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Christopher R. Heier, Ph.D. - Publications

Affiliations: 
2010 Integrated Graduate Program in the Life Sciences Northwestern University, Evanston, IL 
Area:
Molecular Neuroscience, Motor Control, Neurobiology of Disease
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16 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
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  0.324
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  0.706
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  0.332
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  0.339
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  0.358
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  0.715
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  0.314
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  0.699
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  0.669
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  0.721
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  0.718
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  0.545
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  0.685
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