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Prion protein Stock Photos and Images
Chemical structure of a human prion protein molecule (hPrP). hPrP is associated with transmissible spongiform encephalopathies, Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-chemical-structure-of-a-human-prion-protein-molecule-hprp-hprp-is-100699273.htmlRFFRR6XH–Chemical structure of a human prion protein molecule (hPrP). hPrP is associated with transmissible spongiform encephalopathies,
The prion protein (PrP) is a cell surface glycoprotein. The naturally ocuring prion diseases include Creutzfeldt-Jakob disease Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-the-prion-protein-prp-is-a-cell-surface-glycoprotein-the-naturally-73181692.htmlRME71KYT–The prion protein (PrP) is a cell surface glycoprotein. The naturally ocuring prion diseases include Creutzfeldt-Jakob disease
Model of a prion protein. Prions are infectious agents composed entirely of a protein material that can fold in multiple, structurally abstract ways, at least one of which is transmissible to other prion proteins, leading to disease in a manner that is epidemiologically comparable to the spread of viral infection. Prions composed of the prion protein are believed to be the cause of transmissible spongiform encephalopathies among other diseases. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/model-of-a-prion-protein-prions-are-infectious-agents-composed-entirely-of-a-protein-material-that-can-fold-in-multiple-structurally-abstract-ways-at-least-one-of-which-is-transmissible-to-other-prion-proteins-leading-to-disease-in-a-manner-that-is-epidemiologically-comparable-to-the-spread-of-viral-infection-prions-composed-of-the-prion-protein-are-believed-to-be-the-cause-of-transmissible-spongiform-encephalopathies-among-other-diseases-image246588902.htmlRMT952JE–Model of a prion protein. Prions are infectious agents composed entirely of a protein material that can fold in multiple, structurally abstract ways, at least one of which is transmissible to other prion proteins, leading to disease in a manner that is epidemiologically comparable to the spread of viral infection. Prions composed of the prion protein are believed to be the cause of transmissible spongiform encephalopathies among other diseases.
Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. 3D rendering based on protein data Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-associated-with-neurodegenerative-diseases-including-kuru-bse-and-creutzfeldt-jakob-3d-rendering-based-on-protein-data-image227200628.htmlRFR5HTM4–Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. 3D rendering based on protein data
Human prion protein, molecular model Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-molecular-model-image65206205.htmlRFDP2B51–Human prion protein, molecular model
Human prion protein (hPrP), chemical structure. Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Atoms are repre Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-human-prion-protein-hprp-chemical-structure-associated-with-neurodegenerative-140021986.htmlRFJ3PFD6–Human prion protein (hPrP), chemical structure. Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Atoms are repre
Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Combined wireframe and cartoon model. Cartoon and carbon atoms: backbone gradient colouring (blue-teal); other atoms: conventional colour coding. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-associated-with-neurodegenerative-diseases-image150557132.htmlRFJMXD4C–Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Combined wireframe and cartoon model. Cartoon and carbon atoms: backbone gradient colouring (blue-teal); other atoms: conventional colour coding.
Electron microscope image, prion protein fibrils Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/electron-microscope-image-prion-protein-fibrils-image61888926.htmlRFDGK7XP–Electron microscope image, prion protein fibrils
Fungal prion protein Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/fungal-prion-protein-image65209336.htmlRFDP2F4T–Fungal prion protein
Prion protein shown in E. coli, purified and fibrillated at pH 7. Recombinant proteins such as the prion protein shown here are often used to model how proteins respond to each other and sometimes polymerize in neurodegenerative disorders. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/prion-protein-shown-in-e-coli-purified-and-fibrillated-at-ph-7-recombinant-proteins-such-as-the-prion-protein-shown-here-are-often-used-to-model-how-proteins-respond-to-each-other-and-sometimes-polymerize-in-neurodegenerative-disorders-image476707051.htmlRM2JKFTKR–Prion protein shown in E. coli, purified and fibrillated at pH 7. Recombinant proteins such as the prion protein shown here are often used to model how proteins respond to each other and sometimes polymerize in neurodegenerative disorders.
Fungal prion protein. Molecular model of the amyloid form of the HET prion protein. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-fungal-prion-protein-molecular-model-of-the-amyloid-form-of-the-het-73688161.htmlRFE7TP01–Fungal prion protein. Molecular model of the amyloid form of the HET prion protein.
Human prion protein (hPrP), chemical structure. Associated with neurogedenerative diseases, including kuru, BSE, etc Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-chemical-structure-associated-with-neurogedenerative-image62055511.htmlRFDGXTC7–Human prion protein (hPrP), chemical structure. Associated with neurogedenerative diseases, including kuru, BSE, etc
Prionics-Check PrioSTRIP test for detection and isolation of the prion protein, Laboratory of Bacteriology, Departamento de Producción y Sanidad Anima Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/prionics-check-priostrip-test-for-detection-and-isolation-of-the-prion-protein-laboratory-of-bacteriology-departamento-de-produccin-y-sanidad-anima-image611558648.htmlRM2XEXW88–Prionics-Check PrioSTRIP test for detection and isolation of the prion protein, Laboratory of Bacteriology, Departamento de Producción y Sanidad Anima
3d rendering Prions, unlike other infectious agents such as bacteria, viruses, and fungi, do not contain genetic material Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/3d-rendering-prions-unlike-other-infectious-agents-such-as-bacteria-viruses-and-fungi-do-not-contain-genetic-material-image570336194.htmlRF2T3W1HP–3d rendering Prions, unlike other infectious agents such as bacteria, viruses, and fungi, do not contain genetic material
Structure of the protein molecule. Projection on the plane of the biopolymer structure. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-image-structure-of-the-protein-molecule-projection-on-the-plane-of-the-biopolymer-163171602.htmlRFKDD316–Structure of the protein molecule. Projection on the plane of the biopolymer structure.
Structure of human prion, 3D cartoon model isolated, white background Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/structure-of-human-prion-3d-cartoon-model-isolated-white-background-image393159475.htmlRF2DRHXWR–Structure of human prion, 3D cartoon model isolated, white background
Cell Genetically Engineered to Express Prion-like Proteins, Microscopic View Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-cell-genetically-engineered-to-express-prion-like-proteins-microscopic-52017450.htmlRMD0HGP2–Cell Genetically Engineered to Express Prion-like Proteins, Microscopic View
Chemical structure of a human prion protein molecule (hPrP). hPrP is associated with transmissible spongiform encephalopathies, Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/chemical-structure-of-a-human-prion-protein-molecule-hprp-hprp-is-image61817794.htmlRFDGG16A–Chemical structure of a human prion protein molecule (hPrP). hPrP is associated with transmissible spongiform encephalopathies,
types of infectious agents from prions and viruses, to bacteria, fungi, worms, single-celled and unicellular organisms. detailed diagram about Acellul Stock Vectorhttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/types-of-infectious-agents-from-prions-and-viruses-to-bacteria-fungi-worms-single-celled-and-unicellular-organisms-detailed-diagram-about-acellul-image519659534.htmlRF2N5CF12–types of infectious agents from prions and viruses, to bacteria, fungi, worms, single-celled and unicellular organisms. detailed diagram about Acellul
Graphic Representation of a Human Prion Protein Fragment Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-graphic-representation-of-a-human-prion-protein-fragment-27747855.htmlRMBH40JR–Graphic Representation of a Human Prion Protein Fragment
3-dimensional CGI model of the human prion protein Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-3-dimensional-cgi-model-of-the-human-prion-protein-47416897.htmlRMCN40MH–3-dimensional CGI model of the human prion protein
Model of a prion protein. Prions are infectious agents composed entirely of a protein material that can fold in multiple, structurally abstract ways, at least one of which is transmissible to other prion proteins, leading to disease in a manner that is epidemiologically comparable to the spread of viral infection. Prions composed of the prion protein are believed to be the cause of transmissible spongiform encephalopathies among other diseases. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/model-of-a-prion-protein-prions-are-infectious-agents-composed-entirely-of-a-protein-material-that-can-fold-in-multiple-structurally-abstract-ways-at-least-one-of-which-is-transmissible-to-other-prion-proteins-leading-to-disease-in-a-manner-that-is-epidemiologically-comparable-to-the-spread-of-viral-infection-prions-composed-of-the-prion-protein-are-believed-to-be-the-cause-of-transmissible-spongiform-encephalopathies-among-other-diseases-image246588898.htmlRMT952JA–Model of a prion protein. Prions are infectious agents composed entirely of a protein material that can fold in multiple, structurally abstract ways, at least one of which is transmissible to other prion proteins, leading to disease in a manner that is epidemiologically comparable to the spread of viral infection. Prions composed of the prion protein are believed to be the cause of transmissible spongiform encephalopathies among other diseases.
Prionics-Check PrioSTRIP test for detection and isolation of the prion protein, Laboratory of Bacteriology, Departamento de Producción y Sanidad Animal, Neiker Tecnalia, Derio, Bizkaia, Euskadi, Spain. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/prionics-check-priostrip-test-for-detection-and-isolation-of-the-prion-protein-laboratory-of-bacteriology-departamento-de-produccin-y-sanidad-animal-neiker-tecnalia-derio-bizkaia-euskadi-spain-image602272956.htmlRM2WYRW8C–Prionics-Check PrioSTRIP test for detection and isolation of the prion protein, Laboratory of Bacteriology, Departamento de Producción y Sanidad Animal, Neiker Tecnalia, Derio, Bizkaia, Euskadi, Spain.
BOVINE PRION PROTEIN 1dx0 asym r 500 Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-image-bovine-prion-protein-1dx0-asym-r-500-165975964.htmlRMKJ0T10–BOVINE PRION PROTEIN 1dx0 asym r 500
Prion protein, shown in red, can become infectious and cause neurodegenerative disease. Here four nerve cells in a mouse illustrate how infectious prion protein moves within cells along neurites wire-like connections the nerve cells use for communicating with adjacent cells ca. 2019 Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/prion-protein-shown-in-red-can-become-infectious-and-cause-neurodegenerative-disease-here-four-nerve-cells-in-a-mouse-illustrate-how-infectious-prion-protein-moves-within-cells-along-neurites-wire-like-connections-the-nerve-cells-use-for-communicating-with-adjacent-cells-ca-2019-image461146019.htmlRM2HP70CK–Prion protein, shown in red, can become infectious and cause neurodegenerative disease. Here four nerve cells in a mouse illustrate how infectious prion protein moves within cells along neurites wire-like connections the nerve cells use for communicating with adjacent cells ca. 2019
structures of molecules abstract Stock Vectorhttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-structures-of-molecules-abstract-99675924.htmlRFFP4HJC–structures of molecules abstract
A Scientist examining a screen with a segment of brain displayed showing the incidence of CJD on a human brain (indicated with black rings round the white cells). The incidence of Creutzfeldt-Jakob disease (CJD) has been monitored in the UK by the National CJD surveillance unit based at the Western General Hospital in Edinburgh, Scotland. The unit brought together a team of clinical neurologists, neuropathologists and scientists specialising in the investigation of this disease Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/a-scientist-examining-a-screen-with-a-segment-of-brain-displayed-showing-the-incidence-of-cjd-on-a-human-brain-indicated-with-black-rings-round-the-white-cells-the-incidence-of-creutzfeldt-jakob-disease-cjd-has-been-monitored-in-the-uk-by-the-national-cjd-surveillance-unit-based-at-the-western-general-hospital-in-edinburgh-scotland-the-unit-brought-together-a-team-of-clinical-neurologists-neuropathologists-and-scientists-specialising-in-the-investigation-of-this-disease-image350862284.htmlRM2BAR4BT–A Scientist examining a screen with a segment of brain displayed showing the incidence of CJD on a human brain (indicated with black rings round the white cells). The incidence of Creutzfeldt-Jakob disease (CJD) has been monitored in the UK by the National CJD surveillance unit based at the Western General Hospital in Edinburgh, Scotland. The unit brought together a team of clinical neurologists, neuropathologists and scientists specialising in the investigation of this disease
The prion protein, shown in red, can become infectious and cause neurodegenerative disease. Here, four nerve cells in a mouse illustrate how the infectious prion protein moves through cells along neurites' threadlike connections that nerve cells use to communicate with adjacent cells. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/the-prion-protein-shown-in-red-can-become-infectious-and-cause-neurodegenerative-disease-here-four-nerve-cells-in-a-mouse-illustrate-how-the-infectious-prion-protein-moves-through-cells-along-neurites-threadlike-connections-that-nerve-cells-use-to-communicate-with-adjacent-cells-image476707059.htmlRM2JKFTM3–The prion protein, shown in red, can become infectious and cause neurodegenerative disease. Here, four nerve cells in a mouse illustrate how the infectious prion protein moves through cells along neurites' threadlike connections that nerve cells use to communicate with adjacent cells.
Human prion protein, molecular model. Prions are abnormal proteins that cause a group of fatal neurodegenerative diseases including BSE in cows and CJD in humans. Prions do not have a nucleic acid (RNA or DNA) genome for replication. Abnormal infectious p Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-human-prion-protein-molecular-model-prions-are-abnormal-proteins-that-73687884.htmlRFE7TNJ4–Human prion protein, molecular model. Prions are abnormal proteins that cause a group of fatal neurodegenerative diseases including BSE in cows and CJD in humans. Prions do not have a nucleic acid (RNA or DNA) genome for replication. Abnormal infectious p
Human prion protein (hPrP), chemical structure. Associated with neurogedenerative diseases, including kuru, BSE, etc. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-chemical-structure-associated-with-neurogedenerative-image60696595.htmlRFDEMY3F–Human prion protein (hPrP), chemical structure. Associated with neurogedenerative diseases, including kuru, BSE, etc.
Human prion precursor protein, molecular model showing secondary structure. The human prion protein (hPrP) is a prion precursor. Prions are abnormal proteins that are the cause of transmissible spongiform encephalopathies (TSEs) such as BSE in cows, scrap Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-human-prion-precursor-protein-molecular-model-showing-secondary-structure-73687557.htmlRFE7TN6D–Human prion precursor protein, molecular model showing secondary structure. The human prion protein (hPrP) is a prion precursor. Prions are abnormal proteins that are the cause of transmissible spongiform encephalopathies (TSEs) such as BSE in cows, scrap
3d rendering Prions, unlike other infectious agents such as bacteria, viruses, and fungi, do not contain genetic material Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/3d-rendering-prions-unlike-other-infectious-agents-such-as-bacteria-viruses-and-fungi-do-not-contain-genetic-material-image570336191.htmlRF2T3W1HK–3d rendering Prions, unlike other infectious agents such as bacteria, viruses, and fungi, do not contain genetic material
Human prion precursor protein Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-precursor-protein-image65203713.htmlRFDP2801–Human prion precursor protein
Alpha-synuclein protein. May play role in Parkinson's and Alzheimer's disease. Cartoon & stick representation with backbone gradient coloring. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-alpha-synuclein-protein-may-play-role-in-parkinsons-and-alzheimers-136234031.htmlRFHWHYW3–Alpha-synuclein protein. May play role in Parkinson's and Alzheimer's disease. Cartoon & stick representation with backbone gradient coloring.
Prion Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/prion-image407105452.htmlRM2EJ974C–Prion
Isolated prions in the dark background, a 3D rendering of infectious agents that do not contain genetic material, unlike other infectious agents such Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/isolated-prions-in-the-dark-background-a-3d-rendering-of-infectious-agents-that-do-not-contain-genetic-material-unlike-other-infectious-agents-such-image570336197.htmlRF2T3W1HW–Isolated prions in the dark background, a 3D rendering of infectious agents that do not contain genetic material, unlike other infectious agents such
Human prion protein (hPrP), chemical structure. Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Cartoon represe Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-human-prion-protein-hprp-chemical-structure-associated-with-neurodegenerative-140021987.htmlRFJ3PFD7–Human prion protein (hPrP), chemical structure. Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Cartoon represe
Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Space-filling model with conventional colour coding. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-associated-with-neurodegenerative-diseases-image150557125.htmlRFJMXD45–Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Space-filling model with conventional colour coding.
Human prion protein (hPrP), chemical structure. Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Cartoon represe Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-human-prion-protein-hprp-chemical-structure-associated-with-neurodegenerative-140021978.htmlRFJ3PFCX–Human prion protein (hPrP), chemical structure. Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Cartoon represe
Model of a prion protein. Prions are infectious agents composed entirely of a protein material that can fold in multiple, structurally abstract ways, at least one of which is transmissible to other prion proteins, leading to disease in a manner that is epidemiologically comparable to the spread of viral infection. Prions composed of the prion protein are believed to be the cause of transmissible spongiform encephalopathies among other diseases. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/model-of-a-prion-protein-prions-are-infectious-agents-composed-entirely-of-a-protein-material-that-can-fold-in-multiple-structurally-abstract-ways-at-least-one-of-which-is-transmissible-to-other-prion-proteins-leading-to-disease-in-a-manner-that-is-epidemiologically-comparable-to-the-spread-of-viral-infection-prions-composed-of-the-prion-protein-are-believed-to-be-the-cause-of-transmissible-spongiform-encephalopathies-among-other-diseases-image246588900.htmlRMT952JC–Model of a prion protein. Prions are infectious agents composed entirely of a protein material that can fold in multiple, structurally abstract ways, at least one of which is transmissible to other prion proteins, leading to disease in a manner that is epidemiologically comparable to the spread of viral infection. Prions composed of the prion protein are believed to be the cause of transmissible spongiform encephalopathies among other diseases.
Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. 3D rendering based on protein data Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-associated-with-neurodegenerative-diseases-including-kuru-bse-and-creutzfeldt-jakob-3d-rendering-based-on-protein-data-image227200627.htmlRFR5HTM3–Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. 3D rendering based on protein data
Human Prion Protein Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-image353193927.htmlRF2BEHACR–Human Prion Protein
Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. 3D rendering based on protein data Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-associated-with-neurodegenerative-diseases-including-kuru-bse-and-creutzfeldt-jakob-3d-rendering-based-on-protein-data-image402302849.htmlRF2EAEDAW–Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. 3D rendering based on protein data
Structure of the protein molecule. Projection on the plane of the biopolymer structure. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-image-structure-of-the-protein-molecule-projection-on-the-plane-of-the-biopolymer-163171584.htmlRFKDD30G–Structure of the protein molecule. Projection on the plane of the biopolymer structure.
Bloated Cells with Mutant Protein, Microscopic View Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-bloated-cells-with-mutant-protein-microscopic-view-52017173.htmlRMD0HGC5–Bloated Cells with Mutant Protein, Microscopic View
Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-associated-with-neurodegenerative-diseases-image61709637.htmlRFDGB37H–Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob.
Prion Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/prion-image407105482.htmlRM2EJ975E–Prion
Isolated prions in the dark background, a 3D rendering of infectious agents that do not contain genetic material, unlike other infectious agents such Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/isolated-prions-in-the-dark-background-a-3d-rendering-of-infectious-agents-that-do-not-contain-genetic-material-unlike-other-infectious-agents-such-image570336187.htmlRF2T3W1HF–Isolated prions in the dark background, a 3D rendering of infectious agents that do not contain genetic material, unlike other infectious agents such
Prion trafficking: scrapie mouse Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/prion-trafficking-scrapie-mouse-image453671510.htmlRM2HA2EHX–Prion trafficking: scrapie mouse
Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Ball-and-stick model with conventional colour coding. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-associated-with-neurodegenerative-diseases-image150557127.htmlRFJMXD47–Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Ball-and-stick model with conventional colour coding.
Drawing of a prion: infectious protein (encephalopathy agent). Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/drawing-of-a-prion-infectious-protein-encephalopathy-agent-image442065578.htmlRF2GK5R4A–Drawing of a prion: infectious protein (encephalopathy agent).
Prion Isoforms Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/prion-isoforms-image353193984.htmlRF2BEHAET–Prion Isoforms
Prion-like Aggregating Protein in a Cell, Microscopic View Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-prion-like-aggregating-protein-in-a-cell-microscopic-view-52017042.htmlRMD0HG7E–Prion-like Aggregating Protein in a Cell, Microscopic View
Human prion protein (hPrP), chemical structure. Associated with neurogedenerative diseases, including kuru, BSE, etc. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-chemical-structure-associated-with-neurogedenerative-image60696613.htmlRFDEMY45–Human prion protein (hPrP), chemical structure. Associated with neurogedenerative diseases, including kuru, BSE, etc.
Alpha-synuclein protein. May play role in Parkinson's and Alzheimer's disease. Cartoon representation combined with semi-transparent molecular surface Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-alpha-synuclein-protein-may-play-role-in-parkinsons-and-alzheimers-136234051.htmlRFHWHYWR–Alpha-synuclein protein. May play role in Parkinson's and Alzheimer's disease. Cartoon representation combined with semi-transparent molecular surface
Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Cartoon model, secondary structure colouring (helices blue, sheets pink). Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-associated-with-neurodegenerative-diseases-image150557128.htmlRFJMXD48–Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Cartoon model, secondary structure colouring (helices blue, sheets pink).
Drawing of a prion: infectious protein (encephalopathy agent). Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/drawing-of-a-prion-infectious-protein-encephalopathy-agent-image441937819.htmlRF2GK005F–Drawing of a prion: infectious protein (encephalopathy agent).
Prion Amyloid, molecular model Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/prion-amyloid-molecular-model-image353193954.htmlRF2BEHADP–Prion Amyloid, molecular model
Infectious Prion Protein Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-infectious-prion-protein-135011401.htmlRMHRJ8BN–Infectious Prion Protein
Alpha-synuclein protein. May play role in Parkinson's and Alzheimer's disease. Atoms are represented as spheres with conventional color coding. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-alpha-synuclein-protein-may-play-role-in-parkinsons-and-alzheimers-136234056.htmlRFHWHYX0–Alpha-synuclein protein. May play role in Parkinson's and Alzheimer's disease. Atoms are represented as spheres with conventional color coding.
Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Cartoon model, secondary structure colouring (helices blue, sheets pink). Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-associated-with-neurodegenerative-diseases-image150557130.htmlRFJMXD4A–Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Cartoon model, secondary structure colouring (helices blue, sheets pink).
Drawing of a prion: infectious protein (encephalopathy agent). Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/drawing-of-a-prion-infectious-protein-encephalopathy-agent-image442065598.htmlRF2GK5R52–Drawing of a prion: infectious protein (encephalopathy agent).
Infectious Prion Protein Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-infectious-prion-protein-135011405.htmlRMHRJ8BW–Infectious Prion Protein
Alpha-synuclein protein. May play role in Parkinson's and Alzheimer's disease. Cartoon representation with secondary structure coloring (red helices). Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-alpha-synuclein-protein-may-play-role-in-parkinsons-and-alzheimers-136234018.htmlRFHWHYTJ–Alpha-synuclein protein. May play role in Parkinson's and Alzheimer's disease. Cartoon representation with secondary structure coloring (red helices).
Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Stylized cartoon model, secondary structure colouring (helices red, sheets yellow). Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/human-prion-protein-hprp-associated-with-neurodegenerative-diseases-image150557131.htmlRFJMXD4B–Human prion protein (hPrP). Associated with neurodegenerative diseases, including kuru, BSE and Creutzfeldt-Jakob. Stylized cartoon model, secondary structure colouring (helices red, sheets yellow).
Drawing of a prion: infectious protein (encephalopathy agent). Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/drawing-of-a-prion-infectious-protein-encephalopathy-agent-image441937830.htmlRF2GK005X–Drawing of a prion: infectious protein (encephalopathy agent).
Mouse prion protein, molecular model Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-mouse-prion-protein-molecular-model-37885202.htmlRFC5HPXX–Mouse prion protein, molecular model
Microglia, a type of nervous system cell previously suspected of causing retinal damage, has been shown to be beneficial in slowing the progression of prion disease in the brain, and now in the retina. In this image, microglial cells (green) engulf and remove prion-damaged photoreceptors (red), which appears to slow retinal degeneration. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/microglia-a-type-of-nervous-system-cell-previously-suspected-of-causing-retinal-damage-has-been-shown-to-be-beneficial-in-slowing-the-progression-of-prion-disease-in-the-brain-and-now-in-the-retina-in-this-image-microglial-cells-green-engulf-and-remove-prion-damaged-photoreceptors-red-which-appears-to-slow-retinal-degeneration-image476706925.htmlRM2JKFTF9–Microglia, a type of nervous system cell previously suspected of causing retinal damage, has been shown to be beneficial in slowing the progression of prion disease in the brain, and now in the retina. In this image, microglial cells (green) engulf and remove prion-damaged photoreceptors (red), which appears to slow retinal degeneration.
PRION ILLUSTRATION Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-image-prion-illustration-168555242.htmlRMKP69X2–PRION ILLUSTRATION
Mad Cow Disease Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-mad-cow-disease-134987019.htmlRMHRH58Y–Mad Cow Disease
Microglia, shown in green, are part of the immune response that protects the brain. They may play a role in slowing the progression of prions and other neurodegenerative diseases. Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/microglia-shown-in-green-are-part-of-the-immune-response-that-protects-the-brain-they-may-play-a-role-in-slowing-the-progression-of-prions-and-other-neurodegenerative-diseases-image476706919.htmlRM2JKFTF3–Microglia, shown in green, are part of the immune response that protects the brain. They may play a role in slowing the progression of prions and other neurodegenerative diseases.
CREUTZFELDT JAKOB DIS., ARTWORK Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-creutzfeldt-jakob-dis-artwork-49178164.htmlRMCT0770–CREUTZFELDT JAKOB DIS., ARTWORK
CREUTZFELDT JAKOB DIS., ARTWORK Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-creutzfeldt-jakob-dis-artwork-49171559.htmlRMCRYXR3–CREUTZFELDT JAKOB DIS., ARTWORK
RESEARCH Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-research-49184790.htmlRMCT0FKJ–RESEARCH
Mad Cow Disease Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-mad-cow-disease-134987020.htmlRMHRH590–Mad Cow Disease
RESEARCH Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-research-49184792.htmlRMCT0FKM–RESEARCH
CREUTZFELDT JAKOB DISEASE, MRI Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-creutzfeldt-jakob-disease-mri-53858095.htmlRMD3HCFB–CREUTZFELDT JAKOB DISEASE, MRI
Mad Cow Disease Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-mad-cow-disease-134987022.htmlRMHRH592–Mad Cow Disease
CREUTZFELDT JAKOB DISEASE, MRI Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-creutzfeldt-jakob-disease-mri-53858096.htmlRMD3HCFC–CREUTZFELDT JAKOB DISEASE, MRI
CREUTZFELDT JAKOB DISEASE, MRI Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-creutzfeldt-jakob-disease-mri-53858101.htmlRMD3HCFH–CREUTZFELDT JAKOB DISEASE, MRI
CREUTZFELDT JAKOB DISEASE, MRI Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-creutzfeldt-jakob-disease-mri-49163050.htmlRMCRYFY6–CREUTZFELDT JAKOB DISEASE, MRI
CREUTZFELDT JAKOB DISEASE, MRI Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-creutzfeldt-jakob-disease-mri-49162458.htmlRMCRYF62–CREUTZFELDT JAKOB DISEASE, MRI
DIAGNOSING CREUTZFELDT JAKOB DIS Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-diagnosing-creutzfeldt-jakob-dis-49175535.htmlRMCT03W3–DIAGNOSING CREUTZFELDT JAKOB DIS
DIAGNOSING CREUTZFELDT JAKOB DIS Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-diagnosing-creutzfeldt-jakob-dis-49175523.htmlRMCT03TK–DIAGNOSING CREUTZFELDT JAKOB DIS
CREUTZFELDT JAKOB DIS., ARTWORK Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-creutzfeldt-jakob-dis-artwork-25569114.htmlRFBDGNJJ–CREUTZFELDT JAKOB DIS., ARTWORK
CREUTZFELDT JAKOB DIS., ARTWORK Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-creutzfeldt-jakob-dis-artwork-25569117.htmlRFBDGNJN–CREUTZFELDT JAKOB DIS., ARTWORK
CREUTZFELDT JAKOB DIS., ARTWORK Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-creutzfeldt-jakob-dis-artwork-49173969.htmlRMCT01W5–CREUTZFELDT JAKOB DIS., ARTWORK
DIAGNOSING CREUTZFELDT JAKOB DIS Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-diagnosing-creutzfeldt-jakob-dis-49175542.htmlRMCT03WA–DIAGNOSING CREUTZFELDT JAKOB DIS
DIAGNOSING CREUTZFELDT JAKOB DIS Stock Photohttps://www.alamy.com/image-license-details/?v=1https://www.alamy.com/stock-photo-diagnosing-creutzfeldt-jakob-dis-49175540.htmlRMCT03W8–DIAGNOSING CREUTZFELDT JAKOB DIS
