Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Saskia B. Neher"'
Autor:
Kathryn H. Gunn, Saskia B. Neher
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract Lipoprotein lipase (LPL) hydrolyzes triglycerides from circulating lipoproteins, releasing free fatty acids. Active LPL is needed to prevent hypertriglyceridemia, which is a risk factor for cardiovascular disease (CVD). Using cryogenic elect
Externí odkaz:
https://doaj.org/article/06a7b0e095224b0f932095dd0ea3d3ea
Autor:
Ming Jing Wu, Anna Wolska, Benjamin S. Roberts, Ellis M. Pearson, Aspen R. Gutgsell, Alan T. Remaley, Saskia B. Neher
Publikováno v:
Journal of Lipid Research, Vol 59, Iss 12, Pp 2456-2465 (2018)
LPL is a secreted enzyme that hydrolyzes triglycerides from circulating lipoproteins. Individuals lacking LPL suffer from severe hypertriglyceridemia, a risk factor for acute pancreatitis. One potential treatment is to administer recombinant LPL as a
Externí odkaz:
https://doaj.org/article/c4ed15e75e3a431ba9946ec87c0c8a82
Autor:
Kathryn H. Gunn, Saskia B. Neher
Publikováno v:
bioRxiv
Lipoprotein lipase (LPL) hydrolyzes triglycerides from circulating lipoproteins, releasing free fatty acids. Active LPL is needed to prevent hypertriglyceridemia, which is a risk factor for cardiovascular disease (CVD). Using cryogenic electron micro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f860590e2074f5d46d66a9f409fc137
https://doi.org/10.1101/2023.03.21.533650
https://doi.org/10.1101/2023.03.21.533650
Autor:
Robert Risti, Kathryn H. Gunn, Kristofer Hiis-Hommuk, Natjan-Naatan Seeba, Hamed Karimi, Ly Villo, Marko Vendelin, Saskia B. Neher, Aivar Lõokene
Lipoprotein lipase (LPL), a crucial enzyme in the intravascular hydrolysis of triglyceride-rich lipoproteins, is a potential drug target for the treatment of hypertriglyceridemia. The activity and stability of LPL are influenced by a complex ligand n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a9bc87d547470ba937a3d11678a95fa
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0135447 (2015)
Mycobacterium tuberculosis harbors over 160 genes encoding PE/PPE proteins, several of which have roles in the pathogen's virulence. A number of PE/PPE proteins are secreted via Type VII secretion systems known as the ESX secretion systems. One PE pr
Externí odkaz:
https://doaj.org/article/9ef0013cda7144d49e32575daab18155
Publikováno v:
J Cell Sci
Lipoprotein lipase (LPL) is a secreted triglyceride lipase involved in the clearance of very-low-density lipoproteins and chylomicrons from circulation. LPL is expressed primarily in adipose and muscle tissues and transported to the capillary lumen.
Autor:
Aakash Mehta, Kathryn H. Gunn, Samantha S. Stadmiller, Gary J. Pielak, Samantha Piszkiewicz, Thomas C. Boothby, Elizabeth Kuhlman, Kenny H. Nguyen, Alex J. Guseman, Owen Warmuth, Saskia B. Neher, Ashlee M. Propst
Publikováno v:
Protein Sci
Protein-based biological drugs and many industrial enzymes are unstable, making them prohibitively expensive. Some can be stabilized by formulation with excipients, but most still require low temperature storage. In search of new, more robust excipie
Autor:
Mario J. Borgnia, Edward H. Egelman, Fengbin Wang, Benjamin S. Roberts, Saskia B. Neher, Joshua D. Strauss, Kathryn H. Gunn
Publikováno v:
Proc Natl Acad Sci U S A
Lipases are enzymes necessary for the proper distribution and utilization of lipids in the human body. Lipoprotein lipase (LPL) is active in capillaries, where it plays a crucial role in preventing dyslipidemia by hydrolyzing triglycerides from packa
Autor:
Ellis M. Pearson, Ming Jing Wu, Aspen R. Gutgsell, Alan T. Remaley, Anna Wolska, Saskia B. Neher, Benjamin S. Roberts
Publikováno v:
Journal of Lipid Research, Vol 59, Iss 12, Pp 2456-2465 (2018)
LPL is a secreted enzyme that hydrolyzes triglycerides from circulating lipoproteins. Individuals lacking LPL suffer from severe hypertriglyceridemia, a risk factor for acute pancreatitis. One potential treatment is to administer recombinant LPL as a
Publikováno v:
Biochemistry. 56:525-533
Lipoprotein lipase (LPL) is responsible for the hydrolysis of triglycerides from circulating lipoproteins. Whereas most identified mutations in the LPL gene are deleterious, one mutation, LPLS447X, causes a gain of function. This mutation truncates t