Zobrazeno 1 - 10
of 1 481
pro vyhledávání: '"Linda, Partridge"'
Autor:
Huey, Raymond B.
Publikováno v:
The American Naturalist, 2003 Jan . 161(1), i-ii.
Externí odkaz:
https://www.jstor.org/stable/10.1086/367716
Autor:
Maarouf Baghdadi, Tobias Nespital, Carolina Monzó, Joris Deelen, Sebastian Grönke, Linda Partridge
Publikováno v:
Molecular Metabolism, Vol 81, Iss , Pp 101902- (2024)
Objective: Rapamycin, a powerful geroprotective drug, can have detrimental effects when administered chronically. We determined whether intermittent treatment of mice can reduce negative effects while maintaining benefits of chronic treatment. Method
Externí odkaz:
https://doaj.org/article/a82a0bef98704f7ea031b10a51fa7346
Autor:
Ackermann, Martin
Publikováno v:
The Quarterly Review of Biology, 2008 Dec . 83(4), 402-403.
Externí odkaz:
https://www.jstor.org/stable/10.1086/596248
Autor:
Javier Morón-Oset, Lilly Katharina Sophie Fischer, Nathalie Jauré, Pingze Zhang, Annika Julia Jahn, Tessa Supèr, André Pahl, Adrian M. Isaacs, Sebastian Grönke, Linda Partridge
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-28 (2023)
Abstract G4C2 hexanucleotide repeat expansions in a non-coding region of the C9orf72 gene are the most common cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). G4C2 insertion length is variable, and patients can
Externí odkaz:
https://doaj.org/article/f57af59b4b8d485cbaeb003fa4f446ff
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract The Cre-loxP system has been used to generate cell-type specific mutations in mice, allowing researchers to investigate the underlying biological mechanisms of disease. However, the Cre-recombinase alone can induce phenotypes that confound c
Externí odkaz:
https://doaj.org/article/b028f22cecb945f2b689e00e34a8a555
Autor:
Magda L Atilano, Alexander Hull, Catalina-Andreea Romila, Mirjam L Adams, Jacob Wildfire, Enric Ureña, Miranda Dyson, Jorge Ivan-Castillo-Quan, Linda Partridge, Kerri J Kinghorn
Publikováno v:
PLoS Genetics, Vol 19, Iss 12, p e1011063 (2023)
Mutations in the GBA1 gene cause the lysosomal storage disorder Gaucher disease (GD) and are the greatest known genetic risk factors for Parkinson's disease (PD). Communication between the gut and brain and immune dysregulation are increasingly being
Externí odkaz:
https://doaj.org/article/ac15018b4078410a9ca7e92d2fad388d
Publikováno v:
Experimental Gerontology. 42:253-255
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a65372dac2e5d93bbe7d3ca57c3bc48
https://doi.org/10.1016/j.exger.2007.01.002
https://doi.org/10.1016/j.exger.2007.01.002
Akademický článek
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Autor:
Virender K. Sahota, Aelfwin Stone, Nathaniel S. Woodling, Jereme G. Spiers, Joern R. Steinert, Linda Partridge, Hrvoje Augustin
Publikováno v:
Open Biology, Vol 13, Iss 9 (2023)
Alterations in the neuromuscular system underlie several neuromuscular diseases and play critical roles in the development of sarcopenia, the age-related loss of muscle mass and function. Mammalian Myostatin (MST) and GDF11, members of the TGF-β sup
Externí odkaz:
https://doaj.org/article/52604fc9b84246b693fbae8899b28894
Autor:
Linda, Partridge
Publikováno v:
The American naturalist. 161(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f22094633c276d0bbeedf96c11f47ee6
https://pubmed.ncbi.nlm.nih.gov/12650458
https://pubmed.ncbi.nlm.nih.gov/12650458