Joanna M Dragich - Publications

Affiliations: 
 
Area:
Neuroscience, neuropathology, neurodevelopment, neurodegeneration, neurogenetics

18 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
2019 Fox LM, Kim K, Johnson CW, Chen S, Croce KR, Victor MB, Eenjes E, Bosco JR, Randolph LK, Dragatsis I, Dragich JM, Yoo AS, Yamamoto A. Huntington's Disease Pathogenesis Is Modified In Vivo by Alfy/Wdfy3 and Selective Macroautophagy. Neuron. PMID 31899071 DOI: 10.1016/J.Neuron.2019.12.003  0.719
2018 Marsh D, Dragich JM. Autophagy in mammalian neurodevelopment and implications for childhood neurological disorders. Neuroscience Letters. PMID 29665429 DOI: 10.1016/j.neulet.2018.04.017  0.752
2016 Dragich JM, Kuwajima T, Hirose-Ikeda M, Yoon MS, Eenjes E, Bosco JR, Fox LM, Lystad AH, Oo TF, Yarygina O, Mita T, Waguri S, Ichimura Y, Komatsu M, Simonsen A, et al. Autophagy linked FYVE (Alfy/WDFY3) is required for establishing neuronal connectivity in the mammalian brain. Elife. 5. PMID 27648578 DOI: 10.7554/Elife.14810  0.752
2016 Eenjes E, Dragich JM, Kampinga HH, Yamamoto A. Distinguishing aggregate formation and aggregate clearance using cell based assays. Journal of Cell Science. PMID 26818841 DOI: 10.1242/Jcs.179978  0.763
2016 Dragich JM, Kuwajima T, Hirose-Ikeda M, Yoon MS, Eenjes E, Bosco JR, Fox LM, Lystad AH, Oo TF, Yarygina O, Mita T, Waguri S, Ichimura Y, Komatsu M, Simonsen A, et al. Author response: Autophagy linked FYVE (Alfy/WDFY3) is required for establishing neuronal connectivity in the mammalian brain Elife. DOI: 10.7554/Elife.14810.026  0.737
2016 Eenjes E, Dragich JM, Kampinga HH, Yamamoto A. Distinguishing aggregate formation and aggregate clearance using cell-based assays Journal of Cell Science. 129: 1260-1270. DOI: 10.1242/jcs.179978  0.741
2011 Loh DH, Dragich JM, Kudo T, Schroeder AM, Nakamura TJ, Waschek JA, Block GD, Colwell CS. Effects of vasoactive intestinal peptide genotype on circadian gene expression in the suprachiasmatic nucleus and peripheral organs. Journal of Biological Rhythms. 26: 200-9. PMID 21628547 DOI: 10.1177/0748730411401740  0.759
2010 Dragich JM, Loh DH, Wang LM, Vosko AM, Kudo T, Nakamura TJ, Odom IH, Tateyama S, Hagopian A, Waschek JA, Colwell CS. The role of the neuropeptides PACAP and VIP in the photic regulation of gene expression in the suprachiasmatic nucleus. The European Journal of Neuroscience. 31: 864-75. PMID 20180841 DOI: 10.1111/J.1460-9568.2010.07119.X  0.735
2010 Itri JN, Vosko AM, Schroeder A, Dragich JM, Michel S, Colwell CS. Circadian regulation of a-type potassium currents in the suprachiasmatic nucleus. Journal of Neurophysiology. 103: 632-40. PMID 19939959 DOI: 10.1152/Jn.00670.2009  0.718
2009 Wang LM, Dragich JM, Kudo T, Odom IH, Welsh DK, O'Dell TJ, Colwell CS. Expression of the circadian clock gene Period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour. Asn Neuro. 1. PMID 19570032 DOI: 10.1042/An20090020  0.796
2008 Chaudhury D, Loh DH, Dragich JM, Hagopian A, Colwell CS. Select cognitive deficits in vasoactive intestinal peptide deficient mice. Bmc Neuroscience. 9: 63. PMID 18616823 DOI: 10.1186/1471-2202-9-63  0.768
2007 Dragich JM, Kim YH, Arnold AP, Schanen NC. Differential distribution of the MeCP2 splice variants in the postnatal mouse brain. The Journal of Comparative Neurology. 501: 526-42. PMID 17278130 DOI: 10.1002/Cne.21264  0.777
2002 Hammer S, Dorrani N, Dragich J, Kudo S, Schanen C. The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome Mental Retardation and Developmental Disabilities Research Reviews. 8: 94-98. PMID 12112734 DOI: 10.1002/Mrdd.10023  0.737
2001 Kudo S, Nomura Y, Segawa M, Fujita N, Nakao M, Dragich J, Schanen C, Tamura M. Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems Brain and Development. 23: S165-S173. PMID 11738866 DOI: 10.1016/S0387-7604(01)00345-X  0.751
2000 Dragich J, Houwink-Manville I, Schanen C. Rett syndrome: A surprising result of mutation in MECP2 Human Molecular Genetics. 9: 2365-2375. PMID 11005791 DOI: 10.1093/Hmg/9.16.2365  0.751
2000 Jordan-Sciutto KL, Dragich JM, Caltagarone J, Hall DJ, Bowser R. Fetal Alz-50 clone 1 (FAC1) protein interacts with the Myc-associated zinc finger protein (ZF87/MAZ) and alters its transcriptional activity. Biochemistry. 39: 3206-15. PMID 10727212 DOI: 10.1021/Bi992211Q  0.778
1999 Jordan-Sciutto KL, Dragich JM, Rhodes JL, Bowser R. Fetal Alz-50 clone 1, a novel zinc finger protein, binds a specific DNA sequence and acts as a transcriptional regulator. The Journal of Biological Chemistry. 274: 35262-8. PMID 10575013 DOI: 10.1074/Jbc.274.49.35262  0.771
1999 Jordan-Sciutto KL, Dragich JM, Bowser R. DNA binding activity of the fetal Alz-50 clone 1 (FAC1) protein is enhanced by phosphorylation. Biochemical and Biophysical Research Communications. 260: 785-9. PMID 10403843 DOI: 10.1006/Bbrc.1999.0986  0.776
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