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Article ; Online: Analytic thinking predicts accuracy ratings and willingness to share COVID-19 misinformation in Australia.

Nurse, Matthew S / Ross, Robert M / Isler, Ozan / Van Rooy, Dirk

2021 Volume 50, Issue 2, Page(s) 425–434

Abstract: The classical account of reasoning posits that analytic thinking weakens belief in COVID-19 misinformation. We tested this account in a demographically representative sample of 742 Australians. Participants completed a performance-based measure of ... ...

Abstract	The classical account of reasoning posits that analytic thinking weakens belief in COVID-19 misinformation. We tested this account in a demographically representative sample of 742 Australians. Participants completed a performance-based measure of analytic thinking (the Cognitive Reflection Test) and were randomized to groups in which they either rated the perceived accuracy of claims about COVID-19 or indicated whether they would be willing to share these claims. Half of these claims were previously debunked misinformation, and half were statements endorsed by public health agencies. We found that participants with higher analytic thinking levels were less likely to rate COVID-19 misinformation as accurate and were less likely to be willing to share COVID-19 misinformation. These results support the classical account of reasoning for the topic of COVID-19 misinformation and extend it to the Australian context.
MeSH term(s)	Australia ; COVID-19 ; Communication ; Humans ; SARS-CoV-2
Language	English
Publishing date	2021-08-27
Publishing country	United States
Document type	Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
ZDB-ID	185691-1
ISSN	1532-5946 ; 0090-502X
ISSN (online)	1532-5946
ISSN	0090-502X
DOI	10.3758/s13421-021-01219-5
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Article ; Online: The Hydrophobic Patch Directs Cyclin B to Centrosomes to Promote Global CDK Phosphorylation at Mitosis.

Basu, Souradeep / Roberts, Emma L / Jones, Andrew W / Swaffer, Matthew P / Snijders, Ambrosius P / Nurse, Paul

Current biology : CB

2020 Volume 30, Issue 5, Page(s) 883–892.e4

Abstract: ... of substrates, controlling the onset of S phase and M phase [1-3]. However, the patterns of substrate ... of this motif prevents both centrosomal localization of Cdc13 and the onset of mitosis but does not prevent S ...

Abstract	The cyclin-dependent kinases (CDKs) are the major cell-cycle regulators that phosphorylate hundreds of substrates, controlling the onset of S phase and M phase [1-3]. However, the patterns of substrate phosphorylation increase are not uniform, as different substrates become phosphorylated at different times as cells proceed through the cell cycle [4, 5]. In fission yeast, the correct ordering of CDK substrate phosphorylation can be established by the activity of a single mitotic cyclin-CDK complex [6, 7]. Here, we investigate the substrate-docking region, the hydrophobic patch, on the fission yeast mitotic cyclin Cdc13 as a potential mechanism to correctly order CDK substrate phosphorylation. We show that the hydrophobic patch targets Cdc13 to the yeast centrosome equivalent, the spindle pole body (SPB), and disruption of this motif prevents both centrosomal localization of Cdc13 and the onset of mitosis but does not prevent S phase. CDK phosphorylation in mitosis is compromised for approximately half of all mitotic CDK substrates, with substrates affected generally being those that require the highest levels of CDK activity to become phosphorylated and those that are located at the SPB. Our experiments suggest that the hydrophobic patch of mitotic cyclins contributes to CDK substrate selection by directing the localization of Cdc13-CDK to centrosomes and that this localization of CDK contributes to the CDK substrate phosphorylation necessary to ensure proper entry into mitosis. Finally, we show that mutation of the hydrophobic patch prevents cyclin B1 localization to centrosomes in human cells, suggesting that this mechanism of cyclin-CDK spatial regulation may be conserved across eukaryotes.
MeSH term(s)	Cell Line ; Centrosome/metabolism ; Cyclin B1/metabolism ; Cyclin-Dependent Kinases/metabolism ; Humans ; Hydrophobic and Hydrophilic Interactions ; Phosphorylation ; Schizosaccharomyces/metabolism ; Schizosaccharomyces pombe Proteins/metabolism
Chemical Substances	CCNB1 protein, human ; Cyclin B1 ; Schizosaccharomyces pombe Proteins ; Cyclin-Dependent Kinases (EC 2.7.11.22)
Language	English
Publishing date	2020-02-20
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	1071731-6
ISSN	1879-0445 ; 0960-9822
ISSN (online)	1879-0445
ISSN	0960-9822
DOI	10.1016/j.cub.2019.12.053
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Article: Science Communication as a Collective Intelligence Endeavor: A Manifesto and Examples for Implementation.

Holford, Dawn / Fasce, Angelo / Tapper, Katy / Demko, Miso / Lewandowsky, Stephan / Hahn, Ulrike / Abels, Christoph M / Al-Rawi, Ahmed / Alladin, Sameer / Sonia Boender, T / Bruns, Hendrik / Fischer, Helen / Gilde, Christian / Hanel, Paul H P / Herzog, Stefan M / Kause, Astrid / Lehmann, Sune / Nurse, Matthew S / Orr, Caroline /

Pescetelli, Niccolò / Petrescu, Maria / Sah, Sunita / Schmid, Philipp / Sirota, Miroslav / Wulf, Marlene

Science communication

2023 Volume 45, Issue 4, Page(s) 539–554

Abstract: Effective science communication is challenging when scientific messages are informed by a continually updating evidence base and must often compete against misinformation. We argue that we need a new program of science communication as collective ... ...

Abstract	Effective science communication is challenging when scientific messages are informed by a continually updating evidence base and must often compete against misinformation. We argue that we need a new program of science communication as collective intelligence-a collaborative approach, supported by technology. This would have four key advantages over the typical model where scientists communicate as individuals: scientific messages would be informed by (a) a wider base of aggregated knowledge, (b) contributions from a diverse scientific community, (c) participatory input from stakeholders, and (d) better responsiveness to ongoing changes in the state of knowledge.
Language	English
Publishing date	2023-04-04
Publishing country	United States
Document type	Journal Article
ZDB-ID	2014915-3
ISSN	1552-8545 ; 1075-5470
ISSN (online)	1552-8545
ISSN	1075-5470
DOI	10.1177/10755470231162634
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Article ; Online: An ergonomic assessment tool for evaluating the effect of back exoskeletons on injury risk.

Zelik, Karl E / Nurse, Cameron A / Schall, Mark C / Sesek, Richard F / Marino, Matthew C / Gallagher, Sean

Applied ergonomics

2021 Volume 99, Page(s) 103619

Abstract: Low back disorders (LBDs) are a leading injury in the workplace. Back exoskeletons (exos) are wearable assist devices that complement traditional ergonomic controls and reduce LBD risks by alleviating musculoskeletal overexertion. However, there are ... ...

Abstract	Low back disorders (LBDs) are a leading injury in the workplace. Back exoskeletons (exos) are wearable assist devices that complement traditional ergonomic controls and reduce LBD risks by alleviating musculoskeletal overexertion. However, there are currently no ergonomic assessment tools to evaluate risk for workers wearing back exos. Exo-LiFFT, an extension of the Lifting Fatigue Failure Tool, is introduced as a means to unify the etiology of LBDs with the biomechanical function of exos. We present multiple examples demonstrating how Exo-LiFFT can assess or predict the effect of exos on LBD risk without costly, time-consuming electromyography studies. For instance, using simulated and real-world material handling data we show an exo providing a 30 Nm lumbar moment is projected to reduce cumulative back damage by ∼70% and LBD risk by ∼20%. Exo-LiFFT provides a practical, efficient ergonomic assessment tool to assist safety professionals exploring back exos as part of a comprehensive occupational health program.
MeSH term(s)	Biomechanical Phenomena ; Electromyography ; Ergonomics ; Exoskeleton Device ; Humans ; Lifting ; Occupational Diseases/etiology ; Occupational Diseases/prevention & control
Language	English
Publishing date	2021-11-02
Publishing country	England
Document type	Journal Article
ZDB-ID	2003513-5
ISSN	1872-9126 ; 0003-6870
ISSN (online)	1872-9126
ISSN	0003-6870
DOI	10.1016/j.apergo.2021.103619
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Article ; Online: Occurrence and Management of Herbicide Resistance in Annual Vegetable Production Systems in North America

Boyd, Nathan S. / Moretti, Marcelo L. / Sosnoskie, Lynn M. / Singh, Vijay / Kanissery, Ramdas / Sharpe, Shaun / Besançon, Thierry / Culpepper, Stanley / Nurse, Robert / Hatterman-Valenti, Harlene / Mosqueda, Elizabeth / Robinson, Darren / Cutulle, Matthew / Sandhu, Ravneet

Weed Science. 2022 Aug. 5, v. 70, no. 5 p.515-528

2022

Abstract: Herbicide resistance has been studied extensively in agronomic crops across North America but is rarely examined in vegetables. It is widely assumed that the limited number of registered herbicides combined with the adoption of diverse weed management ... ...

Abstract	Herbicide resistance has been studied extensively in agronomic crops across North America but is rarely examined in vegetables. It is widely assumed that the limited number of registered herbicides combined with the adoption of diverse weed management strategies in most vegetable crops effectively inhibits the development of resistance. It is difficult to determine whether resistance is truly less common in vegetable crops or whether the lack of reported cases is due to the lack of resources focused on detection. This review highlights incidences of resistance that are thought to have arisen within vegetable crops. It also includes situations in which herbicide-resistant weeds were likely selected for within agronomic crops but became a problem when vegetables were grown in sequence or in adjacent fields. Occurrence of herbicide resistance can have severe consequences for vegetable growers, and resistance management plans should be adopted to limit selection pressure. This review also highlights resistance management techniques that should slow the development and spread of herbicide resistance in vegetable crops.
Keywords	herbicide resistance ; resistance management ; selection pressure ; vegetable growing ; vegetables ; weed control ; North America ; Integrated weed management ; mode of action ; physical ; chemical ; biological
Language	English
Dates of publication	2022-0805
Size	p. 515-528.
Publishing place	The Weed Science Society of America
Document type	Article ; Online
ZDB-ID	281279-4
ISSN	0043-1745
ISSN	0043-1745
DOI	10.1017/wsc.2022.43
Database	NAL-Catalogue (AGRICOLA)

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Article ; Online: Quantitative Phosphoproteomics Reveals the Signaling Dynamics of Cell-Cycle Kinases in the Fission Yeast Schizosaccharomyces pombe.

Swaffer, Matthew P / Jones, Andrew W / Flynn, Helen R / Snijders, Ambrosius P / Nurse, Paul

Cell reports

2018 Volume 24, Issue 2, Page(s) 503–514

Abstract: ... the temporal organization of phosphorylation during G1/S, as well as the coordination between the NDR-related ...

Abstract	Multiple protein kinases regulate cell-cycle progression, of which the cyclin-dependent kinases (CDKs) are thought to act as upstream master regulators. We have used quantitative phosphoproteomics to analyze the fission yeast cell cycle at sufficiently high temporal resolution to distinguish fine-grain differences in substrate phosphorylation dynamics on a proteome-wide scale. This dataset provides a useful resource for investigating the regulatory dynamics of cell-cycle kinases and their substrates. For example, our analysis indicates that the substrates of different mitotic kinases (CDK, NIMA-related, Polo-like, and Aurora) are phosphorylated in sequential, kinase-specific waves during mitosis. Phosphoproteomics analysis after chemical-genetic manipulation of CDK activity suggests that the timing of these waves is established by the differential dependency of the downstream kinases on upstream CDK. We have also examined the temporal organization of phosphorylation during G1/S, as well as the coordination between the NDR-related kinase Orb6, which controls polarized growth, and other cell-cycle kinases.
MeSH term(s)	Cell Cycle ; Cyclin-Dependent Kinases/metabolism ; Isotope Labeling ; Mitosis ; Phosphoproteins/metabolism ; Phosphorylation ; Protein Kinases/metabolism ; Proteome/metabolism ; Proteomics/methods ; Schizosaccharomyces/cytology ; Schizosaccharomyces/enzymology ; Schizosaccharomyces/metabolism ; Schizosaccharomyces pombe Proteins/metabolism ; Signal Transduction ; Time Factors
Chemical Substances	Phosphoproteins ; Proteome ; Schizosaccharomyces pombe Proteins ; Protein Kinases (EC 2.7.-) ; Cyclin-Dependent Kinases (EC 2.7.11.22)
Language	English
Publishing date	2018-08-25
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2649101-1
ISSN	2211-1247 ; 2211-1247
ISSN (online)	2211-1247
ISSN	2211-1247
DOI	10.1016/j.celrep.2018.06.036
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: CDK Substrate Phosphorylation and Ordering the Cell Cycle.

Swaffer, Matthew P / Jones, Andrew W / Flynn, Helen R / Snijders, Ambrosius P / Nurse, Paul

Cell

2017 Volume 167, Issue 7, Page(s) 1750–1761.e16

Abstract: S phase and mitotic onset are brought about by the action of multiple different cyclin-CDK ... than substrate specificity, drive the temporal ordering of S phase and mitosis. Here, we present a phosphoproteomics-based ...

Abstract	S phase and mitotic onset are brought about by the action of multiple different cyclin-CDK complexes. However, it has been suggested that changes in the total level of CDK kinase activity, rather than substrate specificity, drive the temporal ordering of S phase and mitosis. Here, we present a phosphoproteomics-based systems analysis of CDK substrates in fission yeast and demonstrate that the phosphorylation of different CDK substrates can be temporally ordered during the cell cycle by a single cyclin-CDK. This is achieved by rising CDK activity and the differential sensitivity of substrates to CDK activity over a wide dynamic range. This is combined with rapid phosphorylation turnover to generate clearly resolved substrate-specific activity thresholds, which in turn ensures the appropriate ordering of downstream cell-cycle events. Comparative analysis with wild-type cells expressing multiple cyclin-CDK complexes reveals how cyclin-substrate specificity works alongside activity thresholds to fine-tune the patterns of substrate phosphorylation.
MeSH term(s)	Cell Cycle ; Cyclin-Dependent Kinases/metabolism ; Cyclins/metabolism ; Mitosis ; Phosphorylation ; Schizosaccharomyces/cytology ; Schizosaccharomyces/metabolism ; Schizosaccharomyces pombe Proteins/metabolism
Chemical Substances	Cyclins ; Schizosaccharomyces pombe Proteins ; Cyclin-Dependent Kinases (EC 2.7.11.22)
Language	English
Publishing date	2017-01-10
Publishing country	United States
Document type	Journal Article
ZDB-ID	187009-9
ISSN	1097-4172 ; 0092-8674
ISSN (online)	1097-4172
ISSN	0092-8674
DOI	10.1016/j.cell.2016.11.034
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Article ; Online: Quantitative Phosphoproteomics Reveals the Signaling Dynamics of Cell-Cycle Kinases in the Fission Yeast Schizosaccharomyces pombe

Matthew P. Swaffer / Andrew W. Jones / Helen R. Flynn / Ambrosius P. Snijders / Paul Nurse

Cell Reports, Vol 24, Iss 2, Pp 503-

2018 Volume 514

Abstract: ... also examined the temporal organization of phosphorylation during G1/S, as well as the coordination ...

Abstract	Summary: Multiple protein kinases regulate cell-cycle progression, of which the cyclin-dependent kinases (CDKs) are thought to act as upstream master regulators. We have used quantitative phosphoproteomics to analyze the fission yeast cell cycle at sufficiently high temporal resolution to distinguish fine-grain differences in substrate phosphorylation dynamics on a proteome-wide scale. This dataset provides a useful resource for investigating the regulatory dynamics of cell-cycle kinases and their substrates. For example, our analysis indicates that the substrates of different mitotic kinases (CDK, NIMA-related, Polo-like, and Aurora) are phosphorylated in sequential, kinase-specific waves during mitosis. Phosphoproteomics analysis after chemical-genetic manipulation of CDK activity suggests that the timing of these waves is established by the differential dependency of the downstream kinases on upstream CDK. We have also examined the temporal organization of phosphorylation during G1/S, as well as the coordination between the NDR-related kinase Orb6, which controls polarized growth, and other cell-cycle kinases. : Swaffer et al. use phosphoproteomics at high temporal resolution to determine the fine-grain differences in substrate phosphorylation timing during the fission yeast cell cycle. This global analysis reveals how multiple different cell-cycle kinases contribute to phosphorylation ordering, as well as the hierarchy of mitotic kinases downstream of the master regulator CDK. Keywords: cell cycle, mitosis, CDK, cyclin-dependent kinase, cell-cycle kinases, kinase networks, protein phosphorylation, phosphoproteomics, fission yeast, Schizosaccharomyces pombe
Keywords	Biology (General) ; QH301-705.5
Subject code	571
Language	English
Publishing date	2018-07-01T00:00:00Z
Publisher	Elsevier
Document type	Article ; Online
Database	BASE - Bielefeld Academic Search Engine (life sciences selection)

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Article: Cutaneous stimulation of discrete regions of the sole during locomotion produces "sensory steering" of the foot.

Zehr, E Paul / Nakajima, Tsuyoshi / Barss, Trevor / Klarner, Taryn / Miklosovic, Stefanie / Mezzarane, Rinaldo A / Nurse, Matthew / Komiyama, Tomoyoshi

BMC sports science, medicine & rehabilitation

2014 Volume 6, Page(s) 33

Abstract: Background: While the neural and mechanical effects of whole nerve cutaneous stimulation on human locomotion have been previously studied, there is less information about effects evoked by activation of discrete skin regions on the sole of the foot. ... ...

Abstract	Background: While the neural and mechanical effects of whole nerve cutaneous stimulation on human locomotion have been previously studied, there is less information about effects evoked by activation of discrete skin regions on the sole of the foot. Electrical stimulation of discrete foot regions evokes position-modulated patterns of cutaneous reflexes in muscles acting at the ankle during standing but data during walking are lacking. Here, non-noxious electrical stimulation was delivered to five discrete locations on the sole of the foot (heel, and medial and lateral sites on the midfoot and forefoot) during treadmill walking. EMG activity from muscles acting at the hip, knee and ankle were recorded along with movement at these three joints. Additionally, 3 force sensing resistors measuring continuous force changes were placed at the heel, and the medial and lateral aspects of the right foot sole. All data were sorted based on stimulus occurrence in twelve step-cycle phases, before being averaged together within a phase for subsequent analysis. Methods: Non-noxious electrical stimulation was delivered to five discrete locations on the sole of the foot (heel, and medial and lateral sites on the midfoot and forefoot) during treadmill walking. EMG activity from muscles acting at the hip, knee and ankle were recorded along with movement at these three joints. Additionally, 3 force sensing resistors measuring continuous force changes were placed at the heel, and the medial and lateral aspects of the right foot sole. All data were sorted based on stimulus occurrence in twelve step-cycle phases, before being averaged together within a phase for subsequent analysis. Results: The results demonstrate statistically significant dynamic changes in reflex amplitudes, kinematics and foot sole pressures that are site-specific and phase-dependent. The general trends demonstrate responses producing decreased underfoot pressure at the site of stimulation. Conclusions: The responses to stimulation of discrete locations on the foot sole evoke a kind of "sensory steering" that may promote balance and maintenance of locomotion through the modulation of limb loading and foot placement. These results have implications for using sensory stimulation as a therapeutic modality during gait retraining (e.g. after stroke) as well as for footwear design and implementation of foot sole contact surfaces during gait.
Language	English
Publishing date	2014-08-08
Publishing country	England
Document type	Journal Article
ZDB-ID	2719537-5
ISSN	2052-1847
ISSN	2052-1847
DOI	10.1186/2052-1847-6-33
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Article ; Online: CDK Substrate Phosphorylation and Ordering the Cell Cycle

Swaffer, Matthew P. / Jones, Andrew W. / Flynn, Helen R. / Snijders, Ambrosius P. / Nurse, Paul

Cell. 2016 Dec. 15, v. 167, p. 1750-1761.e16

2016 , Page(s) 1750–1761

Abstract	S phase and mitotic onset are brought about by the action of multiple different cyclin-CDK complexes. However, it has been suggested that changes in the total level of CDK kinase activity, rather than substrate specificity, drive the temporal ordering of S phase and mitosis. Here, we present a phosphoproteomics-based systems analysis of CDK substrates in fission yeast and demonstrate that the phosphorylation of different CDK substrates can be temporally ordered during the cell cycle by a single cyclin-CDK. This is achieved by rising CDK activity and the differential sensitivity of substrates to CDK activity over a wide dynamic range. This is combined with rapid phosphorylation turnover to generate clearly resolved substrate-specific activity thresholds, which in turn ensures the appropriate ordering of downstream cell-cycle events. Comparative analysis with wild-type cells expressing multiple cyclin-CDK complexes reveals how cyclin-substrate specificity works alongside activity thresholds to fine-tune the patterns of substrate phosphorylation.
Keywords	CDK ; cyclin-dependent kinase ; cell cycle ; S phase ; mitosis ; phosphorylation ; kinase ; phosphoproteomics
Language	English
Dates of publication	2016-1215
Size	p. 1750-1761.e16
Publishing place	Elsevier Inc.
Document type	Article ; Online
ZDB-ID	187009-9
ISSN	1097-4172 ; 0092-8674
ISSN (online)	1097-4172
ISSN	0092-8674
DOI	10.1016/j.cell.2016.11.034
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