Temporal and tissue-specific variability of SMN protein levels in mouse models of spinal muscular atrophy

Autor: Groen, EJN, Perenthaler, Elena, Courtney, NL, Jordan, CY, Shorrock, HK, van der Hoorn, D, Huang, YT, Murray, LM, Viero, G, Gillingwater, TH

Publikováno v: Groen, E, Perenthaler, E, Courtney, N, Jordan, C, Shorrock, H, van der Hoorn, D, Huang, Y, Murray, L, Viero, G & Gillingwater, T 2018, ' Temporal and tissue-specific variability of SMN protein levels in mouse models of spinal muscular atrophy ', Human Molecular Genetics . https://doi.org/10.1093/hmg/ddy195
Human Molecular Genetics, 27(16), 2851-2862. Oxford University Press

Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by deleterious variants in SMN1 that lead to a marked decrease in survival motor neuron (SMN) protein expression. Humans have a second SMN gene (SMN2) that is almost identical

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8e46049485f0de49d0de4df3e467c36a
https://hdl.handle.net/20.500.11820/7e272dc0-0fa1-4198-b817-d77c39e7dfc8

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Care transitions by older adults from nursing homes to hospitals: implications for long-term care practice, geriatrics education, and research.

Autor: Murray LM (AUTHOR), Laditka SB (AUTHOR)

Publikováno v: Journal of the American Medical Directors Association. May2010, Vol. 11 Issue 4, p231-238. 8p.

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Isobromotopsentin: a New Bis(indole) Alkaloid From a Deep-Water Marine Sponge Spongosorites sp.

Autor: Murray, LM, Lim, TK, Hooper, JNA, Capon, RJ

Publikováno v: Australian Journal of Chemistry; 1995, Vol. 48 Issue: 12 p2053-2058, 6p