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Disease Models & Mechanisms, ‎1754-8403

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  1. Hearing impairment due to Mir183/96/182 mutations suggests both loss and gain of function effects

    Lewis, M., Di Domenico, F., Ingham, N., Prosser, H. & Steel, K., 14 Dec 2020, (E-pub ahead of print) In: Disease Models & Mechanisms.

    Research output: Contribution to journal › Article › peer-review

  2. Targeted knockout of GABA-A receptor gamma 2 subunit provokes transient light-induced reflex seizures in zebrafish larvae

    Liao, M., Kundap, U., Rosch, R. E., Burrows, D. R. W., Meyer, M. P., Ouled Amar Bencheikh, B., Cossette, P. & Samarut, É., 11 Nov 2019, In: Disease Models & Mechanisms. 12, 11, dmm.040782.

    Research output: Contribution to journal › Article › peer-review

  3. Modelling pancreatic β-cell inflammation in zebrafish identifies the natural product wedelolactone for human islet protection

    Delgadillo-Silva, L. F., Tsakmaki, A., Akhtar, N., Franklin, Z. J., Konantz, J., Bewick, G. A. & Ninov, N., 23 Jan 2019, In: Disease Models & Mechanisms. 12, 1

    Research output: Contribution to journal › Article › peer-review

  4. Adding a temporal dimension to the study of Friedreich's ataxia: the effect of frataxin overexpression in a human cell model

    Vannocci, T., Notario Manzano, R., Beccalli, O., Bettegazzi, B., Grohovaz, F., Cinque, G., De Riso, A., Quaroni, L., Codazzi, F. & Pastore, A., 2018, In: Disease Models & Mechanisms. 11, 6, p. 1-9 dmm.032706.

    Research output: Contribution to journal › Article › peer-review

  5. Cellular dynamics of regeneration reveals role of two distinct Pax7 stem cell populations in larval zebrafish muscle repair

    Pipalia, T. G., Koth, J., Roy, S. D., Hammond, C. L., Kawakami, K. & Hughes, S. M., 5 May 2016, (E-pub ahead of print) In: Disease Models & Mechanisms.

    Research output: Contribution to journal › Article › peer-review

  6. Auditory hair cell defects as potential cause for sensorineural deafness in Wolf-Hirschhorn syndrome

    Ahmed, M., Ura, K. & Streit, A., 1 Sep 2015, In: Disease Models & Mechanisms. 8, 9, p. 1027-1035 9 p.

    Research output: Contribution to journal › Article › peer-review

  7. A gene expression resource generated by genome-wide lacZ profiling in the mouse

    Tuck, E., Estabel, J., Oellrich, A., Maguire, A., Adissu, H. A., Souter, L., Siragher, E., Lillistone, C., Green, A. L. & Jones, H., 20 Aug 2015, (E-pub ahead of print) In: Disease Models & Mechanisms. 8, p. 1467-1478

    Research output: Contribution to journal › Article › peer-review

  8. A new cellular model to follow Friedreich's ataxia development in a time-resolved way

    Vannocci, T., Faggianelli, N., Zaccagnino, S., Della Rosa, I., Adinolfi, S. & Pastore, A., 1 Jul 2015, In: DMM Disease Models and Mechanisms. 8, 7, p. 711-719 9 p.

    Research output: Contribution to journal › Article › peer-review

  9. Conditional deletion of neurogenin-3 using Nkx2.1iCre results in a mouse model for the central control of feeding, activity and obesity

    Anthwal, N., Pelling, M., Claxton, S., Mellitzer, G., Collin, C., Kessaris, N., Richardson, W. D., Gradwohl, G. & Ang, S-L., Sep 2013, In: Disease Models & Mechanisms. 6, 5, p. 1133-1145 13 p.

    Research output: Contribution to journal › Article › peer-review

  10. A new and clinically relevant murine model of solid-organ transplant aspergillosis

    Herbst, S., Shah, A., Carby, M., Chusney, G., Kikkeri, N., Dorling, A., Bignell, E., Shaunak, S. & Armstrong-James, D., May 2013, In: Disease Models & Mechanisms. 6, 3, p. 643-651 9 p.

    Research output: Contribution to journal › Article › peer-review

  11. Deciphering the mechanisms of developmental disorders (DMDD): A new programme for phenotyping embryonic lethal mice

    Mohun, T., Adams, D. J., Baldock, R., Bhattacharya, S., Copp, A. J., Hemberger, M., Houart, C., Hurles, M. E., Robertson, E., Smith, J. C., Weaver, T. & Weninger, W., May 2013, In: Disease Models & Mechanisms. 6, 3, p. 562-566 5 p.

    Research output: Contribution to journal › Article › peer-review

  12. The fraction of strongly bound cross-bridges is increased in mice that carry the myopathy-linked myosin heavy chain mutation MYH4L342Q

    Lindqvist, J., Iwamoto, H., Blanco, G. & Ochala, J., May 2013, (E-pub ahead of print) In: Disease Models & Mechanisms. p. 834-840 7 p.

    Research output: Contribution to journal › Article › peer-review

  13. Mouse genetics for studying mechanisms of deafness and more: an interview with Karen Steel

    Steel, K., Nov 2011, In: Disease Models & Mechanisms. 4, 6, p. 716-718 3 p.

    Research output: Contribution to journal › Editorial › peer-review

  14. Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism

    Sajedi, E., Gaston-Massuet, C., Signore, M., Andoniadou, C. L., Kelberman, D., Castro, S., Etchevers, H. C., Gerrelli, D., Dattani, M. T. & Martinez-Barbera, J. P., Nov 2008, In: Disease Models & Mechanisms. 1, 4-5, p. 241-254 14 p., N/A.

    Research output: Contribution to journal › Article › peer-review

  15. Models of infectious diseases in the fruit fly Drosophila melanogaster

    Dionne, M. S. & Schneider, D. S., 2008, In: Disease Models & Mechanisms. 1, 1, p. 43 - 49 7 p.

    Research output: Contribution to journal › Article › peer-review

  16. Zebrafish myelination: a transparent model for remyelination?

    Buckley, C., Goldsmith, P. & Franklin, R., 2008, In: Disease Models & Mechanisms. 1, 4-5, p. 221-8 8 p., 19093028.

    Research output: Contribution to journal › Article › peer-review

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