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  • 1
    UID:
    (DE-627)1610707052
    Format: XXV, 753 S. , Ill., Kt. , 23 cm
    ISBN: 9781926599106
    Series Statement: Classics of the radical Reformation 12
    Uniform Title: Briefe und Schriften oberdeutscher Täufer, 1527 - 1555 〈engl.〉
    Note: Aus dem Deutschen über. Translation of the "Kunstbuch" (Burgerbibliothek Bern cod. 464), a ms. compilation made in 1561 by Jörg Maler of several writings by the Anabaptist leader Pilgrim Marbeck and his followers. Based on the critical ed. of the ms. published as: Briefe und Schriften oberdeutscher Täufer, 1527-1555 ([Gütersloh] : Gütersloher Verlagshaus, c2007). - Includes bibliographical references and indexes
    Language: English
    Keywords: Oberdeutschland ; Täufer ; Geschichte 1527-1555 ; Quelle
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  • 2
    UID:
    (DE-101)365338095
    Format: XVI, 400 S. , Beil. (35 S. mit Abb.)
    Language: German
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  • 3
    UID:
    (DE-101)1003295037
    Format: [S.l.] @ : [s.n.] @ , [348] Bl. , 4
    Note: [Zwisch. Tit. dat.:] 1843
    Language: German
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  • 4
    Online Resource
    Online Resource
    Dordrecht : Springer Netherlands
    UID:
    (DE-627)1746416106
    Format: 1 online resource (361 pages)
    ISBN: 9789400730120
    Series Statement: Subcellular Biochemistry Ser. v.58
    Content: Intro -- Preface -- Contents -- Abbreviations -- Chapter 1 The Phosphatidylinositol 4-Kinases: Don't Call it a Comeback -- 1.1 Introduction -- 1.2 The Type II PtdIns 4-Kinases -- 1.2.1 PtdIns4KII Gene Family and Domain Structure -- 1.2.2 PtdIns4KII Expression, Localisation and Regulation -- 1.3 The Type III PtdIns 4-Kinases -- 1.3.1 Gene Family and Domain Structure -- 1.3.2 PtdIns4KIII'141 Expression, Localisation and Regulation -- 1.3.3 PtdIns4KIII'142 Expression, Localisation and Regulation -- 1.4 Cellular Functions of PtdIns4Ks -- 1.4.1 PtdIns4Ks in Signalling Pathways -- 1.4.1.1 PtdIns4KIIs in Signalling Pathways -- 1.4.1.2 PtdIns4KIIIs in Signalling Pathways -- 1.4.2 PtdIns4Ks in Intracellular Traffic -- 1.4.2.1 Type II PtdIns4Ks and Intracellular Trafficking Pathways -- 1.4.2.2 PtdIns4KII'141 and Endosomal Traffic -- 1.4.2.3 Type III PtdIns4Ks and Membrane Traffic -- 1.5 PtdIns4K Biology in the Whole Organism -- 1.6 Conclusions -- References -- Chapter 2 PIP Kinases from the Cell Membrane to the Nucleus -- 2.1 Introduction -- 2.2 The Enzymes. Sequence, Structure and Enzymology -- 2.2.1 Sequence and Structure of Phosphatidylinositol Phosphate Kinases -- 2.2.1.1 Sequences of PIP Kinases -- 2.2.1.2 PIP Kinase Structure -- 2.2.2 Enzymology of PIPKs -- 2.3 Membrane Associated PIPKs Drive Cell Migration and Vesicle Trafficking -- 2.3.1 PIPKs Help Regulate Directional Migration -- 2.3.1.1 PIPKs Regulate PIP2 Synthesis at the Leading Edge to Drive Membrane Protrusion -- 2.3.1.2 PIPKIg Regulates the Formation and Maturation of Integrin-mediated Contacts -- 2.3.1.3 Trafficking of Integrin-containing Vesicles to the Leading Edge Is Mediated by PIPKIg and PIP2 -- 2.3.1.4 Rear Retraction of the Cell Requires the Dissociation and Internalization of Integrin and Acto-myosin Contractility.
    Note: Description based on publisher supplied metadata and other sources
    Additional Edition: 9789401781572
    Additional Edition: Erscheint auch als Druck-Ausgabe 9789401781572
    Language: English
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  • 5
    Online Resource
    Online Resource
    Dordrecht : Springer Netherlands
    UID:
    (DE-602)gbv_1651333696
    Format: Online-Ressource (XV, 460p. 44 illus., 23 illus. in color, digital)
    ISBN: 9789400730151
    Series Statement: Subcellular Biochemistry 59
    Additional Edition: ISBN 9789400730144
    Additional Edition: Buchausg. u.d.T. Phosphoinositides ; 2: The diverse biological functions Dordrecht [u.a.] : Springer, 2012 ISBN 9789400730144
    Language: English
    URL: Cover
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  • 6
    UID:
    (DE-605)TT050413163
    ISBN: 9789400730120
    Series Statement: Subcellular Biochemistry 58
    Additional Edition: Erscheint auch als Druck-Ausgabe 9789400730113
    Language: English
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  • 7
    Online Resource
    Online Resource
    Dordrecht : Springer Netherlands
    UID:
    (DE-627)1651396817
    Format: Online-Ressource (XV, 352 p. 32 illus., 13 illus. in color, digital)
    ISBN: 9789400730120 , 1280787333 , 9781280787331
    Series Statement: Subcellular Biochemistry 58
    Content: John D. York
    Content: Phosphoinositides play a major role in cellular signaling and membrane organization. During the last three decades we have learned that enzymes turning over phosphoinositides control vital physiological processes and are involved in the initiation and progression of cancer, inflammation, neurodegenerative, cardiovascular, metabolic disease and more. In two volumes, this book elucidates the crucial mechanisms that control the dynamics of phosphoinositide conversion. Starting out from phosphatidylinositol, a chain of lipid kinases collaborates to generate the oncogenic lipid phosphatidylinositol(3,4,5)-trisphosphate. For every phosphate group added, there are specific lipid kinases - and phosphatases to remove it. Additionally, phospholipases can cleave off the inositol head group and generate poly-phosphoinositols, which act as soluble signals in the cytosol. Volume I untangles the web of these enzymes and their products, and relates them to function in health and disease. Phosphoinositide 3-kinases and 3-phosphatases have received a special focus in volume I, and recent therapeutic developments in human disease are presented along with a historical perspective illustrating the impressive progress in the field.
    Note: Description based upon print version of record , Preface; Contents; Abbreviations; Chapter 1 The Phosphatidylinositol 4-Kinases: Don't Call it a Comeback; 1.1 Introduction; 1.2 The Type II PtdIns 4-Kinases; 1.2.1 PtdIns4KII Gene Family and Domain Structure; 1.2.2 PtdIns4KII Expression, Localisation and Regulation; 1.3 The Type III PtdIns 4-Kinases; 1.3.1 Gene Family and Domain Structure; 1.3.2 PtdIns4KIII'141 Expression, Localisation and Regulation; 1.3.3 PtdIns4KIII'142 Expression, Localisation and Regulation; 1.4 Cellular Functions of PtdIns4Ks; 1.4.1 PtdIns4Ks in Signalling Pathways; 1.4.1.1 PtdIns4KIIs in Signalling Pathways , 1.4.1.2 PtdIns4KIIIs in Signalling Pathways1.4.2 PtdIns4Ks in Intracellular Traffic; 1.4.2.1 Type II PtdIns4Ks and Intracellular Trafficking Pathways; 1.4.2.2 PtdIns4KII'141 and Endosomal Traffic; 1.4.2.3 Type III PtdIns4Ks and Membrane Traffic; 1.5 PtdIns4K Biology in the Whole Organism; 1.6 Conclusions; References; Chapter 2 PIP Kinases from the Cell Membrane to the Nucleus; 2.1 Introduction; 2.2 The Enzymes. Sequence, Structure and Enzymology; 2.2.1 Sequence and Structure of Phosphatidylinositol Phosphate Kinases; 2.2.1.1 Sequences of PIP Kinases; 2.2.1.2 PIP Kinase Structure , 2.2.2 Enzymology of PIPKs2.3 Membrane Associated PIPKs Drive Cell Migration and Vesicle Trafficking; 2.3.1 PIPKs Help Regulate Directional Migration; 2.3.1.1 PIPKs Regulate PIP2 Synthesis at the Leading Edge to Drive Membrane Protrusion; 2.3.1.2 PIPKIg Regulates the Formation and Maturation of Integrin-mediated Contacts; 2.3.1.3 Trafficking of Integrin-containing Vesicles to the Leading Edge Is Mediated by PIPKIg and PIP2; 2.3.1.4 Rear Retraction of the Cell Requires the Dissociation and Internalization of Integrin and Acto-myosin Contractility , 2.3.2 PIP Kinases in Adaptor Protein Complex Assembly and Protein Trafficking2.3.2.1 AP Complexes; 2.3.2.2 PIP Kinases in Regulation of AP Complex Assembly; 2.4 Nuclear Localized PIPKs Regulate Gene Expression and mRNA Processing; 2.4.1 Nuclear PIP Kinases and Phosphoinositides; 2.4.1.1 PIPKs and PIP2 at the Nuclear Envelope; 2.4.1.2 The Intra-nuclear PIPKs and PIP2; 2.4.2 Regulation and Functions of the Nuclear PIPKs; 2.4.2.1 Regulation of the Nuclear PIPKIbold0mu mumu Raw; 2.4.2.2 Regulation of the Nuclear PIPKIIbold0mu mumu bbRawbbbb/IIbold0mu mumu Raw , 2.4.3 Downstream Signaling of the Nuclear PIPK and PIP2References; Chapter 3 The Phospholipase C Isozymes and Their Regulation; 3.1 Introduction; 3.2 Phosphoinositide-specific PLC; 3.3 Catalytic Function and Structure of Conserved Core Domains of PLC; 3.4 Mechanism of PtdIns(4,5)P2 Hydrolysis; 3.5 PLC Subfamilies and Their Regulation; 3.5.1 PLC-d Isozymes; 3.5.1.1 Regulation; 3.5.1.2 Physiology; 3.5.2 PLC-bold0mu mumu Raw Isozymes; 3.5.2.1 Regulation; 3.5.2.2 Physiology; 3.5.3 PLC-bold0mu mumu Raw Isozymes; 3.5.3.1 Regulation; 3.5.3.2 Physiology; 3.5.4 PLC-bold0mu mumu Raw; 3.5.4.1 Regulation , 3.5.4.2 Physiology
    Additional Edition: 9789400730113
    Additional Edition: Buchausg. u.d.T. Phosphoinositides ; 1: Enzymes of synthesis and degradation Dordrecht [u.a.] : Springer, 2012 9789400730113
    Language: English
    Subjects: Biology
    RVK:
    Keywords: Phosphoinositide ; Biologischer Abbau ; Phosphoinositide ; Biosynthese
    URL: Cover
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  • 8
    Online Resource
    Online Resource
    [s.l.] : Springer Netherlands
    UID:
    (DE-627)719233070
    Format: Online Ressource (460 S.)
    Edition: 1. Aufl.
    Edition: Online-Ausg. 2011 Electronic reproduction; Available via World Wide Web
    ISBN: 9400730144
    Series Statement: Subcellular Biochemistry, 59 v.59
    Content: John D. York
    Content: Phosphoinositides play a major role in cellular signaling and membrane organization. During the last three decades we have learned that enzymes turning over phosphoinositides control vital physiological processes and are involved in the initiation and progression of cancer, inflammation, neurodegenerative, cardiovascular, metabolic disease and more. In two volumes, this book elucidates the crucial mechanisms that control the dynamics of phosphoinositide conversion. Starting out from phosphatidylinositol, a chain of lipid kinases collaborates to generate the oncogenic lipid phosphatidylinositol
    Note: Description based upon print version of record , Preface; Contents; Abbreviations; Chapter 1 Ca2+ Signalling by IP3 Receptors; 1.1 Introduction; 1.2 Ca2+ Is a Versatile and Ubiquitous Intracellular Messenger; 1.3 IP3 Receptors: An Overview; 1.4 Activation of IP3 Receptors by Ca2+ and IP3; 1.5 Structure and Function of the IP3 Receptor Pore; 1.6 How Does IP3 Binding Cause the Pore to Open?; 1.7 Clustered IP3 Receptors and Elementary Events; References; Chapter 2 Phosphoinositide Signaling During Membrane Transport in Saccharomyces Cerevisiae; 2.1 Phosphoinositide Metabolism in the Yeast Saccharomyces Cerevisiae , 2.2 Binding Domains and Effector Proteins of PI3P2.2.1 The FYVE Domain; 2.2.2 The Phox Homology (PX) Domain; 2.3 Effectors of PI3,5P2 and Their Roles in Membrane Trafficking; 2.4 Roles for PI4P in Membrane Transport; 2.4.1 Functions of PI4P Synthesized by Pik1p in the Golgi; 2.4.2 Functions of PI4P Synthesized by Stt4p at the Plasma Membrane; 2.5 Roles for PI4,5P2 in Membrane Transport; 2.6 Perspectives and Conclusions; References; Chapter 3 Phosphoinositides in the Mammalian Endo-lysosomal Network; 3.1 Introduction---The Endo-lysosomal Network , 3.2 Subcellular Distribution of Phosphoinositides3.3 Endosomal Phosphoinositide Kinases and Phosphatases; 3.3.1 PtdIns(4,5)P2-to-PtdIns(4)P Switch; 3.3.2 PtdIns-to-PtdIns(3)P Switch; 3.3.3 PtdIns(3)P-to-PtdIns(3,5)P2 Switch; 3.3.4 Other Phosphoinositide Switches; 3.4 Sensing the Phosphoinositide Identity Code; 3.5 PtdIns(4,5)P2 in Endocytosis; 3.5.1 Initiation and Assembly of Clathrin-coat Pits; 3.5.2 Maturation of Clathrin-coated Pits; 3.5.3 Formation of Clathrin-coated Vesicles; 3.6 PtdIns(3)P and MVB Biogenesis; 3.6.1 ESCRT-0; 3.6.2 ESCRT-I and -II; 3.6.3 ESCRT-III , 3.6.4 In Vitro Reconstitution of ESCRT Function3.6.5 ESCRT-independent, Phosphoinositide-mediated Sorting into MVBs; 3.7 Phosphoinositides and Retrograde Transport; 3.7.1 The Retromer Complex; 3.7.1.1 Membrane Deformation Within the Retromer Pathway; 3.7.1.2 Cargo Selection---The Mammalian VPS26-VPS29-VPS35 Sub-complex; 3.7.1.3 Processing of Retromer Tubules; 3.7.2 Phosphoinositide Regulation of Retromer-independent Retrograde Transport; 3.7.3 PtdIns(3,5)P2 in Retrograde Transport; 3.8 Phosphoinositides in Endosomal Recycling; 3.8.1 EHD Proteins and Recycling Tubules , 3.8.2 Sorting Nexins---Another Route for the Generation of Recycling Tubules3.8.3 Sorting Nexins and Cargo Recognition; 3.8.4 Carrier Movement and Fusion with the Plasma Membrane; 3.9 Future Perspectives; References; Chapter 4 Role of PI(4,5)P2 in Vesicle Exocytosis and Membrane Fusion; 4.1 Introduction; 4.2 Background on Membrane Fusion in Vesicle Exocytosis; 4.3 Discovery of a Role for PI(4,5)P2 in Trafficking to the Plasma Membrane; 4.4 A Role for PI(4,5)P2 in the Priming Reactions of Regulated DCV Exocytosis; 4.5 A Role for PI(4,5)P2 in Other Forms of Vesicle Exocytosis , 4.6 Is PI(4,5)P2 Spatially Segregated to Sites of Exocytosis? , Electronic reproduction; Available via World Wide Web
    Additional Edition: 9400730152
    Additional Edition: 9789400730151
    Additional Edition: 9789400795518
    Additional Edition: Print version Phosphoinositides II : The Diverse Biological Functions
    Language: English
    Subjects: Biology
    RVK:
    RVK:
    Keywords: Electronic books
    URL: Volltext  (lizenzpflichtig)
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  • 9
    UID:
    (DE-627)72727340X
    Format: 51 - 93
    Content: The inertial coupling approach for the mo-mentum transfer at the ocean-atmosphere interface, which is based on the assumption of a similarity hypothesis in which the ratio between the water and air reference velocities is equal to the square root of the ratio between the air and water densities, is reviewed using a wave model. In this model, the air and water reference velocities are identified, respectively, with the spectrally weighted phase velocity of the gravity waves and the Stokes velocity at the water roughness length, which are evaluated in terms of the dimensionless frequency limits in Toba's equilibrium spectrum. It is shown that the similarity hypothesis is approximately satisfied by the wave model over the ränge of wave ages encountered in typical sea states, and that the predicted values of the dimensionless surface drift velocity, the dimensionless water reference velocity, and the Charnock constant are in reasonable agreement with observational evidence. The application of the bulk relationship for the surface shear stress, derived from the inertial coupling hypothesis in general circulation modeling, is also discussed.
    Note: Journal Ocean Dynamics, Volume 52, Number 2
    Language: Undetermined
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  • 10
    UID:
    (DE-605)TT050412456
    Edition: 2012
    ISBN: 9789400730151
    Series Statement: Subcellular Biochemistry 59
    Additional Edition: Erscheint auch als Druck-Ausgabe 9789400730144
    Language: English
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