Подписаться
Marshall Hogarth
Marshall Hogarth
Подтвержден адрес электронной почты в домене childrensnational.org
Название
Процитировано
Процитировано
Год
ACTN3 genotype influences muscle performance through the regulation of calcineurin signaling
JT Seto, KGR Quinlan, M Lek, XF Zheng, F Garton, DG MacArthur, ...
The Journal of clinical investigation 123 (10), 4255-4263, 2013
1612013
Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophy
MC Vila, S Rayavarapu, MW Hogarth, JH Van der Meulen, A Horn, ...
Cell Death & Differentiation 24 (2), 330-342, 2017
1302017
Mitochondrial redox signaling enables repair of injured skeletal muscle cells
A Horn, JH Van der Meulen, A Defour, M Hogarth, SC Sreetama, A Reed, ...
Science signaling 10 (495), eaaj1978, 2017
1272017
Fibroadipogenic progenitors are responsible for muscle loss in limb girdle muscular dystrophy 2B
MW Hogarth, A Defour, C Lazarski, E Gallardo, J Diaz Manera, ...
Nature communications 10 (1), 2430, 2019
1172019
TGF-β–driven muscle degeneration and failed regeneration underlie disease onset in a DMD mouse model
DAG Mázala, JS Novak, MW Hogarth, M Nearing, P Adusumalli, CB Tully, ...
JCI insight 5 (6), 2020
1032020
Dysregulation of mitochondrial Ca2+ uptake and sarcolemma repair underlie muscle weakness and wasting in patients and mice lacking MICU1
V Debattisti, A Horn, R Singh, EL Seifert, MW Hogarth, DA Mazala, ...
Cell reports 29 (5), 1274-1286. e6, 2019
832019
Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy
MW Hogarth, PJ Houweling, KC Thomas, H Gordish-Dressman, L Bello, ...
Nature communications 8 (1), 14143, 2017
682017
α-Actinin-3 deficiency is associated with reduced bone mass in human and mouse
N Yang, A Schindeler, MM McDonald, JT Seto, PJ Houweling, M Lek, ...
Bone 49 (4), 790-798, 2011
602011
Annexin A2 links poor myofiber repair with inflammation and adipogenic replacement of the injured muscle
A Defour, S Medikayala, JH Van der Meulen, MW Hogarth, N Holdreith, ...
Human molecular genetics 26 (11), 1979-1991, 2017
542017
Analysis of the ACTN3 heterozygous genotype suggests that α-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashion
MW Hogarth, FC Garton, PJ Houweling, T Tukiainen, M Lek, ...
Human molecular genetics 25 (5), 866-877, 2016
532016
Myoblasts and macrophages are required for therapeutic morpholino antisense oligonucleotide delivery to dystrophic muscle
JS Novak, MW Hogarth, JF Boehler, M Nearing, MC Vila, R Heredia, ...
Nature communications 8 (1), 941, 2017
432017
Effect of endurance exercise on microRNAs in myositis skeletal muscle—A randomized controlled study
JF Boehler, MW Hogarth, MD Barberio, JS Novak, S Ghimbovschi, ...
PLoS One 12 (8), e0183292, 2017
382017
The effect of ACTN3 gene doping on skeletal muscle performance
FC Garton, PJ Houweling, D Vukcevic, LR Meehan, FXZ Lee, M Lek, ...
The American Journal of Human Genetics 102 (5), 845-857, 2018
312018
Elusive sources of variability of dystrophin rescue by exon skipping
MC Vila, MB Klimek, JS Novak, S Rayavarapu, K Uaesoontrachoon, ...
Skeletal muscle 5, 1-12, 2015
312015
Morpholino‐induced exon skipping stimulates cell‐mediated and humoral responses to dystrophin in mdx mice
MC Vila, JS Novak, M Benny Klimek, N Li, M Morales, AG Fritz, K Edwards, ...
The Journal of pathology 248 (3), 339-351, 2019
202019
Cooperative International Neuromuscular Research Group (CINRG); Pegoraro, E.; Hoffman, EP; Head, SI; North, KN Evidence for ACTN3 as a genetic modifier of Duchenne muscular …
MW Hogarth, PJ Houweling, KC Thomas, H Gordish-Dressman, L Bello
Nat. Commun 8, 14143, 2017
192017
Single-cell and spatial transcriptomics identify a macrophage population associated with skeletal muscle fibrosis
G Coulis, D Jaime, C Guerrero-Juarez, JM Kastenschmidt, PK Farahat, ...
Science advances 9 (27), eadd9984, 2023
142023
Pathogenic role and therapeutic potential of fibro-adipogenic progenitors in muscle disease
MW Hogarth, P Uapinyoying, DAG Mázala, JK Jaiswal
Trends in molecular medicine 28 (1), 8-11, 2022
112022
Anoctamin 5 knockout mouse model recapitulates LGMD2L muscle pathology and offers insight into in vivo functional deficits
G Thiruvengadam, SC Sreetama, K Charton, M Hogarth, JS Novak, ...
Journal of Neuromuscular Diseases 8 (s2), S243-S255, 2021
82021
Humoral and cell mediated immune response to new dystrophin after morpholino-induced exon skipping therapy in dystrophin-deficient mdx mice
K Nagaraju, M Vila, J Novak, J Boehler, M Hogarth, A Zhang, T Kinder, ...
NEUROMUSCULAR DISORDERS 28, S90-S90, 2018
12018
В данный момент система не может выполнить эту операцию. Повторите попытку позднее.
Статьи 1–20