Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Patrick B, Reeves"'
Autor:
Finnian R. Mc Causland, João Sérgio Neves, Patrick B. Reeves, Sushrut S. Waikar, Simon Correa, Katherine Scovner Ravi, Suraj Sarvode Mothi
Publikováno v:
Hemodialysis international. International Symposium on Home HemodialysisREFERENCES. 26(1)
INTRODUCTION Intradialytic hypotension (IDH) is a common complication of hemodialysis (HD) and is associated with excess morbidity and mortality. Higher serum phosphate is associated with adverse cardiovascular outcomes in maintenance HD patients; ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::000cbf24bd6fc4b8f1574c74e654f22c
https://pubmed.ncbi.nlm.nih.gov/34236130
https://pubmed.ncbi.nlm.nih.gov/34236130
Publikováno v:
Clinical journal of the American Society of Nephrology : CJASN. 13(8)
Individuals with ESKD requiring maintenance hemodialysis face a unique hemodynamic challenge, typically on a thrice-weekly basis. In an effort to achieve some degree of euvolemia, ultrafiltration goals often involve removal of the equivalent of an en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ef43383ac5ec42063e4476319f4ce9c
https://pubmed.ncbi.nlm.nih.gov/29483138
https://pubmed.ncbi.nlm.nih.gov/29483138
Autor:
Marian DiFiglia, Xueyi Li, Kimberly B Kegel, Matthew P Frosch, Nicholas Masso, Kwadwo A Ansong, Jonathan Alexander, Patrick B Reeves, Hollis McClory, Jeffrey S Kimm, Ellen Sapp, Antonio Valencia
Publikováno v:
Human molecular genetics. 26(21)
A mutation in the huntingtin (Htt) gene produces mutant Htt and Huntington's disease (HD), a neurodegenerative disorder. HD patients have oxidative damage in the brain, but the causes are unclear. Compared with controls, we found brain levels of NADP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::690ea1b6d3be455a643b109dfabbec63
https://pubmed.ncbi.nlm.nih.gov/23223017
https://pubmed.ncbi.nlm.nih.gov/23223017
Autor:
Jonathan Alexander, Ellen Sapp, Marian DiFiglia, Nicholas Masso, Antonio Valencia, Xueyi Li, Patrick B. Reeves, Kimberly B. Kegel
Publikováno v:
NeuroReport. 23:10-15
Patients with Huntington's disease suffer severe neuronal loss and signs of oxidative damage in the brain. Previously we found that primary neurons from embryonic cortex of mice bearing the Huntington's disease mutation (140 glutamines inserted into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ec84a9ed56fbd1c277b4baff857ac1f
https://doi.org/10.1097/wnr.0b013e32834d92e6
https://doi.org/10.1097/wnr.0b013e32834d92e6
Autor:
Neil Aronin, Ellen Sapp, Xueyi Li, Kimberly B. Kegel, Jonathan Alexander, Kathryn Chase, Antonio Valencia, Patrick B. Reeves, Marian DiFiglia
Publikováno v:
Journal of Neuroscience Research. 88:179-190
Patients with Huntington's disease have an expanded polyglutamine tract in huntingtin and suffer severe brain atrophy and neurodegeneration. Because membrane dysfunction can occur in Huntington's disease, we addressed whether mutant huntingtin in bra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbe9cc7769ec8056aa456865366b5f6b
https://doi.org/10.1002/jnr.22184
https://doi.org/10.1002/jnr.22184
Autor:
Edith L. Pfister, Neil Aronin, Phillip D. Zamore, Ellen Sapp, Kallanthottathil G. Rajeev, Marian DiFiglia, Meghan B. Sass, Jennifer Yoder, Rajendra K. Pandey, Miguel Sena-Esteves, Dinah W.Y. Sah, Patrick B. Reeves, Muthiah Manoharan, Kathryn Chase
Publikováno v:
Proceedings of the National Academy of Sciences. 104:17204-17209
Huntington's disease (HD) is an autosomal dominant disease caused by a CAG repeat expansion in the Htt gene (1). Mutant Htt causes neuronal death, dementia, and movement dysfunction; there is no effective treatment. In an inducible transgenic mouse m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87780a26ac550d9657075b52f410f20a
https://doi.org/10.1073/pnas.0708285104
https://doi.org/10.1073/pnas.0708285104
Autor:
Jonathan Alexander, Ellen Sapp, Antonio Valencia, Kimberly B. Kegel, Jeffrey S. Kimm, Hollis McClory, Matthew P. Frosch, Nicholas Masso, Kwadwo A. Ansong, Patrick B. Reeves, Marian DiFiglia, Xueyi Li
Publikováno v:
Hum Mol Genet
A mutation in the huntingtin (Htt) gene produces mutant Htt and Huntington's disease (HD), a neurodegenerative disorder. HD patients have oxidative damage in the brain, but the causes are unclear. Compared with controls, we found brain levels of NADP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8b6727a2bc5352ab54b3392be506c59
https://pubmed.ncbi.nlm.nih.gov/28973680
https://pubmed.ncbi.nlm.nih.gov/28973680
Autor:
Antonio, Valencia, Patrick B, Reeves, Ellen, Sapp, Xueyi, Li, Jonathan, Alexander, Kimberly B, Kegel, Kathryn, Chase, Neil, Aronin, Marian, DiFiglia
Publikováno v:
Journal of neuroscience research. 88(1)
Patients with Huntington's disease have an expanded polyglutamine tract in huntingtin and suffer severe brain atrophy and neurodegeneration. Because membrane dysfunction can occur in Huntington's disease, we addressed whether mutant huntingtin in bra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1977b6c424d60067f3019a939bf2eb93
https://pubmed.ncbi.nlm.nih.gov/19642201
https://pubmed.ncbi.nlm.nih.gov/19642201