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2011, ISBN: 382742657X

Heureka (ich habe es gefunden) soll Archimedes gerufen haben, als er in der Badewanne lag und sah, wie sein Körper das Wasser verdrängte. Unvermittelt war ihm der Zusammenhang klar, er ha… Mehr…

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Evidenzkriterien in den Wissenschaften:

Heureka - neues Buch

ISBN: 9783827426574

"Heureka” (ich habe es gefunden) soll Archimedes gerufen haben, als er in der Badewanne lag und sah, wie sein Körper das Wasser verdrängte. Unvermittelt war ihm der Zusammenhang klar, er … Mehr…

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Heureka - Evidenzkriterien in den Wissenschaften - Eva-Maria Engelen; Christian Fleischhack; C. Giovanni Galizia; Katharina Landfester
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Eva-Maria Engelen; Christian Fleischhack; C. Giovanni Galizia; Katharina Landfester:
Heureka - Evidenzkriterien in den Wissenschaften - neues Buch

2011

ISBN: 9783827426574

Ein Kompendium für den interdisziplinären Gebrauch, eBooks, eBook Download (PDF), 2010, [PU: Spektrum Akademischer Verlag], Seiten: 264, Spektrum Akademischer Verlag, 2011

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Eva-Maria Engelen; Christian Fleischhack; Giovanni Galizia; Katharina Landfester:
Heureka - Evidenzkriterien in den Wissenschaften - Erstausgabe

2011, ISBN: 9783827426574

Ein Kompendium für den interdisziplinären Gebrauch, eBooks, eBook Download (PDF), Auflage, [PU: Spektrum Akademischer Verlag], [ED: 1], Spektrum Akademischer Verlag, 2011

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Heureka - Evidenzkriterien in den Wissenschaften - neues Buch

ISBN: 9783827426574

Heureka - Evidenzkriterien in den Wissenschaften - Ein Kompendium für den interdisziplinären Gebrauch: ab 6.28 € eBooks > Fachthemen & Wissenschaft > Wissenschaften allgemein Spektrum-Aka… Mehr…

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Details zum Buch

Detailangaben zum Buch - Heureka - Evidenzkriterien in den Wissenschaften


EAN (ISBN-13): 9783827426574
ISBN (ISBN-10): 382742657X
Erscheinungsjahr: 2011
Herausgeber: Spektrum Akademischer Verlag
264 Seiten
Sprache: ger/Deutsch

Buch in der Datenbank seit 2009-11-28T20:32:33+01:00 (Vienna)
Detailseite zuletzt geändert am 2024-02-01T08:48:04+01:00 (Vienna)
ISBN/EAN: 9783827426574

ISBN - alternative Schreibweisen:
3-8274-2657-X, 978-3-8274-2657-4
Alternative Schreibweisen und verwandte Suchbegriffe:
Autor des Buches: engelen, galizia, eva maria engel, fleischhack maria, spektrum, giovanni, landfester
Titel des Buches: heureka, nsc kompendium, wissenschaften


Daten vom Verlag:

Autor/in: Eva-Maria Engelen
Titel: Heureka - Evidenzkriterien in den Wissenschaften - Ein Kompendium für den interdisziplinären Gebrauch
Verlag: Spektrum Akademischer Verlag; Spektrum Akademischer Verlag
264 Seiten
Erscheinungsjahr: 2011-12-20
Heidelberg; DE
Gedruckt / Hergestellt in Deutschland.
Sprache: Deutsch
6,28 € (DE)

EA; E107; eBook; Nonbooks, PBS / Naturwissenschaften allgemein; Geschichte der Naturwissenschaften; Verstehen; Geisteswissenschaften; Kulturwissenschaften; Literaturwissenschaft; Naturwissenschaften; Philosophie; Rechtswissenschaften; Soziologie; Wissenschaftsgeschichte; Wissenschaftstheorie; B; History of Science; Science, Humanities and Social Sciences, multidisciplinary; History of Science; Humanities and Social Sciences; History; Interdisziplinäre Studien; BB

Heureka” (ich habe es gefunden) soll Archimedes gerufen haben, als er in der Badewanne lag und sah, wie sein Körper das Wasser verdrängte. Unvermittelt war ihm der Zusammenhang klar, er hatte das Auftriebsgesetz verstanden, was ihm dazu verhalf, den Goldgehalt der Krone des Tyrannen zu bestimmen. Er entstieg der Wanne, rannte nackt durch die Straßen von Syrakus und rief weiterhin „ich habe es gefunden!“ Wie werden in einzelnen Disziplinen Heureka-Effekte hervorgerufen? Wann leuchtet Wissenschaftlern in einem Fach ein Argument, ein Gedanke ein, wie werden sie davon überzeugt? Was sind die disziplinären Standards und wie sieht die Praxis im akademischen Alltag dazu aus? 15 Wissenschaftlerinnen und Wissenschaftler aus den Natur-, Geistes- und Sozialwissenschaften geben hierauf ihre Antworten in einer verständlichen und gut zugänglichen Weise. a:3:{s:4:"NAME";s:7:"Product";s:5:"ATTRS";a:1:{s:9:"datestamp";s:8:"20231222";}s:5:"CHILD";a:14:{i:0;a:2:{s:4:"NAME";s:15:"RecordReference";s:5:"CDATA";s:32:"417af0c7da8d4ff7a230a4522f2724fd";}i:1;a:2:{s:4:"NAME";s:16:"NotificationType";s:5:"CDATA";s:2:"03";}i:2;a:2:{s:4:"NAME";s:17:"ProductIdentifier";s:5:"CHILD";a:3:{i:0;a:2:{s:4:"NAME";s:13:"ProductIDType";s:5:"CDATA";s:2:"01";}i:1;a:2:{s:4:"NAME";s:10:"IDTypeName";s:5:"CDATA";s:10:"VLB_ID_old";}i:2;a:2:{s:4:"NAME";s:7:"IDValue";s:5:"CDATA";s:7:"3964204";}}}i:3;a:2:{s:4:"NAME";s:17:"ProductIdentifier";s:5:"CHILD";a:3:{i:0;a:2:{s:4:"NAME";s:13:"ProductIDType";s:5:"CDATA";s:2:"01";}i:1;a:2:{s:4:"NAME";s:10:"IDTypeName";s:5:"CDATA";s:19:"Publishers Order No";}i:2;a:2:{s:4:"NAME";s:7:"IDValue";s:5:"CDATA";s:17:"978-3-8274-2657-4";}}}i:4;a:2:{s:4:"NAME";s:17:"ProductIdentifier";s:5:"CHILD";a:3:{i:0;a:2:{s:4:"NAME";s:13:"ProductIDType";s:5:"CDATA";s:2:"01";}i:1;a:2:{s:4:"NAME";s:10:"IDTypeName";s:5:"CDATA";s:19:"Publishers Order No";}i:2;a:2:{s:4:"NAME";s:7:"IDValue";s:5:"CDATA";s:8:"80012881";}}}i:5;a:2:{s:4:"NAME";s:17:"ProductIdentifier";s:5:"CHILD";a:2:{i:0;a:2:{s:4:"NAME";s:13:"ProductIDType";s:5:"CDATA";s:2:"02";}i:1;a:2:{s:4:"NAME";s:7:"IDValue";s:5:"CDATA";s:10:"382742657X";}}}i:6;a:2:{s:4:"NAME";s:17:"ProductIdentifier";s:5:"CHILD";a:2:{i:0;a:2:{s:4:"NAME";s:13:"ProductIDType";s:5:"CDATA";s:2:"03";}i:1;a:2:{s:4:"NAME";s:7:"IDValue";s:5:"CDATA";s:13:"9783827426574";}}}i:7;a:2:{s:4:"NAME";s:17:"ProductIdentifier";s:5:"CHILD";a:2:{i:0;a:2:{s:4:"NAME";s:13:"ProductIDType";s:5:"CDATA";s:2:"06";}i:1;a:2:{s:4:"NAME";s:7:"IDValue";s:5:"CDATA";s:25:"10.1007/978-3-8274-2657-4";}}}i:8;a:2:{s:4:"NAME";s:17:"ProductIdentifier";s:5:"CHILD";a:2:{i:0;a:2:{s:4:"NAME";s:13:"ProductIDType";s:5:"CDATA";s:2:"15";}i:1;a:2:{s:4:"NAME";s:7:"IDValue";s:5:"CDATA";s:13:"9783827426574";}}}i:9;a:2:{s:4:"NAME";s:17:"DescriptiveDetail";s:5:"CHILD";a:47:{i:0;a:2:{s:4:"NAME";s:18:"ProductComposition";s:5:"CDATA";s:2:"00";}i:1;a:2:{s:4:"NAME";s:11:"ProductForm";s:5:"CDATA";s:2:"EA";}i:2;a:2:{s:4:"NAME";s:17:"ProductFormDetail";s:5:"CDATA";s:4:"E107";}i:3;a:2:{s:4:"NAME";s:18:"ProductFormFeature";s:5:"CHILD";a:3:{i:0;a:2:{s:4:"NAME";s:22:"ProductFormFeatureType";s:5:"CDATA";s:2:"01";}i:1;a:2:{s:4:"NAME";s:23:"ProductFormFeatureValue";s:5:"CDATA";s:3:"BLU";}i:2;a:2:{s:4:"NAME";s:29:"ProductFormFeatureDescription";s:5:"CDATA";s:3:"47%";}}}i:4;a:2:{s:4:"NAME";s:18:"ProductFormFeature";s:5:"CHILD";a:3:{i:0;a:2:{s:4:"NAME";s:22:"ProductFormFeatureType";s:5:"CDATA";s:2:"01";}i:1;a:2:{s:4:"NAME";s:23:"ProductFormFeatureValue";s:5:"CDATA";s:3:"BRN";}i:2;a:2:{s:4:"NAME";s:29:"ProductFormFeatureDescription";s:5:"CDATA";s:3:"38%";}}}i:5;a:2:{s:4:"NAME";s:18:"ProductFormFeature";s:5:"CHILD";a:3:{i:0;a:2:{s:4:"NAME";s:22:"ProductFormFeatureType";s:5:"CDATA";s:2:"01";}i:1;a:2:{s:4:"NAME";s:23:"ProductFormFeatureValue";s:5:"CDATA";s:3:"GRN";}i:2;a:2:{s:4:"NAME";s:29:"ProductFormFeatureDescription";s:5:"CDATA";s:2:"4%";}}}i:6;a:2:{s:4:"NAME";s:18:"ProductFormFeature";s:5:"CHILD";a:3:{i:0;a:2:{s:4:"NAME";s:22:"ProductFormFeatureType";s:5:"CDATA";s:2:"01";}i:1;a:2:{s:4:"NAME";s:23:"ProductFormFeatureValue";s:5:"CDATA";s:3:"SLV";}i:2;a:2:{s:4:"NAME";s:29:"ProductFormFeatureDescription";s:5:"CDATA";s:2:"2%";}}}i:7;a:2:{s:4:"NAME";s:18:"ProductFormFeature";s:5:"CHILD";a:3:{i:0;a:2:{s:4:"NAME";s:22:"ProductFormFeatureType";s:5:"CDATA";s:2:"01";}i:1;a:2:{s:4:"NAME";s:23:"ProductFormFeatureValue";s:5:"CDATA";s:3:"YEL";}i:2;a:2:{s:4:"NAME";s:29:"ProductFormFeatureDescription";s:5:"CDATA";s:2:"9%";}}}i:8;a:2:{s:4:"NAME";s:22:"ProductFormDescription";s:5:"CDATA";s:5:"eBook";}i:9;a:2:{s:4:"NAME";s:18:"PrimaryContentType";s:5:"CDATA";s:2:"10";}i:10;a:2:{s:4:"NAME";s:20:"CountryOfManufacture";s:5:"CDATA";s:2:"DE";}i:11;a:2:{s:4:"NAME";s:11:"TitleDetail";s:5:"CHILD";a:2:{i:0;a:2:{s:4:"NAME";s:9:"TitleType";s:5:"CDATA";s:2:"01";}i:1;a:2:{s:4:"NAME";s:12:"TitleElement";s:5:"CHILD";a:3:{i:0;a:2:{s:4:"NAME";s:17:"TitleElementLevel";s:5:"CDATA";s:2:"01";}i:1;a:2:{s:4:"NAME";s:9:"TitleText";s:5:"CDATA";s:48:"Heureka - 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eBook; Nonbooks, PBS / Medizin/Klinische Fächer; Genetik, Medizin; Verstehen; Chromosom; DNA; DNA analysis; development; genes; genetics; protein; C; Human Genetics; Medical Genetics; Biomedical and Life Sciences; BB eng 55.00 EUR 1 Chorionic Villus Sampling.- Early Trophoblast Development.- Historical Perspectives.- Techniques of Chorionic Villus Sampling.- Overview.- Transcervical Catheter Aspiration.- Transcervical Endoscopy.- Transcervical Biopsy Forceps.- Transabdominal Sampling.- Sample Processing.- Chromosomal Analysis.- Direct Karyotype Analysis.- Karyotype Analysis of Cultured Villi.- Results of Karyotype Analysis.- Metabolic Analysis of Chorionic Villi.- Overview.- Metabolic Disorders Diagnosed.- Pitfalls of Metabolic Diagnosis.- DNA Analysis of Chorionic Villi.- Overview.- DNA Disorders Diagnosed.- Pitfalls in DNA Diagnosis of Chorionic Villi.- Contraindications to Chorionic Villus Sampling.- Safety of Chorionic Villus Sampling.- Future Applications.- References.- 2 The Molecular Genetics of Hemophilia A and B in Man: Factor VIII and Factor IX Deficiency.- Hemophilia A. Factor VIII Gene.- Cloning and Characterization of Factor VIII Gene and the Deduced Protein Sequence.- Mutations in the Factor VIII Gene in Hemophilia A.- DNA Polymorphisms in the Factor VIII Gene.- Hemophilia B. Factor IX Gene.- Cloning and Characterization of Factor IX Gene.- Mutations in the Factor IX Gene in Hemophilia B.- DNA Polymorphisms in the Factor IX Gene.- X-Chromosome Mapping of Factor VIII and IX Genes.- Lessons from the Study of the Molecular Genetics of Hemophilia.- References.- 3 Cloning of the Duchenne/Becker Muscular Dystrophy Locus.- Background Information: Clinical Aspects of DMD.- Background Information: Biochemical Aspects of DMD.- Chromosomal Map Position.- Strategies to Approach the Gene.- Detection of Deletions in DMD and BMD Patients.- Identification of the DMD Transcript.- The DMD Locus.- The DMD/BMD Protein.- Future Prospects.- References.- 4 Trisomy 21: Molecular and Cytogenetic Studies of Nondisjunction.- Scope of the Problem.- Problems to Be Addressed.- Correct and Complete Ascertainment of Parental Origin of Nondisjunction.- The Maternal Age Conundrum: Is the Maternal Age Effect due to Increased Production of Abnormal Eggs or Decreased Destruction of Abnormal Embryos?.- Identification of Couples at High Risk for Trisomy 21 Offspring..- Is There a Correlation between Crossing Over and Nondisjunction on Chromosome 21?.- The Effect of the Parental Origin of Trisomy on the Phenotype of the Conceptus.- Molecular Cytogenetic Organization of Chromosome 21: Implications for Studies of Nondisjunction.- Organization of DNA Sequences on the Short Arms of the Acrocentric Chromosomes.- The Interspersed 724 Family on the Acrocentric Short Arms.- Isolation of a Large Number of Polymorphic Single-Copy DNA Probes That Span the Long Arm of Chromosome 21.- Lessons from a Pilot Study.- An Experimental Design to Answer the Basic Questions Related to Nondisjunction.- Complete Ascertainment of Parental Origin and Meiotic Stage of Nondisjunction.- The Maternal Age Conundrum: Is the Maternal Age Effect due to Increased Production of Abnormal Eggs or Decreased Destruction of Abnormal Embryos?.- Identification of Couples at High Risk for Trisomy 21 Offspring.- Is There a Correlation between Crossing Over and Nondisjunction on Chromosome 21?.- The Effect of the Parental Origin of Trisomy on the Phenotype of the Conceptus.- Overview.- References.- 5 Molecular Genetics of Human Salivary Proteins and Their Polymorphisms.- Salivary Protein Polymorphisms.- Salivary Amylase (Amy).- B12-Binding Protein (Rs).- Salivary Acid Phosphatase (s-AcP).- Genetic Polymorphisms of Proline-Rich Proteins (PRPs).- Salivary Peroxidase (SAPX).- Parotid Basic Proteins (Pb).- Other Polymorphisms in Human Saliva.- Molecular Genetic Studies.- The Proline-Rich Protein (PRP) Gene Family.- Statherin.- Amylase Gene Family.- Cystatin Gene Family.- References.- Addendum. 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Embryos?.- Identification of Couples at High Risk for Trisomy 21 Offspring..- Is There a Correlation between Crossing Over and Nondisjunction on Chromosome 21?.- The Effect of the Parental Origin of Trisomy on the Phenotype of the Conceptus.- Molecular Cytogenetic Organization of Chromosome 21: Implications for Studies of Nondisjunction.- Organization of DNA Sequences on the Short Arms of the Acrocentric Chromosomes.- The Interspersed 724 Family on the Acrocentric Short Arms.- Isolation of a Large Number of Polymorphic Single-Copy DNA Probes That Span the Long Arm of Chromosome 21.- Lessons from a Pilot Study.- An Experimental Design to Answer the Basic Questions Related to Nondisjunction.- Complete Ascertainment of Parental Origin and Meiotic Stage of Nondisjunction.- The Maternal Age Conundrum: Is the Maternal Age Effect due to Increased Production of Abnormal Eggs or Decreased Destruction of Abnormal Embryos?.- Identification of Couples at High Risk for Trisomy 21 Offspring.- Is There a Correlation between Crossing Over and Nondisjunction on Chromosome 21?.- The Effect of the Parental Origin of Trisomy on the Phenotype of the Conceptus.- Overview.- References.- 5 Molecular Genetics of Human Salivary Proteins and Their Polymorphisms.- Salivary Protein Polymorphisms.- Salivary Amylase (Amy).- B12-Binding Protein (Rs).- Salivary Acid Phosphatase (s-AcP).- Genetic Polymorphisms of Proline-Rich Proteins (PRPs).- Salivary Peroxidase (SAPX).- Parotid Basic Proteins (Pb).- Other Polymorphisms in Human Saliva.- Molecular Genetic Studies.- The Proline-Rich Protein (PRP) Gene Family.- Statherin.- Amylase Gene Family.- Cystatin Gene Family.- References.- 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