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of 55
pro vyhledávání: '"Starr-Moss A"'
Akademický článek
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Autor:
Peterson, Erin, Rudolph, Tori E., Starr‐Moss, Alison, Anderson, Kendall, Lennon, Vanda A., Shelton, G. Diane, Clark, Leigh Anne
Publikováno v:
Animal Genetics; Aug2024, Vol. 55 Issue 4, p702-704, 3p
Autor:
Melissa L. Cox, Jacquelyn M. Evans, Alexander G. Davis, Ling T. Guo, Jennifer R. Levy, Alison N. Starr-Moss, Elina Salmela, Marjo K. Hytönen, Hannes Lohi, Kevin P. Campbell, Leigh Anne Clark, G. Diane Shelton
Publikováno v:
Skeletal Muscle, Vol 7, Iss 1, Pp 1-10 (2017)
Abstract Background Limb-girdle muscular dystrophies (LGMDs) are a heterogeneous group of inherited autosomal myopathies that preferentially affect voluntary muscles of the shoulders and hips. LGMD has been clinically described in several breeds of d
Externí odkaz:
https://doaj.org/article/3b60a22648c040c9b42e49380452a7e9
Autor:
Rinz, Caitlin J., Lennon, Vanda A., James, Fiona, Thoreson, James B., Tsai, Kate L., Starr-Moss, Alison N., Humphries, H. Dale, Guo, Ling T., Palmer, Anthony C., Clark, Leigh Anne *, Shelton, G. Diane **
Publikováno v:
In Neuromuscular Disorders December 2015 25(12):921-927
Autor:
Jacquelyn M Evans, Rooksana E Noorai, Kate L Tsai, Alison N Starr-Moss, Cody M Hill, Kendall J Anderson, Thomas R Famula, Leigh Anne Clark
Publikováno v:
PLoS Genetics, Vol 13, Iss 2, p e1006604 (2017)
Juvenile dermatomyositis (JDM) is a chronic inflammatory myopathy and vasculopathy driven by genetic and environmental influences. Here, we investigated the genetic underpinnings of an analogous, spontaneous disease of dogs also termed dermatomyositi
Externí odkaz:
https://doaj.org/article/306e61d6812241ef856e02531155f0da
Autor:
Caitlin J Rinz, Jonathan Levine, Katie M Minor, Hammon D Humphries, Renee Lara, Alison N Starr-Moss, Ling T Guo, D Colette Williams, G Diane Shelton, Leigh Anne Clark
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e106425 (2014)
Congenital myasthenic syndromes (CMSs) are heterogeneous neuromuscular disorders characterized by skeletal muscle weakness caused by disruption of signal transmission across the neuromuscular junction (NMJ). CMSs are rarely encountered in veterinary
Externí odkaz:
https://doaj.org/article/5479a18746c34b9eb31694733c7300de
Autor:
G. Diane Shelton, Alexander G. Davis, Jennifer R. Levy, Elina Salmela, Hannes Lohi, Alison N. Starr-Moss, Marjo K. Hytönen, Melissa L. Cox, Ling T. Guo, Jacquelyn M. Evans, Kevin P. Campbell, Leigh Anne Clark
Publikováno v:
Skeletal Muscle, Vol 7, Iss 1, Pp 1-10 (2017)
Skeletal muscle, vol 7, iss 1
Skeletal Muscle
Skeletal muscle, vol 7, iss 1
Skeletal Muscle
Background Limb-girdle muscular dystrophies (LGMDs) are a heterogeneous group of inherited autosomal myopathies that preferentially affect voluntary muscles of the shoulders and hips. LGMD has been clinically described in several breeds of dogs, but
Publikováno v:
Genes, Vol 10, Iss 4, p 320 (2019)
Genes
Volume 10
Issue 4
Genes
Volume 10
Issue 4
The lack of an annotated reference sequence for the canine Y chromosome has limited evolutionary studies, as well as our understanding of the role of Y-linked sequences in phenotypes with a sex bias. In genome-wide association studies (GWASs), we obs
Autor:
James B. Thoreson, A. C. Palmer, Kate L. Tsai, Vanda A. Lennon, Caitlin J. Rinz, G. Diane Shelton, H. Dale Humphries, Fiona James, Leigh Anne Clark, Alison N. Starr-Moss, Ling T. Guo
Publikováno v:
Neuromuscular Disorders. 25:921-927
Congenital myasthenic syndromes (CMSs) are a group of rare genetic disorders of the neuromuscular junction resulting in structural or functional causes of fatigable weakness that usually begins early in life. Mutations in pre-synaptic, synaptic and p
Akademický článek
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