| Year |
Citation |
Score |
| 2023 |
Anderson CJ, Cadeddu R, Anderson DN, Huxford JA, VanLuik ER, Odeh K, Pittenger C, Pulst SM, Bortolato M. A novel naïve Bayes approach to identifying grooming behaviors in the force-plate actometric platform. Journal of Neuroscience Methods. 110026. PMID 38029972 DOI: 10.1016/j.jneumeth.2023.110026 |
0.436 |
|
| 2023 |
Anderson CJ, Cadeddu R, Anderson DN, Huxford JA, VanLuik ER, Odeh K, Pittenger C, Pulst SM, Bortolato M. A novel naïve Bayes approach to identifying grooming behaviors in the force-plate actometric platform. Biorxiv : the Preprint Server For Biology. PMID 37503098 DOI: 10.1101/2023.07.08.548198 |
0.437 |
|
| 2023 |
Figueroa KP, Anderson CJ, Paul S, Dansithong W, Gandelman M, Scoles DR, Pulst SM. Slc9a6 mutation causes Purkinje cell loss and ataxia in the shaker rat. Human Molecular Genetics. PMID 36621975 DOI: 10.1093/hmg/ddad004 |
0.519 |
|
| 2021 |
Anderson DN, Dorval AD, Rolston JD, Pulst SM, Anderson CJ. Computational investigation of the impact of deep brain stimulation contact size and shape on neural selectivity. Journal of Neural Engineering. PMID 33721858 DOI: 10.1088/1741-2552/abeeaa |
0.69 |
|
| 2020 |
Lang J, Haas E, Hubener-Schmid J, Anderson CJ, Pulst SM, Giese MA, Ilg W. Detecting and Quantifying Ataxia-Related Motor Impairments in Rodents Using Markerless Motion Tracking With Deep Neural Networks. Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual International Conference. 2020: 3642-3648. PMID 33018791 DOI: 10.1109/EMBC44109.2020.9176701 |
0.465 |
|
| 2020 |
Gandelman M, Dansithong W, Figueroa KP, Paul S, Scoles DR, Pulst SM. Staufen 1 amplifies proapoptotic activation of the unfolded protein response. Cell Death and Differentiation. PMID 32415281 DOI: 10.1038/S41418-020-0553-9 |
0.314 |
|
| 2020 |
Scoles DR, Dansithong W, Pflieger LT, Paul S, Gandelman M, Figueroa KP, Rigo F, Bennett CF, Pulst SM. ALS-associated genes in SCA2 mouse spinal cord transcriptomes. Human Molecular Genetics. PMID 32307524 DOI: 10.1093/Hmg/Ddaa072 |
0.302 |
|
| 2020 |
Anderson CJ, Anderson DN, Pulst SM, Butson CR, Dorval AD. Neural Selectivity, Efficiency, and Dose Equivalence in Deep Brain Stimulation through Pulse Width Tuning and Segmented Electrodes. Brain Stimulation. PMID 32278715 DOI: 10.1016/J.Brs.2020.03.017 |
0.697 |
|
| 2019 |
Brown AS, Meera P, Quinones G, Magri J, Otis TS, Pulst SM, Oro AE. Receptor protein tyrosine phosphatases control Purkinje neuron firing. Cell Cycle (Georgetown, Tex.). 1-7. PMID 31876231 DOI: 10.1080/15384101.2019.1695995 |
0.309 |
|
| 2019 |
Kuo SH, Louis ED, Faust PL, Handforth A, Chang SY, Avlar B, Lang EJ, Pan MK, Miterko LN, Brown AM, Sillitoe RV, Anderson CJ, Pulst SM, Gallagher MJ, Lyman KA, et al. Current Opinions and Consensus for Studying Tremor in Animal Models. Cerebellum (London, England). PMID 31124049 DOI: 10.1007/S12311-019-01037-1 |
0.516 |
|
| 2019 |
Anderson CJ, Figueroa KP, Dorval AD, Pulst SM. Deep cerebellar stimulation reduces ataxic motor symptoms in the shaker rat. Annals of Neurology. PMID 30854718 DOI: 10.1002/Ana.25464 |
0.714 |
|
| 2019 |
Lai RY, Tomishon D, Figueroa KP, Pulst SM, Perlman S, Wilmot G, Gomez CM, Schmahmann JD, Paulson H, Shakkottai VG, Ying SH, Zesiewicz T, Bushara K, Geschwind M, Xia G, et al. Tremor in the Degenerative Cerebellum: Towards the Understanding of Brain Circuitry for Tremor. Cerebellum (London, England). PMID 30830673 DOI: 10.1007/S12311-019-01016-6 |
0.301 |
|
| 2018 |
Pulst SM. The complex structure of genetic variation. Neurology. Genetics. 4: e299. PMID 30588499 DOI: 10.1212/Nxg.0000000000000299 |
0.309 |
|
| 2018 |
Brown AS, Meera P, Altindag B, Chopra R, Perkins EM, Paul S, Scoles DR, Tarapore E, Magri J, Huang H, Jackson M, Shakkottai VG, Otis TS, Pulst SM, Atwood SX, et al. MTSS1/Src family kinase dysregulation underlies multiple inherited ataxias. Proceedings of the National Academy of Sciences of the United States of America. PMID 30530649 DOI: 10.1073/Pnas.1816177115 |
0.341 |
|
| 2018 |
Paul S, Dansithong W, Figueroa KP, Scoles DR, Pulst SM. Staufen1 links RNA stress granules and autophagy in a model of neurodegeneration. Nature Communications. 9: 3648. PMID 30194296 DOI: 10.1038/S41467-018-06041-3 |
0.328 |
|
| 2018 |
Chopra R, Wasserman AH, Pulst SM, De Zeeuw CI, Shakkottai VG. Protein kinase C activity is a protective modifier of Purkinje neuron degeneration in cerebellar ataxia. Human Molecular Genetics. PMID 29432535 DOI: 10.1093/Hmg/Ddy050 |
0.301 |
|
| 2018 |
Scoles DR, Pulst SM. Spinocerebellar Ataxia Type 2. Advances in Experimental Medicine and Biology. 1049: 175-195. PMID 29427103 DOI: 10.1007/978-3-319-71779-1_8 |
0.345 |
|
| 2017 |
Pflieger LT, Dansithong W, Paul S, Scoles D, Figueroa KP, Meera P, Otis TS, Facelli JC, Pulst SM. Gene Co-Expression Network Analysis for Identifying Modules and Functionally Enriched Pathways in SCA2. Human Molecular Genetics. PMID 28525545 DOI: 10.1093/Hmg/Ddx191 |
0.331 |
|
| 2017 |
Scoles DR, Meera P, Schneider MD, Paul S, Dansithong W, Figueroa KP, Hung G, Rigo F, Bennett CF, Otis TS, Pulst SM. Antisense oligonucleotide therapy for spinocerebellar ataxia type 2. Nature. PMID 28405024 DOI: 10.1038/Nature22044 |
0.343 |
|
| 2017 |
Becker LA, Huang B, Bieri G, Ma R, Knowles DA, Jafar-Nejad P, Messing J, Kim HJ, Soriano A, Auburger G, Pulst SM, Taylor JP, Rigo F, Gitler AD. Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice. Nature. PMID 28405022 DOI: 10.1038/Nature22038 |
0.315 |
|
| 2017 |
Wynn DP, Pulst SM. A novel WDR45 mutation in a patient with β-propeller protein-associated neurodegeneration. Neurology. Genetics. 3: e124. PMID 27957548 DOI: 10.1212/Nxg.0000000000000124 |
0.304 |
|
| 2016 |
Li PP, Sun X, Xia G, Arbez N, Paul S, Zhu S, Peng HB, Ross CA, Koeppen AH, Margolis RL, Pulst SM, Ashizawa T, Rudnicki DD. ATXN2-AS, a gene antisense to ATXN2, is associated with SCA2 and ALS. Annals of Neurology. PMID 27531668 DOI: 10.1002/Ana.24761 |
0.315 |
|
| 2016 |
Meera P, Pulst SM, Otis TS. Cellular and circuit mechanisms underlying spinocerebellar ataxias. The Journal of Physiology. PMID 27198167 DOI: 10.1113/Jp271897 |
0.347 |
|
| 2016 |
Pulst SM. Genetics of neurodegenerative diseases. Neurology. Genetics. 2: e52. PMID 27066589 DOI: 10.1212/Nxg.0000000000000052 |
0.319 |
|
| 2016 |
Figueroa KP, Paul S, Calì T, Lopreiato R, Karan S, Frizzarin M, Ames D, Zanni G, Brini M, Dansithong W, Milash B, Scoles DR, Carafoli E, Pulst SM. Spontaneous shaker rat mutant - a new model for X-linked tremor-ataxia. Disease Models & Mechanisms. PMID 27013529 DOI: 10.1242/Dmm.022848 |
0.336 |
|
| 2015 |
Pulst SM. Spotlight on the June 2015 issue. Neurology. Genetics. 1: e11. PMID 27066540 DOI: 10.1212/Nxg.0000000000000011 |
0.307 |
|
| 2015 |
Scoles DR, Ho MH, Dansithong W, Pflieger LT, Petersen LW, Thai KK, Pulst SM. Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat. Plos One. 10: e0128769. PMID 26086378 DOI: 10.1371/Journal.Pone.0128769 |
0.31 |
|
| 2015 |
Dansithong W, Paul S, Figueroa KP, Rinehart MD, Wiest S, Pflieger LT, Scoles DR, Pulst SM. Ataxin-2 regulates RGS8 translation in a new BAC-SCA2 transgenic mouse model. Plos Genetics. 11: e1005182. PMID 25902068 DOI: 10.1371/Journal.Pgen.1005182 |
0.322 |
|
| 2014 |
Gallego-Iradi C, Bickford JS, Khare S, Hall A, Nick JA, Salmasinia D, Wawrowsky K, Bannykh S, Huynh DP, Rincon-Limas DE, Pulst SM, Nick HS, Fernandez-Funez P, Waters MF. KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking. Neurobiology of Disease. 71: 270-9. PMID 25152487 DOI: 10.1016/J.Nbd.2014.08.020 |
0.308 |
|
| 2014 |
Tezenas du Montcel S, Durr A, Bauer P, Figueroa KP, Ichikawa Y, Brussino A, Forlani S, Rakowicz M, Schöls L, Mariotti C, van de Warrenburg BP, Orsi L, Giunti P, Filla A, Szymanski S, ... ... Pulst SM, et al. Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes. Brain : a Journal of Neurology. 137: 2444-55. PMID 24972706 DOI: 10.1093/Brain/Awu174 |
0.308 |
|
| 2014 |
Matilla-Dueñas A, Ashizawa T, Brice A, Magri S, McFarland KN, Pandolfo M, Pulst SM, Riess O, Rubinsztein DC, Schmidt J, Schmidt T, Scoles DR, Stevanin G, Taroni F, Underwood BR, et al. Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias. Cerebellum (London, England). 13: 269-302. PMID 24307138 DOI: 10.1007/S12311-013-0539-Y |
0.314 |
|
| 2013 |
Hansen ST, Meera P, Otis TS, Pulst SM. Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2. Human Molecular Genetics. 22: 271-83. PMID 23087021 DOI: 10.1093/Hmg/Dds427 |
0.325 |
|
| 2012 |
Hekman KE, Yu GY, Brown CD, Zhu H, Du X, Gervin K, Undlien DE, Peterson A, Stevanin G, Clark HB, Pulst SM, Bird TD, White KP, Gomez CM. A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult. Human Molecular Genetics. 21: 5472-83. PMID 23001565 DOI: 10.1093/Hmg/Dds392 |
0.347 |
|
| 2011 |
Fischbeck KH, Pulst SM. Amyotrophic lateral sclerosis and spinocerebellar ataxia 2. Neurology. 76: 2050-1. PMID 21562249 DOI: 10.1212/Wnl.0B013E31821F4498 |
0.306 |
|
| 2011 |
Figueroa KP, Waters MF, Garibyan V, Bird TD, Gomez CM, Ranum LP, Minassian NA, Papazian DM, Pulst SM. Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13). Plos One. 6: e17811. PMID 21479265 DOI: 10.1371/Journal.Pone.0017811 |
0.303 |
|
| 2009 |
Huynh DP, Maalouf M, Silva AJ, Schweizer FE, Pulst SM. Dissociated fear and spatial learning in mice with deficiency of ataxin-2. Plos One. 4: e6235. PMID 19617910 DOI: 10.1371/Journal.Pone.0006235 |
0.733 |
|
| 2009 |
Minassian NA, Lin M, Figueroa KP, Mock AF, Stevanin G, Waters MF, Pulst SM, Papazian DM. Distinct Functional Effects of Kv3.3 Mutations Associated with Spinocerebellar Ataxia Type 13 Biophysical Journal. 96: 328a. DOI: 10.1016/J.Bpj.2008.12.1652 |
0.333 |
|
| 2008 |
Pulst S, med. What Determines Disease Severity in the Spinocerebellar Ataxias Nejm Journal Watch. 2008. DOI: 10.1056/Jn200812300000001 |
0.329 |
|
| 2007 |
Al-Ramahi I, Pérez AM, Lim J, Zhang M, Sorensen R, de Haro M, Branco J, Pulst SM, Zoghbi HY, Botas J. dAtaxin-2 mediates expanded Ataxin-1-induced neurodegeneration in a Drosophila model of SCA1. Plos Genetics. 3: e234. PMID 18166084 DOI: 10.1371/Journal.Pgen.0030234 |
0.331 |
|
| 2007 |
Huynh DP, Nguyen DT, Pulst-Korenberg JB, Brice A, Pulst SM. Parkin is an E3 ubiquitin-ligase for normal and mutant ataxin-2 and prevents ataxin-2-induced cell death. Experimental Neurology. 203: 531-41. PMID 17097639 DOI: 10.1016/J.Expneurol.2006.09.009 |
0.327 |
|
| 2006 |
Willeumier K, Pulst SM, Schweizer FE. Proteasome inhibition triggers activity-dependent increase in the size of the recycling vesicle pool in cultured hippocampal neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 11333-41. PMID 17079661 DOI: 10.1523/Jneurosci.1684-06.2006 |
0.731 |
|
| 2005 |
Waters MF, Fee D, Figueroa KP, Nolte D, Müller U, Advincula J, Coon H, Evidente VG, Pulst SM. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus? Neurology. 65: 1111-3. PMID 16135769 DOI: 10.1212/01.Wnl.0000177490.05162.41 |
0.304 |
|
| 2005 |
Pulst SM, Santos N, Wang D, Yang H, Huynh D, Velazquez L, Figueroa KP. Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset. Brain : a Journal of Neurology. 128: 2297-303. PMID 16000334 DOI: 10.1093/Brain/Awh586 |
0.343 |
|
| 2004 |
Fee DB, So YT, Barraza C, Figueroa KP, Pulst SM. Phenotypic variability associated with Arg26Gln mutation in caveolin3. Muscle & Nerve. 30: 375-8. PMID 15318349 DOI: 10.1002/Mus.20092 |
0.314 |
|
| 2004 |
Matsuura T, Fang P, Lin X, Khajavi M, Tsuji K, Rasmussen A, Grewal RP, Achari M, Alonso ME, Pulst SM, Zoghbi HY, Nelson DL, Roa BB, Ashizawa T. Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10. American Journal of Human Genetics. 74: 1216-24. PMID 15127363 DOI: 10.1086/421526 |
0.321 |
|
| 2003 |
Huynh DP, Scoles DR, Nguyen D, Pulst SM. The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI. Human Molecular Genetics. 12: 2587-97. PMID 12925569 DOI: 10.1093/Hmg/Ddg269 |
0.314 |
|
| 2003 |
Huynh DP, Yang HT, Vakharia H, Nguyen D, Pulst SM. Expansion of the polyQ repeat in ataxin-2 alters its Golgi localization, disrupts the Golgi complex and causes cell death. Human Molecular Genetics. 12: 1485-96. PMID 12812977 DOI: 10.1093/Hmg/Ddg175 |
0.333 |
|
| 2001 |
Konakova M, Pulst SM. Immunocytochemical characterization of torsin proteins in mouse brain. Brain Research. 922: 1-8. PMID 11730696 DOI: 10.1016/S0006-8993(01)03014-1 |
0.322 |
|
| 2001 |
Cholfin JA, Sobrido MJ, Perlman S, Pulst SM, Geschwind DH. The SCA12 mutation as a rare cause of spinocerebellar ataxia. Archives of Neurology. 58: 1833-5. PMID 11708992 DOI: 10.1001/Archneur.58.11.1833 |
0.334 |
|
| 2001 |
Figueroa KP, Chan P, Schöls L, Tanner C, Riess O, Perlman SL, Geschwind DH, Pulst SM. Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia. Archives of Neurology. 58: 1649-53. PMID 11594924 DOI: 10.1001/Archneur.58.10.1649 |
0.314 |
|
| 2001 |
Bruder CE, Hirvelä C, Tapia-Paez I, Fransson I, Segraves R, Hamilton G, Zhang XX, Evans DG, Wallace AJ, Baser ME, Zucman-Rossi J, Hergersberg M, Boltshauser E, Papi L, Rouleau GA, ... ... Pulst SM, et al. High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH. Human Molecular Genetics. 10: 271-82. PMID 11159946 DOI: 10.1093/Hmg/10.3.271 |
0.318 |
|
| 2000 |
Huynh DP, Scoles DR, Ho TH, Del Bigio MR, Pulst SM. Parkin is associated with actin filaments in neuronal and nonneural cells. Annals of Neurology. 48: 737-44. PMID 11079537 DOI: 10.1002/1531-8249(200011)48:5<737::Aid-Ana7>3.0.Co;2-D |
0.337 |
|
| 2000 |
Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, et al. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nature Genetics. 26: 191-4. PMID 11017075 DOI: 10.1038/79911 |
0.301 |
|
| 2000 |
Huynh DP, Figueroa K, Hoang N, Pulst SM. Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human. Nature Genetics. 26: 44-50. PMID 10973246 DOI: 10.1038/79162 |
0.338 |
|
| 2000 |
Pulst SM, Filla A. Ataxias on the march from Quebec to Tunisia. Neurology. 54: 1400-1. PMID 10751244 DOI: 10.1212/Wnl.54.7.1400 |
0.33 |
|
| 1999 |
Simon DK, Pulst SM, Sutton JP, Browne SE, Beal MF, Johns DR. Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation. Neurology. 53: 1787-93. PMID 10563629 DOI: 10.1212/Wnl.53.8.1787 |
0.3 |
|
| 1999 |
Kuo AA, Pulst SM, Eliashiv DS, Adams CR. Electrical inexcitability of nerves and muscles in severe infantile spinal muscular atrophy. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 122. PMID 10454872 DOI: 10.1136/Jnnp.67.1.122 |
0.312 |
|
| 1999 |
Pulst SM. Genetic linkage analysis. Archives of Neurology. 56: 667-72. PMID 10369304 DOI: 10.1001/Archneur.56.6.667 |
0.306 |
|
| 1999 |
Huynh DP, Del Bigio MR, Ho DH, Pulst SM. Expression of ataxin-2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2. Annals of Neurology. 45: 232-41. PMID 9989626 DOI: 10.1002/1531-8249(199902)45:2<232::Aid-Ana14>3.0.Co;2-7 |
0.324 |
|
| 1999 |
Zu L, Figueroa KP, Grewal R, Pulst SM. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22. American Journal of Human Genetics. 64: 594-9. PMID 9973298 DOI: 10.1086/302247 |
0.307 |
|
| 1998 |
Grewal RP, Tayag E, Figueroa KP, Zu L, Durazo A, Nunez C, Pulst SM. Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia. Neurology. 51: 1423-6. PMID 9818872 DOI: 10.1212/Wnl.51.5.1423 |
0.338 |
|
| 1998 |
Nechiporuk T, Huynh DP, Figueroa K, Sahba S, Nechiporuk A, Pulst SM. The mouse SCA2 gene: cDNA sequence, alternative splicing and protein expression. Human Molecular Genetics. 7: 1301-9. PMID 9668173 DOI: 10.1093/Hmg/7.8.1301 |
0.306 |
|
| 1998 |
Gouw LG, Castañeda MA, McKenna CK, Digre KB, Pulst SM, Perlman S, Lee MS, Gomez C, Fischbeck K, Gagnon D, Storey E, Bird T, Jeri FR, Ptácek LJ. Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmission. Human Molecular Genetics. 7: 525-32. PMID 9467013 DOI: 10.1093/Hmg/7.3.525 |
0.315 |
|
| 1997 |
Riess O, Laccone FA, Gispert S, Schöls L, Zühlke C, Vieira-Saecker AM, Herlt S, Wessel K, Epplen JT, Weber BH, Kreuz F, Chahrokh-Zadeh S, Meindl A, Lunkes A, Aguiar J, ... ... Pulst SM, et al. SCA2 trinucleotide expansion in German SCA patients. Neurogenetics. 1: 59-64. PMID 10735276 DOI: 10.1007/S100480050009 |
0.334 |
|
| 1997 |
Geschwind DH, Perlman S, Figueroa KP, Karrim J, Baloh RW, Pulst SM. Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations. Neurology. 49: 1247-51. PMID 9371902 DOI: 10.1212/Wnl.49.5.1247 |
0.318 |
|
| 1997 |
Adams C, Starkman S, Pulst SM. Clinical and molecular analysis of a pedigree of southern Italian ancestry with spinocerebellar ataxia type 2. Neurology. 49: 1163-6. PMID 9339711 DOI: 10.1212/Wnl.49.4.1163 |
0.317 |
|
| 1997 |
Schöls L, Gispert S, Vorgerd M, Menezes Vieira-Saecker AM, Blanke P, Auburger G, Amoiridis G, Meves S, Epplen JT, Przuntek H, Pulst SM, Riess O. Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds. Archives of Neurology. 54: 1073-80. PMID 9311350 DOI: 10.1001/Archneur.1997.00550210011007 |
0.335 |
|
| 1997 |
Sutton JP, Pulst SM. Atypical parkinsonism in a family of Portuguese ancestry: absence of CAG repeat expansion in the MJD1 gene. Neurology. 48: 1285-90. PMID 9153459 DOI: 10.1212/Wnl.48.5.1285 |
0.312 |
|
| 1997 |
Huynh DP, Mautner V, Baser ME, Stavrou D, Pulst SM. Immunohistochemical detection of schwannomin and neurofibromin in vestibular schwannomas, ependymomas and meningiomas. Journal of Neuropathology and Experimental Neurology. 56: 382-90. PMID 9100669 DOI: 10.1097/00005072-199704000-00007 |
0.309 |
|
| 1996 |
Huynh DP, Ho VV, Pulst SM. Characterization and expression of presenilin 1 in mouse brain. Neuroreport. 7: 2423-8. PMID 8981396 DOI: 10.1097/00001756-199611040-00004 |
0.317 |
|
| 1996 |
Pulst SM, Nechiporuk A, Nechiporuk T, Gispert S, Chen XN, Lopes-Cendes I, Pearlman S, Starkman S, Orozco-Diaz G, Lunkes A, DeJong P, Rouleau GA, Auburger G, Korenberg JR, Figueroa C, et al. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nature Genetics. 14: 269-76. PMID 8896555 DOI: 10.1038/Ng1196-269 |
0.305 |
|
| 1996 |
Baser ME, Ragge NK, Riccardi VM, Janus T, Gantz B, Pulst SM. Phenotypic variability in monozygotic twins with neurofibromatosis 2. American Journal of Medical Genetics. 64: 563-7. PMID 8870923 DOI: 10.1002/(Sici)1096-8628(19960906)64:4<563::Aid-Ajmg7>3.0.Co;2-Q |
0.313 |
|
| 1996 |
Scoles DR, Baser ME, Pulst SM. A missense mutation in the neurofibromatosis 2 gene occurs in patients with mild and severe phenotypes. Neurology. 47: 544-6. PMID 8757035 DOI: 10.1212/Wnl.47.2.544 |
0.301 |
|
| 1994 |
Huynh DP, Nechiporuk T, Pulst SM. Alternative transcripts in the mouse neurofibromatosis type 2 (NF2) gene are conserved and code for schwannomins with distinct C-terminal domains. Human Molecular Genetics. 3: 1075-9. PMID 7981675 DOI: 10.1093/Hmg/3.7.1075 |
0.319 |
|
| 1994 |
Sainz J, Huynh DP, Figueroa K, Ragge NK, Baser ME, Pulst SM. Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas. Human Molecular Genetics. 3: 885-91. PMID 7951231 DOI: 10.1093/Hmg/3.6.885 |
0.304 |
|
| 1993 |
Rouleau GA, Merel P, Lutchman M, Sanson M, Zucman J, Marineau C, Hoang-Xuan K, Demczuk S, Desmaze C, Plougastel B, Pulst SM, Lenoir G, Bijlsma E, Fashold R, Dumanski J, et al. Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2 Nature. 363: 515-521. PMID 8379998 DOI: 10.1038/363515A0 |
0.321 |
|
| 1989 |
Brown RO, Pulst SM, Mayeri E. Neuroendocrine bag cells of Aplysia are activated by bag cell peptide-containing neurons in the pleural ganglion. Journal of Neurophysiology. 61: 1142-52. PMID 2746315 DOI: 10.1152/Jn.1989.61.6.1142 |
0.719 |
|
| 1988 |
Pulst SM, Gusman D, Mayeri E. Immunostaining for peptides of the egg-laying hormone/bag cell peptide precursor protein in the head ganglia of Aplysia. Neuroscience. 27: 363-71. PMID 3200446 DOI: 10.1016/0306-4522(88)90244-8 |
0.664 |
|
| 1987 |
Pulst SM, Rothman BS, Mayeri E. Presence of immunoreactive alpha-bag cell peptide[1-8] in bag cell neurons of Aplysia suggests novel carboxypeptidase processing of neuropeptides. Neuropeptides. 10: 249-59. PMID 3683775 DOI: 10.1016/0143-4179(87)90075-8 |
0.74 |
|
| 1986 |
Pulst SM, Gusman D, Rothman BS, Mayeri E. Coexistence of egg-laying hormone and alpha-bag cell peptide in bag cell neurons of Aplysia indicates that they are a peptidergic multitransmitter system. Neuroscience Letters. 70: 40-5. PMID 2877421 DOI: 10.1016/0304-3940(86)90434-9 |
0.745 |
|
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