GLORIA

GEOMAR Library Ocean Research Information Access

X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    CO2 Conversion and Utilization : Photocatalytic and Electrochemical Methods and Applications. (2023)
    Newark :John Wiley & Sons, Incorporated,
    Details
    Keywords: Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (362 pages)
    Edition: 1st ed.
    ISBN: 9783527841783
    URL: https://ebookcentral.proquest.com/lib/geomar/detail.action?docID=7276411
    Language: English
    Note: Cover -- Title Page -- Copyright -- Contents -- Preface -- Chapter 1 Measurement Systems and Parameters for CO2 Photo/Electro‐Conversion -- 1.1 Introduction -- 1.2 The Measurement Systems for CO2 Photo/Electro‐Conversion -- 1.2.1 The Measurement Systems of Photocatalytic CO2 Reduction -- 1.2.1.1 CO2 Reduction System Under Liquid‐Phase Reaction System -- 1.2.1.2 CO2 Reduction System in Gas‐Phase Reaction System -- 1.2.1.3 Detection of CO2 Reduction Products -- 1.2.2 The Measurement Systems of Electrocatalytic CO2 Reduction -- 1.2.2.1 Electrocatalytic CO2 Reduction Reaction Test in H‐Cell -- 1.2.2.2 Electrocatalytic CO2 Reduction Reaction Test in Flow Cell -- 1.2.2.3 Electrocatalytic CO2 Reduction Reaction Test in MEA -- 1.2.3 The Measurement Systems of Photo‐Electro‐Catalytic CO2 Reduction -- 1.2.3.1 Basic Device for Photocatalytic CO2 Reduction Experiment -- 1.2.3.2 Other Devices for Photocatalytic CO2 Reduction -- 1.2.3.3 Detection of CO2 Reduction Reaction Products -- 1.3 The Parameters for CO2 Photo‐Conversion -- 1.3.1 The Parameters of Photocatalytic CO2 Reduction -- 1.3.1.1 Evaluation Parameters of Photocatalytic CO2 Reduction Activity -- 1.3.1.2 Evaluation Parameters of Photocatalytic CO2 Reduction Selectivity -- 1.3.1.3 Evaluation Parameters of Photocatalytic CO2 Reduction Stability -- 1.3.2 The Parameters of Electrocatalytic CO2 Reduction -- 1.3.3 The Parameters of Photo‐Electro‐Catalytic CO2 Reduction -- 1.3.3.1 Overpotential -- 1.3.3.2 Total Photocurrent Density (jph) and Partial Photocurrent Density (jA) -- 1.3.3.3 Faraday Efficiency (FE) -- 1.3.3.4 Solar Energy Conversion Efficiency -- 1.3.3.5 Apparent Quantum Yield (AQY) -- 1.3.3.6 Electrochemical Active Area (ECSA) -- 1.3.3.7 Electrochemical Impedance (EIS) -- 1.3.3.8 Tafel Slope (Tafel) -- 1.3.3.9 Photocatalytic Stability -- References. , Chapter 2 CO2 Photo/Electro‐Conversion Mechanism -- 2.1 Introduction -- 2.2 CO2 Photo‐Conversion Mechanism -- 2.3 CO2 Electro‐Conversion Mechanism -- 2.3.1 Thermodynamics of CO2 Reduction -- 2.3.2 Pathways of Electrochemical CO2 Reduction -- 2.3.2.1 Electrochemical CO2 Reduction to CO -- 2.3.2.2 Electrochemical CO2 Reduction to Formate -- 2.3.2.3 Electrochemical CO2 Reduction to Products Beyond CO -- 2.4 Summary and Perspectives -- References -- Chapter 3 Cu‐Based Metal Materials for Electrocatalytic CO2 Reduction -- 3.1 Introduction -- 3.2 Cu‐Based Metal Materials for Electrocatalytic CO2 Reduction -- 3.2.1 Cu Materials for Electrocatalytic CO2 Reduction -- 3.2.2 Cu‐Based Bimetal Materials for Electrocatalytic CO2 Reduction -- 3.2.2.1 Cu-Au -- 3.2.2.2 Cu-Ag -- 3.2.2.3 Cu-Pd -- 3.2.2.4 Cu-Sn -- 3.2.2.5 Cu-Bi -- 3.2.2.6 Cu-In -- 3.2.2.7 Cu-Al -- 3.2.2.8 Cu-Zn -- 3.2.3 Cu‐Based Trimetallic Materials for Electrocatalytic CO2 Reduction -- 3.3 Conclusion and Outlook -- Acknowledgment -- References -- Chapter 4 Cu‐Free Metal Materials for Electrocatalytic CO2 Conversion -- 4.1 Introduction -- 4.2 CO‐Producing Metals -- 4.2.1 Au‐Based Electrocatalysts -- 4.2.2 Ag‐Based Electrocatalysts -- 4.2.3 Pd‐Based Electrocatalysts -- 4.2.4 Zn‐Based Electrocatalysts -- 4.3 HCOOH‐Producing Metals -- 4.3.1 Sn‐Based Electrocatalysts -- 4.3.2 Bi‐Based Electrocatalysts -- 4.3.3 In‐Based Electrocatalysts -- References -- Chapter 5 Organic-Inorganic Hybrid Materials for CO2 Photo/Electro‐Conversion -- 5.1 Hybrid Materials for Photocatalytic CO2 Reduction Reaction (CO2RR) -- 5.1.1 Photocatalytic CO2RR on p‐type Semiconductor/Molecule Catalysts -- 5.1.2 Photocatalytic CO2RR on Carbon Nitride (C3N4)‐supported Molecular Catalysts -- 5.1.3 Photocatalytic CO2RR on Polyoxometalates (POMs)‐based Catalysts -- 5.2 Hybrid Materials for Electrochemical CO2RR. , 5.2.1 Electrochemical CO2RR on Carbon‐supported Molecular Catalysts -- 5.2.2 Electrochemical CO2RR on TiO2‐based Hybrid Materials -- 5.3 Hybrid Materials for Photoelectrochemical (PEC) CO2RR -- 5.4 Challenge and Opportunity -- References -- Chapter 6 Metal-Organic Framework Materials for CO2 Photo‐/Electro‐Conversion -- 6.1 Introduction -- 6.2 Photocatalysis -- 6.2.1 MOFs with Photoactive Organic Ligands -- 6.2.2 MOFs with Photoactive Metal Nodes -- 6.2.3 MOF‐Based Hybrid System -- 6.3 Electrocatalysis -- 6.3.1 MOFs with Active Sites at Organic Ligands -- 6.3.2 MOFs with Active Sites at Metal Nodes -- 6.3.3 MOF‐Based Hybrid System -- 6.4 Photoelectrocatalysis -- 6.5 Conclusion and Outlook -- Acknowledgment -- References -- Chapter 7 Covalent Organic Frameworks for CO2 Photo/Electro‐Conversion -- 7.1 Introduction -- 7.2 COFs for Photocatalytic CO2 Reduction -- 7.2.1 Imine‐Linked COFs -- 7.2.2 Ketoenamine COFs -- 7.2.3 Carbon-Carbon Double Bond‐Linked COFs -- 7.2.4 Dioxin‐Linked COFs -- 7.2.5 Azine‐Linked and Hydrazone‐Linked COFs -- 7.3 COFs for Electrocatalytic CO2 Reduction -- 7.3.1 Porphyrin‐Based COFs -- 7.3.2 Phthalocyanine‐Based COFs -- 7.3.3 Other COFs -- 7.4 Challenges and Perspectives -- References -- Chapter 8 Single/Dual‐Atom Catalysts for CO2 Photo/Electro‐Conversion -- 8.1 Introduction -- 8.2 Synthetic Methods of Single/Dual‐Atom Catalysts -- 8.2.1 Single‐Atom Photocatalysts -- 8.2.2 Dual‐Atom Photocatalysts -- 8.2.3 Single‐Atom Electro‐Catalysts -- 8.2.4 Dual‐Atom Electro‐Catalysts -- 8.3 CO2 Photo‐Conversion -- 8.4 CO2 Electro‐Conversion -- 8.5 Summary and Perspective -- References -- Chapter 9 Homogeneous Catalytic CO2 Photo/Electro‐Conversion -- 9.1 Introduction -- 9.2 Homogeneous Catalytic CO2 Electro‐Conversion -- 9.2.1 The Structure Homogeneous Electrocatalytic CO2 Reduction System. , 9.2.2 Products in Homogeneous Electrocatalytic CO2 Reduction -- 9.2.3 Characterizing the Performance of Molecular Electrocatalysts -- 9.2.3.1 Selectivity -- 9.2.3.2 Activity -- 9.2.3.3 Overpotential (η) -- 9.2.3.4 Stability -- 9.2.4 Catalysts for Homogeneous Electrocatalytic CO2 Reduction -- 9.3 Homogeneous Photocatalytic CO2 Reduction -- 9.3.1 Mechanism of Homogeneous Photocatalytic CO2 Reduction -- 9.3.2 Characterizing the Performance of Photocatalysis -- 9.3.3 Photosensitizers Used in Homogeneous Photocatalytic CO2 Reduction -- 9.3.4 Sacrificial Electron Donors in Homogeneous Photocatalytic CO2 Reduction -- 9.3.5 Catalysts Used in Homogeneous Photocatalytic CO2 Reduction -- 9.4 Summary and Perspective -- Acknowledgments -- References -- Chapter 10 High‐Entropy Alloys for CO2 Photo/Electro‐Conversion -- 10.1 Introduction -- 10.2 Reaction Pathways and Evaluation Parameters of Electrochemical CO2RR -- 10.2.1 Reaction Pathways of CO2RR -- 10.2.2 Evaluation Parameters of Electrochemical CO2RR -- 10.2.2.1 Faraday Efficiency -- 10.2.2.2 Current Density -- 10.2.2.3 Turnover Number (TON) -- 10.2.2.4 Turnover Frequency (TOF) -- 10.2.2.5 Overpotential -- 10.3 Characteristics and Synthesis of HEAs -- 10.3.1 Characteristics of HEAs -- 10.3.1.1 The Cocktail Effect -- 10.3.1.2 The Sluggish Diffusion Effect -- 10.3.1.3 The High‐entropy Effect -- 10.3.1.4 The Lattice Distortion Effect -- 10.3.1.5 The Phase Structure -- 10.3.2 Synthesis of HEAs -- 10.3.2.1 Top‐Down Method -- 10.3.2.2 Down-Top Method -- 10.4 High‐Entropy Alloys for CO2RR -- 10.5 Summary and Outlook -- References -- Chapter 11 Semiconductor Composite Materials for Photocatalytic CO2 Reduction -- 11.1 Introduction -- 11.2 TiO2‐Based Composite Photocatalysts -- 11.2.1 Mixed‐Phase TiO2 Composites -- 11.2.2 Metal‐Modified TiO2 -- 11.2.3 Nonmetallic‐Modified TiO2. , 11.2.4 Organic Photosensitizer‐Modified TiO2 -- 11.2.5 Composited TiO2 Catalyst -- 11.3 Metal Oxides/Hydroxides‐Based Composite Photocatalysts -- 11.3.1 Binary Metal Oxide -- 11.3.2 Ternary Metal Oxide -- 11.3.3 Oxide Perovskite -- 11.3.4 Transition Metal Hydroxide -- 11.3.5 Layered Double Hydroxides (LDHs) -- 11.4 Metal Chalcogenides/Nitrides‐Based Composite Photocatalysts -- 11.4.1 Metal Chalcogenides‐Based Composite Photocatalysts -- 11.4.2 Metal Nitrides‐Based Composite Photocatalysts -- 11.5 C3N4‐Based Composite Photocatalysts -- 11.5.1 Change the Morphology and Structure -- 11.5.2 Doped Elements and Other Structural Units -- 11.5.3 Influence of Cocatalyst -- 11.5.4 Constructing Heterojunction -- 11.6 MOFs‐Derived Composite Photocatalysts -- 11.6.1 Tunable Frame Structure -- 11.6.2 High Specific Surface Area Enhances CO2 Adsorption -- 11.6.3 MOFs‐Derived Composite Photocatalysts -- 11.7 Nonmetal‐Based Composite Photocatalysts -- 11.7.1 Graphene Oxide‐Based Composite Photocatalysts -- 11.7.2 SiC‐Based Composite Photocatalysts -- 11.7.3 BN‐Based Composite Photocatalysts -- 11.7.4 Black Phosphorus‐Based Composite Photocatalysts -- 11.7.5 COFs‐Based Composite Photocatalysts -- 11.7.6 CMPs‐Based Composite Photocatalysts -- 11.8 Conclusions and Perspectives -- References -- Chapter 12 Carbon‐Based Materials for CO2 Photo/Electro‐Conversion -- 12.1 Advances of Carbon‐Based Materials -- 12.1.1 Heteroatom‐Doped Carbon -- 12.1.2 Metal‐Based Carbon Composites -- 12.1.3 Carbon-Carbon Composites -- 12.1.4 Pore Construction -- 12.2 Background of CO2 Conversion -- 12.3 EC CO2 Conversion -- 12.3.1 Heteroatom‐Doped Carbon in EC CO2 Conversion -- 12.3.2 Metal‐Modified Carbon Materials in EC CO2 Conversion -- 12.3.3 Carbon-Carbon Composites in EC CO2 Conversion -- 12.3.4 Pore Engineering in EC CO2 Conversion -- 12.4 PC CO2 Reduction. , 12.4.1 Heteroatom‐Doped Carbon in PC CO2 Conversion.
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
    GEOMAR EBL
  • 2
    Electronic Resource
    Electronic Resource
    A new model of positronium formation: Resonant positronium formation (1990)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 1021-1029 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: "Resonant model,'' a new model of positronium (Ps) formation is proposed. The first stage of Ps formation is the inelastic collisions of e+ through formation of an intermediate state (M*.e+) by resonant energy absorption and e+ attachment. The second stage of Ps formation involves thermalized e+ and loosely bound electrons (excess electrons, excited molecules, and certain anions) through resonant electron transfer. Experimental results are reviewed from the viewpoint of the new model comparing it with the older models, the Ore model and the spur model.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.459166
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Effect of paramagnetic particles on the lifetime of o-Ps in positron spur
    Amsterdam : Elsevier
    International Journal of Radiation Applications & Instrumentation. Part C, 28 (1986), S. 55-57 
    Details
    ISSN: 1359-0197
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Physics
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/1359-0197(86)90036-6
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    On the probability of positronium formation in liquid molecular substances-An improvement of the spur model
    Amsterdam : Elsevier
    International Journal of Radiation Applications & Instrumentation. Part C, 28 (1986), S. 59-64 
    Details
    ISSN: 1359-0197
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Physics
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/1359-0197(86)90037-8
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    Parallel study between positronium yield and emission spectra in perfluorobenzene and cyclohexane mixtures-Influence of excited states on positronium yield
    Amsterdam : Elsevier
    International Journal of Radiation Applications & Instrumentation. Part C, 28 (1986), S. 65-68 
    Details
    ISSN: 1359-0197
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Physics
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/1359-0197(86)90038-X
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 6
    Electronic Resource
    Electronic Resource
    Effect of dose rate on emulsion and microemulsion polymerization of styrene (1998)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 257-262 
    Details
    ISSN: 0887-624X
    Keywords: nucleation mechanism ; emulsion polymerization ; microemulsion polymerization ; irradiation polymerization ; styrene ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Emulsion and microemulsion polymerization of styrene were initiated with a gamma ray to study the effect of dose rate on polymerization. In both systems, there is an apparent plateau of polymerization rate in the curve of reaction rate vs. conversion. It was shown that emulsion polymerization conformed to the Smith-Ewart theory very well. Changing the dose rate in interval 2 had no great influence on polymerization rate, but it changed the average lifetime of radicals in polymer particles and affected the molecular weight of polymer produced. For microemulsion polymerization it was assumed that in the plateau it is the number of growing polymer particles being kept constant, not the number of polymer particles. When the dose rate was changed while the polymerization came into the constant period, the polymerization rate and the molecular weight of the polymer varied with the dose rate. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 257-262, 1998
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
  • 7
    Electronic Resource
    Electronic Resource
    Polymerization of butyl acrylate in anionic microemulsion (1996)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1657-1661 
    Details
    ISSN: 0887-624X
    Keywords: butyl acrylate ; microemulsion polymerization ; polymerization kinetics ; nucleation mechanisms ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Butyl acrylate was initiated with KPS or BPO to polymerize at high monomer concentration in the microemulsions with SBOA (sodium 12-butinoyloxy-9-octadecenate) as emulsifier. The microemulsion remained clear or reddish. It was found that the constant polymerization period appeared in most microemulsions and the length of it varied with the concentration of monomer and the initiating rate. When microemulsions were initiated with KPS, the overall polymerization rate increased with the emulsifier concentration; while initiator was BPO, it showed the inverse tendency. It was attributed to the difference between the initiating mechanism of the two initiators. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
  • 8
    Electronic Resource
    Electronic Resource
    Microemulsion polymerization of butyl acrylate initiated by γ rays (1996)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1179-1183 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Radiation polymerization of butyl acrylate was carried out in a microemulsion stabilized with sodium 12-butinoyloxy-9-octadecenate (SBOA). The stable and reddish latex with high polymer content and low emulsifier content was successfully produced in this way. It was found that, for most cases, the polymerization rate shows three intervals: the increasing period, the plateau period, and the decreasing period. The length of the nucleation period becomes longer at a higher dose rate (D) and lower emulsifier content (E). The plateau region of polymerization rate is lengthened with the increase of monomer and emulsifier content and shortened with the increase of dose rate. It was shown that monomer content, emulsifier content, and dose rate have great effects on Rp (the polymerization rate in the plateau region, or the maximum polymerization rate during polymerization) and Mn (the molecular weight of the polymer). Rp ∞ [M0.93D1.27[E]-1.07; Mn ∞ [M]0.65D0.28[E]-1.66. The polymerization mechanism is discussed based on these results. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
  • 9
    Electronic Resource
    Electronic Resource
    Studies on the phase separation of polyetherimide-modified epoxy resin, 1. Effect of curing rate on the phase structure (1997)
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 198 (1997), S. 1865-1872 
    Details
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of the curing rate on the phase structure of a new polyetherimide-modified epoxy systems was studied. Through changing cure agents and cure temperature, selecting different molecular weights and end groups of the polyetherimide (PEI) polymers, the curing rates, the phase separation processes and the morphology of the cured blends were observed employing differential scanning calorimetry, time-resolved light scattering and scanning electron microscopy. The highly active cure agent 4,4′-oxydianiline leads to phase separation in the early stage of spinodal decomposition and to a co-continuous phase structure. As to the 4,4′-diaminodiphenyl sulfone cured systems, not only the curing rate, but the mobility of the PEI molecule also affected the final morphology of the PEI-modified epoxy resin.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1997.021980615
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 10
    facet.materialart.
    Unknown
    FoxO3 inactivation promotes human cholangiocarcinoma tumorigenesis and chemoresistance via Keap1-Nrf2 signaling (2016)
    Wiley-Blackwell
    Details
    Publication Date: 2016-02-10
    Description: FoxO transcription factors have been reported to play pivotal roles in tumorigenesis and drug resistance. The mechanistic insights underlying the tumor suppression function of FoxOs in human cancers remain largely unknown. Aberrant expression and activation of Nrf2 often correlate with chemoresistance and poor prognosis. Here, we report that FoxO3 directs the basal transcription of Keap1, an adaptor protein that bridges Nrf2 to Cul3 for degradation. FoxO3 depletion resulted in Keap1 down-regulation, thereby activating Nrf2 signaling. We further demonstrated that the inhibition of FoxO3-Keap1 axis accounts for Nrf2 induction and activation induced by constitutively active AKT signaling or tumor necrosis factor α (TNFα) treatment. Unlike previous findings, we showed FoxO3 silencing led to decreased reactive oxygen species (ROS) production, therefore protecting cells from oxidative stress-induced killing in an Nrf2-dependent manner. Importantly, FoxO3 deficiency strongly potentiated tumor formation in nude mice and rendered cholangiocarcinoma (CCA) xenografts resistant to cisplatin-induced cell death via activating Nrf2. Additionally, we found that clinical CCA samples displayed FoxO3-Keap1 down-regulation and Nrf2 hyperactivation, underscoring the essential roles of these proteins in CCA development. Conclusion ：Our results unravel a unique mechanism underlying the tumor suppressor function of FoxO3 via constraining Nrf2 signaling. This article is protected by copyright. All rights reserved.
    Print ISSN: 0270-9139
    Electronic ISSN: 1527-3350
    Topics: Medicine
    Published by Wiley-Blackwell on behalf of The American Association for the Study of Liver Diseases.
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
    PAPER CURRENT
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...