يعرض 1 - 20 نتائج من 38 نتيجة بحث عن '"Bailey, M.E.S."', وقت الاستعلام: 0.45s تنقيح النتائج
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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal

    وصف الملف: text

    Relation: https://eprints.gla.ac.uk/90348/1/90348.pdf; Celis-Morales, C. A. , Ghouri, N. , Bailey, M.E.S. , Sattar, N. and Gill, J. M.R. (2013) Should physical activity recommendations be ethnicity-specific? Evidence from a cross-sectional study of south Asian and European men. PLoS ONE , 8(12), e82568. (doi:10.1371/journal.pone.0082568 ) (PMID:24349313) (PMCID:PMC3859604)

  7. 7
    Academic Journal

    وصف الملف: text

    Relation: https://eprints.gla.ac.uk/56990/1/56990.pdf; Celis-Morales, C.A. , Perez-Bravo, F., Ibañes, L., Sanzana, R., Hormazabal, E., Ulloa, N., Calvo, C., Bailey, M.E.S. and Gill, J.M.R. (2011) Insulin resistance in Chileans of European and indigenous descent: evidence for an ethnicity x environment interaction. PLoS ONE , 6(9), e24690. (doi:10.1371/journal.pone.0024690 ) (PMID:21931814) (PMCID:PMC3169638)

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    Academic Journal
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    Academic Journal
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    Academic Journal

    Relation: Wang, G. et al. (2013) Association analysis of ACE and ACTN3 in elite caucasian and east Asian swimmers. Medicine and Science in Sports and Exercise , 45(5), pp. 892-900. (doi:10.1249/MSS.0b013e31827c501f )

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    Academic Journal

    Relation: Gadalla, K.K.E. et al. (2013) Improved survival and reduced phenotypic severity following AAV9/MECP2 gene transfer to neonatal and juvenile male Mecp2 knockout mice. Molecular Therapy , 21(1), pp. 18-30. (doi:10.1038/mt.2012.200 ) (PMID:23011033) (PMCID:PMC3536818)

  12. 12
    Academic Journal

    Relation: Winchester, C. L. and Hamilton, G. M. and Morris, B. and Pratt, J. A. and Hunter, R. and Bailey, M.E.S (2011 ) Using next generation sequencing to investigate DPYSL2 gene variants in schizophrenia. Journal of Psychopharmacology , 25 (8 Supp). A67-A67. ISSN 1461-7285

  13. 13
    Academic Journal

    وصف الملف: text

    Relation: https://eprints.gla.ac.uk/44341/1/Koni_et_al_IJO_final_author_MS.pdf; Koni, A.C., Scott, R.A. , Wang, G. , Bailey, M.E.S. , Peplies, J., Bammann, K. and Pitsiladis, Y.P. (2011) DNA yield and quality of saliva samples and suitability for large scale epidemiological studies in children. International Journal of Obesity , 35(Suppl.), S113-S118.

  14. 14
    Academic Journal

    Relation: Gadalla, K.K.E., Bailey, M.E.S. and Cobb, S.R. (2011) MeCP2 and Rett syndrome: reversibility and potential avenues for therapy. Biochemical Journal , 439(1), pp. 1-14. (doi:10.1042/BJ20110648 )

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    Academic Journal

    Relation: Weng, S.-M., McLeod, F., Bailey, M.E.S. and Cobb, S.R. (2011) Synaptic plasticity deficits in an experimental model of Rett Syndrome: LTP saturation and its pharmacological reversal. Neuroscience , 180, pp. 314-321. (doi:10.1016/j.neuroscience.2011.01.061 )

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    Academic Journal

    المساهمون: 臺北護理健康大學語言治療與聽力學系

    مصطلحات موضوعية: MECP2, Rett syndrome, memantine, LTP, plasticity

    Time: 13

    وصف الملف: 141 bytes; text/html

    Relation: Neuroscience, 180, 314-321; http://140.131.94.7/handle/987654321/6263

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    Academic Journal

    وصف الملف: text

    Relation: https://eprints.gla.ac.uk/40609/1/Scott-EJHG-FTOfinalauthorMS.pdf; Scott, R.A. et al. (2010) FTO genotype and adiposity in children: physical activity levels influence the effect of the risk genotype in adolescent males. European Journal of Human Genetics , 18(12), pp. 1339-1343. (doi:10.1038/ejhg.2010.131 ) (PMID:20717169) (PMCID:PMC3002848)

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    Academic Journal

    وصف الملف: text

    Relation: http://eprints.gla.ac.uk/44344/1/id44344.pdf; Neul, J.L. et al. (2010) Rett Syndrome: Revised diagnostic criteria and nomenclature. Annals of Neurology , 68(6), pp. 944-950. (doi:10.1002/ana.22124 )

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    Academic Journal

    مصطلحات موضوعية: QH426 Genetics

    وصف الملف: text

    Relation: http://eprints.gla.ac.uk/25678/1/25678.pdf; Wilson, R.H. , Moran, C.N., Cole, J. , Pitsiladis, Y.P. and Bailey, M.E.S. (2010) Evolutionary history of the ADRB2 gene in humans. American Journal of Human Genetics , 86(3), pp. 490-493. (doi:10.1016/j.ajhg.2010.01.031 ) (PMID:20215008) (PMCID:PMC2833374)

  20. 20
    Academic Journal

    وصف الملف: text

    Relation: http://eprints.gla.ac.uk/42536/1/Bailey_MES_J_Laryn_Oto_.pdf; Morrison, A. W., Bailey, M.E.S. and Morrison, G. A. J. (2009) Familial Ménière's disease: clinical and genetic aspects. Journal of Laryngology and Otology , 123(01), pp. 29-37. (doi:10.1017/S0022215108002788 )