Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Christine M. Wooley"'
Autor:
Robert A. Maue, Brent T. Harris, Ivan A. Borbon, Christine M. Wooley, Maximillian A. Rogers, David J. Graber, Catherine C.Y. Chang, Robert W. Burgess, Leslie P. Henderson, Robert P. Erickson, Theodore P. Trouard, Marie T. Vanier, Carlos A. A. Penatti, Kevin L. Seburn, Bing Wang, John Totenhagen, Benjamin S. Szwergold, Ta-Yuan Chang, Donna M. Porter
Publikováno v:
Human Molecular Genetics. 21:730-750
We have identified a point mutation in Npc1 that creates a novel mouse model (Npc1(nmf164)) of Niemann-Pick type C1 (NPC) disease: a single nucleotide change (A to G at cDNA bp 3163) that results in an aspartate to glycine change at position 1005 (D1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3183f2b0e75b63b8fff7fd0c1c1717d6
https://doi.org/10.1093/hmg/ddr505
https://doi.org/10.1093/hmg/ddr505
Publikováno v:
Physiology & Behavior. 96:350-361
WOOLEY, C.M., S. XING, R.W. BURGESS, G.A. COX, AND K.L. SEBURN. Age, experience and genetic background influence treadmill walking in mice. PHYSIOL. BEHAV. XX(X), XXX-XXX, 2008 – The use of a treadmill to gather data for gait analysis in mice is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0df5eeb86ae3c3aa5cd0dd9dc541ac58
https://doi.org/10.1016/j.physbeh.2008.10.020
https://doi.org/10.1016/j.physbeh.2008.10.020
Autor:
Wayne N. Frankel, Christine M. Wooley, Gregory A. Cox, Kevin L. Seburn, Ajit Kale, Roger B. Sher
Publikováno v:
Muscle & Nerve. 32:43-50
The effective treatment or cure of motoneuron disease will require understanding the disease processes that precede irreversible cell loss. To study these early stages, and to evaluate potential treatments in relevant animal models, requires a sensit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9167b9c2c31a94d7906c9bd9d9378d76
https://doi.org/10.1002/mus.20228
https://doi.org/10.1002/mus.20228
Autor:
Elena Kudryashova, Christine M. Wooley, Melissa J. Spencer, Kimberly A. Huebsch, Roger B. Sher, Gregory A. Cox, Kevin L. Seburn
Publikováno v:
Human molecular genetics. 14(19)
Human tibial muscular dystrophy (TMD) and limb-girdle muscular dystrophy 2J (LGMD2J) are caused by mutations in the giant sarcomeric protein titin (TTN) adjacent to a binding site for the muscle-specific protease calpain 3 (CAPN3). Muscular dystrophy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7279c9015973e8c5b8f82a82297c5d6e
https://pubmed.ncbi.nlm.nih.gov/16115818
https://pubmed.ncbi.nlm.nih.gov/16115818