Wilfried Rossoll - Publications

Mayo Clinic Florida 
Motor Neuron DIseases

31 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 McEachin ZT, Gendron TF, Raj N, García-Murias M, Banerjee A, Purcell RH, Ward PJ, Todd TW, Merritt-Garza ME, Jansen-West K, Hales CM, García-Sobrino T, Quintáns B, Holler CJ, Taylor G, ... ... Rossoll W, et al. Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36. Neuron. PMID 32375063 DOI: 10.1016/j.neuron.2020.04.011  0.92
2020 Todd TW, McEachin ZT, Chew J, Burch AR, Jansen-West K, Tong J, Yue M, Song Y, Castanedes-Casey M, Kurti A, Dunmore JH, Fryer JD, Zhang YJ, San Millan B, Teijeira Bautista S, ... ... Rossoll W, et al. Hexanucleotide Repeat Expansions in c9FTD/ALS and SCA36 Confer Selective Patterns of Neurodegeneration In Vivo. Cell Reports. 31: 107616. PMID 32375043 DOI: 10.1016/j.celrep.2020.107616  0.92
2020 Fallini C, Khalil B, Smith CL, Rossoll W. Traffic jam at the nuclear pore: All roads lead to nucleocytoplasmic transport defects in ALS/FTD. Neurobiology of Disease. 104835. PMID 32179176 DOI: 10.1016/j.nbd.2020.104835  0.64
2019 Rossoll W, Bassell GJ. Crosstalk of Local Translation and Mitochondria: Powering Plasticity in Axons and Dendrites. Neuron. 101: 204-206. PMID 30653934 DOI: 10.1016/j.neuron.2018.12.027  0.92
2018 Chou CC, Zhang Y, Umoh ME, Vaughan SW, Lorenzini I, Liu F, Sayegh M, Donlin-Asp PG, Chen YH, Duong DM, Seyfried NT, Powers MA, Kukar T, Hales CM, Gearing M, ... ... Rossoll W, et al. TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD. Nature Neuroscience. PMID 29311743 DOI: 10.1038/s41593-017-0047-3  0.76
2017 Donlin-Asp PG, Rossoll W, Bassell GJ. Spatially and temporally regulating translation via mRNA-binding proteins in cellular and neuronal function. Febs Letters. PMID 28295262 DOI: 10.1002/1873-3468.12621  0.92
2017 Donlin-Asp PG, Fallini C, Campos J, Chou CC, Merritt ME, Phan HC, Bassell GJ, Rossoll W. The Survival of Motor Neuron Protein Acts as a Molecular Chaperone for mRNP Assembly. Cell Reports. 18: 1660-1673. PMID 28199839 DOI: 10.1016/j.celrep.2017.01.059  0.92
2016 Wang ET, Taliaferro JM, Lee JA, Sudhakaran IP, Rossoll W, Gross C, Moss KR, Bassell GJ. Dysregulation of mRNA Localization and Translation in Genetic Disease. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 11418-11426. PMID 27911744 DOI: 10.1523/JNEUROSCI.2352-16.2016  0.92
2016 Holler CJ, Taylor G, McEachin ZT, Deng Q, Watkins WJ, Hudson K, Easley CA, Hu WT, Hales CM, Rossoll W, Bassell GJ, Kukar T. Trehalose upregulates progranulin expression in human and mouse models of GRN haploinsufficiency: a novel therapeutic lead to treat frontotemporal dementia. Molecular Neurodegeneration. 11: 46. PMID 27341800 DOI: 10.1186/s13024-016-0114-3  0.64
2016 Donlin-Asp PG, Bassell GJ, Rossoll W. A role for the survival of motor neuron protein in mRNP assembly and transport. Current Opinion in Neurobiology. 39: 53-61. PMID 27131421 DOI: 10.1016/j.conb.2016.04.004  0.92
2016 Fallini C, Donlin-Asp PG, Rouanet JP, Bassell GJ, Rossoll W. Deficiency of the Survival of Motor Neuron Protein Impairs mRNA Localization and Local Translation in the Growth Cone of Motor Neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 3811-20. PMID 27030765 DOI: 10.1523/JNEUROSCI.2396-15.2016  0.92
2015 Chou CC, Alexeeva OM, Yamada S, Pribadi A, Zhang Y, Mo B, Williams KR, Zarnescu DC, Rossoll W. PABPN1 suppresses TDP-43 toxicity in ALS disease models. Human Molecular Genetics. PMID 26130692 DOI: 10.1093/hmg/ddv238  0.64
2014 Fallini C, Rouanet JP, Donlin-Asp PG, Guo P, Zhang H, Singer RH, Rossoll W, Bassell GJ. Dynamics of survival of motor neuron (SMN) protein interaction with the mRNA-binding protein IMP1 facilitates its trafficking into motor neuron axons. Developmental Neurobiology. 74: 319-32. PMID 23897586 DOI: 10.1002/dneu.22111  0.64
2012 Wu CH, Fallini C, Ticozzi N, Keagle PJ, Sapp PC, Piotrowska K, Lowe P, Koppers M, McKenna-Yasek D, Baron DM, Kost JE, Gonzalez-Perez P, Fox AD, Adams J, Taroni F, ... ... Rossoll W, et al. Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis. Nature. 488: 499-503. PMID 22801503 DOI: 10.1038/nature11280  0.92
2012 Dammer EB, Fallini C, Gozal YM, Duong DM, Rossoll W, Xu P, Lah JJ, Levey AI, Peng J, Bassell GJ, Seyfried NT. Coaggregation of RNA-binding proteins in a model of TDP-43 proteinopathy with selective RGG motif methylation and a role for RRM1 ubiquitination. Plos One. 7: e38658. PMID 22761693 DOI: 10.1371/journal.pone.0038658  0.64
2012 Fallini C, Bassell GJ, Rossoll W. The ALS disease protein TDP-43 is actively transported in motor neuron axons and regulates axon outgrowth. Human Molecular Genetics. 21: 3703-18. PMID 22641816 DOI: 10.1093/hmg/dds205  0.64
2012 Fallini C, Bassell GJ, Rossoll W. Spinal muscular atrophy: the role of SMN in axonal mRNA regulation. Brain Research. 1462: 81-92. PMID 22330725 DOI: 10.1016/j.brainres.2012.01.044  0.64
2011 Fallini C, Zhang H, Su Y, Silani V, Singer RH, Rossoll W, Bassell GJ. The survival of motor neuron (SMN) protein interacts with the mRNA-binding protein HuD and regulates localization of poly(A) mRNA in primary motor neuron axons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 3914-25. PMID 21389246 DOI: 10.1523/JNEUROSCI.3631-10.2011  0.64
2011 Peter CJ, Evans M, Thayanithy V, Taniguchi-Ishigaki N, Bach I, Kolpak A, Bassell GJ, Rossoll W, Lorson CL, Bao ZZ, Androphy EJ. The COPI vesicle complex binds and moves with survival motor neuron within axons. Human Molecular Genetics. 20: 1701-11. PMID 21300694 DOI: 10.1093/hmg/ddr046  0.64
2010 Fallini C, Bassell GJ, Rossoll W. High-efficiency transfection of cultured primary motor neurons to study protein localization, trafficking, and function. Molecular Neurodegeneration. 5: 17. PMID 20406490 DOI: 10.1186/1750-1326-5-17  0.64
2010 Glinka M, Herrmann T, Funk N, Havlicek S, Rossoll W, Winkler C, Sendtner M. The heterogeneous nuclear ribonucleoprotein-R is necessary for axonal beta-actin mRNA translocation in spinal motor neurons. Human Molecular Genetics. 19: 1951-66. PMID 20167579 DOI: 10.1093/hmg/ddq073  0.64
2009 Rossoll W, Bassell GJ. Spinal muscular atrophy and a model for survival of motor neuron protein function in axonal ribonucleoprotein complexes. Results and Problems in Cell Differentiation. 48: 289-326. PMID 19343312 DOI: 10.1007/400_2009_4  0.64
2008 Oprea GE, Kröber S, McWhorter ML, Rossoll W, Müller S, Krawczak M, Bassell GJ, Beattie CE, Wirth B. Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy. Science (New York, N.Y.). 320: 524-7. PMID 18440926 DOI: 10.1126/science.1155085  0.64
2006 Zhang H, Xing L, Rossoll W, Wichterle H, Singer RH, Bassell GJ. Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 8622-32. PMID 16914688 DOI: 10.1523/JNEUROSCI.3967-05.2006  0.64
2006 Ito Y, Wiese S, Funk N, Chittka A, Rossoll W, Bömmel H, Watabe K, Wegner M, Sendtner M. Sox10 regulates ciliary neurotrophic factor gene expression in Schwann cells. Proceedings of the National Academy of Sciences of the United States of America. 103: 7871-6. PMID 16684879 DOI: 10.1073/pnas.0602332103  0.64
2005 Götz R, Wiese S, Takayama S, Camarero GC, Rossoll W, Schweizer U, Troppmair J, Jablonka S, Holtmann B, Reed JC, Rapp UR, Sendtner M. Bag1 is essential for differentiation and survival of hematopoietic and neuronal cells. Nature Neuroscience. 8: 1169-78. PMID 16116448 DOI: 10.1038/nn1524  0.64
2004 Grohmann K, Rossoll W, Kobsar I, Holtmann B, Jablonka S, Wessig C, Stoltenburg-Didinger G, Fischer U, Hübner C, Martini R, Sendtner M. Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1). Human Molecular Genetics. 13: 2031-42. PMID 15269181 DOI: 10.1093/hmg/ddh222  0.64
2003 Rossoll W, Jablonka S, Andreassi C, Kröning AK, Karle K, Monani UR, Sendtner M. Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons. The Journal of Cell Biology. 163: 801-12. PMID 14623865 DOI: 10.1083/jcb.200304128  0.64
2002 Bommel H, Xie G, Rossoll W, Wiese S, Jablonka S, Boehm T, Sendtner M. Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease. The Journal of Cell Biology. 159: 563-9. PMID 12446740 DOI: 10.1083/jcb.200208001  0.64
2002 Jablonka S, Holtmann B, Meister G, Bandilla M, Rossoll W, Fischer U, Sendtner M. Gene targeting of Gemin2 in mice reveals a correlation between defects in the biogenesis of U snRNPs and motoneuron cell death. Proceedings of the National Academy of Sciences of the United States of America. 99: 10126-31. PMID 12091709 DOI: 10.1073/pnas.152318699  0.64
2002 Rossoll W, Kröning AK, Ohndorf UM, Steegborn C, Jablonka S, Sendtner M. Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons? Human Molecular Genetics. 11: 93-105. PMID 11773003  0.64
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