Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jessica L. Buescher"'
Publikováno v:
Molecular Vision, Vol 25, Iss 1, Pp 165-173 (2019)
Purpose: The evolutionarily conserved retinal homeobox (Rax) transcription factor is essential for normal eye development in all vertebrates. Despite Rax’s biologic significance, the molecular mechanisms underlying Rax molecular function as a trans
Externí odkaz:
https://doaj.org/article/9ede55c38b4e4a8cb6b2f3c0a9eba100
Autor:
Jessica L. Buescher, Laura P. Musselman, Christina A. Wilson, Tieming Lang, Madeline Keleher, Thomas J. Baranski, Jennifer G. Duncan
Publikováno v:
Disease Models & Mechanisms, Vol 6, Iss 5, Pp 1123-1132 (2013)
SUMMARY Worldwide epidemiologic studies have repeatedly demonstrated an association between prenatal nutritional environment, birth weight and susceptibility to adult diseases including obesity, cardiovascular disease and type 2 diabetes. Despite adv
Externí odkaz:
https://doaj.org/article/df523c717da14ecc8fe1cc69f885dce0
Autor:
Jennifer G. Duncan, Laura Palanker Musselman, Thomas J. Baranski, Jessica L. Buescher, Madeline Rose Keleher, Tieming Lang, Christina A. Wilson
Publikováno v:
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 6, Iss 5, Pp 1123-1132 (2013)
Disease Models & Mechanisms, Vol 6, Iss 5, Pp 1123-1132 (2013)
Summary Worldwide epidemiologic studies have repeatedly demonstrated an association between prenatal nutritional environment, birth weight and susceptibility to adult diseases including obesity, cardiovascular disease and type 2 diabetes. Despite adv
Publikováno v:
Journal of Biological Chemistry. 285:7957-7963
Glycogen synthase kinase-3 (GSK-3) isoforms, GSK-3alpha and GSK-3beta, are serine/threonine kinases involved in numerous cellular processes and diverse diseases, including Alzheimer disease, cancer, and diabetes. GSK-3 isoforms function redundantly i
Autor:
Thong C. Ma, Jessica L. Buescher, Benjamin Oatis, Jason A. Funk, Andrew J. Nash, Raeann L. Carrier, Kari R. Hoyt
Publikováno v:
Neuroscience Letters. 411:98-103
Huntington's disease (HD) is a hereditary neurodegenerative disease that leads to striatal degeneration and a severe movement disorder. We used a transgenic mouse model of HD (the R6/2 line with approximately 150 glutamine repeats) to test a new ther
Autor:
Anthony P. Popkie, Bradley W. Doble, Brian K. Kaspar, Carlos Henrique Miranda, Jessica L. Buescher, Christopher J. Phiel
Publikováno v:
Alzheimer's & Dementia. 4
Alzheimer’s BACE1. Increased expression of RTN3 in culture reduces the production of -amyloid peptide (A ). However, RTN3 can also form high-molecular-weight RTN3 aggregates upon aberrant accumulation, and the increased RTN3 aggregation correlates
Publikováno v:
Alzheimer's & Dementia. 4
Publikováno v:
Neurobiology of Aging. 25:S531