| Year |
Citation |
Score |
| 2019 |
Randazzo D, Khalique U, Belanto JJ, Kenea A, Talsness DM, Olthoff JT, Tran MD, Zaal KJ, Pak K, Pinal-Fernandez I, Mammen AL, Sackett D, Ervasti JM, Ralston E. Persistent upregulation of the β-tubulin tubb6, linked to muscle regeneration, is a source of microtubule disorganization in dystrophic muscle. Human Molecular Genetics. PMID 30753428 DOI: 10.1093/Hmg/Ddz035 |
0.776 |
|
| 2018 |
Randazzo D, Khalique U, Belanto JJ, Kenea A, Talsness DM, Olthoff JT, Tran MD, Zaal KJ, Pak K, Pinal-Fernandez I, Mammen AL, Sackett D, Ervasti JM, Ralston E. Persistent upregulation of the β-tubulin tubb6, linked to muscle regeneration, is a source of microtubule disorganization in dystrophic muscle. Human Molecular Genetics. PMID 30535187 DOI: 10.1093/hmg/ddy418 |
0.779 |
|
| 2018 |
Olthoff JT, Lindsay A, Abo-Zahrah R, Baltgalvis KA, Patrinostro X, Belanto JJ, Yu DY, Perrin BJ, Garry DJ, Rodney GG, Lowe DA, Ervasti JM. Loss of peroxiredoxin-2 exacerbates eccentric contraction-induced force loss in dystrophin-deficient muscle. Nature Communications. 9: 5104. PMID 30504831 DOI: 10.1038/S41467-018-07639-3 |
0.675 |
|
| 2017 |
McCourt JL, Talsness DM, Lindsay A, Arpke RW, Chatterton PD, Nelson DM, Chamberlain CM, Olthoff JT, Belanto JJ, McCourt PM, Kyba M, Lowe DA, Ervasti JM. Mouse models of two missense mutations in actin binding domain 1 of dystrophin associated with Duchenne or Becker muscular dystrophy. Human Molecular Genetics. PMID 29194514 DOI: 10.1093/Hmg/Ddx414 |
0.766 |
|
| 2017 |
Cermak T, Curtin SJ, Gil-Humanes J, Čegan R, Kono TJY, Konečná E, Belanto JJ, Starker CG, Mathre JW, Greenstein RL, Voytas DF. A multi-purpose toolkit to enable advanced genome engineering in plants. The Plant Cell. PMID 28522548 DOI: 10.1105/Tpc.16.00922 |
0.303 |
|
| 2016 |
Belanto JJ, Olthoff JT, Mader TL, Chamberlain CM, Nelson DM, McCourt PM, Talsness DM, Gundersen GG, Lowe DA, Ervasti JM. Independent variability of microtubule perturbations associated with dystrophinopathy. Human Molecular Genetics. 25: 4951-4961. PMID 28171583 DOI: 10.1093/Hmg/Ddw318 |
0.78 |
|
| 2016 |
Belanto JJ, Olthoff JT, Mader TL, Chamberlain CM, Nelson DM, McCourt PM, Talsness DM, Gunderson GG, Lowe DA, Ervasti JM. Independent variability of microtubule perturbations associated with dystrophinopathy. Human Molecular Genetics. PMID 27638889 DOI: 10.1093/hmg/ddw318 |
0.785 |
|
| 2016 |
Olthoff JT, Belanto JJ, Lindsay A, Rodney GG, Lowe DA, Ervasti JM. Peroxiredoxin II Deficiency Contributes to Contraction-Induced Force Loss in the mdx Model of Duchenne Muscular Dystrophy Free Radical Biology and Medicine. 100: S107. DOI: 10.1016/J.Freeradbiomed.2016.10.273 |
0.712 |
|
| 2015 |
Filareto A, Rinaldi F, Arpke RW, Darabi R, Belanto JJ, Toso EA, Miller AZ, Ervasti JM, McIvor RS, Kyba M, Perlingeiro RC. Pax3-induced expansion enables the genetic correction of dystrophic satellite cells. Skeletal Muscle. 5: 36. PMID 26504514 DOI: 10.1186/S13395-015-0061-7 |
0.673 |
|
| 2015 |
Talsness DM, Belanto JJ, Ervasti JM. Disease-proportional proteasomal degradation of missense dystrophins. Proceedings of the National Academy of Sciences of the United States of America. PMID 26392559 DOI: 10.1073/Pnas.1508755112 |
0.76 |
|
| 2015 |
McCourt JL, Rhett KK, Jaeger MA, Belanto JJ, Talsness DM, Ervasti JM. In vitro stability of therapeutically relevant, internally truncated dystrophins. Skeletal Muscle. 5: 13. PMID 25954502 DOI: 10.1186/S13395-015-0040-Z |
0.741 |
|
| 2015 |
Simionescu-Bankston A, Pichavant C, Canner JP, Apponi LH, Wang Y, Steeds C, Olthoff JT, Belanto JJ, Ervasti JM, Pavlath GK. Creatine kinase B is necessary to limit myoblast fusion during myogenesis. American Journal of Physiology. Cell Physiology. 308: C919-31. PMID 25810257 DOI: 10.1152/Ajpcell.00029.2015 |
0.688 |
|
| 2015 |
McCourt JL, Rhett KK, Jaeger MA, Belanto JJ, Talsness DM, Ervasti JM. In vitro stability of therapeutically relevant, internally truncated dystrophins Skeletal Muscle. 5. DOI: 10.1186/s13395-015-0040-z. |
0.718 |
|
| 2014 |
Belanto JJ, Mader TL, Eckhoff MD, Strandjord DM, Banks GB, Gardner MK, Lowe DA, Ervasti JM. Microtubule binding distinguishes dystrophin from utrophin. Proceedings of the National Academy of Sciences of the United States of America. 111: 5723-8. PMID 24706788 DOI: 10.1073/Pnas.1323842111 |
0.719 |
|
| 2011 |
Henderson DM, Belanto JJ, Li B, Heun-Johnson H, Ervasti JM. Internal deletion compromises the stability of dystrophin. Human Molecular Genetics. 20: 2955-63. PMID 21558423 DOI: 10.1093/Hmg/Ddr199 |
0.741 |
|
| 2010 |
Belanto JJ, Diaz-Perez SV, Magyar CE, Maxwell MM, Yilmaz Y, Topp K, Boso G, Jamieson CH, Cacalano NA, Jamieson CA. Dexamethasone induces dysferlin in myoblasts and enhances their myogenic differentiation. Neuromuscular Disorders : Nmd. 20: 111-21. PMID 20080405 DOI: 10.1016/J.Nmd.2009.12.003 |
0.348 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2016 |
Osborn MJ, Belanto JJ, Tolar J, Voytas DF. Gene editing and its application for hematological diseases. International Journal of Hematology. 104: 18-28. PMID 27233509 DOI: 10.1007/S12185-016-2017-Z |
0.271 |
|
| 2017 |
Abudayyeh OO, Gootenberg JS, Essletzbichler P, Han S, Joung J, Belanto JJ, Verdine V, Cox DBT, Kellner MJ, Regev A, Lander ES, Voytas DF, Ting AY, Zhang F. RNA targeting with CRISPR-Cas13. Nature. PMID 28976959 DOI: 10.1038/Nature24049 |
0.227 |
|
| 2011 |
Jamieson C, Petrigliano F, Belanto J, Virk M, Coppola G, Tchieu J, Fu E, Magyar C, Raheem O, Kazarian M, Morris S, Cacalano N, Geschwind D, Tetradis S, Jamieson C, et al. 1451 GENOME-WIDE EXPRESSION PROFILING OF CASTRATION-RESISTANT PROSTATE CANCER XENOGRAFTS IN THE BONE-NICHE REVEALED UP-REGULATION OF THE ANTI-APOPTOSIS GENE, YWHAZ, A NETWORK MODULE HUB GENE Journal of Urology. 185. DOI: 10.1016/J.Juro.2011.02.1364 |
0.069 |
|
| Hide low-probability matches. |