简介:转变生长因素贝它(发信号的TGF-尾)/bonemorphogenic蛋白质(BMP)涉及绝大多数细胞的过程并且在所有metazoans的全部生活期间是根本上重要的。TGF-尾/BMP活动的解除管制几乎总是导致发展缺点或疾病,包括癌症。TGF-尾/BMP小径的合适的工作与另外的发信号的小径取决于它的组成、广泛的通讯,导致synergistic或对抗效果和最后理想的生物结果。如此的发信号的串音的性质是压倒性地复杂的并且高度上下文依赖者。这里,我们考察在TGF-尾/BMP和激活Mitogen的蛋白质kinase,phosphatidylinositol-3kinase/Akt,Wnt,刺猬,槽口,和interleukin/interferon-gamma/tumor坏死factor-alpha的发信号的小径之间的串音的不同模式cytokines,与内在的分子的机制上的一个重音。
简介:Monoclonal(mAb)成功地被用于长期的疾病的治疗,例如癌症,发炎和有免疫力的疾病。与在抗体工程的技术进展,当有减少的immunogenicity的高亲密关系治疗学在聚光灯下面变得,小重组体抗体的开发碎裂。设计重组体抗体碎片的一种流行格式是单个链的改正变量(scFv)分子,父母抗体的VH和VL区域被一个多肽连接器一起在连接。scFv碎片保留目标特性和未经触动的抗体,和罐头的抗原绑定亲密关系被在房间从单个cDNA表示VH和VL区域的宫外的联盟者遗传上在大数量设计并且生产。由于它的更小的尺寸,scFv分子表演在肿瘤穿入改进了pharmacokinetics并且被主人免疫系统更好容忍。
简介:抽象本地配偶比赛理论在传花粉给预言那后代性比率微量黄蜂当仅仅有一个女创立者时,是偏导女性的,并且在增加的后代性增加女创立者密度结果比率。另外的女创立者和离合器尺寸的信息被建议了是对在本地配偶竞争下面的性比率调整的主要贴近的解释。我们的焦点是在一只传花粉给的微量黄蜂显示出性比率调整的机制,CeratosolensolmsiMayr,机能上地雌雄异体的微量的obligatepollinator,Ficushispida悬崖,与这块地里的控制实验。首先,我们在不同oviposition序列从一pollinator和后代获得了后代,并且发现那后代性比率与离合器尺寸减少了,并且pollinators在一回的开始生产了大多数他们的男后代,列在后面由主要女性。第二,我们发现那后代性比率与女创立者密度增加了,并且pollinators做了在oviposition补丁以另外的女性调整他们的后代性比率。我们建议当oviposition地点是不有限的时,pollinators将主要以离合器尺寸变化的另外的女创立者独立人士调整他们的后代性比率,而当oviposition地点是有限的时,调整离合器尺寸可以被用来调整性比率。
简介:BACKGROUND:Previousstudiesreportedthatfrontal-temporal-parietal-occipitalpathologicalchangesanddiseasedrangeintherightcerbralhemispherewerecorrelatedwithneglect.Butstudiesonthecorrelationofneglectwithdiseasedregionandareainpatientswhosufferfrominitialattackofsinglefocusofcerebralinfarction(CI)inleftandrightcerebralhemispheresarefew.OBJECTIVE:ToobservethestatusofneglectinpatientswhosufferfromsinglefocusofCIincerebralhemisphereandanalyzethecorrelationofneglectwithdiseasedregionandareaofCI.DESIGN:CaseanalysisSETTING:TreatmentCenterforCardiocerebrovascularDisease,SecondHospitalofXiamencity;DepartmentofNeurology,FirstHospitalAffiliatedtoBaotouMedicalCollege.PARTICIPANTS:AlltheCIpatientshospitalizedintheDepartmentofNeurology.FirstHospitalAffiliatedtoBaotouMedicalCollegefromJune1998toMay2001wereretrieved.Inclusivecriteria:①PatientswhosufferedfrominitialattackofCI.whichwasconfirmedbyskullCTorMRIwithin24hoursafteronsetandpresentedsinglefocusincerebralhemisphere.②beconsciousandcouldcooperateintheexamination.③didnotreceiveformaleducation,butcoulddoaccountsandsomesimplewritingandreading.④Patientswithhomonymoushemianopiawereexcludedthroughtheexaminationofperimeter.⑤Informedconsentswereobtainedfromallthepatients.Among67patientswhomettheinclusivecriteria.33sufferedfromCIintheleftcerebralhemisphereand34intherightcerebralhemisphere.METHODS:①PatientsreceivedneglectsupplementexaminationandChineseaphasiaexaminationwithin2.5to3monthsaftertheattackofCI.Thediagnosticcriteriaofneglectinthetestsoflinecancellation.1inebisectionandcopyingthefigureswereasfollows:InthelinecancellationtestbasedonthemethodofAlbert.patientswhocouldnotcanceloneormorelineswereregardedasabnormal.InthelinebisectiontestbasedonthemethodofPeter.patientswholeftdeviated1.16%
简介:Researchshowsthatthemortalityrateamongpeoplewithschizophreniaisuptofourtimeshigherthanthatinthegeneralpopulation.Thesubsequenthighcomorbiditiesandsocietalcostofschizophrenianecessitatefindingbetter,moreeffectivetreatmentsandstrategiesforprevention.Oneofthecurrentobstaclesarethecomplicatedgeneetiologiesthatareinvolvedinthepathophyslologyofschizophrenia.Sofar,anincreasingnumberofclinicalandexperimentalstudiesshowlinksbetweenschizophreniatreatmentandgeneticconditions.Here,weanalyzetheliteratureonschizophreniagenetics,withaparticularfocusonthebrain,themindandenvironmentalinsults.Anoverlapofschlzophrenlawithotherpsychoticdisordershasalsobeentakenintoaccuntwithanattempttofindaparallelrelationshipbetweengeneticsandtreatment.Finally,wesummarizeallthepresent-daytreatmentoptionsforschizophrenialikeclozapineandelectroconvulslvetherapyandalsotakeintoconsiderationtherelativelyunexploredroleoftraditionalChinesemedicine.
简介:EXPERIENCESOFTHEOPENING-UPANDEXPLOITATIONOFVARIOUSINTERIORREGIONSBYINDIA,PAKISTANANDOTHERCOUNTRIESHeDao-long;LiuXiao-fengandX...
简介:Intheefforttodevelopacomprehensiveapproachtobetterandgoodjobs,itisatopicofhotdebateastowhethertheintroduction(temporarilyoronapermanentbasis)ofstatutorylegislation―differentfromthegenerallawapplyingtosubordinateworkers―mayencourageemployersandemployeestooperatewithintheformaleconomyandinthecontextofregularcontractsofemployment.Theessayanalyzesfromacomparativepointofviewnotthetraditionalformsofnon-standardemployment,butthosespecialworkingarrangements,thatmayinvolveveryshorthours(“marginal”parttime:generally,fewerthan15hoursperweek)ornopredictablefixedhours,andthoseaccordingtowhichtheemployerhasnoobligationtoprovideasetnumberofhoursofwork.Theconclusionisthatextremelyatypicalformsofworkappeartogiveananswertothechallengesofthemarketlaboroftheurbaneconomiesofthe21stcentury,butthatspeciallegalprovisionsareneededtoguaranteeindividualrighttofairwagesandtoprotectpersonallifeofemployees.
简介:MutationsintheGJB2genearethemostfrequentlyfoundmutationsinpatientswithnonsyndromichearingimpairment.However,themutationspectrumandprevalenceofmutationsvaryamongdifferentethnicgroups.Everyyear,30,000babiesarebornwithcongenitalhearingimpairmentinChina.Inordertoprovideappropriategenetictestingandcounselingtothefamily,weinvestigatedthemolecularetiologyofnonsyndromicdeafnessin135unrelatedschoolchildrenattendingChifengMunicipalSpecialEducationSchoolinInnerMongolia,China.ThecodingexonoftheGJB2genewasPCRamplifiedandsequenced.Inaddition,the12SrRNAgeneandtRNAser(UCN)ofmitochondrialgenomewerescreenedformutationsresponsibleforhearingimpairment.SixtyfourGJB2mutantalleles,including60confirmedpathogenicallelesand4unclassifiedvariants,wereidentifiedin31.1%(42/135)ofthesubjects.Twentytwosubjectscarriedtwopathogenicmutationsand20subjectscarriedonemutantallele,includingonesubjectwithoneautosomaldominantmutation.The235delCwasthemostcommonmutationaccountingfor65.6%(42/64)GJB2mutantalleles.WhencomparedtootherAsianpopulations,oursubjectcohorthadhigherfrequencyof235delCmutationthantheJapanesepopulation.TheGJB2mutantallelesaccountfor23.7%(64/270)ofallchromosomesresponsiblefornonsyndromichearingimpairment.Testingofthe4mostprevalentdeleteriousframeshiftmutations(235delC,299_300delAT,176_191del16,and560_605ins46)inthiscohortdetected90%ofallGJB2mutantalleles.TheseresultsdemonstratethateffectivegenetictestingoftheGJB2geneforpatientsandfamilieswithnonsyndromichearingimpairmentispossibleintheChinesepopulation.Sincethemostcommon309kbGJB6deletionisnotdetectedandonlyone1555A>GmutationinmitochondrialDNAisdetectedinourpatients,investigationofmutationsinothernucleargenesand/orenvironmentalfactorsresponsiblefornonsyndromichearingimpairmentintheChinesepopulationis
简介:SystematicgeochemicalstudiesoftheProterozoicLengjiaxiGroupinnortheasternHunanProvincesuggestthattheLengjiaxiGroupisaAu-As-Sb-Wassociation-typeAu-bearingturbiditeformation.ThecontentsofAu,As,Sb,W,Cr,Mn,PbandZnintheturbiditeformationaremorethantwotimesashighastheaveragecontentsoftraceelementsintheuppercontinentalcrust.ThelowabundanceofAgandtheclosecorrelationbetweenAuandAsaretwoimportantcharacteristicfeatures.IntheAu-bearingturbiditeformationtheenrichmentofgoldisduetotheextensiveoccurrenceofAu-bearingpyrites.HighercontentsofAu,W,SbandAginthegreywackeindicatethattheyalsoexistintheformofheavyminerals.Au,Ag,As,Sb,WandREEintheAu-bearingturbiditeformationhaveaclosegeneticrelationwiththechemistryofthegolddeposits.