Zobrazeno 1 - 3
of 3
pro vyhledávání: '"S. W. Reddel"'
Autor:
G. Perez-Siles, M. Ellis, A. Ashe, B. Grosz, S. Vucic, M. C. Kiernan, K. A. Morris, S. W. Reddel, M. L. Kennerson
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Spinal Muscular Atrophy (SMA) is a heterogeneous group of neuromuscular diseases characterized by degeneration of anterior horn cells of the spinal cord, leading to muscular atrophy and weakness. Although the major cause of SMA is autosomal recessive
Externí odkaz:
https://doaj.org/article/6324a42e1da947ec8f90dabe93e5418e
Autor:
G, Perez-Siles, M, Ellis, A, Ashe, B, Grosz, S, Vucic, M C, Kiernan, K A, Morris, S W, Reddel, M L, Kennerson
Publikováno v:
Frontiers in Genetics
Spinal Muscular Atrophy (SMA) is a heterogeneous group of neuromuscular diseases characterized by degeneration of anterior horn cells of the spinal cord, leading to muscular atrophy and weakness. Although the major cause of SMA is autosomal recessive
Publikováno v:
The Journal of physiology. 588(Pt 17)
The postsynaptic muscle-specific kinase (MuSK) coordinates formation of the neuromuscular junction (NMJ) during embryonic development. Here we have studied the effects of MuSK autoantibodies upon the NMJ in adult mice. Daily injections of IgG from fo