02300nam 2200397 450 99655287230331620231125022351.03-9874006-5-X10.5771/9783987400650(CKB)5840000000406442(NjHacI)995840000000406442(EXLCZ)99584000000040644220231125d2023 uy 0gerur|||||||||||txtrdacontentcrdamediacrrdacarrierAdam und Embryo Ein Beitrag zur Erforschung der Adamsgeschichte in jüdischen, christlichen und islamischen Texten bis zum Ende des ersten Jahrtausends /Thomas Eich, Doru Constantin DorofteiBaden-Baden :Ergon,2023.1 online resource (340 pages)Recht, Ethik und Gesellschaft im Vorderen Orient ;33-9874006-4-1 Titelei/Inhaltsverzeichnis -- Einleitung -- Teil I Zur Entwicklung der Adamsgeschichte bis zum 7. Jahrhundert -- Teil II Zur koranischen Embyrologie -- Teil III Nu?fa, ?alaqa und mu?ga in außerkoranischem Textmaterial -- Bibliographie -- Appendix A: Findet sich im Korantext nicht doch die Idee der Individualbeseelung? -- Appendix B: Der Koran und die Infantizid-Debatte: zum Begriff maw?uda in Q 81:8.Das Buch analysiert kritisch die Idee, im Korantext des 7. Jahrhunderts fänden sich Passagen, die damalige medizinische Ideen von der Entstehung der Menschen durch Schwangerschaft reflektieren. Es zeigt sich, dass der Koran diesbezüglich auf ein reiches Erbe an Motiven zurückgreift, wobei sich eine aus jüdisch-palästinensischen Texten des 6. Jahrhunderts bekannte Vorstellung als zentral erweist: das Wachstum eines jeden Embryos laufe so ab, wie Gott den ersten Menschen erschaffen habe. Das Bild von "Adam und Embryo" begleitete die frühislamische Geistesgeschichte noch über mehrere Jahrhunderte, bevor es allmählich in Vergessenheit geriet.Human beingsHuman beings.222.11092Eich Thomas1439262Constantin Doroftei DoruNjHacINjHaclBOOK996552872303316Adam und Embryo3601526UNISA02257nam 2200505 450 991055275060332120220925125722.01-5261-5966-X10.7765/9781526159663(CKB)5670000000210914(NjHacI)995670000000210914(DE-B1597)659008(DE-B1597)9781526159663(EXLCZ)99567000000021091420220925d2021 uy 0engur|||||||||||txtrdacontentcrdamediacrrdacarrierAnglophobia in fascist Italy /Jacopo PiliManchester :Manchester University Press,2021.1 online resource (215 pages)This book is freely available in digital formats thanks to a generous grant from the Andrew W. Mellon Foundation.Anglophobia in Fascist Italy traces the origins and development of anti-British sentiment in Fascist Italy, as Britain turned from being an ally in the First World War to an enemy in the Second. The book demonstrates that Fascist ideologues framed Britain as a stagnant and decaying country and the polar opposite of Fascism's new civilisation, to the point that the regime's assessment of British political resolve and military might were distorted by ideological bias. The book offers a thorough analysis of diplomatic, military and journalistic sources and demonstrates that anti-British tropes had permeated Italy to a greater degree than was previously believed.FascismItalyHistory20th centuryItalyForeign relationsGreat BritainAnglo-Italian relations.Benito Mussolini.European relations in the Interwar Years.Fascist Italy.Italian history.Second World War.military attachés.racist theories.totalitarianism.war propoganda.FascismHistory945.091Pili Jacopo1260779NjHacINjHaclBOOK9910552750603321Anglophobia in fascist Italy2922175UNINA03974nam 2200937z- 450 991055748470332120210501(CKB)5400000000042985(oapen)https://directory.doabooks.org/handle/20.500.12854/69300(oapen)doab69300(EXLCZ)99540000000004298520202105d2020 |y 0engurmn|---annantxtrdacontentcrdamediacrrdacarrierGenomics and Models of Nerve Sheath TumorsBasel, SwitzerlandMDPI - Multidisciplinary Digital Publishing Institute20201 online resource (172 p.)3-03943-489-6 3-03943-490-X Nerve sheath tumors can be a significant cause of morbidity for many patients. These include benign tumors such as schwannomas, diffuse and plexiform neurofibromas, and atypical neurofibromas, as well as the aggressive soft tissue sarcoma known as the malignant peripheral nerve sheath tumor (MPNST). Nerve sheath tumors occur sporadically and in the context of the clinical neuro-genetic tumor predisposition syndromes neurofibromatosis type 1 (NF1) and type 2 (NF2). Historically, the mainstay of treatment for nerve sheath tumors has been surgery. However, for both benign and malignant nerve sheath tumors, there is a high recurrence rate, highlighting the pressing need for novel therapies. As we have entered the genomic era, the hope is that an improved understanding of the genetics, and therefore the biology, of these tumors will ultimately lead to therapies that result in better outcomes. In this Special Issue, we include both review articles and original research related to the genomic understanding and modeling of schwannomas, plexiform and diffuse neurofibromas, atypical neurofibromas, and malignant peripheral nerve sheath tumors as well as genomic methods being developed and applied to advance our understanding of these tumors.Medicine and Nursingbicssccancercapmatinibchemopreventionclinical geneticsCOX-2 inhibitorCRISPR/Cas9doxorubicingenetically engineered mouse modelsgenomicsheterogeneitykinasekinome adaptationkinome reprogramminglatent variablesmachine learningmalignancymalignant peripheral nerve sheath tumormalignant peripheral nerve sheath tumorsmebendazole (MBZ)MEKMETmetaVIPERmouse modelsMPNSTnerve sheath tumornerve sheath tumorsneurofibromatosisneurofibromatosis 1 (NF1)neurofibromatosis type 1neurofibromatosis type 1 syndromeneurofibromin 1next generation sequencingNF1pathologyplexiform neurofibromaspolycomb repressive complexPRC2random forestsarcomaSchwann cellssupervised learningtramtransfer learningtumor deconvolutiontumor evolutiontumor microenvironmentMedicine and NursingHirbe Angela Cedt1312695Pratilas Christine AedtDodd Rebecca DedtHirbe Angela CothPratilas Christine AothDodd Rebecca DothBOOK9910557484703321Genomics and Models of Nerve Sheath Tumors3030922UNINA