| Year |
Citation |
Score |
| 2012 |
Rooney JE, Knapp JR, Hodges BL, Wuebbles RD, Burkin DJ. Laminin-111 protein therapy reduces muscle pathology and improves viability of a mouse model of merosin-deficient congenital muscular dystrophy. The American Journal of Pathology. 180: 1593-602. PMID 22322301 DOI: 10.1016/J.Ajpath.2011.12.019 |
0.794 |
|
| 2011 |
Doe JA, Wuebbles RD, Allred ET, Rooney JE, Elorza M, Burkin DJ. Transgenic overexpression of the α7 integrin reduces muscle pathology and improves viability in the dy(W) mouse model of merosin-deficient congenital muscular dystrophy type 1A. Journal of Cell Science. 124: 2287-97. PMID 21652631 DOI: 10.1242/Jcs.083311 |
0.656 |
|
| 2009 |
Welser JV, Rooney JE, Cohen NC, Gurpur PB, Singer CA, Evans RA, Haines BA, Burkin DJ. Myotendinous junction defects and reduced force transmission in mice that lack alpha7 integrin and utrophin. The American Journal of Pathology. 175: 1545-54. PMID 19729483 DOI: 10.2353/Ajpath.2009.090052 |
0.771 |
|
| 2009 |
Rooney JE, Gurpur PB, Burkin DJ. Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy. Proceedings of the National Academy of Sciences of the United States of America. 106: 7991-6. PMID 19416897 DOI: 10.1073/Pnas.0811599106 |
0.84 |
|
| 2009 |
Rooney JE, Gurpur PB, Yablonka-Reuveni Z, Burkin DJ. Laminin-111 restores regenerative capacity in a mouse model for alpha7 integrin congenital myopathy. The American Journal of Pathology. 174: 256-64. PMID 19074617 DOI: 10.2353/Ajpath.2009.080522 |
0.856 |
|
| 2006 |
Rooney JE, Welser JV, Dechert MA, Flintoff-Dye NL, Kaufman SJ, Burkin DJ. Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin. Journal of Cell Science. 119: 2185-95. PMID 16684813 DOI: 10.1242/Jcs.02952 |
0.766 |
|
| 2005 |
Flintoff-Dye NL, Welser J, Rooney J, Scowen P, Tamowski S, Hatton W, Burkin DJ. Role for the alpha7beta1 integrin in vascular development and integrity. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 234: 11-21. PMID 16003770 DOI: 10.1002/Dvdy.20462 |
0.75 |
|
| 1993 |
Fertala A, Westerhausen A, Morris G, Rooney JE, Prockop DJ. Two cysteine substitutions in procollagen I: a glycine replacement near the N-terminus of alpha 1(I) chain causes lethal osteogenesis imperfecta and a glycine replacement in the alpha 2(I) chain markedly destabilizes the triple helix. The Biochemical Journal. 289: 195-9. PMID 8424758 DOI: 10.1042/Bj2890195 |
0.376 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2020 |
Pham HT, Kram V, Dar QA, Komori T, Ji Y, Mohassel P, Rooney J, Li L, Kilts TM, Bonnemann C, Lamande S, Young MF. Collagen VIα2 chain deficiency causes trabecular bone loss by potentially promoting osteoclast differentiation through enhanced TNFα signaling. Scientific Reports. 10: 13749. PMID 32792616 DOI: 10.1038/s41598-020-70730-7 |
0.206 |
|
| 2020 |
Foley AR, Zou Y, Dunford JE, Rooney J, Chandra G, Xiong H, Straub V, Voit T, Romero N, Donkervoort S, Hu Y, Markello T, Horn A, Qebibo L, Dastgir J, et al. GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome. Annals of Neurology. PMID 32403198 DOI: 10.1002/Ana.25772 |
0.155 |
|
| 2015 |
Zukosky K, Meilleur K, Traynor BJ, Dastgir J, Medne L, Devoto M, Collins J, Rooney J, Zou Y, Yang ML, Gibbs JR, Meier M, Stetefeld J, Finkel RS, Schessl J, et al. Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family. Jama Neurology. 72: 689-98. PMID 25938801 DOI: 10.1001/Jamaneurol.2015.37 |
0.086 |
|
| 1989 |
Ganguly A, Rooney JE, Hosomi S, Zeiger AR, Prockop DJ. Detection and location of single-base mutations in large DNA fragments by immunomicroscopy. Genomics. 4: 530-8. PMID 2744763 DOI: 10.1016/0888-7543(89)90276-0 |
0.044 |
|
| Hide low-probability matches. |