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  1. AU=Klimovich Pavel V.
  2. AU="Jingbo Chen"
  3. AU="Viazlo, Oleksander"
  4. AU="Toshiki Iwabuchi"
  5. AU="Dissanayake, Lakmali"
  6. AU="Michael Denkinger"
  7. AU="Abilio J. F. N. Sobral"
  8. AU="Geller, Alan"
  9. AU=Petrat Sren
  10. AU="Sterling, Shanique"
  11. AU="Qi, Zeqiang"
  12. AU="Thongstisubskul, A"
  13. AU="Daniel C. Schneider, PhD"
  14. AU="Völker, Christoph"
  15. AU="El Aoud, S"
  16. AU="Yi, Tongpei"
  17. AU="Anil K. Mantha"
  18. AU="Artzner, Christoph"
  19. AU=Diana Giovanni
  20. AU="Kinloch, Sabine"
  21. AU="Nuertey, David"
  22. AU="Ojubolamo, Olakunle"

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  1. Artikel: Implicit-descriptor ligand-based virtual screening by means of collaborative filtering.

    Srinivas, Raghuram / Klimovich, Pavel V / Larson, Eric C

    Journal of cheminformatics

    2018  Band 10, Heft 1, Seite(n) 56

    Abstract: Current ligand-based machine learning methods in virtual screening rely heavily on molecular fingerprinting for preprocessing, i.e., explicit description of ligands' structural and physicochemical properties in a vectorized form. Of particular importance ...

    Abstract Current ligand-based machine learning methods in virtual screening rely heavily on molecular fingerprinting for preprocessing, i.e., explicit description of ligands' structural and physicochemical properties in a vectorized form. Of particular importance to current methods are the extent to which molecular fingerprints describe a particular ligand and what metric sufficiently captures similarity among ligands. In this work, we propose and evaluate methods that do not require explicit feature vectorization through fingerprinting, but, instead, provide implicit descriptors based only on other known assays. Our methods are based upon well known collaborative filtering algorithms used in recommendation systems. Our implicit descriptor method does not require any fingerprint similarity search, which makes the method free of the bias arising from the empirical nature of the fingerprint models. We show that implicit methods significantly outperform traditional machine learning methods, and the main strengths of implicit methods are their resilience to target-ligand sparsity and high potential for spotting promiscuous ligands.
    Sprache Englisch
    Erscheinungsdatum 2018-11-22
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 2486539-4
    ISSN 1758-2946
    ISSN 1758-2946
    DOI 10.1186/s13321-018-0310-y
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: A Python tool to set up relative free energy calculations in GROMACS.

    Klimovich, Pavel V / Mobley, David L

    Journal of computer-aided molecular design

    2015  Band 29, Heft 11, Seite(n) 1007–1014

    Abstract: Free energy calculations based on molecular dynamics (MD) simulations have seen a tremendous growth in the last decade. However, it is still difficult and tedious to set them up in an automated manner, as the majority of the present-day MD simulation ... ...

    Abstract Free energy calculations based on molecular dynamics (MD) simulations have seen a tremendous growth in the last decade. However, it is still difficult and tedious to set them up in an automated manner, as the majority of the present-day MD simulation packages lack that functionality. Relative free energy calculations are a particular challenge for several reasons, including the problem of finding a common substructure and mapping the transformation to be applied. Here we present a tool, alchemical-setup.py, that automatically generates all the input files needed to perform relative solvation and binding free energy calculations with the MD package GROMACS. When combined with Lead Optimization Mapper (LOMAP; Liu et al. in J Comput Aided Mol Des 27(9):755-770, 2013), recently developed in our group, alchemical-setup.py allows fully automated setup of relative free energy calculations in GROMACS. Taking a graph of the planned calculations and a mapping, both computed by LOMAP, our tool generates the topology and coordinate files needed to perform relative free energy calculations for a given set of molecules, and provides a set of simulation input parameters. The tool was validated by performing relative hydration free energy calculations for a handful of molecules from the SAMPL4 challenge (Mobley et al. in J Comput Aided Mol Des 28(4):135-150, 2014). Good agreement with previously published results and the straightforward way in which free energy calculations can be conducted make alchemical-setup.py a promising tool for automated setup of relative solvation and binding free energy calculations.
    Mesh-Begriff(e) Energy Metabolism ; Molecular Dynamics Simulation ; Software ; Thermodynamics
    Sprache Englisch
    Erscheinungsdatum 2015-11
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 808166-9
    ISSN 1573-4951 ; 0920-654X
    ISSN (online) 1573-4951
    ISSN 0920-654X
    DOI 10.1007/s10822-015-9873-0
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Implicit-descriptor ligand-based virtual screening by means of collaborative filtering

    Raghuram Srinivas / Pavel V. Klimovich / Eric C. Larson

    Journal of Cheminformatics, Vol 10, Iss 1, Pp 1-

    2018  Band 20

    Abstract: Abstract Current ligand-based machine learning methods in virtual screening rely heavily on molecular fingerprinting for preprocessing, i.e., explicit description of ligands’ structural and physicochemical properties in a vectorized form. Of particular ... ...

    Abstract Abstract Current ligand-based machine learning methods in virtual screening rely heavily on molecular fingerprinting for preprocessing, i.e., explicit description of ligands’ structural and physicochemical properties in a vectorized form. Of particular importance to current methods are the extent to which molecular fingerprints describe a particular ligand and what metric sufficiently captures similarity among ligands. In this work, we propose and evaluate methods that do not require explicit feature vectorization through fingerprinting, but, instead, provide implicit descriptors based only on other known assays. Our methods are based upon well known collaborative filtering algorithms used in recommendation systems. Our implicit descriptor method does not require any fingerprint similarity search, which makes the method free of the bias arising from the empirical nature of the fingerprint models. We show that implicit methods significantly outperform traditional machine learning methods, and the main strengths of implicit methods are their resilience to target-ligand sparsity and high potential for spotting promiscuous ligands.
    Schlagwörter Ligand-based virtual screening ; Collaborative filtering ; Drug discovery ; Computational pharmacology ; Information technology ; T58.5-58.64 ; Chemistry ; QD1-999
    Thema/Rubrik (Code) 006
    Sprache Englisch
    Erscheinungsdatum 2018-11-01T00:00:00Z
    Verlag BMC
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  4. Artikel ; Online: Films enriched with semiconducting single-walled carbon nanotubes by aerosol N2O etching

    Alekseeva, Аlena A. / Krasnikov, Dmitry V. / Livshits, Grigoriy B. / Romanov, Stepan A. / Popov, Zakhar I. / Varlamova, Liubov A. / Sukhanova, Ekaterina V. / Klimovich, Andrei S. / Sorokin, Pavel B. / Savilov, Serguei V. / Nasibulin, Albert G.

    Carbon. 2023 Aug., v. 212 p.118094-

    2023  

    Abstract: Semiconducting single-walled carbon nanotubes (SWCNTs) are of particular interest to electronics. As most of synthesis methods yield 1/3 of metallic SWCNTs, the route for a purely semiconducting species is a complex multistep procedure. Herein, we report ...

    Abstract Semiconducting single-walled carbon nanotubes (SWCNTs) are of particular interest to electronics. As most of synthesis methods yield 1/3 of metallic SWCNTs, the route for a purely semiconducting species is a complex multistep procedure. Herein, we report a simple one-step method for selective etching of metallic SWCNTs in the aerosol phase with nitrous oxide. Our approach is based on a tandem of two flow reactors, where the first one is needed to produce individual SWCNTs, and the second one is to eliminate metallic SWCNTs due to their faster oxidization rate. The oxidant (N₂O) adsorption on the SWCNT surface was modelled by DFTB taking into account geometric characteristics of the nanotube and its electronic properties, resulting in less N₂O adsorption energy for metallic SWCNTs of some chiralities than for semiconducting ones. Thus, we obtained SWCNT films enriched with semiconducting nanotubes up to optical selectivity of 97% by treatment of pristine SWCNT aerosols for 6 s at 600 °C in an atmosphere of 30% N₂O. The treated films show a turnaround of the temperature dependence of the resistance. As a proof of the concept, enriched SWCNT films were utilized as a channel material for thin film field effect transistors, which show an average improvement of ON/OFF current ratio from 1- 10 to 10 - 10⁴ for the same open state resistance for the statistical sampling based on more than 7500 devices.
    Schlagwörter adsorption ; aerosols ; carbon ; carbon nanotubes ; electronics ; energy ; films (materials) ; geometry ; nitrous oxide ; oxidants ; semiconductors ; temperature ; Tandem reactor ; Semiconducting carbon nanotubes ; Selective etching ; Field effect transistors ; DFTB
    Sprache Englisch
    Erscheinungsverlauf 2023-08
    Umfang p. 118094
    Erscheinungsort Elsevier Ltd
    Dokumenttyp Artikel ; Online
    ISSN 0008-6223
    DOI 10.1016/j.carbon.2023.118094
    Datenquelle NAL Katalog (AGRICOLA)

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  5. Artikel ; Online: Perspective: Alchemical free energy calculations for drug discovery.

    Mobley, David L / Klimovich, Pavel V

    The Journal of chemical physics

    2012  Band 137, Heft 23, Seite(n) 230901

    Abstract: Computational techniques see widespread use in pharmaceutical drug discovery, but typically prove unreliable in predicting trends in protein-ligand binding. Alchemical free energy calculations seek to change that by providing rigorous binding free ... ...

    Abstract Computational techniques see widespread use in pharmaceutical drug discovery, but typically prove unreliable in predicting trends in protein-ligand binding. Alchemical free energy calculations seek to change that by providing rigorous binding free energies from molecular simulations. Given adequate sampling and an accurate enough force field, these techniques yield accurate free energy estimates. Recent innovations in alchemical techniques have sparked a resurgence of interest in these calculations. Still, many obstacles stand in the way of their routine application in a drug discovery context, including the one we focus on here, sampling. Sampling of binding modes poses a particular challenge as binding modes are often separated by large energy barriers, leading to slow transitions. Binding modes are difficult to predict, and in some cases multiple binding modes may contribute to binding. In view of these hurdles, we present a framework for dealing carefully with uncertainty in binding mode or conformation in the context of free energy calculations. With careful sampling, free energy techniques show considerable promise for aiding drug discovery.
    Mesh-Begriff(e) Drug Design ; Drug Discovery ; Entropy ; Ligands ; Models, Chemical ; Molecular Dynamics Simulation ; Protein Binding ; Proteins/chemistry ; Thermodynamics
    Chemische Substanzen Ligands ; Proteins
    Sprache Englisch
    Erscheinungsdatum 2012-12-26
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/1.4769292
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Pathomorphological Markers of Overcoming Radioresistance in the Treatment of Cervical Cancer

    Pavel Yu. Andreev / Daniil Yu. Bugrimov / Andrey A. Filin / Olga V. Kashaeva / Natalya V. Korotkikh / Andrey A. Klimovich

    International Journal of Biomedicine, Vol 10, Iss 2, Pp 120-

    2020  Band 123

    Abstract: The aim of this study was to study pathomorphological markers of decreasing radioresistance of cervical tumor tissue during radiation therapy and the administration of sodium deoxyribonucleate. Methods and Results: The object of the study was patients ... ...

    Abstract The aim of this study was to study pathomorphological markers of decreasing radioresistance of cervical tumor tissue during radiation therapy and the administration of sodium deoxyribonucleate. Methods and Results: The object of the study was patients with diagnosed cervical cancer (T1/FIGOIB, T1a1-2/FIGOIA1-2, and T1b1-2/FIGOIB1-2; NX0 and M0). All patients in the study were divided into 2 groups. The main group (MG) included 40 patients receiving combination of standard chemoradiotherapy with sodium deoxyribonucleate (5ml intramuscularly for 20 days). The comparison group (CG) included 23 patients receiving only standard chemoradiotherapy. Histological and immunohistochemical analysis was performed. Conclusion: Against the background of complex therapy, the TLR9 expression indices in the patients of the MG were 24%-36% higher than the indices in the patients of the CG. The inclusion of sodium deoxyribonucleate—a TLR9 agonist—in the chemoradiotherapy regimen for cervical cancer has great potential for stimulating the TLR9 expression in immunocompetent cells of the tumor microenvironment.
    Schlagwörter radioresistance ; tlr9 expression ; cervical cancer ; pathomorphological markers ; Medicine ; R
    Thema/Rubrik (Code) 610
    Sprache Englisch
    Erscheinungsdatum 2020-06-01T00:00:00Z
    Verlag International Medical Research and Development Corporation
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  7. Artikel ; Online: Guidelines for the analysis of free energy calculations.

    Klimovich, Pavel V / Shirts, Michael R / Mobley, David L

    Journal of computer-aided molecular design

    2015  Band 29, Heft 5, Seite(n) 397–411

    Abstract: Free energy calculations based on molecular dynamics simulations show considerable promise for applications ranging from drug discovery to prediction of physical properties and structure-function studies. But these calculations are still difficult and ... ...

    Abstract Free energy calculations based on molecular dynamics simulations show considerable promise for applications ranging from drug discovery to prediction of physical properties and structure-function studies. But these calculations are still difficult and tedious to analyze, and best practices for analysis are not well defined or propagated. Essentially, each group analyzing these calculations needs to decide how to conduct the analysis and, usually, develop its own analysis tools. Here, we review and recommend best practices for analysis yielding reliable free energies from molecular simulations. Additionally, we provide a Python tool, alchemical-analysis.py, freely available on GitHub as part of the pymbar package (located at http://github.com/choderalab/pymbar), that implements the analysis practices reviewed here for several reference simulation packages, which can be adapted to handle data from other packages. Both this review and the tool covers analysis of alchemical calculations generally, including free energy estimates via both thermodynamic integration and free energy perturbation-based estimators. Our Python tool also handles output from multiple types of free energy calculations, including expanded ensemble and Hamiltonian replica exchange, as well as standard fixed ensemble calculations. We also survey a range of statistical and graphical ways of assessing the quality of the data and free energy estimates, and provide prototypes of these in our tool. We hope this tool and discussion will serve as a foundation for more standardization of and agreement on best practices for analysis of free energy calculations.
    Mesh-Begriff(e) Computer Simulation ; Drug Design ; Drug Discovery ; Entropy ; Guidelines as Topic ; Models, Chemical ; Molecular Dynamics Simulation
    Sprache Englisch
    Erscheinungsdatum 2015-05
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 808166-9
    ISSN 1573-4951 ; 0920-654X
    ISSN (online) 1573-4951
    ISSN 0920-654X
    DOI 10.1007/s10822-015-9840-9
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: Predicting hydration free energies using all-atom molecular dynamics simulations and multiple starting conformations.

    Klimovich, Pavel V / Mobley, David L

    Journal of computer-aided molecular design

    2010  Band 24, Heft 4, Seite(n) 307–316

    Abstract: Molecular dynamics simulations in explicit solvent were applied to predict the hydration free energies for 23 small organic molecules in blind SAMPL2 test. We found good agreement with experimental results, with an RMS error of 2.82 kcal/mol over the ... ...

    Abstract Molecular dynamics simulations in explicit solvent were applied to predict the hydration free energies for 23 small organic molecules in blind SAMPL2 test. We found good agreement with experimental results, with an RMS error of 2.82 kcal/mol over the whole set and 1.86 kcal/mol over all the molecules except several hydroxyl-rich compounds where we find evidence for a systematic error in the force field. We tested two different solvent models, TIP3P and TIP4P-Ew, and obtained very similar hydration free energies for these two models; the RMS difference was 0.64 kcal/mol. We found that preferred conformation of the carboxylic acids in water differs from that in vacuum. Surprisingly, this conformational change is not adequately sampled on simulation timescales, so we apply an umbrella sampling technique to include free energies associated with the conformational change. Overall, the results of this test reveal that the force field parameters for some groups of molecules (such as hydroxyl-rich compounds) still need to be improved, but for most compounds, accuracy was consistent with that seen in our previous tests.
    Mesh-Begriff(e) Molecular Conformation ; Molecular Dynamics Simulation ; Organic Chemicals/chemistry ; Thermodynamics ; Water/chemistry
    Chemische Substanzen Organic Chemicals ; Water (059QF0KO0R)
    Sprache Englisch
    Erscheinungsdatum 2010-04-06
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 808166-9
    ISSN 1573-4951 ; 0920-654X
    ISSN (online) 1573-4951
    ISSN 0920-654X
    DOI 10.1007/s10822-010-9343-7
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: A Bicistronic Plasmid Encoding Brain-Derived Neurotrophic Factor and Urokinase Plasminogen Activator Stimulates Peripheral Nerve Regeneration After Injury.

    Karagyaur, Maxim / Rostovtseva, Alexandra / Semina, Ekaterina / Klimovich, Polina / Balabanyan, Vadim / Makarevich, Pavel / Popov, Vladimir / Stambolsky, Dmitry / Tkachuk, Vsevolod

    The Journal of pharmacology and experimental therapeutics

    2019  Band 372, Heft 3, Seite(n) 248–255

    Abstract: Timely nerve restoration is an important factor for the successful regeneration of tissues and organs. It is known that axon regeneration following nerve injury is a multifactorial process that depends on the local expression of neurotrophins, including ... ...

    Abstract Timely nerve restoration is an important factor for the successful regeneration of tissues and organs. It is known that axon regeneration following nerve injury is a multifactorial process that depends on the local expression of neurotrophins, including brain-derived neurotrophic factor (BDNF). Along with the survival of neurons, the active reorganization of the extracellular matrix is an important step for the growth of axons to their targets. Urokinase serine protease is part of the plasminogen activator system, which provides the vectoriality of the process of fibrinolysis and matrix reorganization, facilitating the growth of nerves to their targets. Based on this and in view of the results of our previous studies, we suggest that a combined bicistronic plasmid encoding the complementary proteins BDNF and urokinase may be beneficial in nerve regeneration. The ability of this bicistronic plasmid to stimulate nerve restoration was confirmed by in vitro stimulation of Neuro2a neurite growth and in vivo nerve conductivity and histology studies. To our knowledge, this is the first article that demonstrates the effectiveness of a bicistronic plasmid containing the human genes BDNF and urokinase plasminogen activator in the regeneration of the injured peripheral nerve. The results obtained demonstrate that plasmid vectors encoding several complementary-active therapeutic proteins may serve as a basis for developing prospective treatments for a wide range of multicomponent neural system disorders, such as nerve trauma. SIGNIFICANCE STATEMENT: This study is the first to show the effectiveness of using a bicistronic plasmid encoding complementary-active human protein brain-derived neurotrophic factor and urokinase plasminogen activator in the regeneration of the crushed peripheral nerve in a murine model.
    Mesh-Begriff(e) Animals ; Brain-Derived Neurotrophic Factor/administration & dosage ; Brain-Derived Neurotrophic Factor/genetics ; Cell Line, Tumor ; Disease Models, Animal ; HEK293 Cells ; Humans ; Injections, Intramuscular ; Male ; Mice ; Mice, Inbred C57BL ; Nerve Regeneration/genetics ; Peripheral Nervous System Diseases/genetics ; Peripheral Nervous System Diseases/therapy ; Plasmids ; Transfection ; Urokinase-Type Plasminogen Activator/administration & dosage ; Urokinase-Type Plasminogen Activator/genetics
    Chemische Substanzen Brain-Derived Neurotrophic Factor ; Urokinase-Type Plasminogen Activator (EC 3.4.21.73)
    Sprache Englisch
    Erscheinungsdatum 2019-12-30
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 3106-9
    ISSN 1521-0103 ; 0022-3565
    ISSN (online) 1521-0103
    ISSN 0022-3565
    DOI 10.1124/jpet.119.261594
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel: Investigation of Evolutionary History and Origin of the Tre1 Family Suggests a Role in Regulating Hemocytes Cells Infiltration of the Blood–Brain Barrier

    Kubick, Norwin / Klimovich, Pavel / Bieńkowska, Irmina / Poznanski, Piotr / Łazarczyk, Marzena / Sacharczuk, Mariusz / Mickael, Michel-Edwar

    Insects. 2021 Sept. 29, v. 12, no. 10

    2021  

    Abstract: Understanding the evolutionary relationship between immune cells and the blood–brain barrier (BBB) is important to devise therapeutic strategies. In vertebrates, immune cells follow either a paracellular or a transcellular pathway to infiltrate the BBB. ... ...

    Abstract Understanding the evolutionary relationship between immune cells and the blood–brain barrier (BBB) is important to devise therapeutic strategies. In vertebrates, immune cells follow either a paracellular or a transcellular pathway to infiltrate the BBB. In Drosophila, glial cells form the BBB that regulates the access of hemocytes to the brain. However, it is still not known which diapedesis route hemocytes cells follow. In vertebrates, paracellular migration is dependent on PECAM1, while transcellular migration is dependent on the expression of CAV1. Interestingly Drosophila genome lacks both genes. Tre1 family (Tre1, moody, and Dmel_CG4313) play a diverse role in regulating transepithelial migration in Drosophila. However, its evolutionary history and origin are not yet known. We performed phylogenetic analysis, together with HH search, positive selection, and ancestral reconstruction to investigate the Tre1 family. We found that Tre1 exists in Mollusca, Arthropoda, Ambulacraria, and Scalidophora. moody is shown to be a more ancient protein and it has existed since Cnidaria emergence and has a homolog (e.g., GPCR84) in mammals. The third family member (Dmel_CG4313) seems to only exist in insects. The origin of the family seems to be related to the rhodopsin-like family and in particular family α. We found that opsin is the nearest receptor to have a common ancestor with the Tre1 family that has diverged in sponges. We investigated the positive selection of the Tre1 family using PAML. Tre1 seems to have evolved under negative selection, whereas moody has evolved during positive selection. The sites that we found under positive selection are likely to play a role in the speciation of function in the case of moody. We have identified an SH3 motif, in Tre1 and, moody and Dmel_CG4313. SH3 is known to play a fundamental role in regulating actin movement in a Rho-dependent manner in PECAM1. Our results suggest that the Tre1 family could be playing an important role in paracellular diapedesis in Drosophila.
    Schlagwörter Cnidaria ; Drosophila ; Mollusca ; actin ; ancestry ; blood-brain barrier ; brain ; hemocytes ; opsin ; phylogeny ; therapeutics
    Sprache Englisch
    Erscheinungsverlauf 2021-0929
    Erscheinungsort Multidisciplinary Digital Publishing Institute
    Dokumenttyp Artikel
    ZDB-ID 2662247-6
    ISSN 2075-4450
    ISSN 2075-4450
    DOI 10.3390/insects12100882
    Datenquelle NAL Katalog (AGRICOLA)

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