يعرض 1 - 8 نتائج من 8 نتيجة بحث عن '"Nitric Oxide Synthase Type I/genetics"', وقت الاستعلام: 0.89s تنقيح النتائج
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    المساهمون: CHU Lille, Lille Neurosciences & Cognition - U 1172 (LilNCog), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), FHU 1,000 Days for Health [Lille], Université de Lille, Université de Lausanne = University of Lausanne (UNIL), National and Kapodistrian University of Athens (NKUA), Lausanne University Hospital, Institute of Experimental Medicine [Budapest] (KOKI), Hungarian Academy of Sciences (MTA), Université de Genève = University of Geneva (UNIGE), Oxford Brookes University, Newcastle University [Newcastle], Poznan University of Medical Sciences [Poland] (PUMS), University of Applied Sciences of Eastern Switzerland (FHO), Universidade do Porto = University of Porto, Instituto de Patologia e Imunologia Molecular da Universidade do Porto (IPATIMUP), Geneva University Hospitals and Geneva University, University Children’s Hospital Zurich, Bern University Hospital [Berne] (Inselspital), University of Bern, Hôpital Jeanne de Flandres, Université de Lille, Droit et Santé-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Neurocentre Magendie : Physiopathologie de la Plasticité Neuronale (U1215 Inserm - UB), Université de Bordeaux (UB)-Institut François Magendie-Institut National de la Santé et de la Recherche Médicale (INSERM), Universidad de Córdoba = University of Córdoba [Córdoba], Instituto Maimonides de Investigación Biomédica de Cordoba (IMIBIC), Universidad de Córdoba = University of Córdoba [Córdoba]-Hospital Universitario Reina Sofía, Instituto de Salud Carlos III [Madrid] (ISC), University College of London [London] (UCL), Wolfson Institute for Biomedical Research (WIBR), Université de Clermont-Ferrand, ANR-17-CE16-0015,GRAND,Vieillissement et démence: un rôle hormonal?(2017), Prevot, Vincent

    المصدر: Science Translational Medicine
    Science Translational Medicine, 2022, 14 (665), pp.eabh2369. ⟨10.1126/scitranslmed.abh2369⟩
    Science translational medicine, vol. 14, no. 665, pp. eabh2369

    وصف الملف: application/pdf

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    المساهمون: Pharmacology and Personalised Medicine, RS: FHML non-thematic output

    المصدر: Casas, A I, Hassan, A A, Larsen, S J, Gomez-Rangel, V, Elbatreek, M, Kleikers, P W M, Guney, E, Egea, J, López, M G, Baumbach, J & Schmidt, H H H W 2019, ' From single drug targets to synergistic network pharmacology in ischemic stroke ', Proceedings of the National Academy of Sciences of the United States of America, vol. 116, no. 14, pp. 7129-7136 . https://doi.org/10.1073/pnas.1820799116
    Proceedings of the National Academy of Sciences of the United States of America
    Proceedings of the National Academy of Sciences of the United States of America, 116(14), 7129-7136. National Academy of Sciences
    Proceedings of the National Academy of Sciences

    وصف الملف: application/pdf

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    المصدر: Translational Psychiatry
    Lescai, F, Als, T D, Li, Q, Nyegaard, M, Andorsdottir, G, Biskopstø, M, Hedemand, A, Fiorentino, A, O'Brien, N, Jarram, A, Liang, J, Grove, J, Pallesen, J, Eickhardt, E, Mattheisen, M, Bolund, L, Demontis, D, Wang, A G, McQuillin, A, Mors, O, Wang, J & Børglum, A D 2017, ' Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder ', Translational Psychiatry, vol. 7, e1034 . https://doi.org/10.1038/tp.2017.3
    Lescai, F, Als, T D, Li, Q, Nyegaard, M, Andorsdottir, G, Biskopstø, M, Hedemand, A, Fiorentino, A, O'Brien, N L, Jarram, A, Liang, T J, Grove, J, Pallesen, J, Eickhardt, E, Mattheisen, M, Bolund, L, Demontis, D, Wang, A G, McQuillin, A, Mors, O, Wang, J & Børglum, A D 2017, ' Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder ', Translational Psychiatry, vol. 7, no. 2, pp. e1034 . https://doi.org/10.1038/tp.2017.3

    وصف الملف: application/pdf

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    مورد إلكتروني

    المصدر: Lescai , F , Als , T D , Li , Q , Nyegaard , M , Andorsdottir , G , Biskopstø , M , Hedemand , A , Fiorentino , A , O'Brien , N , Jarram , A , Liang , J , Grove , J , Pallesen , J , Eickhardt , E , Mattheisen , M , Bolund , L , Demontis , D , Wang , A G , McQuillin , A , Mors , O , Wang , J & Børglum , A D 2017 , ' Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder ' , Translational Psychiatry , vol. 7 , e1034 .

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    مورد إلكتروني

    المصدر: Lescai , F , Als , T D , Li , Q , Nyegaard , M , Andorsdottir , G , Biskopstø , M , Hedemand , A , Fiorentino , A , O'Brien , N , Jarram , A , Liang , J , Grove , J , Pallesen , J , Eickhardt , E , Mattheisen , M , Bolund , L , Demontis , D , Wang , A G , McQuillin , A , Mors , O , Wang , J & Børglum , A D 2017 , ' Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder ' , Translational Psychiatry , vol. 7 , e1034 .