يعرض 1 - 10 نتائج من 2,887 نتيجة بحث عن '"Proteins genetics"', وقت الاستعلام: 1.40s تنقيح النتائج
  1. 1
  2. 2

    المصدر: Rübsam, H, Krönauer, C, Abel, N B, Ji, H, Lironi, D, Hansen, S B, Nadzieja, M, Kolte, M V, Abel, D, de Jong, N, Madsen, L H, Liu, H, Stougaard, J, Radutoiu, S & Andersen, K R 2023, ' Nanobody-driven signaling reveals the core receptor complex in root nodule symbiosis ', Science (New York, N.Y.), vol. 379, no. 6629, pp. 272-277 . https://doi.org/10.1126/science.ade9204

    وصف الملف: application/pdf

  3. 3

    المساهمون: Neurology, Pathology, Amsterdam Neuroscience - Neurodegeneration, Netherlands Institute for Neuroscience (NIN)

    المصدر: Netherlands Brain Bank 2022, ' Isoform-specific patterns of tau burden and neuronal degeneration in MAPT-associated frontotemporal lobar degeneration ', Acta Neuropathologica, vol. 144, no. 6, pp. 1065-1084 . https://doi.org/10.1007/s00401-022-02487-4
    Acta Neuropathologica, 144(6), 1065-1084. Springer-Verlag
    Acta Neuropathologica, 144(6), 1065-1084. Springer Verlag
    Acta Neuropathologica, 144(6), 1065-1084. Springer Verlag GmbH

  4. 4

    المساهمون: Lee, Sunwoo [0000-0003-2806-3268], Pérez-Dueñas, Belén [0000-0002-4979-2788], Banka, Siddharth [0000-0002-8527-2210], Kurian, Manju A [0000-0003-3529-5075], Maher, Eamonn R [0000-0002-6226-6918], Apollo - University of Cambridge Repository, Maher, Eamonn [0000-0002-6226-6918]

    المصدر: Lee, S, Ochoa, E, Barwick, K, Cif, L, Rodger, F, Docquier, F, Pérez-Dueñas, B, Clark, G, Martin, E, Banka, S, Kurian, M A & Maher, E R 2022, ' Comparison of methylation episignatures in KMT2B-and KMT2D-related human disorders ', Epigenomics, vol. 14, no. 9, pp. 537-547 . https://doi.org/10.2217/epi-2021-0521

    وصف الملف: text/xml; application/zip; application/pdf

  5. 5

    المؤلفون: Oddsson, Asmundur, Sulem, Patrick, Sveinbjornsson, Gardar, Arnadottir, Gudny A, Steinthorsdottir, Valgerdur, Halldorsson, Gisli H, Atlason, Bjarni A, Oskarsson, Gudjon R, Helgason, Hannes, Nielsen, Henriette Svarre, Westergaard, David, Karjalainen, Juha M, Katrinardottir, Hildigunnur, Fridriksdottir, Run, Jensson, Brynjar O, Tragante, Vinicius, Ferkingstad, Egil, Jonsson, Hakon, Gudjonsson, Sigurjon A, Beyter, Doruk, Moore, Kristjan H S, Thordardottir, Helga B, Kristmundsdottir, Snaedis, Stefansson, Olafur A, Rantapää-Dahlqvist, Solbritt, Sonderby, Ida Elken, Didriksen, Maria, Stridh, Pernilla, Haavik, Jan, Tryggvadottir, Laufey, Frei, Oleksandr, Walters, G Bragi, Kockum, Ingrid, Hjalgrim, Henrik, Olafsdottir, Thorunn A, Selbaek, Geir, Nyegaard, Mette, Erikstrup, Christian, Brodersen, Thorsten, Saevarsdottir, Saedis, Olsson, Tomas, Nielsen, Kaspar Rene, Haraldsson, Asgeir, Bruun, Mie Topholm, Hansen, Thomas Folkmann, Steingrimsdottir, Thora, Jacobsen, Rikke Louise, Lie, Rolv T, Djurovic, Srdjan, Alfredsson, Lars, Lopez de Lapuente Portilla, Aitzkoa, Brunak, Soren, Melsted, Pall, Halldorsson, Bjarni V, Saemundsdottir, Jona, Magnusson, Olafur Th, Padyukov, Leonid, Banasik, Karina, Rafnar, Thorunn, Askling, Johan, Klareskog, Lars, Pedersen, Ole Birger, Masson, Gisli, Havdahl, Alexandra, Nilsson, Bjorn, Andreassen, Ole A, Daly, Mark, Ostrowski, Sisse Rye, Jonsdottir, Ingileif, Stefansson, Hreinn, Holm, Hilma, Helgason, Agnar, Thorsteinsdottir, Unnur, Stefansson, Kari, Gudbjartsson, Daniel F

    المصدر: Oddsson, A, Sulem, P, Sveinbjornsson, G, Arnadottir, G A, Steinthorsdottir, V, Halldorsson, G H, Atlason, B A, Oskarsson, G R, Helgason, H, Nielsen, H S, Westergaard, D, Karjalainen, J M, Katrinardottir, H, Fridriksdottir, R, Jensson, B O, Tragante, V, Ferkingstad, E, Jonsson, H, Gudjonsson, S A, Beyter, D, Moore, K H S, Thordardottir, H B, Kristmundsdottir, S, Stefansson, O A, Rantapää-Dahlqvist, S, Sonderby, I E, Didriksen, M, Stridh, P, Haavik, J, Tryggvadottir, L, Frei, O, Walters, G B, Kockum, I, Hjalgrim, H, Olafsdottir, T A, Selbaek, G, Nyegaard, M, Erikstrup, C, Brodersen, T, Saevarsdottir, S, Olsson, T, Nielsen, K R, Haraldsson, A, Bruun, M T, Hansen, T F, DBDS Genomic Consortium, Steingrimsdottir, T, Jacobsen, R L, Lie, R T, Djurovic, S, Alfredsson, L, Lopez de Lapuente Portilla, A, Brunak, S, Melsted, P, Halldorsson, B V, Saemundsdottir, J, Magnusson, O T, Padyukov, L, Banasik, K, Rafnar, T, Askling, J, Klareskog, L, Pedersen, O B, Masson, G, Havdahl, A, Nilsson, B, Andreassen, O A, Daly, M, Ostrowski, S R, Jonsdottir, I, Stefansson, H, Holm, H, Helgason, A, Thorsteinsdottir, U, Stefansson, K & Gudbjartsson, D F 2023, ' Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality ', Nature Communications, vol. 14, no. 1, 3453 . https://doi.org/10.1038/s41467-023-38951-2

    وصف الملف: application/pdf

  6. 6
  7. 7
  8. 8

    المصدر: Pairo-Castineira, E, Rawlik, K, Bretherick, A D, Qi, T, Wu, Y, Nassiri, I, McConkey, G A, Zechner, M, Klaric, L, Griffiths, F, Oosthuyzen, W, Kousathanas, A, Richmond, A, Millar, J, Russell, C D, Malinauskas, T, Thwaites, R, Morrice, K, Keating, S, Maslove, D M, Nichol, A D, Semple, M G, Knight, J, Shankar-Hari, M, Summers, C, Hinds, C, Horby, P, Ling, L, McAuley, D F, Montgomery, H, Openshaw, P J M, Begg, C, Walsh, T S, Tenesa, A, Flores, C, Riancho, J A, Rojas-Martinez, A, Lapunzina, P, Yang, J, Ponting, C P, Wilson, J F, Vitart, V, Abedalthagafi, M S, Luchessi, A, Parra, E J, Cruz, R, Carracedo, A, Fawkes, A, Murphy, L, Rowan, K, Pereira, A C, Law, A, Fairfax, B P, Clohisey Hendry, S & Baillie, J K 2023, ' GWAS and meta-analysis identifies 49 genetic variants underlying critical Covid-19 ', Nature, vol. 617, no. 7962, pp. 764-768 . https://doi.org/10.1038/s41586-023-06034-3

    وصف الملف: application/pdf

  9. 9
  10. 10