Search Results - Griffiths, L.
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Actin Nemaline Myopathy Mouse Reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression by Ravenscroft, G., Jackaman, Connie, Sewry, C., Mcnamara, E., Squire, S., Potter, A., Papadimitriou, J., Griffiths, L., Bakker, A., Davies, K., Laing, N., Nowak, K.
Published 2011Get full text
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Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality by Adewuyi, Emmanuel, Mehta, D., Sapkota, Y., Yoshihara, K., Nyegaard, M., Steinthorsdottir, V., Morris, A.P., Fassbender, A., Rahmioglu, N., Vivo, I.D., Buring, J.E., Zhang, F., Edwards, T.L., Jones, S., Dorien, Peterse, D., Rexrode, K.M., Ridker, P.M., Schork, A.J., MacGregor, S., Martin, N.G., Becker, C.M., Adachi, S., Enomoto, T., Takahashi, A., Kamatani, Y., Matsuda, K., Kubo, M., Thorleifsson, G., Geirsson, R.T., Thorsteinsdottir, U., Wallace, L.M., Yang, J., Velez Edwards, D.R., Low, S.K., Zondervan, K.T., Missmer, S.A., D’Hooghe, T., Stefansson, K., Tung, J.Y., Montgomery, G.W., Chasman, D.I., Nyholt, D.R., Agee, M., Alipanahi, B., Auton, A., Bell, R.K., Bryc, K., Elson, S.L., Fontanillas, P., Furlotte, N.A., Huber, K.E., Kleinman, A., Litterman, N.K., McIntyre, M.H., Mountain, J.L., Noblin, E.S., Northover, C.A.M., Pitts, S.J., Sathirapongsasuti, J.F., Sazonova, O.V., Auta, A., Nyegaard, M., Wilson, C.H., Griffiths, L.R.
Published 2021Get full text