Rachelle H. Crosbie
Affiliations: | University of California, Los Angeles, Los Angeles, CA |
Website:
https://www.ibp.ucla.edu/faculty/rachelle-crosbie/Google:
"Rachelle Crosbie"Bio:
aka Rachelle H. Crosbie-Watson
https://books.google.com/books?id=2p8vAQAAIAAJ
Mean distance: 35622
Cross-listing: Cell Biology Tree
Parents
Sign in to add mentor| Emil Reisler | grad student | 1994 | UCLA (Chemistry Tree) | |
| (Structural determinants of actin function and their effects on the components of the motile apparatus) | ||||
| Kevin P. Campbell | post-doc | University of Iowa | ||
Children
Sign in to add trainee| Janine M. Bekker | grad student | 2005 | UCLA |
| Angela K. Peter | grad student | 2007 | UCLA |
| Jamie L. Marshall | grad student | 2012 | UCLA (Cell Biology Tree) |
| Michelle S. Parvatiyar | post-doc | 2013-2018 | UCLA (Chemistry Tree) |
BETA: Related publications
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Publications
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| Helzer D, Kannan P, Reynolds JC, et al. (2024) Role of microenvironment on muscle stem cell function in health, adaptation, and disease. Current Topics in Developmental Biology. 158: 179-201 |
| Stearns-Reider KM, Hicks MR, Hammond KG, et al. (2023) Myoscaffolds reveal laminin scarring is detrimental for stem cell function while sarcospan induces compensatory fibrosis. Npj Regenerative Medicine. 8: 16 |
| McCourt JL, Stearns-Reider KM, Mamsa H, et al. (2023) Multi-omics analysis of sarcospan overexpression in mdx skeletal muscle reveals compensatory remodeling of cytoskeleton-matrix interactions that promote mechanotransduction pathways. Skeletal Muscle. 13: 1 |
| Mamsa H, Stark RL, Shin KM, et al. (2021) Sarcospan increases laminin binding capacity of α-dystroglycan to ameliorate DMD independent of Galgt2. Human Molecular Genetics |
| Gibbs EM, McCourt JL, Shin KM, et al. (2021) Loss of sarcospan exacerbates pathology in mdx mice, but does not affect utrophin amelioration of disease. Human Molecular Genetics |
| Gibbs EM, McCourt JL, Shin KM, et al. (2021) Loss of sarcospan exacerbates pathology in mdx mice, but does not affect utrophin amelioration of disease. Human Molecular Genetics |
| Shu C, Parfenova L, Mokhonova E, et al. (2020) High-throughput screening identifies modulators of sarcospan that stabilize muscle cells and exhibit activity in the mouse model of Duchenne muscular dystrophy. Skeletal Muscle. 10: 26 |
| Moore TM, Lin AJ, Strumwasser AR, et al. (2020) Mitochondrial Dysfunction Is an Early Consequence of Partial or Complete Dystrophin Loss in Mice. Frontiers in Physiology. 11: 690 |
| Lee CC, Hoang A, Segovia D, et al. (2020) Enhanced Methods for Needle Biopsy and Cryopreservation of Skeletal Muscle in Older Adults. Journal of Cytology & Histology. 11 |
| Shu C, Kaxon-Rupp AN, Collado JR, et al. (2019) Development of a high-throughput screen to identify small molecule enhancers of sarcospan for the treatment of Duchenne muscular dystrophy. Skeletal Muscle. 9: 32 |