Federica Montanaro - Publications

Affiliations: 
Biochemistry Ohio State University, Columbus, Columbus, OH 
Area:
Biochemistry

20 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Bourdon A, François V, Zhang L, Lafoux A, Fraysse B, Toumaniantz G, Larcher T, Girard T, Ledevin M, Lebreton C, Hivonnait A, Creismeas A, Allais M, Marie B, Guguin J, ... ... Montanaro F, et al. Evaluation of the dystrophin carboxy-terminal domain for micro-dystrophin gene therapy in cardiac and skeletal muscles in the DMD rat model. Gene Therapy. PMID 35105949 DOI: 10.1038/s41434-022-00317-6  0.309
2019 Omairi S, Hau KL, Collins-Hooper H, Scott C, Vaiyapuri S, Torelli S, Montanaro F, Matsakas A, Patel K. Regulation of the dystrophin-associated glycoprotein complex composition by the metabolic properties of muscle fibres. Scientific Reports. 9: 2770. PMID 30808964 DOI: 10.1038/s41598-019-39532-4  0.381
2013 He WA, Berardi E, Cardillo VM, Acharyya S, Aulino P, Thomas-Ahner J, Wang J, Bloomston M, Muscarella P, Nau P, Shah N, Butchbach ME, Ladner K, Adamo S, Rudnicki MA, ... ... Montanaro F, et al. NF-κB-mediated Pax7 dysregulation in the muscle microenvironment promotes cancer cachexia. The Journal of Clinical Investigation. 123: 4821-35. PMID 24084740 DOI: 10.1172/Jci68523  0.454
2013 Johnson EK, Li B, Yoon JH, Flanigan KM, Martin PT, Ervasti J, Montanaro F. Identification of new dystroglycan complexes in skeletal muscle. Plos One. 8: e73224. PMID 23951345 DOI: 10.1371/Journal.Pone.0073224  0.454
2013 Penton CM, Thomas-Ahner JM, Johnson EK, McAllister C, Montanaro F. Muscle side population cells from dystrophic or injured muscle adopt a fibro-adipogenic fate. Plos One. 8: e54553. PMID 23336007 DOI: 10.1371/Journal.Pone.0054553  0.448
2012 Johnson EK, Zhang L, Adams ME, Phillips A, Freitas MA, Froehner SC, Green-Church KB, Montanaro F. Proteomic analysis reveals new cardiac-specific dystrophin-associated proteins. Plos One. 7: e43515. PMID 22937058 DOI: 10.1371/Journal.Pone.0043515  0.424
2012 Yoon JH, Johnson E, Xu R, Martin LT, Martin PT, Montanaro F. Comparative proteomic profiling of dystroglycan-associated proteins in wild type, mdx, and Galgt2 transgenic mouse skeletal muscle. Journal of Proteome Research. 11: 4413-24. PMID 22775139 DOI: 10.1021/Pr300328R  0.484
2011 Beastrom N, Lu H, Macke A, Canan BD, Johnson EK, Penton CM, Kaspar BK, Rodino-Klapac LR, Zhou L, Janssen PM, Montanaro F. mdx(⁵cv) mice manifest more severe muscle dysfunction and diaphragm force deficits than do mdx Mice. The American Journal of Pathology. 179: 2464-74. PMID 21893021 DOI: 10.1016/J.Ajpath.2011.07.009  0.377
2011 Leblanc E, Trensz F, Haroun S, Drouin G, Bergeron E, Penton CM, Montanaro F, Roux S, Faucheux N, Grenier G. BMP-9-induced muscle heterotopic ossification requires changes to the skeletal muscle microenvironment. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 26: 1166-77. PMID 21611960 DOI: 10.1002/Jbmr.311  0.451
2011 Alexander MS, Kawahara G, Kho AT, Howell MH, Pusack TJ, Myers JA, Montanaro F, Zon LI, Guyon JR, Kunkel LM. Isolation and transcriptome analysis of adult zebrafish cells enriched for skeletal muscle progenitors. Muscle & Nerve. 43: 741-50. PMID 21337346 DOI: 10.1002/Mus.21972  0.408
2009 Kaspar RW, Allen HD, Ray WC, Alvarez CE, Kissel JT, Pestronk A, Weiss RB, Flanigan KM, Mendell JR, Montanaro F. Analysis of dystrophin deletion mutations predicts age of cardiomyopathy onset in becker muscular dystrophy. Circulation. Cardiovascular Genetics. 2: 544-51. PMID 20031633 DOI: 10.1161/Circgenetics.109.867242  0.333
2005 Guyon JR, Mosley AN, Jun SJ, Montanaro F, Steffen LS, Zhou Y, Nigro V, Zon LI, Kunkel LM. Delta-sarcoglycan is required for early zebrafish muscle organization. Experimental Cell Research. 304: 105-15. PMID 15707578 DOI: 10.1016/J.Yexcr.2004.10.032  0.395
2004 Montanaro F, Liadaki K, Schienda J, Flint A, Gussoni E, Kunkel LM. Demystifying SP cell purification: viability, yield, and phenotype are defined by isolation parameters. Experimental Cell Research. 298: 144-54. PMID 15242769 DOI: 10.1016/J.Yexcr.2004.04.010  0.374
2004 Tomczak KK, Marinescu VD, Ramoni MF, Sanoudou D, Montanaro F, Han M, Kunkel LM, Kohane IS, Beggs AH. Expression profiling and identification of novel genes involved in myogenic differentiation The Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 18: 403-405. PMID 14688207 DOI: 10.1096/Fj.03-0568Fje  0.325
2003 Montanaro F, Liadaki K, Volinski J, Flint A, Kunkel LM. Skeletal muscle engraftment potential of adult mouse skin side population cells Proceedings of the National Academy of Sciences of the United States of America. 100: 9336-9341. PMID 12886022 DOI: 10.1073/Pnas.1133179100  0.398
2003 Montanaro F, Carbonetto S. Targeting dystroglycan in the brain Neuron. 37: 193-196. PMID 12546815 DOI: 10.1016/S0896-6273(03)00032-1  0.417
1999 Montanaro F, Lindenbaum M, Carbonetto S. α-dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability Journal of Cell Biology. 145: 1325-1340. PMID 10366602 DOI: 10.1083/Jcb.145.6.1325  0.364
1998 Jacobson C, Montanaro F, Lindenbaum M, Carbonetto S, Ferns M. α-Dystroglycan functions in acetylcholine receptor aggregation but is not a coreceptor for agrin-MuSK signaling Journal of Neuroscience. 18: 6340-6348. PMID 9698325 DOI: 10.1523/Jneurosci.18-16-06340.1998  0.348
1995 Montanaro F, Carbonetto S, Campbell KP, Lindenbaum M. Dystroglycan expression in the wild type and mdx mouse neural retina: synaptic colocalization with dystrophin, dystrophin-related protein but not laminin. Journal of Neuroscience Research. 42: 528-38. PMID 8568939 DOI: 10.1002/Jnr.490420411  0.378
1994 Gee SH, Montanaro F, Lindenbaum MH, Carbonetto S. Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor. Cell. 77: 675-86. PMID 8205617 DOI: 10.1016/0092-8674(94)90052-3  0.342
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