フォロー
Russell J Butterfield
Russell J Butterfield
確認したメール アドレス: hsc.utah.edu
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引用先
引用先
Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study
C Darryl, E Bertini, KJ Swoboda, WL Hwu, TO Crawford, RS Finkel, ...
Neuromuscular Disorders 29 (11), 842-856, 2019
6112019
Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
CM McDonald, C Campbell, RE Torricelli, RS Finkel, KM Flanigan, ...
The Lancet 390 (10101), 1489-1498, 2017
4802017
New genetic loci that control susceptibility and symptoms of experimental allergic encephalomyelitis in inbred mice
RJ Butterfield, JD Sudweeks, EP Blankenhorn, R Korngold, JC Marini, ...
The Journal of Immunology 161 (4), 1860-1867, 1998
1861998
Population-based prevalence of myotonic dystrophy type 1 using genetic analysis of statewide blood screening program
NE Johnson, RJ Butterfield, K Mayne, T Newcomb, C Imburgia, D Dunn, ...
Neurology 96 (7), e1045-e1053, 2021
1372021
Genetic analysis of disease subtypes and sexual dimorphisms in mouse experimental allergic encephalomyelitis (EAE): relapsing/remitting and monophasic remitting/nonrelapsing …
RJ Butterfield, EP Blankenhorn, RJ Roper, JF Zachary, RW Doerge, ...
The Journal of Immunology 162 (5), 3096-3102, 1999
1281999
Identification of genetic loci controlling the characteristics and severity of brain and spinal cord lesions in experimental allergic encephalomyelitis
RJ Butterfield, EP Blankenhorn, RJ Roper, JF Zachary, RW Doerge, ...
The American journal of pathology 157 (2), 637-645, 2000
1202000
Position of Glycine Substitutions in the Triple Helix of COL6A1, COL6A2, and COL6A3 is Correlated with Severity and Mode of Inheritance in Collagen VI …
RJ Butterfield, AR Foley, J Dastgir, S Asman, DM Dunn, Y Zou, Y Hu, ...
Human mutation 34 (11), 1558-1567, 2013
1032013
Effect of different corticosteroid dosing regimens on clinical outcomes in boys with Duchenne muscular dystrophy: a randomized clinical trial
M Guglieri, K Bushby, MP McDermott, KA Hart, R Tawil, WB Martens, ...
Jama 327 (15), 1456-1468, 2022
1012022
Gender, age, and season at immunization uniquely influence the genetic control of susceptibility to histopathological lesions and clinical signs of experimental allergic …
C Teuscher, JY Bunn, PD Fillmore, RJ Butterfield, JF Zachary, ...
The American journal of pathology 165 (5), 1593-1602, 2004
1002004
Genetic analysis of the influence of pertussis toxin on experimental allergic encephalomyelitis susceptibility: an environmental agent can override genetic checkpoints
EP Blankenhorn, RJ Butterfield, R Rigby, L Cort, D Giambrone, ...
The Journal of Immunology 164 (6), 3420-3425, 2000
902000
Sequence polymorphisms in the chemokines Scya1 (TCA-3), Scya2 (monocyte chemoattractant protein (MCP)-1), and Scya12 (MCP-5) are candidates for eae7, a locus controlling …
C Teuscher, RJ Butterfield, RZ Ma, JF Zachary, RW Doerge, ...
The Journal of Immunology 163 (4), 2262-2266, 1999
891999
Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy
BEP Ostrander, RJ Butterfield, BS Pedersen, AJ Farrell, RM Layer, ...
NPJ genomic medicine 3 (1), 22, 2018
872018
The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID‐19 pandemic
A Veerapandiyan, KR Wagner, S Apkon, CM McDonald, KD Mathews, ...
Muscle & Nerve 62 (1), 41-45, 2020
812020
Genetic control of susceptibility to experimental Lyme arthritis is polygenic and exhibits consistent linkage to multiple loci on chromosome 5 in four independent mouse crosses
RJ Roper, JJ Weis, BA McCracken, CB Green, Y Ma, KS Weber, ...
Genes & Immunity 2 (7), 388-397, 2001
812001
p53 convergently activates Dux/DUX4 in embryonic stem cells and in facioscapulohumeral muscular dystrophy cell models
EJ Grow, BD Weaver, CM Smith, J Guo, P Stein, SC Shadle, ...
Nature genetics 53 (8), 1207-1220, 2021
782021
Developing standardized corticosteroid treatment for Duchenne muscular dystrophy
M Guglieri, K Bushby, MP McDermott, KA Hart, R Tawil, WB Martens, ...
Contemporary clinical trials 58, 34-39, 2017
772017
Association study of exon variants in the NF-κB and TGFβ pathways identifies CD40 as a modifier of Duchenne muscular dystrophy
L Bello, KM Flanigan, RB Weiss, DM Dunn, KJ Swoboda, E Gappmaier, ...
The American Journal of Human Genetics 99 (5), 1163-1171, 2016
752016
Congenital muscular dystrophy and congenital myopathy
RJ Butterfield
CONTINUUM: Lifelong Learning in Neurology 25 (6), 1640-1661, 2019
682019
Repeated intravenous cardiosphere-derived cell therapy in late-stage Duchenne muscular dystrophy (HOPE-2): a multicentre, randomised, double-blind, placebo-controlled, phase 2 …
CM McDonald, E Marbán, S Hendrix, N Hogan, RR Smith, M Eagle, ...
The Lancet 399 (10329), 1049-1058, 2022
672022
Congenital lethal motor neuron disease with a novel defect in ribosome biogenesis
RJ Butterfield, TJ Stevenson, L Xing, TM Newcomb, B Nelson, W Zeng, ...
Neurology 82 (15), 1322-1330, 2014
652014
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