SIROCCO Research Area: mice

The following SIROCCO partners are involved in Small RNA research in mice.

SIROCCO mice Publications

The p38 MAPK pathway is essential for skeletogenesis and bone homeostasis in mice.

Greenblatt MB, Shim JH, Zou W, Sitara D, Schweitzer M, Hu D, Lotinun S, Sano Y, Baron R, Park JM, Arthur S, Xie M, Schneider MD, Zhai B, Gygi S, Davis R, Glimcher LH. The p38 MAPK pathway is essential for skeletogenesis and bone homeostasis in mice. J Clin Invest. 2010 Jul 1;120(7):2457-73. doi: 10.1172/JCI42285. Epub 2010 Jun 14.

An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

Lewis MA, Quint E, Glazier AM, Fuchs H, De Angelis MH, Langford C, van Dongen S, Abreu-Goodger C, Piipari M, Redshaw N, Dalmay T, Moreno-Pelayo MA, Enright AJ, Steel KP. An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice. Nat Genet. 2009 May;41(5):614-8. Epub 2009 Apr 12.

Life-long benefit of AAV/antisense-mediated exon skipping in dystrophic mice

Denti M. A., Incitti T., Sthandier O., Nicoletti C., De Angelis F.G., Rizzato E., Auricchio A, Musarò A, Bozzoni I. (2008) Life-long benefit of AAV/antisense-mediated exon skipping in dystrophic mice, Hum. Gene
Ther., 19: 601-608

Long-term benefit of adeno-associated virus/antisense-mediated exon skipping in dystrophic mice

Denti MA, Incitti T, Sthandier O, Nicoletti C, De Angelis FG, Rizzuto E, Auricchio A, Musarò A, Bozzoni I.
Long-term benefit of adeno-associated virus/antisense-mediated exon skipping in dystrophic mice.
Hum Gene Ther. 2008 Jun;19(6):601-8.

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