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Ionization of atomic hydrogen by 30 1000 keV antiprotons.

Physical review letters

Charlton M, Kirsebom K, Knudsen H, Mikkelsen U, Moller SP, Morenzoni E, Paludan K, Slevin J, Uggerhoj E.
PMID: 10058558
Phys Rev Lett. 1995 Jun 05;74(23):4627-4630. doi: 10.1103/PhysRevLett.74.4627.

No abstract available.

Cite
Charlton M, Kirsebom K, Knudsen H, et al. Ionization of atomic hydrogen by 30 1000 keV antiprotons. Phys Rev Lett. 1995;74(23):4627-4630doi: 10.1103/PhysRevLett.74.4627.
Charlton, M., Kirsebom, K., Knudsen, H., Mikkelsen, U., Moller, S. P., Morenzoni, E., Paludan, K., Slevin, J., & Uggerhoj, E. (1995). Ionization of atomic hydrogen by 30 1000 keV antiprotons. Physical review letters, 74(23), 4627-4630. https://doi.org/10.1103/PhysRevLett.74.4627
Charlton, et al. "Ionization of atomic hydrogen by 30 1000 keV antiprotons." Physical review letters vol. 74,23 (1995): 4627-4630. doi: https://doi.org/10.1103/PhysRevLett.74.4627
Charlton M, Kirsebom K, Knudsen H, Mikkelsen U, Moller SP, Morenzoni E, Paludan K, Slevin J, Uggerhoj E. Ionization of atomic hydrogen by 30 1000 keV antiprotons. Phys Rev Lett. 1995 Jun 05;74(23):4627-4630. doi: 10.1103/PhysRevLett.74.4627. PMID: 10058558.
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Innate immunological pathways in COVID-19 pathogenesis.

Science immunology

Paludan SR, Mogensen TH.
PMID: 34995097
Sci Immunol. 2022 Jan 07;7(67):eabm5505. doi: 10.1126/sciimmunol.abm5505. Epub 2022 Jan 07.

[Figure: see text].

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Paludan SR, Mogensen TH. Innate immunological pathways in COVID-19 pathogenesis. Sci Immunol. 2022;7(67):eabm5505doi: 10.1126/sciimmunol.abm5505.
Paludan, S. R., & Mogensen, T. H. (2022). Innate immunological pathways in COVID-19 pathogenesis. Science immunology, 7(67), eabm5505. https://doi.org/10.1126/sciimmunol.abm5505
Paludan, Søren R, and Mogensen, Trine H. "Innate immunological pathways in COVID-19 pathogenesis." Science immunology vol. 7,67 (2022): eabm5505. doi: https://doi.org/10.1126/sciimmunol.abm5505
Paludan SR, Mogensen TH. Innate immunological pathways in COVID-19 pathogenesis. Sci Immunol. 2022 Jan 07;7(67):eabm5505. doi: 10.1126/sciimmunol.abm5505. Epub 2022 Jan 07. PMID: 34995097.
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Innate immunological pathways in COVID-19 pathogenesis.

Science immunology

Paludan SR, Mogensen TH.
PMID: 34995097
Sci Immunol. 2022 Jan 07;7(67):eabm5505. doi: 10.1126/sciimmunol.abm5505. Epub 2022 Jan 07.

[Figure: see text].

Cite
Paludan SR, Mogensen TH. Innate immunological pathways in COVID-19 pathogenesis. Sci Immunol. 2022;7(67):eabm5505doi: 10.1126/sciimmunol.abm5505.
Paludan, S. R., & Mogensen, T. H. (2022). Innate immunological pathways in COVID-19 pathogenesis. Science immunology, 7(67), eabm5505. https://doi.org/10.1126/sciimmunol.abm5505
Paludan, Søren R, and Mogensen, Trine H. "Innate immunological pathways in COVID-19 pathogenesis." Science immunology vol. 7,67 (2022): eabm5505. doi: https://doi.org/10.1126/sciimmunol.abm5505
Paludan SR, Mogensen TH. Innate immunological pathways in COVID-19 pathogenesis. Sci Immunol. 2022 Jan 07;7(67):eabm5505. doi: 10.1126/sciimmunol.abm5505. Epub 2022 Jan 07. PMID: 34995097.
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B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation.

Frontiers in immunology

Green K, Wittenborn TR, Fahlquist-Hagert C, Terczynska-Dyla E, van Campen N, Jensen L, Reinert L, Hartmann R, Paludan SR, Degn SE.
PMID: 34938294
Front Immunol. 2021 Dec 06;12:782558. doi: 10.3389/fimmu.2021.782558. eCollection 2021.

Germinal centers (GCs) are induced microanatomical structures wherein B cells undergo affinity maturation to improve the quality of the antibody response. Although GCs are crucial to appropriate humoral responses to infectious challenges and vaccines, many questions remain about the...

Cite
Green K, Wittenborn TR, Fahlquist-Hagert C, et al. B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation. Front Immunol. 2021;12:782558doi: 10.3389/fimmu.2021.782558.
Green, K., Wittenborn, T. R., Fahlquist-Hagert, C., Terczynska-Dyla, E., van Campen, N., Jensen, L., Reinert, L., Hartmann, R., Paludan, S. R., & Degn, S. E. (2021). B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation. Frontiers in immunology, 12782558. https://doi.org/10.3389/fimmu.2021.782558
Green, Kenneth, et al. "B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation." Frontiers in immunology vol. 12 (2021): 782558. doi: https://doi.org/10.3389/fimmu.2021.782558
Green K, Wittenborn TR, Fahlquist-Hagert C, Terczynska-Dyla E, van Campen N, Jensen L, Reinert L, Hartmann R, Paludan SR, Degn SE. B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation. Front Immunol. 2021 Dec 06;12:782558. doi: 10.3389/fimmu.2021.782558. eCollection 2021. PMID: 34938294; PMCID: PMC8685402.
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Erratum: STING Mediates Lupus via the Activation of Conventional Dendritic Cell Maturation and Plasmacytoid Dendritic Cell Differentiation.

iScience

Thim-Uam A, Prabakaran T, Tansakul M, Makjaroen J, Wongkongkathep P, Chantaravisoot N, Saethang T, Leelahavanichkul A, Benjachat T, Paludan SR, Pisitkun T, Pisitkun P.
PMID: 33196029
iScience. 2020 Nov 01;23(11):101706. doi: 10.1016/j.isci.2020.101706. eCollection 2020 Nov 20.

[This corrects the article DOI: 10.1016/j.isci.2020.101530.].

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Thim-Uam A, Prabakaran T, Tansakul M, et al. Erratum: STING Mediates Lupus via the Activation of Conventional Dendritic Cell Maturation and Plasmacytoid Dendritic Cell Differentiation. iScience. 2020;23(11):101706doi: 10.1016/j.isci.2020.101706.
Thim-Uam, A., Prabakaran, T., Tansakul, M., Makjaroen, J., Wongkongkathep, P., Chantaravisoot, N., Saethang, T., Leelahavanichkul, A., Benjachat, T., Paludan, S. R., Pisitkun, T., & Pisitkun, P. (2020). Erratum: STING Mediates Lupus via the Activation of Conventional Dendritic Cell Maturation and Plasmacytoid Dendritic Cell Differentiation. iScience, 23(11), 101706. https://doi.org/10.1016/j.isci.2020.101706
Thim-Uam, Arthid, et al. "Erratum: STING Mediates Lupus via the Activation of Conventional Dendritic Cell Maturation and Plasmacytoid Dendritic Cell Differentiation." iScience vol. 23,11 (2020): 101706. doi: https://doi.org/10.1016/j.isci.2020.101706
Thim-Uam A, Prabakaran T, Tansakul M, Makjaroen J, Wongkongkathep P, Chantaravisoot N, Saethang T, Leelahavanichkul A, Benjachat T, Paludan SR, Pisitkun T, Pisitkun P. Erratum: STING Mediates Lupus via the Activation of Conventional Dendritic Cell Maturation and Plasmacytoid Dendritic Cell Differentiation. iScience. 2020 Nov 01;23(11):101706. doi: 10.1016/j.isci.2020.101706. eCollection 2020 Nov 20. PMID: 33196029; PMCID: PMC7644739.
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Author Correction: STEEP mediates STING ER exit and activation of signaling.

Nature immunology

Zhang BC, Nandakumar R, Reinert LS, Huang J, Laustsen A, Gao ZL, Sun CL, Jensen SB, Troldborg A, Assil S, Berthelsen MF, Scavenius C, Zhang Y, Windross SJ, Olagnier D, Prabakaran T, Bodda C, Narita R, Cai Y, Zhang CG, Stenmark H, Doucet CM, Noda T, Guo Z, Goldbach-Mansky R, Hartmann R, Chen ZJ, Enghild JJ, Bak RO, Thomsen MK, Paludan SR.
PMID: 32929276
Nat Immunol. 2020 Nov;21(11):1468-1469. doi: 10.1038/s41590-020-0803-5.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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Zhang BC, Nandakumar R, Reinert LS, et al. Author Correction: STEEP mediates STING ER exit and activation of signaling. Nat Immunol. 2020;21(11):1468-1469doi: 10.1038/s41590-020-0803-5.
Zhang, B. C., Nandakumar, R., Reinert, L. S., Huang, J., Laustsen, A., Gao, Z. L., Sun, C. L., Jensen, S. B., Troldborg, A., Assil, S., Berthelsen, M. F., Scavenius, C., Zhang, Y., Windross, S. J., Olagnier, D., Prabakaran, T., Bodda, C., Narita, R., Cai, Y., Zhang, C. G., Stenmark, H., Doucet, C. M., Noda, T., Guo, Z., Goldbach-Mansky, R., Hartmann, R., Chen, Z. J., Enghild, J. J., Bak, R. O., Thomsen, M. K., & Paludan, S. R. (2020). Author Correction: STEEP mediates STING ER exit and activation of signaling. Nature immunology, 21(11), 1468-1469. https://doi.org/10.1038/s41590-020-0803-5
Zhang, Bao-Cun, et al. "Author Correction: STEEP mediates STING ER exit and activation of signaling." Nature immunology vol. 21,11 (2020): 1468-1469. doi: https://doi.org/10.1038/s41590-020-0803-5
Zhang BC, Nandakumar R, Reinert LS, Huang J, Laustsen A, Gao ZL, Sun CL, Jensen SB, Troldborg A, Assil S, Berthelsen MF, Scavenius C, Zhang Y, Windross SJ, Olagnier D, Prabakaran T, Bodda C, Narita R, Cai Y, Zhang CG, Stenmark H, Doucet CM, Noda T, Guo Z, Goldbach-Mansky R, Hartmann R, Chen ZJ, Enghild JJ, Bak RO, Thomsen MK, Paludan SR. Author Correction: STEEP mediates STING ER exit and activation of signaling. Nat Immunol. 2020 Nov;21(11):1468-1469. doi: 10.1038/s41590-020-0803-5. PMID: 32929276.
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B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation.

Frontiers in immunology

Green K, Wittenborn TR, Fahlquist-Hagert C, Terczynska-Dyla E, van Campen N, Jensen L, Reinert L, Hartmann R, Paludan SR, Degn SE.
PMID: 34938294
Front Immunol. 2021 Dec 06;12:782558. doi: 10.3389/fimmu.2021.782558. eCollection 2021.

Germinal centers (GCs) are induced microanatomical structures wherein B cells undergo affinity maturation to improve the quality of the antibody response. Although GCs are crucial to appropriate humoral responses to infectious challenges and vaccines, many questions remain about the...

Cite
Green K, Wittenborn TR, Fahlquist-Hagert C, et al. B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation. Front Immunol. 2021;12:782558doi: 10.3389/fimmu.2021.782558.
Green, K., Wittenborn, T. R., Fahlquist-Hagert, C., Terczynska-Dyla, E., van Campen, N., Jensen, L., Reinert, L., Hartmann, R., Paludan, S. R., & Degn, S. E. (2021). B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation. Frontiers in immunology, 12782558. https://doi.org/10.3389/fimmu.2021.782558
Green, Kenneth, et al. "B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation." Frontiers in immunology vol. 12 (2021): 782558. doi: https://doi.org/10.3389/fimmu.2021.782558
Green K, Wittenborn TR, Fahlquist-Hagert C, Terczynska-Dyla E, van Campen N, Jensen L, Reinert L, Hartmann R, Paludan SR, Degn SE. B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation. Front Immunol. 2021 Dec 06;12:782558. doi: 10.3389/fimmu.2021.782558. eCollection 2021. PMID: 34938294; PMCID: PMC8685402.
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The chromosomal arrangement of six soybean leghemoglobin genes.

The EMBO journal

Bojsen K, Abildsten D, Jensen EØ, Paludan K, Marcker KA.
PMID: 16453470
EMBO J. 1983;2(7):1165-8.

Clones containing six leghemoglobin (Lb) genes have been isolated from two genomic libraries of soybean. They encompass two independent DNA regions: a 40-kb region containing four genes in the order 5' Lba-Lbc(1)-[unk]Lb-Lbc(3) 3' with the same transcriptional polarity, and...

Cite
Bojsen K, Abildsten D, Jensen EØ, et al. The chromosomal arrangement of six soybean leghemoglobin genes. EMBO J. 1983;2(7):1165-8
Bojsen, K., Abildsten, D., Jensen, E. �. �., Paludan, K., & Marcker, K. A. (1983). The chromosomal arrangement of six soybean leghemoglobin genes. The EMBO journal, 2(7), 1165-8.
Bojsen, K, et al. "The chromosomal arrangement of six soybean leghemoglobin genes." The EMBO journal vol. 2,7 (1983): 1165-8.
Bojsen K, Abildsten D, Jensen EØ, Paludan K, Marcker KA. The chromosomal arrangement of six soybean leghemoglobin genes. EMBO J. 1983;2(7):1165-8. PMID: 16453470; PMCID: PMC555251.
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STING orchestrates the crosstalk between polyunsaturated fatty acid metabolism and inflammatory responses.

Cell metabolism

Vila IK, Chamma H, Steer A, Saccas M, Taffoni C, Turtoi E, Reinert LS, Hussain S, Marines J, Jin L, Bonnefont X, Hubert M, Schwartz O, Paludan SR, Van Simaeys G, Doumont G, Sobhian B, Vlachakis D, Turtoi A, Laguette N.
PMID: 34986331
Cell Metab. 2022 Jan 04;34(1):125-139.e8. doi: 10.1016/j.cmet.2021.12.007.

Concerted alteration of immune and metabolic homeostasis underlies several inflammation-related pathologies, ranging from metabolic syndrome to infectious diseases. Here, we explored the coordination of nucleic acid-dependent inflammatory responses and metabolic homeostasis. We reveal that the STING (stimulator of interferon...

Cite
Vila IK, Chamma H, Steer A, et al. STING orchestrates the crosstalk between polyunsaturated fatty acid metabolism and inflammatory responses. Cell Metab. 2022;34(1):125-139.e8doi: 10.1016/j.cmet.2021.12.007.
Vila, I. K., Chamma, H., Steer, A., Saccas, M., Taffoni, C., Turtoi, E., Reinert, L. S., Hussain, S., Marines, J., Jin, L., Bonnefont, X., Hubert, M., Schwartz, O., Paludan, S. R., Van Simaeys, G., Doumont, G., Sobhian, B., Vlachakis, D., Turtoi, A., & Laguette, N. (2022). STING orchestrates the crosstalk between polyunsaturated fatty acid metabolism and inflammatory responses. Cell metabolism, 34(1), 125-139.e8. https://doi.org/10.1016/j.cmet.2021.12.007
Vila, Isabelle K, et al. "STING orchestrates the crosstalk between polyunsaturated fatty acid metabolism and inflammatory responses." Cell metabolism vol. 34,1 (2022): 125-139.e8. doi: https://doi.org/10.1016/j.cmet.2021.12.007
Vila IK, Chamma H, Steer A, Saccas M, Taffoni C, Turtoi E, Reinert LS, Hussain S, Marines J, Jin L, Bonnefont X, Hubert M, Schwartz O, Paludan SR, Van Simaeys G, Doumont G, Sobhian B, Vlachakis D, Turtoi A, Laguette N. STING orchestrates the crosstalk between polyunsaturated fatty acid metabolism and inflammatory responses. Cell Metab. 2022 Jan 04;34(1):125-139.e8. doi: 10.1016/j.cmet.2021.12.007. PMID: 34986331; PMCID: PMC8733004.
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STING orchestrates the crosstalk between polyunsaturated fatty acid metabolism and inflammatory responses.

Cell metabolism

Vila IK, Chamma H, Steer A, Saccas M, Taffoni C, Turtoi E, Reinert LS, Hussain S, Marines J, Jin L, Bonnefont X, Hubert M, Schwartz O, Paludan SR, Van Simaeys G, Doumont G, Sobhian B, Vlachakis D, Turtoi A, Laguette N.
PMID: 34986331
Cell Metab. 2022 Jan 04;34(1):125-139.e8. doi: 10.1016/j.cmet.2021.12.007.

Concerted alteration of immune and metabolic homeostasis underlies several inflammation-related pathologies, ranging from metabolic syndrome to infectious diseases. Here, we explored the coordination of nucleic acid-dependent inflammatory responses and metabolic homeostasis. We reveal that the STING (stimulator of interferon...

Cite
Vila IK, Chamma H, Steer A, et al. STING orchestrates the crosstalk between polyunsaturated fatty acid metabolism and inflammatory responses. Cell Metab. 2022;34(1):125-139.e8doi: 10.1016/j.cmet.2021.12.007.
Vila, I. K., Chamma, H., Steer, A., Saccas, M., Taffoni, C., Turtoi, E., Reinert, L. S., Hussain, S., Marines, J., Jin, L., Bonnefont, X., Hubert, M., Schwartz, O., Paludan, S. R., Van Simaeys, G., Doumont, G., Sobhian, B., Vlachakis, D., Turtoi, A., & Laguette, N. (2022). STING orchestrates the crosstalk between polyunsaturated fatty acid metabolism and inflammatory responses. Cell metabolism, 34(1), 125-139.e8. https://doi.org/10.1016/j.cmet.2021.12.007
Vila, Isabelle K, et al. "STING orchestrates the crosstalk between polyunsaturated fatty acid metabolism and inflammatory responses." Cell metabolism vol. 34,1 (2022): 125-139.e8. doi: https://doi.org/10.1016/j.cmet.2021.12.007
Vila IK, Chamma H, Steer A, Saccas M, Taffoni C, Turtoi E, Reinert LS, Hussain S, Marines J, Jin L, Bonnefont X, Hubert M, Schwartz O, Paludan SR, Van Simaeys G, Doumont G, Sobhian B, Vlachakis D, Turtoi A, Laguette N. STING orchestrates the crosstalk between polyunsaturated fatty acid metabolism and inflammatory responses. Cell Metab. 2022 Jan 04;34(1):125-139.e8. doi: 10.1016/j.cmet.2021.12.007. PMID: 34986331.
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Characterization of DNA-protein complexes by nanoparticle tracking analysis and their association with systemic lupus erythematosus.

Proceedings of the National Academy of Sciences of the United States of America

Juul-Madsen K, Troldborg A, Wittenborn TR, Axelsen MG, Zhao H, Klausen LH, Luecke S, Paludan SR, Stengaard-Pedersen K, Dong M, Møller HJ, Thiel S, Jensen H, Schuck P, Sutherland DS, Degn SE, Vorup-Jensen T.
PMID: 34301873
Proc Natl Acad Sci U S A. 2021 Jul 27;118(30). doi: 10.1073/pnas.2106647118.

Nanotechnology enables investigations of single biomacromolecules, but technical challenges have limited the application in liquid biopsies, for example, blood plasma. Nonetheless, tools to characterize single molecular species in such samples represent a significant unmet need with the increasing appreciation...

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Juul-Madsen K, Troldborg A, Wittenborn TR, et al. Characterization of DNA-protein complexes by nanoparticle tracking analysis and their association with systemic lupus erythematosus. Proc Natl Acad Sci U S A. 2021;118(30)doi: 10.1073/pnas.2106647118.
Juul-Madsen, K., Troldborg, A., Wittenborn, T. R., Axelsen, M. G., Zhao, H., Klausen, L. H., Luecke, S., Paludan, S. R., Stengaard-Pedersen, K., Dong, M., Møller, H. J., Thiel, S., Jensen, H., Schuck, P., Sutherland, D. S., Degn, S. E., & Vorup-Jensen, T. (2021). Characterization of DNA-protein complexes by nanoparticle tracking analysis and their association with systemic lupus erythematosus. Proceedings of the National Academy of Sciences of the United States of America, 118(30), . https://doi.org/10.1073/pnas.2106647118
Juul-Madsen, Kristian, et al. "Characterization of DNA-protein complexes by nanoparticle tracking analysis and their association with systemic lupus erythematosus." Proceedings of the National Academy of Sciences of the United States of America vol. 118,30 (2021). doi: https://doi.org/10.1073/pnas.2106647118
Juul-Madsen K, Troldborg A, Wittenborn TR, Axelsen MG, Zhao H, Klausen LH, Luecke S, Paludan SR, Stengaard-Pedersen K, Dong M, Møller HJ, Thiel S, Jensen H, Schuck P, Sutherland DS, Degn SE, Vorup-Jensen T. Characterization of DNA-protein complexes by nanoparticle tracking analysis and their association with systemic lupus erythematosus. Proc Natl Acad Sci U S A. 2021 Jul 27;118(30). doi: 10.1073/pnas.2106647118. PMID: 34301873; PMCID: PMC8325352.
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A serum-stable RNA aptamer specific for SARS-CoV-2 neutralizes viral entry.

Proceedings of the National Academy of Sciences of the United States of America

Valero J, Civit L, Dupont DM, Selnihhin D, Reinert LS, Idorn M, Israels BA, Bednarz AM, Bus C, Asbach B, Peterhoff D, Pedersen FS, Birkedal V, Wagner R, Paludan SR, Kjems J.
PMID: 34876524
Proc Natl Acad Sci U S A. 2021 Dec 14;118(50). doi: 10.1073/pnas.2112942118.

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has created an urgent need for new technologies to treat COVID-19. Here we report a 2'-fluoro protected RNA aptamer that binds with high affinity to the receptor binding domain (RBD)...

Cite
Valero J, Civit L, Dupont DM, et al. A serum-stable RNA aptamer specific for SARS-CoV-2 neutralizes viral entry. Proc Natl Acad Sci U S A. 2021;118(50)doi: 10.1073/pnas.2112942118.
Valero, J., Civit, L., Dupont, D. M., Selnihhin, D., Reinert, L. S., Idorn, M., Israels, B. A., Bednarz, A. M., Bus, C., Asbach, B., Peterhoff, D., Pedersen, F. S., Birkedal, V., Wagner, R., Paludan, S. R., & Kjems, J. (2021). A serum-stable RNA aptamer specific for SARS-CoV-2 neutralizes viral entry. Proceedings of the National Academy of Sciences of the United States of America, 118(50), . https://doi.org/10.1073/pnas.2112942118
Valero, Julián, et al. "A serum-stable RNA aptamer specific for SARS-CoV-2 neutralizes viral entry." Proceedings of the National Academy of Sciences of the United States of America vol. 118,50 (2021). doi: https://doi.org/10.1073/pnas.2112942118
Valero J, Civit L, Dupont DM, Selnihhin D, Reinert LS, Idorn M, Israels BA, Bednarz AM, Bus C, Asbach B, Peterhoff D, Pedersen FS, Birkedal V, Wagner R, Paludan SR, Kjems J. A serum-stable RNA aptamer specific for SARS-CoV-2 neutralizes viral entry. Proc Natl Acad Sci U S A. 2021 Dec 14;118(50). doi: 10.1073/pnas.2112942118. PMID: 34876524.
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