| Year |
Citation |
Score |
| 2020 |
Kapur M, Ganguly A, Nagy G, Adamson SI, Chuang JH, Frankel WN, Ackerman SL. Expression of the Neuronal tRNA n-Tr20 Regulates Synaptic Transmission and Seizure Susceptibility. Neuron. PMID 32853550 DOI: 10.1016/J.Neuron.2020.07.023 |
0.383 |
|
| 2020 |
Griffin EN, Ackerman SL. Lipid Metabolism and Axon Degeneration: An ACOX1 Balancing Act. Neuron. 106: 551-553. PMID 32437651 DOI: 10.1016/J.Neuron.2020.04.030 |
0.361 |
|
| 2018 |
Vo MN, Terrey M, Lee JW, Roy B, Moresco JJ, Sun L, Fu H, Liu Q, Weber TG, Yates JR, Fredrick K, Schimmel P, Ackerman SL. ANKRD16 prevents neuron loss caused by an editing-defective tRNA synthetase. Nature. PMID 29769718 DOI: 10.1038/S41586-018-0137-8 |
0.396 |
|
| 2018 |
Kapur M, Ackerman SL. mRNA Translation Gone Awry: Translation Fidelity and Neurological Disease. Trends in Genetics : Tig. PMID 29352613 DOI: 10.1016/J.Tig.2017.12.007 |
0.321 |
|
| 2017 |
Kapur M, Monaghan CE, Ackerman SL. Regulation of mRNA Translation in Neurons-A Matter of Life and Death. Neuron. 96: 616-637. PMID 29096076 DOI: 10.1016/J.Neuron.2017.09.057 |
0.359 |
|
| 2017 |
Ackerman SL. Abstract IA13: Ribosome stalling and disease Cancer Research. 77. DOI: 10.1158/1538-7445.Transcontrol16-Ia13 |
0.325 |
|
| 2016 |
Ishimura R, Nagy G, Dotu I, Chuang JH, Ackerman SL. Activation of GCN2 kinase by ribosome stalling links translation elongation with translation initiation. Elife. 5. PMID 27085088 DOI: 10.7554/Elife.14295 |
0.37 |
|
| 2016 |
Garrett AM, Jucius TJ, Sigaud LP, Tang FL, Xiong WC, Ackerman SL, Burgess RW. Analysis of Expression Pattern and Genetic Deletion of Netrin5 in the Developing Mouse. Frontiers in Molecular Neuroscience. 9: 3. PMID 26858598 DOI: 10.3389/Fnmol.2016.00003 |
0.392 |
|
| 2015 |
Poliak S, Morales D, Croteau LP, Krawchuk D, Palmesino E, Morton S, Jean-François C, Charron F, Dalva MB, Ackerman SL, Kao TJ, Kania A. Synergistic integration of Netrin and ephrin axon guidance signals by spinal motor neurons. Elife. 4. PMID 26633881 DOI: 10.7554/Elife.10841 |
0.32 |
|
| 2015 |
Liu Y, Lee JW, Ackerman SL. Mutations in the microtubule-associated protein 1A (Map1a) gene cause Purkinje cell degeneration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 4587-98. PMID 25788676 DOI: 10.1523/Jneurosci.2757-14.2015 |
0.435 |
|
| 2015 |
Jia Y, Jucius TJ, Cook SA, Ackerman SL. Loss of Clcc1 results in ER stress, misfolded protein accumulation, and neurodegeneration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 3001-9. PMID 25698737 DOI: 10.1523/Jneurosci.3678-14.2015 |
0.4 |
|
| 2015 |
Poliak S, Morales D, Croteau L, Krawchuk D, Palmesino E, Morton S, Cloutier J, Charron F, Dalva MB, Ackerman SL, Kao T, Kania A. Author response: Synergistic integration of Netrin and ephrin axon guidance signals by spinal motor neurons Elife. DOI: 10.7554/Elife.10841.021 |
0.319 |
|
| 2014 |
Liu Y, Satz JS, Vo MN, Nangle LA, Schimmel P, Ackerman SL. Deficiencies in tRNA synthetase editing activity cause cardioproteinopathy. Proceedings of the National Academy of Sciences of the United States of America. 111: 17570-5. PMID 25422440 DOI: 10.1073/Pnas.1420196111 |
0.376 |
|
| 2014 |
Ishimura R, Nagy G, Dotu I, Zhou H, Yang XL, Schimmel P, Senju S, Nishimura Y, Chuang JH, Ackerman SL. RNA function. Ribosome stalling induced by mutation of a CNS-specific tRNA causes neurodegeneration. Science (New York, N.Y.). 345: 455-9. PMID 25061210 DOI: 10.1126/Science.1249749 |
0.379 |
|
| 2014 |
Srivatsa S, Parthasarathy S, Britanova O, Bormuth I, Donahoo AL, Ackerman SL, Richards LJ, Tarabykin V. Unc5C and DCC act downstream of Ctip2 and Satb2 and contribute to corpus callosum formation. Nature Communications. 5: 3708. PMID 24739528 DOI: 10.1038/Ncomms4708 |
0.367 |
|
| 2013 |
Nagy G, Ackerman SL. Cholesterol metabolism and Rett syndrome pathogenesis. Nature Genetics. 45: 965-7. PMID 23985682 DOI: 10.1038/Ng.2738 |
0.338 |
|
| 2013 |
Liu Y, Zaun HC, Orlowski J, Ackerman SL. CHP1-mediated NHE1 biosynthetic maturation is required for Purkinje cell axon homeostasis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 12656-69. PMID 23904602 DOI: 10.1523/Jneurosci.0406-13.2013 |
0.365 |
|
| 2013 |
Natarajan S, Li Y, Miller EE, Shih DJ, Taylor MD, Stearns TM, Bronson RT, Ackerman SL, Yoon JK, Yun K. Notch1-induced brain tumor models the sonic hedgehog subgroup of human medulloblastoma. Cancer Research. 73: 5381-90. PMID 23852537 DOI: 10.1158/0008-5472.Can-13-0033 |
0.311 |
|
| 2012 |
Jia Y, Mu JC, Ackerman SL. Mutation of a U2 snRNA gene causes global disruption of alternative splicing and neurodegeneration. Cell. 148: 296-308. PMID 22265417 DOI: 10.1016/J.Cell.2011.11.057 |
0.39 |
|
| 2011 |
Zhao L, Spassieva SD, Jucius TJ, Shultz LD, Shick HE, Macklin WB, Hannun YA, Obeid LM, Ackerman SL. A deficiency of ceramide biosynthesis causes cerebellar purkinje cell neurodegeneration and lipofuscin accumulation. Plos Genetics. 7: e1002063. PMID 21625621 DOI: 10.1371/Journal.Pgen.1002063 |
0.407 |
|
| 2011 |
Kim D, Ackerman SL. The UNC5C netrin receptor regulates dorsal guidance of mouse hindbrain axons Journal of Neuroscience. 31: 2167-2179. PMID 21307253 DOI: 10.1523/Jneurosci.5254-10.2011 |
0.378 |
|
| 2011 |
Stum M, McLaughlin HM, Kleinbrink EL, Miers KE, Ackerman SL, Seburn KL, Antonellis A, Burgess RW. An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations. Molecular and Cellular Neurosciences. 46: 432-43. PMID 21115117 DOI: 10.1016/J.Mcn.2010.11.006 |
0.42 |
|
| 2010 |
Zhao L, Rosales C, Seburn K, Ron D, Ackerman SL. Alteration of the unfolded protein response modifies neurodegeneration in a mouse model of Marinesco-Sjögren syndrome. Human Molecular Genetics. 19: 25-35. PMID 19801575 DOI: 10.1093/Hmg/Ddp464 |
0.351 |
|
| 2008 |
Ackerman SL, Cox GA. From ER to Eph Receptors: New Roles for VAP Fragments Cell. 133: 949-951. PMID 18555770 DOI: 10.1016/J.Cell.2008.05.028 |
0.3 |
|
| 2008 |
Ishimura R, Martin GR, Ackerman SL. Loss of apoptosis-inducing factor results in cell-type-specific neurogenesis defects. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 4938-48. PMID 18463247 DOI: 10.1523/Jneurosci.0229-08.2008 |
0.397 |
|
| 2008 |
Renaud J, Kerjan G, Sumita I, Zagar Y, Georget V, Kim D, Fouquet C, Suda K, Sanbo M, Suto F, Ackerman SL, Mitchell KJ, Fujisawa H, Chédotal A. Plexin-A2 and its ligand, Sema6A, control nucleus-centrosome coupling in migrating granule cells. Nature Neuroscience. 11: 440-9. PMID 18327254 DOI: 10.1038/Nn2064 |
0.306 |
|
| 2008 |
Hu Z, Shanker S, MacLean JA, Ackerman SL, Wilkinson MF. The RHOX5 homeodomain protein mediates transcriptional repression of the netrin-1 receptor gene Unc5c. The Journal of Biological Chemistry. 283: 3866-76. PMID 18077458 DOI: 10.1074/Jbc.M706717200 |
0.373 |
|
| 2007 |
Dillon AK, Jevince AR, Hinck L, Ackerman SL, Lu X, Tessier-Lavigne M, Kaprielian Z. UNC5C is required for spinal accessory motor neuron development. Molecular and Cellular Neurosciences. 35: 482-9. PMID 17543537 DOI: 10.1016/J.Mcn.2007.04.011 |
0.343 |
|
| 2006 |
Lee JW, Beebe K, Nangle LA, Jang J, Longo-Guess CM, Cook SA, Davisson MT, Sundberg JP, Schimmel P, Ackerman SL. Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration. Nature. 443: 50-5. PMID 16906134 DOI: 10.1038/Nature05096 |
0.401 |
|
| 2006 |
Burgess RW, Jucius TJ, Ackerman SL. Motor axon guidance of the mammalian trochlear and phrenic nerves: dependence on the netrin receptor Unc5c and modifier loci. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 5756-66. PMID 16723533 DOI: 10.1523/Jneurosci.0736-06.2006 |
0.346 |
|
| 2006 |
Xie Y, Hong Y, Ma XY, Ren XR, Ackerman S, Mei L, Xiong WC. DCC-dependent phospholipase C signaling in netrin-1-induced neurite elongation. The Journal of Biological Chemistry. 281: 2605-11. PMID 16321979 DOI: 10.1074/Jbc.M512767200 |
0.331 |
|
| 2005 |
Xie Y, Ding YQ, Hong Y, Feng Z, Navarre S, Xi CX, Zhu XJ, Wang CL, Ackerman SL, Kozlowski D, Mei L, Xiong WC. Phosphatidylinositol transfer protein-alpha in netrin-1-induced PLC signalling and neurite outgrowth. Nature Cell Biology. 7: 1124-32. PMID 16244667 DOI: 10.1038/Ncb1321 |
0.408 |
|
| 2005 |
Zhao L, Longo-Guess C, Harris BS, Lee JW, Ackerman SL. Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP. Nature Genetics. 37: 974-9. PMID 16116427 DOI: 10.1038/Ng1620 |
0.405 |
|
| 2005 |
van Empel VPM, Bertrand AT, van der Nagel R, Kostin S, Doevendans PA, Crijns HJ, de Wit E, Sluiter W, Ackerman SL, De Windt LJ. Downregulation of apoptosis-inducing factor in harlequin mutant mice sensitizes the myocardium to oxidative stress-related cell death and pressure overload-induced decompensation Circulation Research. 96: e92-e101. PMID 15933268 DOI: 10.1161/01.Res.0000172081.30327.28 |
0.336 |
|
| 2004 |
Munroe RJ, Ackerman SL, Schimenti JC. Genomewide two-generation screens for recessive mutations by ES cell mutagenesis Mammalian Genome. 15: 960-965. PMID 15599554 DOI: 10.1007/S00335-004-2406-0 |
0.326 |
|
| 2004 |
Herrup K, Neve R, Ackerman SL, Copani A. Divide and die: cell cycle events as triggers of nerve cell death. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 9232-9. PMID 15496657 DOI: 10.1523/Jneurosci.3347-04.2004 |
0.311 |
|
| 2004 |
Schwarting GA, Raitcheva D, Bless EP, Ackerman SL, Tobet S. Netrin 1-mediated chemoattraction regulates the migratory pathway of LHRH neurons European Journal of Neuroscience. 19: 11-20. PMID 14750959 DOI: 10.1111/J.1460-9568.2004.03094.X |
0.392 |
|
| 2003 |
Klein JA, Ackerman SL. Oxidative stress, cell cycle, and neurodegeneration Journal of Clinical Investigation. 111: 785-793. PMID 12639981 DOI: 10.1172/Jci18182 |
0.313 |
|
| 2002 |
Klein JA, Longo-Guess CM, Rossmann MP, Seburn KL, Hurd RE, Frankel WN, Bronson RT, Ackerman SL. The harlequin mouse mutation downregulates apoptosis-inducing factor Nature. 419: 367-374. PMID 12353028 DOI: 10.1038/Nature01034 |
0.409 |
|
| 2002 |
Park C, Falls W, Finger JH, Longo-Guess CM, Ackerman SL. Deletion in Catna2, encoding αN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation Nature Genetics. 31: 279-284. PMID 12089526 DOI: 10.1038/Ng908 |
0.376 |
|
| 2002 |
Park C, Finger JH, Cooper JA, Ackerman SL. The cerebellar deficient folia (cdf) gene acts intrinsically in Purkinje cell migrations Genesis. 32: 32-41. PMID 11835672 DOI: 10.1002/Gene.10024 |
0.419 |
|
| 2002 |
Finger JH, Bronson RT, Harris B, Johnson K, Przyborski SA, Ackerman SL. The netrin 1 receptors Unc5h3 and Dcc are necessary at multiple choice points for the guidance of corticospinal tract axons. The Journal of Neuroscience. 22: 10346-10356. DOI: 10.1523/Jneurosci.22-23-10346.2002 |
0.367 |
|
| 2001 |
Barclay J, Balaguero N, Mione M, Ackerman SL, Letts VA, Brodbeck J, Canti C, Meir A, Page KM, Kusumi K, Perez-Reyes E, Lander ES, Frankel WN, Gardiner RM, Dolphin AC, et al. Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 6095-104. PMID 11487633 DOI: 10.1523/Jneurosci.21-16-06095.2001 |
0.322 |
|
| 2001 |
Beierbach E, Park C, Ackerman SL, Goldowitz D, Hawkes R. Abnormal dispersion of a purkinje cell subset in the mouse mutant cerebellar deficient folia (cdf). The Journal of Comparative Neurology. 436: 42-51. PMID 11413545 DOI: 10.1002/Cne.1052 |
0.317 |
|
| 2001 |
Chen Z, Karaplis AC, Ackerman SL, Pogribny IP, Melnyk S, Lussier-Cacan S, Chen MF, Pai A, John SW, Smith RS, Bottiglieri T, Bagley P, Selhub J, Rudnicki MA, James SJ, et al. Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition. Human Molecular Genetics. 10: 433-43. PMID 11181567 DOI: 10.1093/Hmg/10.5.433 |
0.327 |
|
| 2001 |
Näf D, Wilson LA, Bergstrom RA, Smith RS, Goodwin NC, Verkerk A, van Ommen GJ, Ackerman SL, Frankel WN, Schimenti JC. Mouse models for the Wolf-Hirschhorn deletion syndrome. Human Molecular Genetics. 10: 91-8. PMID 11152656 DOI: 10.1093/Hmg/10.2.91 |
0.323 |
|
| 2000 |
Park C, Longo CM, Ackerman SL. Genetic and physical mapping of the cerebellar deficient folia (cdf) locus on mouse chromosome 6 Genomics. 69: 135-138. PMID 11013084 DOI: 10.1006/Geno.2000.6322 |
0.33 |
|
| 2000 |
Goldowitz D, Hamre KM, Przyborski SA, Ackerman SL. Granule cells and cerebellar boundaries: analysis of Unc5h3 mutant chimeras. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 20: 4129-37. PMID 10818148 DOI: 10.1523/Jneurosci.20-11-04129.2000 |
0.364 |
|
| 1998 |
Ackerman SL, Knowles BB. Cloning and mapping of the UNC5C gene to human chromosome 4q21-q23. Genomics. 52: 205-8. PMID 9782087 DOI: 10.1006/Geno.1998.5425 |
0.338 |
|
| 1998 |
Przyborski SA, Knowles BB, Handel MA, Gurwitch SA, Ackerman SL. Differential expression of the zinc finger gene Zfp105 during spermatogenesis. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 758-62. PMID 9716663 DOI: 10.1007/S003359900859 |
0.328 |
|
| 1997 |
Ackerman SL, Kozak LP, Przyborski SA, Rund LA, Boyer BB, Knowles BB. The mouse rostral cerebellar malformation gene encodes an UNC-5-like protein. Nature. 386: 838-42. PMID 9126743 DOI: 10.1038/386838A0 |
0.443 |
|
| 1997 |
Leonardo ED, Hinck L, Masu M, Keino-Masu K, Ackerman SL, Tessier-Lavigne M. Vertebrate homologues of C. elegans UNC-5 are candidate netrin receptors. Nature. 386: 833-8. PMID 9126742 DOI: 10.1038/386833A0 |
0.386 |
|
| 1996 |
Hwang S, Benjamin LE, Oh B, Rothstein JL, Ackerman SL, Beddington RS, Solter D, Knowles BB. Genetic mapping and embryonic expression of a novel, maternally transcribed gene Mem3. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 586-90. PMID 8678978 DOI: 10.1007/S003359900174 |
0.306 |
|
| 1994 |
Ackerman SL, Knowles BB, Andrews PW. Gene regulation during neuronal and non-neuronal differentiation of NTERA2 human teratocarcinoma-derived stem cells Molecular Brain Research. 25: 157-162. PMID 7984043 DOI: 10.1016/0169-328X(94)90293-3 |
0.358 |
|
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