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Christine Didonato - Publications

Affiliations: 
Northwestern University, Evanston, IL 
Area:
Molecular Neuroscience, Motor Control, Neurobiology of Disease
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29 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
2023 Glascock J, Darras BT, Crawford TO, Sumner CJ, Kolb SJ, DiDonato C, Elsheikh B, Howell K, Farwell W, Valente M, Petrillo M, Tingey J, Jarecki J. Identifying Biomarkers of Spinal Muscular Atrophy for Further Development. Journal of Neuromuscular Diseases. PMID 37458045 DOI: 10.3233/JND-230054  0.462
2021 Ojala KS, Reedich EJ, DiDonato CJ, Meriney SD. In Search of a Cure: The Development of Therapeutics to Alter the Progression of Spinal Muscular Atrophy. Brain Sciences. 11. PMID 33562482 DOI: 10.3390/brainsci11020194  0.359
2020 Reedich EJ, Kalski M, Armijo N, Cox GA, DiDonato CJ. Spinal motor neuron loss occurs through a p53-and-p21-independent mechanism in the Smn mouse model of spinal muscular atrophy. Experimental Neurology. 337: 113587. PMID 33382987 DOI: 10.1016/j.expneurol.2020.113587  0.471
2020 Harada Y, Rao VK, Arya K, Kuntz NL, DiDonato CJ, Napchan-Pomerantz G, Agarwal A, Stefans V, Katsuno M, Veerapandiyan A. Combination molecular therapies for type 1 spinal muscular atrophy. Muscle & Nerve. PMID 32710634 DOI: 10.1002/Mus.27034  0.368
2019 Quinlan KA, Reedich E, Arnold WD, Puritz A, Cavarsan CF, Heckman CJ, DiDonato CJ. Hyperexcitability precedes motoneuron loss in the mouse model of spinal muscular atrophy. Journal of Neurophysiology. PMID 31365319 DOI: 10.1152/jn.00652.2018  0.457
2017 Cherry JJ, DiDonato CJ, Androphy EJ, Calo A, Potter K, Custer SK, Du S, Foley TL, Gopalsamy A, Reedich EJ, Gordo SM, Gordon W, Hosea N, Jones LH, Krizay DK, et al. In vitro and in vivo effects of 2,4 diaminoquinazoline inhibitors of the decapping scavenger enzyme DcpS: Context-specific modulation of SMN transcript levels. Plos One. 12: e0185079. PMID 28945765 DOI: 10.1371/Journal.Pone.0185079  0.477
2016 Genç B, Jara JH, Schultz MC, Manuel M, Stanford MJ, Gautam M, Klessner JL, Sekerkova G, Heller DB, Cox GA, Heckman CJ, DiDonato CJ, Özdinler PH. Absence of UCHL 1 function leads to selective motor neuropathy. Annals of Clinical and Translational Neurology. 3: 331-45. PMID 27231703 DOI: 10.1002/Acn3.298  0.382
2015 Singh NN, Lee BM, DiDonato CJ, Singh RN. Mechanistic principles of antisense targets for the treatment of spinal muscular atrophy. Future Medicinal Chemistry. PMID 26381381 DOI: 10.4155/fmc.15.101  0.321
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  0.744
2014 Keil JM, Seo J, Howell MD, Hsu WH, Singh RN, DiDonato CJ. A short antisense oligonucleotide ameliorates symptoms of severe mouse models of spinal muscular atrophy. Molecular Therapy. Nucleic Acids. 3: e174. PMID 25004100 DOI: 10.1038/Mtna.2014.23  0.462
2013 Sivanesan S, Howell MD, Didonato CJ, Singh RN. Antisense oligonucleotide mediated therapy of spinal muscular atrophy. Translational Neuroscience. 4. PMID 24265944 DOI: 10.2478/S13380-013-0109-2  0.443
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, ... ... DiDonato CJ, 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  0.764
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  0.75
2011 Gogliotti RG, Lutz C, Jorgensen M, Huebsch K, Koh S, Didonato CJ. Characterization of a commonly used mouse model of SMA reveals increased seizure susceptibility and heightened fear response in FVB/N mice. Neurobiology of Disease. 43: 142-51. PMID 21396450 DOI: 10.1016/j.nbd.2011.03.002  0.74
2010 Hammond SM, Gogliotti RG, Rao V, Beauvais A, Kothary R, DiDonato CJ. Mouse survival motor neuron alleles that mimic SMN2 splicing and are inducible rescue embryonic lethality early in development but not late. Plos One. 5: e15887. PMID 21249120 DOI: 10.1371/Journal.Pone.0015887  0.784
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  0.709
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  0.768
2010 Gogliotti RG, Hammond SM, Lutz C, Didonato CJ. Molecular and phenotypic reassessment of an infrequently used mouse model for spinal muscular atrophy. Biochemical and Biophysical Research Communications. 391: 517-22. PMID 19961830 DOI: 10.1016/J.Bbrc.2009.11.090  0.784
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  0.747
2008 Gavrilina TO, McGovern VL, Workman E, Crawford TO, Gogliotti RG, DiDonato CJ, Monani UR, Morris GE, Burghes AH. Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect. Human Molecular Genetics. 17: 1063-75. PMID 18178576 DOI: 10.1093/Hmg/Ddm379  0.774
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  0.718
2007 Schmid A, DiDonato CJ. Animal models of spinal muscular atrophy. Journal of Child Neurology. 22: 1004-12. PMID 17761656 DOI: 10.1177/0883073807305667  0.473
2007 Kostova FV, Williams VC, Heemskerk J, Iannaccone S, Didonato C, Swoboda K, Maria BL. Spinal muscular atrophy: classification, diagnosis, management, pathogenesis, and future research directions. Journal of Child Neurology. 22: 926-45. PMID 17761647 DOI: 10.1177/0883073807305662  0.376
2003 DiDonato CJ, Parks RJ, Kothary R. Development of a gene therapy strategy for the restoration of survival motor neuron protein expression: implications for spinal muscular atrophy therapy. Human Gene Therapy. 14: 179-88. PMID 12614569 DOI: 10.1089/104303403321070874  0.439
2002 Young PJ, DiDonato CJ, Hu D, Kothary R, Androphy EJ, Lorson CL. SRp30c-dependent stimulation of survival motor neuron (SMN) exon 7 inclusion is facilitated by a direct interaction with hTra2 beta 1. Human Molecular Genetics. 11: 577-87. PMID 11875052 DOI: 10.1093/Hmg/11.5.577  0.348
2001 DiDonato CJ, Lorson CL, De Repentigny Y, Simard L, Chartrand C, Androphy EJ, Kothary R. Regulation of murine survival motor neuron (Smn) protein levels by modifying Smn exon 7 splicing. Human Molecular Genetics. 10: 2727-36. PMID 11726560 DOI: 10.1093/Hmg/10.23.2727  0.466
1999 DiDonato CJ, Brun T, Simard LR. Complete nucleotide sequence, genomic organization, and promoter analysis of the murine survival motor neuron gene (Smn) Mammalian Genome. 10: 638-641. PMID 10341102 DOI: 10.1007/s003359901061  0.331
1997 DiDonato CJ, Chen XN, Noya D, Korenberg JR, Nadeau JH, Simard LR. Cloning, characterization, and copy number of the murine survival motor neuron gene: homolog of the spinal muscular atrophy-determining gene. Genome Research. 7: 339-52. PMID 9110173 DOI: 10.1101/Gr.7.4.339  0.367
1997 DiDonato CJ, Ingraham SE, Mendell JR, Prior TW, Lenard S, Moxley RT, Florence J, Burghes AHM. Deletion and conversion in spinal muscular atrophy patients: Is there a relationship to severity? Annals of Neurology. 41: 230-237. PMID 9029072 DOI: 10.1002/ana.410410214  0.353
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