Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rory M. Weston"'
Autor:
Megan A. O’Brien, Rory M. Weston, Nihar U. Sheth, Steven Bradley, John Bigbee, Ashutosh Pandey, Robert W. Williams, Jennifer T. Wolstenholme, Michael F. Miles
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Alcoholism is a complex behavioral disorder characterized by loss of control in limiting intake, and progressive compulsion to seek and consume ethanol. Prior studies have suggested that the characteristic behaviors associated with escalation of drug
Externí odkaz:
https://doaj.org/article/9b0ee6e80a1e4e28b6d511a72bf85f56
Publikováno v:
PLoS ONE, Vol 16, Iss 7, p e0246224 (2021)
PLoS ONE
PLoS ONE
Chloride intracellular channels (CLICs) are a unique family of evolutionarily conserved metamorphic proteins, switching between stable conformations based on redox conditions. CLICs have been implicated in a wide variety biological processes includin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de09231706fe8c9d780f03274fcf665b
https://doi.org/10.1371/journal.pone.0246224
https://doi.org/10.1371/journal.pone.0246224
Autor:
Robert M. Bragg, Sydney R. Coffey, Rory M. Weston, Seth A. Ament, Jeffrey P. Cantle, Shawn Minnig, Cory C. Funk, Dominic D. Shuttleworth, Emily L. Woods, Bonnie R. Sullivan, Lindsey Jones, Anne Glickenhaus, John S. Anderson, Michael D. Anderson, Stephen B. Dunnett, Vanessa C. Wheeler, Marcy E. MacDonald, Simon P. Brooks, Nathan D. Price, Jeffrey B. Carroll
Publikováno v:
Scientific Reports. 7
Scientific Reports 7: Article number: 41570; published online: 08 February 2017; updated: 28 March 2017 This Article contains a typographical error in the Methods section, under the subheading “Library construction, RNA Sequencing and RNASeq analys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1496f6ddb4740ddb933aa001eac951fa
https://doi.org/10.1038/srep44960
https://doi.org/10.1038/srep44960
Autor:
Lindsey Jones, Sydney R. Coffey, Vanessa C. Wheeler, Marcy E. MacDonald, Anne Glickenhaus, Stephen B. Dunnett, Jeffrey P. Cantle, Seth A. Ament, Rory M. Weston, Emily L. Woods, Robert M. Bragg, Jeffrey B. Carroll, Dominic D. Shuttleworth, Nathan D. Price, Michael D. Anderson, Bonnie R. Sullivan, Simon Philip Brooks, John S. Anderson, Cory C. Funk, Shawn Minnig
Publikováno v:
Scientific Reports
We investigated the appearance and progression of disease-relevant signs in the B6.HttQ111/+mouse, a genetically precise model of the mutation that causes Huntington’s disease (HD). We find that B6.HttQ111/+mice are healthy, show no overt signs of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ac77a6ea7b8894d52d032ff928730f2
https://pubmed.ncbi.nlm.nih.gov/28350386
https://pubmed.ncbi.nlm.nih.gov/28350386
Autor:
J Rodier, Rory M. Weston, LG Boros, Anne Glickenhaus, Sydney R. Coffey, Marcy E. MacDonald, Jeffrey B. Carroll
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 85:A19-A20
Background We are interested in mapping and understanding phenotypes that precede the development of overt signs of Huntington’s disease, in hopes of identifying pathways with the potential to be disease-modifying. Notably, the Huntington’s disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0f9f43e3c7e87828c63ef31fbcc93d2
https://doi.org/10.1136/jnnp-2014-309032.58
https://doi.org/10.1136/jnnp-2014-309032.58
Autor:
Rory M. Weston, Marcy E. MacDonald, Clary B. Clish, Amy Deik, Jolene R. Guide, Elisa Fossale, Jeffrey B. Carroll, Jamshid Arjomand, Seung Kwak
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 8, p e0134465 (2015)
PLoS ONE, Vol 10, Iss 8, p e0134465 (2015)
The HTT CAG expansion mutation causes Huntington's Disease and is associated with a wide range of cellular consequences, including altered metabolism. The mutant allele is expressed widely, in all tissues, but the striatum and cortex are especially v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93321289e0838e887cc8b43b36da359c
https://doi.org/10.1371/journal.pone.0134465
https://doi.org/10.1371/journal.pone.0134465
Publikováno v:
Journal of Vision. 11:1012-1012
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a7198c124b049feae38b6daf5b36fa4
https://doi.org/10.1167/11.11.1012
https://doi.org/10.1167/11.11.1012
Autor:
Jeffrey B Carroll, Amy Deik, Elisa Fossale, Rory M Weston, Jolene R Guide, Jamshid Arjomand, Seung Kwak, Clary B Clish, Marcy E MacDonald
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0134465 (2015)
The HTT CAG expansion mutation causes Huntington's Disease and is associated with a wide range of cellular consequences, including altered metabolism. The mutant allele is expressed widely, in all tissues, but the striatum and cortex are especially v
Externí odkaz:
https://doaj.org/article/a8690f7be1554d12945d9a4d73f05bec