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Literature for DOID 12377: spinal muscular atrophy
Xenbase Articles
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Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy.,
Winkler C,Eggert C,Gradl D,Meister G,Giegerich M,Wedlich D,Laggerbauer B,Fischer U,
Genes Dev. October 1, 2005; 19(19):1549-5477.
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Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements., Wang YH,Griffith J, Genomics. January 20, 1995; 25(2):1089-8646. |
Reduced levels of survival motor neuron protein leads to aberrant motoneuron growth in a Xenopus model of muscular atrophy.,
Ymlahi-Ouazzani Q,J Bronchain O,Paillard E,Ballagny C,Chesneau A,Jadaud A,Mazabraud A,Pollet N,
Neurogenetics. February 1, 2010; 11(1):1364-6745.
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Functional characterization of SMN evolution in mouse models of SMA.,
Osman EY,Bolding MR,Villalón E,Kaifer KA,Lorson ZC,Tisdale S,Hao Y,Conant GC,Pires JC,Pellizzoni L,Lorson CL,
Sci Rep. July 1, 2019; 9(1):2045-2322.
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