|
XB--489159
Papers associated with smn1 (and Disease Ontology)
???pagination.result.count???
???pagination.result.page??? 1
| Sort Newest To Oldest | Sort Oldest To Newest |
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): 9472.  |
|
Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryos., Willsey HR, Walentek P, Exner CRT, Xu Y, Xu Y, Lane AB, Harland RM, Heald R, Santama N., Dev Biol. October 15, 2018; 442 (2): 276-287.  |
|
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): 27-40.  |
|
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): 2320-30.  |
???pagination.result.page??? 1