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  1. Book ; Article ; Online: The current landscape of coronavirus-host protein-protein interactions

    Perrin-Coccon, Laure / Diaz, Olivier / Jacquemin, Clémence / Barthel, Valentine / Ogire, Eva / Ramière, Christophe / André, Patrice / Lotteau, Vincent / Vidalain, Pierre-Olivier

    https://hal.archives-ouvertes.fr/hal-02874650 ; 2020

    2020  

    Abstract: In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat ... ...

    Abstract In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat for both domestic and wild animals. Members of this viral family have the longest genome of all RNA viruses, and express up to 29 proteins establishing complex interactions with the host proteome. Deciphering these interactions is essential to identify cellular pathways hijacked by these viruses to replicate and escape innate immunity. Virus-host interactions also provide key information to select targets for antiviral drug development. Here, we have manually curated the literature to assemble a unique dataset of 1311 coronavirus-host protein-protein interactions. Functional enrichment and network-based analyses showed coronavirus connections to RNA processing and translation, DNA damage and pathogen sensing, interferon production, and metabolic pathways. In particular, this global analysis pinpointed overlooked interactions with translation modulators (GIGYF2-EIF4E2), components of the nuclear pore, proteins involved in mitochondria homeostasis (PHB, PHB2, STOML2), and methylation pathways (MAT2A/B). Finally, interactome data provided a rational for the antiviral activity of some drugs inhibiting coronaviruses replication. Altogether, this work describing the current landscape of coronavirus-host interactions provides valuable hints for understanding the pathophysiology of coronavirus infections and developing effective antiviral therapies.
    Keywords [SDV]Life Sciences [q-bio] ; [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ; covid19
    Subject code 612
    Language English
    Publishing date 2020-06-19
    Publisher HAL CCSD
    Publishing country fr
    Document type Book ; Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  2. Book ; Article ; Online: The current landscape of coronavirus-host protein-protein interactions

    Perrin-Coccon, Laure / Diaz, Olivier / Jacquemin, Clémence / Barthel, Valentine / Ogire, Eva / Ramière, Christophe / André, Patrice / Lotteau, Vincent / Vidalain, Pierre-Olivier

    https://hal.archives-ouvertes.fr/hal-02874650 ; 2020

    2020  

    Abstract: In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat ... ...

    Abstract In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat for both domestic and wild animals. Members of this viral family have the longest genome of all RNA viruses, and express up to 29 proteins establishing complex interactions with the host proteome. Deciphering these interactions is essential to identify cellular pathways hijacked by these viruses to replicate and escape innate immunity. Virus-host interactions also provide key information to select targets for antiviral drug development. Here, we have manually curated the literature to assemble a unique dataset of 1311 coronavirus-host protein-protein interactions. Functional enrichment and network-based analyses showed coronavirus connections to RNA processing and translation, DNA damage and pathogen sensing, interferon production, and metabolic pathways. In particular, this global analysis pinpointed overlooked interactions with translation modulators (GIGYF2-EIF4E2), components of the nuclear pore, proteins involved in mitochondria homeostasis (PHB, PHB2, STOML2), and methylation pathways (MAT2A/B). Finally, interactome data provided a rational for the antiviral activity of some drugs inhibiting coronaviruses replication. Altogether, this work describing the current landscape of coronavirus-host interactions provides valuable hints for understanding the pathophysiology of coronavirus infections and developing effective antiviral therapies.
    Keywords [SDV]Life Sciences [q-bio] ; [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ; covid19
    Subject code 612
    Language English
    Publishing date 2020-07-28
    Publisher HAL CCSD
    Publishing country fr
    Document type Book ; Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  3. Book ; Article ; Online: The current landscape of coronavirus-host protein-protein interactions

    Perrin-Coccon, Laure / Diaz, Olivier / Jacquemin, Clémence / Barthel, Valentine / Ogire, Eva / Ramière, Christophe / André, Patrice / Lotteau, Vincent / Vidalain, Pierre-Olivier

    https://hal.archives-ouvertes.fr/hal-02874650 ; 2020

    2020  

    Abstract: In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat ... ...

    Abstract In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat for both domestic and wild animals. Members of this viral family have the longest genome of all RNA viruses, and express up to 29 proteins establishing complex interactions with the host proteome. Deciphering these interactions is essential to identify cellular pathways hijacked by these viruses to replicate and escape innate immunity. Virus-host interactions also provide key information to select targets for antiviral drug development. Here, we have manually curated the literature to assemble a unique dataset of 1311 coronavirus-host protein-protein interactions. Functional enrichment and network-based analyses showed coronavirus connections to RNA processing and translation, DNA damage and pathogen sensing, interferon production, and metabolic pathways. In particular, this global analysis pinpointed overlooked interactions with translation modulators (GIGYF2-EIF4E2), components of the nuclear pore, proteins involved in mitochondria homeostasis (PHB, PHB2, STOML2), and methylation pathways (MAT2A/B). Finally, interactome data provided a rational for the antiviral activity of some drugs inhibiting coronaviruses replication. Altogether, this work describing the current landscape of coronavirus-host interactions provides valuable hints for understanding the pathophysiology of coronavirus infections and developing effective antiviral therapies.
    Keywords [SDV]Life Sciences [q-bio] ; [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ; covid19
    Subject code 612
    Language English
    Publishing date 2020-07-28
    Publisher HAL CCSD
    Publishing country fr
    Document type Book ; Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  4. Book ; Article ; Online: The current landscape of coronavirus-host protein-protein interactions

    Perrin-Coccon, Laure / Diaz, Olivier / Jacquemin, Clémence / Barthel, Valentine / Ogire, Eva / Ramière, Christophe / André, Patrice / Lotteau, Vincent / Vidalain, Pierre-Olivier

    https://hal.archives-ouvertes.fr/hal-02874650 ; 2020

    2020  

    Abstract: In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat ... ...

    Abstract In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat for both domestic and wild animals. Members of this viral family have the longest genome of all RNA viruses, and express up to 29 proteins establishing complex interactions with the host proteome. Deciphering these interactions is essential to identify cellular pathways hijacked by these viruses to replicate and escape innate immunity. Virus-host interactions also provide key information to select targets for antiviral drug development. Here, we have manually curated the literature to assemble a unique dataset of 1311 coronavirus-host protein-protein interactions. Functional enrichment and network-based analyses showed coronavirus connections to RNA processing and translation, DNA damage and pathogen sensing, interferon production, and metabolic pathways. In particular, this global analysis pinpointed overlooked interactions with translation modulators (GIGYF2-EIF4E2), components of the nuclear pore, proteins involved in mitochondria homeostasis (PHB, PHB2, STOML2), and methylation pathways (MAT2A/B). Finally, interactome data provided a rational for the antiviral activity of some drugs inhibiting coronaviruses replication. Altogether, this work describing the current landscape of coronavirus-host interactions provides valuable hints for understanding the pathophysiology of coronavirus infections and developing effective antiviral therapies.
    Keywords [SDV]Life Sciences [q-bio] ; [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ; covid19
    Subject code 612
    Language English
    Publishing date 2020-06-19
    Publisher HAL CCSD
    Publishing country fr
    Document type Book ; Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  5. Book ; Article ; Online: The current landscape of coronavirus-host protein-protein interactions

    Perrin-Coccon, Laure / Diaz, Olivier / Jacquemin, Clémence / Barthel, Valentine / Ogire, Eva / Ramière, Christophe / André, Patrice / Lotteau, Vincent / Vidalain, Pierre-Olivier

    https://hal.archives-ouvertes.fr/hal-02874650 ; 2020

    2020  

    Abstract: In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat ... ...

    Abstract In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat for both domestic and wild animals. Members of this viral family have the longest genome of all RNA viruses, and express up to 29 proteins establishing complex interactions with the host proteome. Deciphering these interactions is essential to identify cellular pathways hijacked by these viruses to replicate and escape innate immunity. Virus-host interactions also provide key information to select targets for antiviral drug development. Here, we have manually curated the literature to assemble a unique dataset of 1311 coronavirus-host protein-protein interactions. Functional enrichment and network-based analyses showed coronavirus connections to RNA processing and translation, DNA damage and pathogen sensing, interferon production, and metabolic pathways. In particular, this global analysis pinpointed overlooked interactions with translation modulators (GIGYF2-EIF4E2), components of the nuclear pore, proteins involved in mitochondria homeostasis (PHB, PHB2, STOML2), and methylation pathways (MAT2A/B). Finally, interactome data provided a rational for the antiviral activity of some drugs inhibiting coronaviruses replication. Altogether, this work describing the current landscape of coronavirus-host interactions provides valuable hints for understanding the pathophysiology of coronavirus infections and developing effective antiviral therapies.
    Keywords [SDV]Life Sciences [q-bio] ; [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ; covid19
    Subject code 612
    Language English
    Publishing date 2020-07-28
    Publisher HAL CCSD
    Publishing country fr
    Document type Book ; Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  6. Book ; Article ; Online: The current landscape of coronavirus-host protein-protein interactions

    Perrin-Coccon, Laure / Diaz, Olivier / Jacquemin, Clémence / Barthel, Valentine / Ogire, Eva / Ramière, Christophe / André, Patrice / Lotteau, Vincent / Vidalain, Pierre-Olivier

    https://hal.archives-ouvertes.fr/hal-02874650 ; 2020

    2020  

    Abstract: In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat ... ...

    Abstract In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat for both domestic and wild animals. Members of this viral family have the longest genome of all RNA viruses, and express up to 29 proteins establishing complex interactions with the host proteome. Deciphering these interactions is essential to identify cellular pathways hijacked by these viruses to replicate and escape innate immunity. Virus-host interactions also provide key information to select targets for antiviral drug development. Here, we have manually curated the literature to assemble a unique dataset of 1311 coronavirus-host protein-protein interactions. Functional enrichment and network-based analyses showed coronavirus connections to RNA processing and translation, DNA damage and pathogen sensing, interferon production, and metabolic pathways. In particular, this global analysis pinpointed overlooked interactions with translation modulators (GIGYF2-EIF4E2), components of the nuclear pore, proteins involved in mitochondria homeostasis (PHB, PHB2, STOML2), and methylation pathways (MAT2A/B). Finally, interactome data provided a rational for the antiviral activity of some drugs inhibiting coronaviruses replication. Altogether, this work describing the current landscape of coronavirus-host interactions provides valuable hints for understanding the pathophysiology of coronavirus infections and developing effective antiviral therapies.
    Keywords [SDV]Life Sciences [q-bio] ; [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ; covid19
    Subject code 612
    Language English
    Publishing date 2020-07-28
    Publisher HAL CCSD
    Publishing country fr
    Document type Book ; Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  7. Book ; Article ; Online: The current landscape of coronavirus-host protein-protein interactions

    Perrin-Coccon, Laure / Diaz, Olivier / Jacquemin, Clémence / Barthel, Valentine / Ogire, Eva / Ramière, Christophe / André, Patrice / Lotteau, Vincent / Vidalain, Pierre-Olivier

    https://hal.archives-ouvertes.fr/hal-02874650 ; 2020

    2020  

    Abstract: In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat ... ...

    Abstract In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat for both domestic and wild animals. Members of this viral family have the longest genome of all RNA viruses, and express up to 29 proteins establishing complex interactions with the host proteome. Deciphering these interactions is essential to identify cellular pathways hijacked by these viruses to replicate and escape innate immunity. Virus-host interactions also provide key information to select targets for antiviral drug development. Here, we have manually curated the literature to assemble a unique dataset of 1311 coronavirus-host protein-protein interactions. Functional enrichment and network-based analyses showed coronavirus connections to RNA processing and translation, DNA damage and pathogen sensing, interferon production, and metabolic pathways. In particular, this global analysis pinpointed overlooked interactions with translation modulators (GIGYF2-EIF4E2), components of the nuclear pore, proteins involved in mitochondria homeostasis (PHB, PHB2, STOML2), and methylation pathways (MAT2A/B). Finally, interactome data provided a rational for the antiviral activity of some drugs inhibiting coronaviruses replication. Altogether, this work describing the current landscape of coronavirus-host interactions provides valuable hints for understanding the pathophysiology of coronavirus infections and developing effective antiviral therapies.
    Keywords [SDV]Life Sciences [q-bio] ; [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ; covid19
    Subject code 612
    Language English
    Publishing date 2020-07-28
    Publisher HAL CCSD
    Publishing country fr
    Document type Book ; Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  8. Book ; Article ; Online: The current landscape of coronavirus-host protein-protein interactions

    Perrin-Coccon, Laure / Diaz, Olivier / Jacquemin, Clémence / Barthel, Valentine / Ogire, Eva / Ramière, Christophe / André, Patrice / Lotteau, Vincent / Vidalain, Pierre-Olivier

    https://hal.archives-ouvertes.fr/hal-02874650 ; 2020

    2020  

    Abstract: In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat ... ...

    Abstract In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat for both domestic and wild animals. Members of this viral family have the longest genome of all RNA viruses, and express up to 29 proteins establishing complex interactions with the host proteome. Deciphering these interactions is essential to identify cellular pathways hijacked by these viruses to replicate and escape innate immunity. Virus-host interactions also provide key information to select targets for antiviral drug development. Here, we have manually curated the literature to assemble a unique dataset of 1311 coronavirus-host protein-protein interactions. Functional enrichment and network-based analyses showed coronavirus connections to RNA processing and translation, DNA damage and pathogen sensing, interferon production, and metabolic pathways. In particular, this global analysis pinpointed overlooked interactions with translation modulators (GIGYF2-EIF4E2), components of the nuclear pore, proteins involved in mitochondria homeostasis (PHB, PHB2, STOML2), and methylation pathways (MAT2A/B). Finally, interactome data provided a rational for the antiviral activity of some drugs inhibiting coronaviruses replication. Altogether, this work describing the current landscape of coronavirus-host interactions provides valuable hints for understanding the pathophysiology of coronavirus infections and developing effective antiviral therapies.
    Keywords [SDV]Life Sciences [q-bio] ; [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ; covid19
    Subject code 612
    Language English
    Publishing date 2020-06-19
    Publisher HAL CCSD
    Publishing country fr
    Document type Book ; Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  9. Book ; Article ; Online: The current landscape of coronavirus-host protein-protein interactions

    Perrin-Coccon, Laure / Diaz, Olivier / Jacquemin, Clémence / Barthel, Valentine / Ogire, Eva / Ramière, Christophe / André, Patrice / Lotteau, Vincent / Vidalain, Pierre-Olivier

    https://hal.archives-ouvertes.fr/hal-02874650 ; 2020

    2020  

    Abstract: In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat ... ...

    Abstract In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat for both domestic and wild animals. Members of this viral family have the longest genome of all RNA viruses, and express up to 29 proteins establishing complex interactions with the host proteome. Deciphering these interactions is essential to identify cellular pathways hijacked by these viruses to replicate and escape innate immunity. Virus-host interactions also provide key information to select targets for antiviral drug development. Here, we have manually curated the literature to assemble a unique dataset of 1311 coronavirus-host protein-protein interactions. Functional enrichment and network-based analyses showed coronavirus connections to RNA processing and translation, DNA damage and pathogen sensing, interferon production, and metabolic pathways. In particular, this global analysis pinpointed overlooked interactions with translation modulators (GIGYF2-EIF4E2), components of the nuclear pore, proteins involved in mitochondria homeostasis (PHB, PHB2, STOML2), and methylation pathways (MAT2A/B). Finally, interactome data provided a rational for the antiviral activity of some drugs inhibiting coronaviruses replication. Altogether, this work describing the current landscape of coronavirus-host interactions provides valuable hints for understanding the pathophysiology of coronavirus infections and developing effective antiviral therapies.
    Keywords [SDV]Life Sciences [q-bio] ; [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ; covid19
    Subject code 612
    Language English
    Publishing date 2020-07-28
    Publisher HAL CCSD
    Publishing country fr
    Document type Book ; Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  10. Book ; Article ; Online: The current landscape of coronavirus-host protein-protein interactions

    Perrin-Coccon, Laure / Diaz, Olivier / Jacquemin, Clémence / Barthel, Valentine / Ogire, Eva / Ramière, Christophe / André, Patrice / Lotteau, Vincent / Vidalain, Pierre-Olivier

    https://hal.archives-ouvertes.fr/hal-02874650 ; 2020

    2020  

    Abstract: In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat ... ...

    Abstract In less than twenty years, three deadly coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2, have emerged in human population causing hundreds to hundreds of thousands of deaths. Other coronaviruses are causing epizootic representing a significant threat for both domestic and wild animals. Members of this viral family have the longest genome of all RNA viruses, and express up to 29 proteins establishing complex interactions with the host proteome. Deciphering these interactions is essential to identify cellular pathways hijacked by these viruses to replicate and escape innate immunity. Virus-host interactions also provide key information to select targets for antiviral drug development. Here, we have manually curated the literature to assemble a unique dataset of 1311 coronavirus-host protein-protein interactions. Functional enrichment and network-based analyses showed coronavirus connections to RNA processing and translation, DNA damage and pathogen sensing, interferon production, and metabolic pathways. In particular, this global analysis pinpointed overlooked interactions with translation modulators (GIGYF2-EIF4E2), components of the nuclear pore, proteins involved in mitochondria homeostasis (PHB, PHB2, STOML2), and methylation pathways (MAT2A/B). Finally, interactome data provided a rational for the antiviral activity of some drugs inhibiting coronaviruses replication. Altogether, this work describing the current landscape of coronavirus-host interactions provides valuable hints for understanding the pathophysiology of coronavirus infections and developing effective antiviral therapies.
    Keywords [SDV]Life Sciences [q-bio] ; [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ; [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ; covid19
    Subject code 612
    Language English
    Publishing date 2020-06-19
    Publisher HAL CCSD
    Publishing country fr
    Document type Book ; Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

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