: 1-7.",{"doi":1747},"10.1016\u002F0021-9150(83)90002-3",{"id":24,"text":1749,"url":24,"identifiers":1750},"Rosseneu M, Vercaemst R, Vinaimont N, Van Tomont P, Henderson LO, Herbert PN. Quantitative determination of human plasma apolipoprotein Al by laser immunonephelometry. Clin Chem 1981;27:856-9.",{"doi":1751},"10.1093\u002Fclinchem\u002F27.6.856",{"id":24,"text":1753,"url":24,"identifiers":1754},"Rosseneu M, Vinaimont R, Dekeersgieter W, Belpaire F. Standardisation of immunoassays for the quantitation of plasma apoB protein. Anal Biochem 1981:116:204-10.",{},{"id":24,"text":1756,"url":24,"identifiers":1757},"Funke H, Assman G. Influence of triglyceride-rich lipoproteins in nephelometric determination of apolipoprotein Al. Clin Chem 1982;28:1 153-8.",{},{"id":24,"text":1759,"url":24,"identifiers":1760},"Heuck CC, Schlief G. Nephelometry of apolipoprotein B in human serum. Clin Chem 1970;25:221-6.",{"doi":1761},"10.1093\u002Fclinchem\u002F25.2.221",{"id":24,"text":1763,"url":24,"identifiers":1764},"Van Stiphout WAHJ, Hofman A, Kruijssen HACM, Vermeeren R, Groot PHE. Is the ratio of apoB\u002FapoA I an early predictor of coronary atherosclerosis? Atherosclerosis 1986;62:179-82.",{"doi":1765},"10.1016\u002F0021-9150(86)90065-1",{"id":1767,"createTime":1768,"updateTime":1768,"relativeEntities":1769,"slug":1770,"properties":1771,"entityType":109,"verifyStatus":110,"verifyTime":1768,"verifyNote":111,"languages":1786,"translateLanguages":24,"viewCount":25,"primaryUrl":1787,"fullTextUrl":24,"authors":1788,"publicationType":133,"publisherRelationship":1962,"citationCount":2006,"citationInfo":2007,"publishDate":2010,"publishYear":2008,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":2011,"openAccess":24,"references":2012,"isForceReanalyzing":187},"eb77846b-f25a-4bc2-a672-60b8f74389c1","2025-02-09T21:35:41.492+00:00",[],"Upregulation-of-Twist-in-oesophageal-squamous-cell-carcinoma-is-associated-with-neoplastic-transformation-and-distant-metastasis",{"mag":1772,"pmc":1774,"openalex":1776,"abstract":1778,"title":1780,"pm":1782,"doi":1784},{"VOID":1773},"2164765173",{"VOID":1775},"1994533",{"VOID":1777},"W2164765173",{"EN":1779},"\u003Cjats:p>\u003Cjats:bold>Background:\u003C\u002Fjats:bold>The antiapoptotic and epithelial–mesenchymal transition activities of Twist have been implicated in the neoplastic transformation and the development of metastasis, respectively. Upregulation of Twist, described in several types of human cancer, also acts as a prognostic marker of poor outcome.\u003C\u002Fjats:p>\u003Cjats:p>\u003Cjats:bold>Aim:\u003C\u002Fjats:bold>To investigate Twist expression in oesophageal squamous cell carcinoma (SCC) and its prognostic value in a Chinese cohort of patients with oesophageal SCC.\u003C\u002Fjats:p>\u003Cjats:p>\u003Cjats:bold>Methods:\u003C\u002Fjats:bold>Twist expression in primary oesophageal SCC of 87 Chinese patients was investigated by immunohistochemical staining. Twist protein level in one immortalised normal oesophageal epithelial cell line and six oesophageal SCC cell lines was measured by western blot analysis.\u003Cjats:italic>Twist\u003C\u002Fjats:italic>mRNA level in 30 pairs of frozen specimens of primary oesophageal SCC and non-neoplastic oesophageal epithelium from the upper resection margin of corresponding oesophagectomy specimen was also determined by semiquantitative reverse transcription-PCR.\u003C\u002Fjats:p>\u003Cjats:p>\u003Cjats:bold>Results:\u003C\u002Fjats:bold>It was found that Twist was upregulated in oesophageal SCC cell lines, and its mRNA and protein levels were both increased in oesophageal SCC and the non-neoplastic oesophageal epithelium (p<0.001). In addition, a high level of Twist expression in oesophageal SCC was significantly associated with a greater risk for the patient of developing distant metastasis within 1 year of oesophagectomy (OR 3.462, 95% CI 1.201 to 9.978; p = 0.022).\u003C\u002Fjats:p>\u003Cjats:p>\u003Cjats:bold>Conclusions:\u003C\u002Fjats:bold>Our results suggest that upregulation of Twist plays a role in the neoplastic transformation to oesophageal SCC and subsequent development of distant metastasis. Twist may serve as a useful prognostic marker for predicting the development of distant metastasis in oesophageal SCC.\u003C\u002Fjats:p>",{"EN":1781},"Upregulation of Twist in oesophageal squamous cell carcinoma is associated with neoplastic transformation and distant 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