Human Molecular Genetics, 0964-6906

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  1. TCF7L2 is a master regulator of insulin production and processing.

    Zhou, Y., Park, S-Y., Su, J., Bailey, K., Ottosson Laakso, E., Liliya Shcherbina, Nikolay Oskolkov, Enming Zhang, Thevenin, T., Fadista, J., Bennet, H., Petter Vikman, Nils Wierup, Malin Fex, Rung, J., Claes Wollheim, Nobrega, M., Erik Renström, Leif Groop & Ola Hansson, 2014, In : Human Molecular Genetics. 23, 24, p. 6419-6431

    Research output: Contribution to journalArticle

  2. Survival of pancreatic beta cells is partly controlled by a TCF7L2-p53-p53INP1-dependent pathway.

    Zhou, Y., Enming Zhang, Berggreen, C., Jing, X., Osmark, P., Stefan Lang, Corrado Cilio, Olga Göransson, Leif Groop, Erik Renström & Ola Hansson, 2012, In : Human Molecular Genetics. 21, p. 196-207

    Research output: Contribution to journalArticle

  3. Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations

    Yoneyama, S., Guo, Y., Lanktree, M. B., Barnes, M. R., Elbers, C. C., Karczewski, K. J., Padmanabhan, S., Bauer, F., Baumert, J., Beitelshees, A., Berenson, G. S., Boer, J. M. A., Burke, G., Cade, B., Chen, W., Cooper-Dehoff, R. M., Gaunt, T. R., Gieger, C., Gong, Y., Gorski, M. & 54 othersHeard-Costa, N., Johnson, T., Lamonte, M. J., Mcdonough, C., Monda, K. L., Onland-Moret, N. C., Nelson, C. P., O'Connell, J. R., Ordovas, J., Peter, I., Peters, A., Shaffer, J., Shen, H., Smith, E., Speilotes, L., Thomas, F., Thorand, B., Verschuren, W. M. M., Anand, S. S., Dominiczak, A., Davidson, K. W., Hegele, R. A., Heid, I., Hofker, M. H., Huggins, G. S., Illig, T., Johnson, J. A., Kirkland, S., Koenig, W., Langaee, T. Y., Mccaffery, J., Olle Melander, Mitchell, B. D., Munroe, P., Murray, S. S., Papanicolaou, G., Redline, S., Reilly, M., Samani, N. J., Schork, N. J., Van der Schouw, Y. T., Shimbo, D., Shuldiner, A. R., Tobin, M. D., Wijmenga, C., Yusuf, S., Hakonarson, H., Lange, L. A., Demerath, E. W., Fox, C. S., North, K. E., Reiner, A. P., Keating, B. & Taylor, K. C., 2014, In : Human Molecular Genetics. 23, 9, p. 2498-2510

    Research output: Contribution to journalArticle

  4. Selective neuroprotective effects of the S18Y polymorphic variant of UCH-L1 in the dopaminergic system

    Xilouri, M., Kyratzi, E., Pitychoutis, P. M., Papadopoulou-Daifoti, Z., Perier, C., Vila, M., Maniati, M., Ulusoy, A., Deniz Kirik, Park, D. S., Wada, K. & Stefanis, L., 2012, In : Human Molecular Genetics. 21, 4, p. 874-889

    Research output: Contribution to journalArticle

  5. Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegeneration.

    Wiesner, D., Sinniger, J., Henriques, A., Dieterlé, S., Müller, H-P., Rasche, V., Ferger, B., Dirrig-Grosch, S., Rana Soylu, Åsa Petersén, Walther, P., Linkus, B., Kassubek, J., Wong, P. C., Ludolph, A. C. & Dupuis, L., 2015, In : Human Molecular Genetics. 24, 8, p. 2228-2240

    Research output: Contribution to journalArticle

  6. DNA-BASED MUTATION ANALYSIS OF BRUTONS TYROSINE KINASE GENE IN PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA

    VORECHOVSKY, I., Mauno Vihinen, DESAINTBASILE, G., HONSOVA, S., HAMMARSTROM, L., MULLER, S., NILSSON, L., FISCHER, A. & SMITH, CIE., 1995, In : Human Molecular Genetics. 4, 1, p. 51-58

    Research output: Contribution to journalArticle

  7. A genome wide scan for early onset primary hypertension in Scandinavians.

    von Wowern, F., Kristina Bengtsson Boström, Lindgren, C., Marju Orho-Melander, Fyhrquist, F., Lindblad, U., Lennart Råstam, Forsblom, C., Kanninen, T., Almgren, P., Burri, P., Katzman, P., Leif Groop, Hulthén, U. L. & Olle Melander, 2003, In : Human Molecular Genetics. 12, 16, p. 2077-2081

    Research output: Contribution to journalArticle

  8. Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration

    Vlachantoni, D., Bramall, A. N., Murphy, M. P., Taylor, R. W., Shu, X., Tulloch, B., van Veen, T., Turnbull, D. M., McInnes, R. R. & Wright, A. F., 2011, In : Human Molecular Genetics. 20, 2, p. 322-335

    Research output: Contribution to journalArticle

  9. Altered expression and distribution of cathepsins in neuronopathic forms of Gaucher disease and in other sphingolipidoses

    Vitner, E. B., Dekel, H., Zigdon, H., Shachar, T., Farfel-Becker, T., Eilam, R., Stefan Karlsson & Futerman, A. H., 2010, In : Human Molecular Genetics. 19, 18, p. 3583-3590

    Research output: Contribution to journalArticle

  10. Novel expression and transcriptional regulation of FoxJ1 during oro-facial morphogenesis

    Venugopalan, S. R., Amen, M. A., Wang, J., Wong, L., Cavender, A. C., D'Souza, R. N., Mikael Åkerlund, Brody, S. L., Hjalt, T. & Amendt, B. A., 2008, In : Human Molecular Genetics. 17, 23, p. 3643-3654

    Research output: Contribution to journalArticle

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