| Year | Citation | Score | |||
|---|---|---|---|---|---|
| 2023 | Urzi A, Lahmann I, Nguyen LVN, Rost BR, García-Pérez A, Lelievre N, Merritt-Garza ME, Phan HC, Bassell GJ, Rossoll W, Diecke S, Kunz S, Schmitz D, Gouti M. Efficient generation of a self-organizing neuromuscular junction model from human pluripotent stem cells. Nature Communications. 14: 8043. PMID 38114482 DOI: 10.1038/s41467-023-43781-3 | 0.586 | |||
| 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 | 0.572 | |||
| 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 | 0.64 | |||
| 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 | 0.452 | |||
| 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 | 0.624 | |||
| 2018 | Price PL, Morderer D, Rossoll W. RNP Assembly Defects in Spinal Muscular Atrophy. Advances in Neurobiology. 20: 143-171. PMID 29916019 DOI: 10.1007/978-3-319-89689-2_6 | 0.62 | |||
| 2018 | Khalil B, Morderer D, Price PL, Liu F, Rossoll W. mRNP assembly, axonal transport, and local translation in neurodegenerative diseases. Brain Research. PMID 29462608 DOI: 10.1016/J.Brainres.2018.02.018 | 0.526 | |||
| 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 | 0.442 | |||
| 2017 | Coyne AN, Lorenzini I, Chou CC, Torvund M, Rogers RS, Starr A, Zaepfel BL, Levy J, Johannesmeyer J, Schwartz JC, Nishimune H, Zinsmaier K, Rossoll W, Sattler R, Zarnescu DC. Post-transcriptional Inhibition of Hsc70-4/HSPA8 Expression Leads to Synaptic Vesicle Cycling Defects in Multiple Models of ALS. Cell Reports. 21: 110-125. PMID 28978466 DOI: 10.1016/J.Celrep.2017.09.028 | 0.51 | |||
| 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 | 0.639 | |||
| 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 | 0.734 | |||
| 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 | 0.635 | |||
| 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 | 0.643 | |||
| 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 | 0.72 | |||
| 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 | 0.756 | |||
| 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 | 0.44 | |||
| 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 | 0.764 | |||
| 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 | 0.649 | |||
| 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 | 0.614 | |||
| 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 | 0.757 | |||
| 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 | 0.76 | |||
| 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 | 0.756 | |||
| 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 | 0.749 | |||
| 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 | 0.739 | |||
| 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 | 0.695 | |||
| 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 | 0.763 | |||
| 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 | 0.722 | |||
| 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 | 0.738 | |||
| 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 | 0.566 | |||
| 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 | 0.595 | |||
| 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 | 0.719 | |||
| 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 | 0.633 | |||
| 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 | 0.651 | |||
| 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 | 0.688 | |||
| 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 DOI: 10.1093/Hmg/11.1.93 | 0.718 | |||
| 2000 | Jablonka S, Rossoll W, Schrank B, Sendtner M. The role of SMN in spinal muscular atrophy. Journal of Neurology. 247: I37-42. PMID 10795885 DOI: 10.1007/S004150050555 | 0.619 | |||
| 2000 | Jablonka S, Schrank B, Kralewski M, Rossoll W, Sendtner M. Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III. Human Molecular Genetics. 9: 341-6. PMID 10655542 DOI: 10.1093/Hmg/9.3.341 | 0.695 | |||
| 2000 | Monani UR, Sendtner M, Coovert DD, Parsons DW, Andreassi C, Le TT, Jablonka S, Schrank B, Rossoll W, Rossol W, Prior TW, Morris GE, Burghes AH. The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy. Human Molecular Genetics. 9: 333-9. PMID 10655541 DOI: 10.1093/Hmg/9.3.333 | 0.644 | |||
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