Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Darren M. Hutt"'
Autor:
Chao Wang, Samantha M. Scott, Kanagaraj Subramanian, Salvatore Loguercio, Pei Zhao, Darren M. Hutt, Nicole Y. Farhat, Forbes D. Porter, William E. Balch
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
How epigenetics coordinate with genetics to impact protein fitness is unknown. Here, using a Variation Spatial Profiling strategy and machine learning, the authors map HDAC impact on a full set of Niemann pick C1 disease variants to quantitate an una
Externí odkaz:
https://doaj.org/article/cdd46cddd7bd45bbba719375caab04d4
Autor:
Nina H. Pipalia, Kanagaraj Subramanian, Shu Mao, Harold Ralph, Darren M. Hutt, Samantha M. Scott, William E. Balch, Frederick R. Maxfield
Publikováno v:
Journal of Lipid Research, Vol 58, Iss 4, Pp 695-708 (2017)
Niemann-Pick C (NPC) disease is an autosomal recessive disorder that leads to excessive storage of cholesterol and other lipids in late endosomes and lysosomes. The large majority of NPC disease is caused by mutations in NPC1, a large polytopic membr
Externí odkaz:
https://doaj.org/article/0b6bea2e63ea4fa5ae88777be3306dfd
Publikováno v:
Journal of Lipid Research, Vol 42, Iss 1, Pp 79-87 (2001)
The effects of different acylglycerides on the conformation and charge of apolipoprotein A-I (apoA-I) have been investigated in reconstituted high density lipoproteins (LpA-I). Various amounts of diacylglycerol (DG) and triacylglycerol (TG) were inco
Externí odkaz:
https://doaj.org/article/98202c3509184ca399c1dbd6e464b083
Autor:
Salvatore Loguercio, Nicole Y. Farhat, Kanagaraj Subramanian, Pei Zhao, Darren M. Hutt, Forbes D. Porter, Samantha M. Scott, William E. Balch, Chao Wang
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Nature Communications
Nature communications, vol 10, iss 1
Nature Communications
Nature communications, vol 10, iss 1
To understand the impact of epigenetics on human misfolding disease, we apply Gaussian-process regression (GPR) based machine learning (ML) (GPR-ML) through variation spatial profiling (VSP). VSP generates population-based matrices describing the spa
Autor:
Chao Wang, William E. Balch, Samantha M. Scott, Jason E. Gestwicki, Pei Zhao, Hao Shao, Darren M. Hutt, Shuhong Sun
Publikováno v:
Hum Mol Genet
Human molecular genetics, vol 29, iss 1
Human molecular genetics, vol 29, iss 1
Genetic diversity provides a rich repository for understanding the role of proteostasis in the management of the protein fold in human biology. Failure in proteostasis can trigger multiple disease states, affecting both human health and lifespan. Nie
Autor:
Nina R. Ortiz, Laura J. Blair, Marc B. Cox, Jeffrey C. Sivils, David S. Culbertson, Jane Dyson, Ashley N Payan, Dan Finley, Jazzmin Jovonna Owens, Jason E. Gestwicki, Szu Yu Kuo, William E. Balch, Jaideep Chaudhary, Jay Singh, Darren M. Hutt, Chad A. Dickey, Naihsuan Guy, Bradley D. Tait, Shravan Kumar Komaragiri
Publikováno v:
Cell chemical biology, vol 27, iss 3
Cell Chem Biol
Cell Chem Biol
Summary Hsp90 plays an important role in health and is a therapeutic target for managing misfolding disease. Compounds that disrupt co-chaperone delivery of clients to Hsp90 target a subset of Hsp90 activities, thereby minimizing the toxicity of pan-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c800b824e420391f461894a73274c69
https://escholarship.org/uc/item/3k55j4vx
https://escholarship.org/uc/item/3k55j4vx
Autor:
Judith A Coppinger, Darren M Hutt, Abbas Razvi, Atanas V Koulov, Sandra Pankow, John R Yates, William E Balch
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e37682 (2012)
Protein folding is the primary role of proteostasis network (PN) where chaperone interactions with client proteins determine the success or failure of the folding reaction in the cell. We now address how the Phe508 deletion in the NBD1 domain of the
Externí odkaz:
https://doaj.org/article/c58f48318e9d4af4b9a801a25a808a6e
Publikováno v:
Journal of Molecular Biology. 430:2951-2973
The advent of precision medicine for genetic diseases has been hampered by the large number of variants that cause familial and somatic disease, a complexity that is further confounded by the impact of genetic modifiers. To begin to understand differ
Autor:
Kanagaraj Subramanian, William E. Balch, Harold Ralph, Darren M. Hutt, Nina H. Pipalia, Frederick R. Maxfield, Shu Mao, Samantha M. Scott
Publikováno v:
Journal of Lipid Research, Vol 58, Iss 4, Pp 695-708 (2017)
Niemann-Pick C (NPC) disease is an autosomal recessive disorder that leads to excessive storage of cholesterol and other lipids in late endosomes and lysosomes. The large majority of NPC disease is caused by mutations in NPC1, a large polytopic membr
Autor:
Salvatore Loguercio, Alexander V. Misharin, Richard I. Morimoto, Ziyan Lu, Alexandra C. McQuattie-Pimentel, Hiam Abdala-Valencia, Thomas Stoeger, Karen M. Ridge, G. R. Scott Budinger, William E. Balch, Darren M. Hutt, Navdeep S. Chandel, Alexandre Rosa Campos, Nikita Joshi, Rogan A. Grant, Jacob I. Sznajder
Aging is associated with an increased risk for the development of many diseases. This is exemplified by the increased incidence of lung injury, muscle dysfunction and cognitive impairment in the elderly following influenza infection. Because the infe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eeeb7eb3b81492b85c6f6487c1a6be0
https://doi.org/10.1101/769737
https://doi.org/10.1101/769737