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John T. Olthoff
John T. Olthoff
University of Minnesota
Biology
Duchenne muscular dystrophy
Actin
Molecular biology
Dystrophin
6
Papers
92
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Persistent upregulation of the β-tubulin tubb6, linked to muscle regeneration, is a source of microtubule disorganization in dystrophic muscle
2019
Human Molecular Genetics
Davide Randazzo
Umara Khalique
Joseph J. Belanto
Aster Kenea
Dana M Talsness
John T. Olthoff
Michelle Tran
Kristien Zaal
Katherine Pak
Iago Pinal-Fernandez
Andrew L. Mammen
Dan L. Sackett
James M. Ervasti
Evelyn Ralston
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Citations (17)
Mouse models of two missense mutations in actin-binding domain 1 of dystrophin associated with duchenne or becker muscular dystrophy
2018
Human Molecular Genetics
Jackie L McCourt
Dana M Talsness
Angus Lindsay
Robert W. Arpke
Paul D Chatterton
D’anna M Nelson
Christopher M. Chamberlain
John T. Olthoff
Joseph J. Belanto
Preston M. McCourt
Michael Kyba
Dawn A. Lowe
James M. Ervasti
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Citations (14)
Loss of peroxiredoxin-2 exacerbates eccentric contraction-induced force loss in dystrophin-deficient muscle
2018
Nature Communications
John T. Olthoff
Angus Lindsay
Reem Abo-Zahrah
Kristen A. Baltgalvis
Xiaobai Patrinostro
Joseph J. Belanto
Dae-Yeul Yu
Benjamin J. Perrin
Daniel J. Garry
George G. Rodney
Dawn A. Lowe
James M. Ervasti
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Citations (21)
Peroxiredoxin II Deficiency Contributes to Contraction-Induced Force Loss in the mdx Model of Duchenne Muscular Dystrophy
2016
Free Radical Biology and Medicine
John T. Olthoff
Joseph J. Belanto
Angus Lindsay
George G. Rodney
Dawn A. Lowe
James M. Ervasti
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Independent variability of microtubule perturbations associated with dystrophinopathy
2016
Human Molecular Genetics
Joseph J. Belanto
John T. Olthoff
Tara L. Mader
Christopher M. Chamberlain
D’anna M Nelson
Preston M. McCourt
Dana M Talsness
Gregg G. Gundersen
Dawn A. Lowe
James M. Ervasti
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Citations (30)
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