Year |
Citation |
Score |
2020 |
Spurney C, Panigrahi A, Heier C, Tully C, Hamann K, Gordish-Dressman H, Soslow J, Olivieri L. NOVEL SERUM PROTEIN BIOMARKERS SIGNIFICANTLY UP-REGULATED IN LGE NEGATIVE DMD SUBJECTS Journal of the American College of Cardiology. 75: 1061. DOI: 10.1016/S0735-1097(20)31688-0 |
0.325 |
|
2015 |
Fiorillo AA, Heier CR, Novak JS, Tully CB, Brown KJ, Uaesoontrachoon K, Vila MC, Ngheim PP, Bello L, Kornegay JN, Angelini C, Partridge TA, Nagaraju K, Hoffman EP. TNF-α-Induced microRNAs Control Dystrophin Expression in Becker Muscular Dystrophy. Cell Reports. 12: 1678-90. PMID 26321630 DOI: 10.1016/J.Celrep.2015.07.066 |
0.324 |
|
2015 |
Heier CR, DiDonato CJ. ECG in neonate mice with spinal muscular atrophy allows assessment of drug efficacy. Frontiers in Bioscience (Elite Edition). 7: 107-16. PMID 25553367 DOI: 10.2741/E721 |
0.705 |
|
2015 |
Dillingham BC, Knoblach SM, Many GM, Harmon BT, Mullen AM, Heier CR, Bello L, McCall JM, Hoffman EP, Connor EM, Nagaraju K, Reeves EK, Damsker JM. VBP15, a novel anti-inflammatory, is effective at reducing the severity of murine experimental autoimmune encephalomyelitis. Cellular and Molecular Neurobiology. 35: 377-87. PMID 25392236 DOI: 10.1007/S10571-014-0133-Y |
0.333 |
|
2014 |
Heier CR, Guerron AD, Korotcov A, Lin S, Gordish-Dressman H, Fricke S, Sze RW, Hoffman EP, Wang P, Nagaraju K. Non-invasive MRI and spectroscopy of mdx mice reveal temporal changes in dystrophic muscle imaging and in energy deficits. Plos One. 9: e112477. PMID 25390038 DOI: 10.1371/Journal.Pone.0112477 |
0.368 |
|
2013 |
Heier CR, Damsker JM, Yu Q, Dillingham BC, Huynh T, Van der Meulen JH, Sali A, Miller BK, Phadke A, Scheffer L, Quinn J, Tatem K, Jordan S, Dadgar S, Rodriguez OC, et al. VBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects. Embo Molecular Medicine. 5: 1569-85. PMID 24014378 DOI: 10.1002/Emmm.201302621 |
0.34 |
|
2013 |
Huynh T, Uaesoontrachoon K, Quinn JL, Tatem KS, Heier CR, Van Der Meulen JH, Yu Q, Harris M, Nolan CJ, Haegeman G, Grounds MD, Nagaraju K. Selective modulation through the glucocorticoid receptor ameliorates muscle pathology in mdx mice. The Journal of Pathology. 231: 223-35. PMID 23794417 DOI: 10.1002/Path.4231 |
0.359 |
|
2013 |
Gogliotti RG, Cardona H, Singh J, Bail S, Emery C, Kuntz N, Jorgensen M, Durens M, Xia B, Barlow C, Heier CR, Plasterer HL, Jacques V, Kiledjian M, Jarecki J, et al. The DcpS inhibitor RG3039 improves survival, function and motor unit pathologies in two SMA mouse models. Human Molecular Genetics. 22: 4084-101. PMID 23736298 DOI: 10.1093/Hmg/Ddt258 |
0.717 |
|
2013 |
Damsker JM, Dillingham BC, Rose MC, Balsley MA, Heier CR, Watson AM, Stemmy EJ, Jurjus RA, Huynh T, Tatem K, Uaesoontrachoon K, Berry DM, Benton AS, Freishtat RJ, Hoffman EP, et al. VBP15, a glucocorticoid analogue, is effective at reducing allergic lung inflammation in mice. Plos One. 8: e63871. PMID 23667681 DOI: 10.1371/Journal.Pone.0063871 |
0.315 |
|
2012 |
Baudy AR, Reeves EK, Damsker JM, Heier C, Garvin LM, Dillingham BC, McCall J, Rayavarapu S, Wang Z, Vandermeulen JH, Sali A, Jahnke V, Duguez S, DuBois D, Rose MC, et al. Δ-9,11 modification of glucocorticoids dissociates nuclear factor-κB inhibitory efficacy from glucocorticoid response element-associated side effects. The Journal of Pharmacology and Experimental Therapeutics. 343: 225-32. PMID 22743576 DOI: 10.1124/Jpet.112.194340 |
0.325 |
|
2012 |
Gogliotti RG, Quinlan KA, Barlow CB, Heier CR, Heckman CJ, Didonato CJ. Motor neuron rescue in spinal muscular atrophy mice demonstrates that sensory-motor defects are a consequence, not a cause, of motor neuron dysfunction. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 3818-29. PMID 22423102 DOI: 10.1523/Jneurosci.5775-11.2012 |
0.7 |
|
2010 |
Heier CR, Hampton TG, Wang D, Didonato CJ. Development of electrocardiogram intervals during growth of FVB/N neonate mice. Bmc Physiology. 10: 16. PMID 20735846 DOI: 10.1186/1472-6793-10-16 |
0.668 |
|
2010 |
Heier CR, Satta R, Lutz C, DiDonato CJ. Arrhythmia and cardiac defects are a feature of spinal muscular atrophy model mice. Human Molecular Genetics. 19: 3906-18. PMID 20693262 DOI: 10.1093/Hmg/Ddq330 |
0.72 |
|
2009 |
Heier CR, DiDonato CJ. Translational readthrough by the aminoglycoside geneticin (G418) modulates SMN stability in vitro and improves motor function in SMA mice in vivo. Human Molecular Genetics. 18: 1310-22. PMID 19150990 DOI: 10.1093/Hmg/Ddp030 |
0.716 |
|
2008 |
Heier C, Hammond S, Gogliotti R, DiDonato C. G.P.4.12 Translational readthrough modulates SMN stability: Potential for aminoglycosides as an SMA therapy Neuromuscular Disorders. 18: 763-764. DOI: 10.1016/J.Nmd.2008.06.139 |
0.544 |
|
2007 |
Heier CR, Gogliotti RG, DiDonato CJ. SMN transcript stability: could modulation of messenger RNA degradation provide a novel therapy for spinal muscular atrophy? Journal of Child Neurology. 22: 1013-8. PMID 17761657 DOI: 10.1177/0883073807305669 |
0.687 |
|
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