Hana M. Odeh, Ph.D. - Publications

2004 University of Michigan, Ann Arbor, Ann Arbor, MI 
Genetics, Molecular Biology, Neuroscience Biology, Audiology

14 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 Guo L, Mann JR, Mauna JC, Copley KE, Wang H, Rubien JD, Odeh HM, Lin J, Lee BL, Ganser L, Robinson E, Kim KM, Murthy AC, Paul T, Portz B, et al. Defining RNA oligonucleotides that reverse deleterious phase transitions of RNA-binding proteins with prion-like domains. Biorxiv : the Preprint Server For Biology. PMID 37732211 DOI: 10.1101/2023.09.04.555754  0.636
2023 Balendra R, Ruiz de Los Mozos I, Odeh HM, Glaria I, Milioto C, Wilson KM, Ule AM, Hallegger M, Masino L, Martin S, Patani R, Shorter J, Ule J, Isaacs AM. Transcriptome-wide RNA binding analysis of C9orf72 poly(PR) dipeptides. Life Science Alliance. 6. PMID 37438085 DOI: 10.26508/lsa.202201824  0.647
2023 Rhine K, Odeh HM, Shorter J, Myong S. Regulation of Biomolecular Condensates by Poly(ADP-ribose). Chemical Reviews. PMID 37115110 DOI: 10.1021/acs.chemrev.2c00851  0.521
2022 Odeh HM, Shorter J. Aggregates of TDP-43 protein spiral into view. Nature. 601: 29-30. PMID 34880481 DOI: 10.1038/d41586-021-03605-0  0.458
2021 Odeh HM, Fare CM, Shorter J. Nuclear-import receptors counter deleterious phase transitions in neurodegenerative disease. Journal of Molecular Biology. 167220. PMID 34464655 DOI: 10.1016/j.jmb.2021.167220  0.758
2021 Hallegger M, Chakrabarti AM, Lee FCY, Lee BL, Amalietti AG, Odeh HM, Copley KE, Rubien JD, Portz B, Kuret K, Huppertz I, Rau F, Patani R, Fawzi NL, Shorter J, et al. TDP-43 condensation properties specify its RNA-binding and regulatory repertoire. Cell. PMID 34380047 DOI: 10.1016/j.cell.2021.07.018  0.714
2020 Hutten S, Usluer S, Bourgeois B, Simonetti F, Odeh HM, Fare CM, Czuppa M, Hruska-Plochan M, Hofweber M, Polymenidou M, Shorter J, Edbauer D, Madl T, Dormann D. Nuclear Import Receptors Directly Bind to Arginine-Rich Dipeptide Repeat Proteins and Suppress Their Pathological Interactions. Cell Reports. 33: 108538. PMID 33357437 DOI: 10.1016/j.celrep.2020.108538  0.76
2020 Cook CN, Wu Y, Odeh HM, Gendron TF, Jansen-West K, Del Rosso G, Yue M, Jiang P, Gomes E, Tong J, Daughrity LM, Avendano NM, Castanedes-Casey M, Shao W, Oskarsson B, et al. poly(GR) aggregation induces TDP-43 proteinopathy. Science Translational Medicine. 12. PMID 32878979 DOI: 10.1126/Scitranslmed.Abb3774  0.641
2020 Odeh HM, Shorter J. Arginine-rich dipeptide-repeat proteins as phase disruptors in C9-ALS/FTD. Emerging Topics in Life Sciences. PMID 32639008 DOI: 10.1042/ETLS20190167  0.541
2020 Odeh HM, Shorter J. The Sense of Targeting Nonsense-Mediated Decay in C9-ALS/FTD. Neuron. 106: 6-9. PMID 32272067 DOI: 10.1016/J.Neuron.2020.03.017  0.535
2018 Odeh HM, Coyaud E, Raught B, Matunis MJ. The SUMO-Specific Isopeptidase SENP2 is Targeted to Intracellular Membranes via a Predicted N-Terminal Amphipathic α-Helix. Molecular Biology of the Cell. mbcE17070445. PMID 29874116 DOI: 10.1091/Mbc.E17-07-0445  0.593
2010 Odeh H, Hunker KL, Belyantseva IA, Azaiez H, Avenarius MR, Zheng L, Peters LM, Gagnon LH, Hagiwara N, Skynner MJ, Brilliant MH, Allen ND, Riazuddin S, Johnson KR, Raphael Y, et al. Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse. American Journal of Human Genetics. 86: 148-60. PMID 20137774 DOI: 10.1016/J.Ajhg.2010.01.016  0.664
2004 Odeh H, Hagiwara N, Skynner M, Mitchem KL, Beyer LA, Allen ND, Brilliant MH, Lebart MC, Dolan DF, Raphael Y, Kohrman DC. Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus. Audiology & Neuro-Otology. 9: 303-14. PMID 15347914 DOI: 10.1159/000080701  0.646
2003 Karolyi IJ, Probst FJ, Beyer L, Odeh H, Dootz G, Cha KB, Martin DM, Avraham KB, Kohrman D, Dolan DF, Raphael Y, Camper SA. Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia. Human Molecular Genetics. 12: 2797-805. PMID 12966030 DOI: 10.1093/Hmg/Ddg308  0.643
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