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1دورية أكاديمية
المؤلفون: Doust, Catherine, Fontanillas, Pierre, Bell, Robert K., Pennell, Craig E., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Eising, Else, Fletez-Brant, Kipper, Freyman, W, Gandhi, PM, Heilbron, K, Hicks, B, Hinds, DA, Jewett, EM, Jiang, Y, Kukar, K, Lin, KH, Gordon, Scott D., Lowe, M, McCreight, J, McIntyre, MH, Micheletti, SJ, Moreno, ME, Mountain, JL, Nandakumar, P, Noblin, ES, O’Connell, J, Petrakovitz, AA, Wang, Zhengjun, Poznik, GD, Schumacher, M, Shastri, AJ, Shelton, JF, Shi, J, Shringarpure, S, Tran, V, Tung, JY, Wang, X, Wang, W, Alagöz, Gökberk, Weldon, CH, Wilton, P, Hernandez, A, Wong, Carol A., Tchakouté, CT, Abbondanza, F, Allegrini, AG, Andlauer, TFM, Barr, CL, Bernard, M, Molz, Barbara, Blokland, K, Bonte, M, Boomsma, DI, Bourgeron, T, Brandeis, D, Carreiras, M, Ceroni, F, Csépe, V, Dale, PS, de Jong, PF, Aslibekyan, Stella, Démonet, JF, de Zeeuw, EL, Feng, Y, Franken, MCJ, Gerritse, M, Gialluisi, A, Guger, SL, Hayiou-Thomas, ME, Hernández-Cabrera, J, Hottenga, JJ, Auton, Adam, Hulme, C, Jansen, PR, Kere, J, Kerr, EN, Koomar, T, Landerl, K, Leonard, GT, Liao, Z, Lovett, MW, Lyytinen, H, Babalola, Elizabeth, Martinelli, A, Maurer, U, Michaelson, JJ, Mirza-Schreiber, N, Moll, K, Morgan, AT, Müller-Myhsok, B, Newbury, DF, Nöthen, MM, Paus, T
المساهمون: The University of Newcastle. College of Health, Medicine & Wellbeing, School of Medicine and Public Health
مصطلحات موضوعية: dyslexia, genetic, ambidexterity, chromosome
العلاقة: Nature Genetics Vol. 54, p. 1621-1629; http://hdl.handle.net/1959.13/1493197Test; uon:53505
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2دورية أكاديمية
المؤلفون: Puan, KJ, San Luis, B, Yusof, N, Kumar, D, Andiappan, AK, Lee, W, Cajic, S, Vuckovic, D, Chan, JD, Döllner, T, Hou, HW, Jiang, Y, Tian, C, Agee, M, Aslibekyan, S, Auton, A, Babalola, E, Bell, RK, Bielenberg, J, Bryc, K, Bullis, E, Cameron, B, Coker, D, Partida, GC, Dhamija, D, Das, S, Elson, SL, Filshtein, T, Fletez-Brant, K, Fontanillas, P, Freyman, W, Gandhi, PM, Heilbron, K, Hicks, B, Hinds, DA, Huber, KE, Jewett, EM, Kleinman, A, Kukar, K, Lane, V, Lin, KH, Lowe, M, Luff, MK, McCreight, JC, McIntyre, MH, McManus, KF, Micheletti, SJ, Moreno, ME, Mountain, JL, Mozaffari, SV, Nandakumar, P., Noblin, ES, O’Connell, J, Petrakovitz, AA, Poznik, GD, Schumacher, M, Shastri, AJ, Shelton, JF, Shi, J, Shringarpure, S, Tran, V, Tung, JY, Wang, X, Wang W, Weldon, CH, Wilton, P, Rapp, E, Poidinger, M, Wang, DY, Soranzo, N, Lee, B, Rötzschke, O
المساهمون: BIOLOGICAL SCIENCES, DEPT OF OPHTHALMOLOGY
المصدر: Elements
مصطلحات موضوعية: Base Sequence, Basophils, Cells, Cultured, Cohort Studies, E-Selectin, Fucosyltransferases, Gene Expression, Gene Expression Profiling, Humans, Leukocyte Count, Leukocyte Rolling, Polymorphism, Single Nucleotide, Sequence Homology, Nucleic Acid, Sialyl Lewis X Antigen
العلاقة: Puan, KJ, San Luis, B, Yusof, N, Kumar, D, Andiappan, AK, Lee, W, Cajic, S, Vuckovic, D, Chan, JD, Döllner, T, Hou, HW, Jiang, Y, Tian, C, Agee, M, Aslibekyan, S, Auton, A, Babalola, E, Bell, RK, Bielenberg, J, Bryc, K, Bullis, E, Cameron, B, Coker, D, Partida, GC, Dhamija, D, Das, S, Elson, SL, Filshtein, T, Fletez-Brant, K, Fontanillas, P, Freyman, W, Gandhi, PM, Heilbron, K, Hicks, B, Hinds, DA, Huber, KE, Jewett, EM, Kleinman, A, Kukar, K, Lane, V, Lin, KH, Lowe, M, Luff, MK, McCreight, JC, McIntyre, MH, McManus, KF, Micheletti, SJ, Moreno, ME, Mountain, JL, Mozaffari, SV, Nandakumar, P., Noblin, ES, O’Connell, J, Petrakovitz, AA, Poznik, GD, Schumacher, M, Shastri, AJ, Shelton, JF, Shi, J, Shringarpure, S, Tran, V, Tung, JY, Wang, X, Wang W, Weldon, CH, Wilton, P, Rapp, E, Poidinger, M, Wang, DY, Soranzo, N, Lee, B, Rötzschke, O (2021-12-01). FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expression. Communications Biology 4 (1) : 832-. ScholarBank@NUS Repository. https://doi.org/10.1038/s42003-021-02295-8Test; https://scholarbank.nus.edu.sg/handle/10635/227547Test