受强制性开放获取政策约束的文章 - Jeff Carroll了解详情
可在其他位置公开访问的文章：30 篇
Potent and selective antisense oligonucleotides targeting single-nucleotide polymorphisms in the Huntington disease gene/allele-specific silencing of mutant huntingtin
JB Carroll, SC Warby, AL Southwell, CN Doty, S Greenlee, N Skotte, ...
Molecular Therapy 19 (12), 2178-2185, 2011
强制性开放获取政策： Canadian Institutes of Health Research
CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup
SC Warby, A Montpetit, AR Hayden, JB Carroll, SL Butland, H Visscher, ...
The American Journal of Human Genetics 84 (3), 351-366, 2009
强制性开放获取政策： Canadian Institutes of Health Research
Age-dependent alterations of corticostriatal activity in the YAC128 mouse model of Huntington disease
PR Joshi, NP Wu, VM André, DM Cummings, C Cepeda, JA Joyce, ...
Journal of Neuroscience 29 (8), 2414-2427, 2009
强制性开放获取政策： US National Institutes of Health
Automated deformation analysis in the YAC128 Huntington disease mouse model
JP Lerch, JB Carroll, S Spring, LN Bertram, C Schwab, MR Hayden, ...
Neuroimage 39 (1), 32-39, 2008
强制性开放获取政策： Canadian Institutes of Health Research
Cholesterol defect is marked across multiple rodent models of Huntington's disease and is manifest in astrocytes
M Valenza, V Leoni, JM Karasinska, L Petricca, J Fan, J Carroll, ...
Journal of Neuroscience 30 (32), 10844-10850, 2010
强制性开放获取政策： US National Institutes of Health, Fondazione Telethon, Italy
In vivo evaluation of candidate allele-specific mutant huntingtin gene silencing antisense oligonucleotides
AL Southwell, NH Skotte, HB Kordasiewicz, ME Østergaard, AT Watt, ...
Molecular Therapy 22 (12), 2093-2106, 2014
强制性开放获取政策： Canadian Institutes of Health Research
Activated caspase-6 and caspase-6-cleaved fragments of huntingtin specifically colocalize in the nucleus
SC Warby, CN Doty, RK Graham, JB Carroll, YZ Yang, RR Singaraja, ...
Human molecular genetics 17 (15), 2390-2404, 2008
强制性开放获取政策： Canadian Institutes of Health Research
Allele-specific suppression of mutant huntingtin using antisense oligonucleotides: providing a therapeutic option for all Huntington disease patients
NH Skotte, AL Southwell, ME Østergaard, JB Carroll, SC Warby, CN Doty, ...
PloS one 9 (9), e107434, 2014
强制性开放获取政策： Canadian Institutes of Health Research
Cortical thickness measured from MRI in the YAC128 mouse model of Huntington's disease
JP Lerch, JB Carroll, A Dorr, S Spring, AC Evans, MR Hayden, JG Sled, ...
Neuroimage 41 (2), 243-251, 2008
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
Cleavage at the 586 amino acid caspase-6 site in mutant huntingtin influences caspase-6 activation in vivo
RK Graham, Y Deng, J Carroll, K Vaid, C Cowan, MA Pouladi, M Metzler, ...
Journal of Neuroscience 30 (45), 15019-15029, 2010
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
A fully humanized transgenic mouse model of Huntington disease
AL Southwell, SC Warby, JB Carroll, CN Doty, NH Skotte, W Zhang, ...
Human molecular genetics 22 (1), 18-34, 2013
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
Antisense oligonucleotides extend survival of prion-infected mice
GJ Raymond, HT Zhao, B Race, LD Raymond, K Williams, EE Swayze, ...
JCI insight 4 (16), 2019
强制性开放获取政策： US National Science Foundation, US National Institutes of Health
Prion protein lowering is a disease-modifying therapy across prion disease stages, strains and endpoints
EV Minikel, HT Zhao, J Le, J O’Moore, R Pitstick, S Graffam, GA Carlson, ...
Nucleic acids research 48 (19), 10615-10631, 2020
强制性开放获取政策： US National Science Foundation, US National Institutes of Health
Wild-type HTT modulates the enzymatic activity of the neuronal palmitoyl transferase HIP14
K Huang, SS Sanders, R Kang, JB Carroll, L Sutton, J Wan, R Singaraja, ...
Human Molecular Genetics 20 (17), 3356-3365, 2011
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
Natural history of disease in the YAC128 mouse reveals a discrete signature of pathology in Huntington disease
JB Carroll, JP Lerch, S Franciosi, A Spreeuw, N Bissada, RM Henkelman, ...
Neurobiology of disease 43 (1), 257-265, 2011
强制性开放获取政策： Canadian Institutes of Health Research
Transcriptional regulatory networks underlying gene expression changes in Huntington's disease
SA Ament, JR Pearl, JP Cantle, RM Bragg, PJ Skene, SR Coffey, ...
Molecular systems biology 14 (3), e7435, 2018
强制性开放获取政策： US National Science Foundation, US National Institutes of Health
Single-nucleus RNA-seq reveals dysregulation of striatal cell identity due to huntington's disease mutations
S Malaiya, M Cortes-Gutierrez, BR Herb, SR Coffey, SRW Legg, ...
Journal of Neuroscience 41 (25), 5534-5552, 2021
强制性开放获取政策： US National Institutes of Health
High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington’s disease CAG knock-in mice across multiple genetic backgrounds
SA Ament, JR Pearl, A Grindeland, J St. Claire, JC Earls, M Kovalenko, ...
Human molecular genetics 26 (5), 913-922, 2017
强制性开放获取政策： US National Science Foundation, US National Institutes of Health
Huntingtin structure is orchestrated by HAP40 and shows a polyglutamine expansion-specific interaction with exon 1
RJ Harding, JC Deme, JF Hevler, S Tamara, A Lemak, JP Cantle, ...
Communications Biology 4 (1), 1374, 2021
强制性开放获取政策： US Department of Energy, US National Institutes of Health, Genome Canada …
Mice lacking caspase-2 are protected from behavioral changes, but not pathology, in the YAC128 model of Huntington disease
JB Carroll, AL Southwell, RK Graham, JP Lerch, DE Ehrnhoefer, LP Cao, ...
Molecular neurodegeneration 6, 1-13, 2011
强制性开放获取政策： Austrian Science Fund, Canadian Institutes of Health Research
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