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Steven S. Scherer, MD PhD - Publications

Affiliations: 
Neurology University of Pennsylvania, Philadelphia, PA, United States 
Area:
Peripheral nerve
Website:
http://www.med.upenn.edu/ins/faculty/scherer.htm

127 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
2021 Guo MH, Bardakjian TM, Brzozowski MR, Scherer SS, Quinn C, Elman L, Orthmann-Murphy J, Tropea TF, Ellis CA, Gonzalez-Alegre P. Temporal trends and yield of clinical diagnostic genetic testing in adult neurology. American Journal of Medical Genetics. Part A. PMID 34075706 DOI: 10.1002/ajmg.a.62372  0.702
2020 Motley WW, Züchner S, Scherer SS. Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathy. Neurology. Genetics. 6: e496. PMID 32802955 DOI: 10.1212/Nxg.0000000000000496  0.345
2020 Sase S, Almad AA, Boecker CA, Guedes-Dias P, Li JJ, Takanohashi A, Patel A, McCaffrey T, Patel H, Sirdeshpande D, Curiel J, Shih-Hwa Liu J, Padiath Q, Holzbaur EL, Scherer SS, et al. mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model. Elife. 9. PMID 32463361 DOI: 10.7554/Elife.52986  0.342
2020 Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA, ... ... Scherer SS, et al. Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. Nature Genetics. PMID 32367058 DOI: 10.1038/S41588-020-0615-4  0.332
2020 Li JJ, Sarute N, Lancaster E, Otkiran-Clare G, Fagla BM, Ross SR, Scherer SS. A recessive Trim2 mutation causes an axonal neuropathy in mice. Neurobiology of Disease. 104845. PMID 32205255 DOI: 10.1016/J.Nbd.2020.104845  0.415
2020 Sase S, Almad AA, Boecker CA, Guedes-Dias P, Li JJ, Takanohashi A, Patel A, McCaffrey T, Patel H, Sirdeshpande D, Curiel J, Liu JS, Padiath Q, Holzbaur EL, Scherer SS, et al. Author response: TUBB4A mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model Elife. DOI: 10.7554/Elife.52986.Sa2  0.309
2019 Lee DC, Dankwa L, Edmundson C, Cornblath DR, Scherer SS. Yield of next-generation neuropathy gene panels in axonal neuropathies. Journal of the Peripheral Nervous System : Jpns. PMID 31701603 DOI: 10.1111/Jns.12356  0.302
2019 Lee DC, Meyer-Schuman R, Bacon C, Shy ME, Antonellis A, Scherer SS. A recurrent GARS mutation causes distal hereditary motor neuropathy. Journal of the Peripheral Nervous System : Jpns. PMID 31628756 DOI: 10.1111/Jns.12353  0.318
2019 Horga A, Bugiardini E, Manole A, Bremner F, Jaunmuktane Z, Dankwa L, Rebelo AP, Woodward CE, Hargreaves IP, Cortese A, Pittman AM, Brandner S, Polke JM, Pitceathly RDS, Züchner S, ... ... Scherer SS, et al. Autosomal dominant optic atrophy and cataract "plus" phenotype including axonal neuropathy. Neurology. Genetics. 5: e322. PMID 31119193 DOI: 10.1212/Nxg.0000000000000322  0.331
2019 Pareyson D, Stojkovic T, Reilly MM, Leonard-Louis S, Laurà M, Blake J, Parman Y, Battaloglu E, Tazir M, Bellatache M, Bonello-Palot N, Lévy N, Sacconi S, Guimarães-Costa R, Attarian S, ... ... Scherer SS, et al. A multicentre retrospective study of Charcot-Marie-Tooth disease type 4B (CMT4B) due to mutations in Myotubularin-related proteins (MTMRs). Annals of Neurology. PMID 31070812 DOI: 10.1002/Ana.25500  0.356
2019 Phillips J, Courel S, Rebelo AP, Bis-Brewer DM, Bardakjian T, Dankwa L, Hamedani AG, Züchner S, Scherer SS. POLG mutations presenting as CMT. Journal of the Peripheral Nervous System : Jpns. PMID 30843307 DOI: 10.1111/Jns.12313  0.353
2018 Dankwa L, Richardson J, Motley WW, Scavina M, Courel S, Bardakjian T, Züchner S, Scherer SS. A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 family. Neuromuscular Disorders : Nmd. PMID 30642740 DOI: 10.1016/J.Nmd.2018.12.008  0.357
2018 Meister-Broekema M, Freilich R, Jagadeesan C, Rauch JN, Bengoechea R, Motley WW, Kuiper EFE, Minoia M, Furtado GV, van Waarde MAWH, Bird SJ, Rebelo A, Zuchner S, Pytel P, Scherer SS, et al. Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks. Nature Communications. 9: 5342. PMID 30559338 DOI: 10.1038/S41467-018-07718-5  0.302
2018 Allard DE, Wang Y, Li JJ, Conley B, Xu EW, Sailer D, Kimpston C, Notini R, Smith CJ, Koseoglu E, Starmer J, Zeng XL, Howard JF, Hoke A, Scherer SS, et al. Schwann cell-derived periostin promotes autoimmune peripheral polyneuropathy via macrophage recruitment. The Journal of Clinical Investigation. PMID 30222134 DOI: 10.1172/Jci99308  0.338
2018 Lancaster E, Li J, Hanania T, Liem R, Scheideler MA, Scherer SS. Myelinated axons fail to develop properly in a genetically authentic mouse model of Charcot-Marie-Tooth disease type 2E. Experimental Neurology. PMID 29940160 DOI: 10.1016/J.Expneurol.2018.06.010  0.393
2018 Lassuthova P, Rebelo AP, Ravenscroft G, Lamont PJ, Davis MR, Manganelli F, Feely SM, Bacon C, Brožková DŠ, Haberlova J, Mazanec R, Tao F, Saghira C, Abreu L, Courel S, ... ... Scherer SS, et al. Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2. American Journal of Human Genetics. 102: 505-514. PMID 29499166 DOI: 10.1016/J.Ajhg.2018.01.023  0.37
2018 Dankwa L, Richardson J, Motley WW, Züchner S, Scherer SS. A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A family. Journal of the Peripheral Nervous System : Jpns. PMID 29341354 DOI: 10.1111/Jns.12248  0.371
2017 Zhao HT, Damle S, Ikeda-Lee K, Kuntz S, Li J, Mohan A, Kim A, Hung G, Scheideler MA, Scherer SS, Svaren J, Swayze EE, Kordasiewicz HB. PMP22 antisense oligonucleotides reverse Charcot-Marie-Tooth disease type 1A features in rodent models. The Journal of Clinical Investigation. PMID 29202483 DOI: 10.1172/Jci96499  0.361
2017 Abrams CK, Goman M, Wong S, Scherer SS, Kleopa KA, Peinado A, Freidin MM. Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations. Scientific Reports. 7: 40166. PMID 28071741 DOI: 10.1038/Srep40166  0.412
2016 Kagiava A, Sargiannidou I, Theophilidis G, Karaiskos C, Richter J, Bashiardes S, Schiza N, Nearchou M, Christodoulou C, Scherer SS, Kleopa KA. Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy. Proceedings of the National Academy of Sciences of the United States of America. PMID 27035961 DOI: 10.1073/Pnas.1522202113  0.401
2016 Motley WW, Palaima P, Yum SW, Gonzalez MA, Tao F, Wanschitz JV, Strickland AV, Löscher WN, De Vriendt E, Koppi S, Medne L, Janecke AR, Jordanova A, Zuchner S, Scherer SS. De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease. Brain : a Journal of Neurology. PMID 27009151 DOI: 10.1093/Brain/Aww055  0.369
2016 Thomas FP, Guergueltcheva V, Gondim FA, Tournev I, Rao CV, Ishpekova B, Kinsella LJ, Pan Y, Geller TJ, Litvinenko I, De Jonghe P, Scherer SS, Jordanova A. Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy. Journal of Neurology. PMID 26725087 DOI: 10.1007/S00415-015-7989-8  0.342
2016 Auer-Grumbach M, Bennett DLH, Andersen P, Harms MB, Reilly MM, Weishaupt J, Strom TM, Walther T, Scherer SS, Zuchner S, Martini R, Senderek J. Rare Coding Variants In The Mme Gene, Encoding The Metalloprotease Neprilysin, Are Linked To Late-Onset Axonal Neuropathies Journal of the Peripheral Nervous System. 21: 235-235. DOI: 10.1111/Jns.12181  0.324
2015 Sanmaneechai O, Feely S, Scherer SS, Herrmann DN, Burns J, Muntoni F, Li J, Siskind CE, Day JW, Laura M, Sumner CJ, Lloyd TE, Ramchandren S, Shy RR, Grider T, et al. Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene. Brain : a Journal of Neurology. 138: 3180-92. PMID 26310628 DOI: 10.1093/Brain/Awv241  0.383
2015 Sargiannidou I, Kagiava A, Bashiardes S, Richter J, Christodoulou C, Scherer SS, Kleopa KA. Intraneural GJB1 gene delivery improves nerve pathology in a model of X-linked Charcot-Marie-Tooth disease. Annals of Neurology. 78: 303-16. PMID 26010264 DOI: 10.1002/Ana.24441  0.407
2015 Baets J, Duan X, Wu Y, Smith G, Seeley WW, Mademan I, McGrath NM, Beadell NC, Khoury J, Botuyan MV, Mer G, Worrell GA, Hojo K, DeLeon J, Laura M, ... ... Scherer SS, et al. Defects of mutant DNMT1 are linked to a spectrum of neurological disorders. Brain : a Journal of Neurology. 138: 845-61. PMID 25678562 DOI: 10.1093/Brain/Awv010  0.348
2015 Fridman V, Bundy B, Reilly MM, Pareyson D, Bacon C, Burns J, Day J, Feely S, Finkel RS, Grider T, Kirk CA, Herrmann DN, Laurá M, Li J, Lloyd T, ... ... Scherer SS, et al. CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 873-8. PMID 25430934 DOI: 10.1136/Jnnp-2014-308826  0.333
2014 Abrams CK, Scherer SS, Flores-Obando R, Freidin MM, Wong S, Lamantea E, Farina L, Scaioli V, Pareyson D, Salsano E. A new mutation in GJC2 associated with subclinical leukodystrophy. Journal of Neurology. 261: 1929-38. PMID 25059390 DOI: 10.1007/S00415-014-7429-1  0.435
2014 King CH, Lancaster E, Salomon D, Peles E, Scherer SS. Kv7.2 regulates the function of peripheral sensory neurons. The Journal of Comparative Neurology. 522: 3262-80. PMID 24687876 DOI: 10.1002/Cne.23595  0.602
2014 Foley AR, Menezes MP, Pandraud A, Gonzalez MA, Al-Odaib A, Abrams AJ, Sugano K, Yonezawa A, Manzur AY, Burns J, Hughes I, McCullagh BG, Jungbluth H, Lim MJ, Lin JP, ... ... Scherer SS, et al. Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2. Brain : a Journal of Neurology. 137: 44-56. PMID 24253200 DOI: 10.1093/Brain/Awt315  0.367
2013 Caramins M, Colebatch JG, Bainbridge MN, Scherer SS, Abrams CK, Hackett EL, Freidin MM, Jhangiani SN, Wang M, Wu Y, Muzny DM, Lindeman R, Gibbs RA. Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1). Human Molecular Genetics. 22: 4329-38. PMID 23773993 DOI: 10.1093/Hmg/Ddt282  0.328
2012 Kleopa KA, Abrams CK, Scherer SS. How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease? Brain Research. 1487: 198-205. PMID 22771394 DOI: 10.1016/J.Brainres.2012.03.068  0.459
2012 Ferguson TA, Scherer SS. Neuronal cadherin (NCAD) increases sensory neurite formation and outgrowth on astrocytes. Neuroscience Letters. 522: 108-12. PMID 22698587 DOI: 10.1016/J.Neulet.2012.06.013  0.316
2012 King CH, Scherer SS. Kv7.5 is the primary Kv7 subunit expressed in C-fibers. The Journal of Comparative Neurology. 520: 1940-50. PMID 22134895 DOI: 10.1002/Cne.23019  0.591
2012 Abrams CK, Scherer SS. Gap junctions in inherited human disorders of the central nervous system. Biochimica Et Biophysica Acta. 1818: 2030-47. PMID 21871435 DOI: 10.1016/J.Bbamem.2011.08.015  0.416
2011 Shroff S, Mierzwa A, Scherer SS, Peles E, Arevalo JC, Chao MV, Rosenbluth J. Paranodal permeability in "myelin mutants". Glia. 59: 1447-57. PMID 21618613 DOI: 10.1002/Glia.21188  0.342
2011 Potter KA, Kern MJ, Fullbright G, Bielawski J, Scherer SS, Yum SW, Li JJ, Cheng H, Han X, Venkata JK, Khan PA, Rohrer B, Hama H. Central nervous system dysfunction in a mouse model of FA2H deficiency. Glia. 59: 1009-21. PMID 21491498 DOI: 10.1002/Glia.21172  0.342
2011 Lancaster E, Huijbers MG, Bar V, Boronat A, Wong A, Martinez-Hernandez E, Wilson C, Jacobs D, Lai M, Walker RW, Graus F, Bataller L, Illa I, Markx S, Strauss KA, ... ... Scherer SS, et al. Investigations of caspr2, an autoantigen of encephalitis and neuromyotonia. Annals of Neurology. 69: 303-11. PMID 21387375 DOI: 10.1002/Ana.22297  0.356
2011 Zhang J, Scherer SS, Yum SW. Dominant Cx26 mutants associated with hearing loss have dominant-negative effects on wild type Cx26. Molecular and Cellular Neurosciences. 47: 71-8. PMID 21040787 DOI: 10.1016/J.Mcn.2010.10.002  0.355
2010 Wasseff S, Abrams CK, Scherer SS. A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes. Neuron Glia Biology. 6: 213-23. PMID 21375791 DOI: 10.1017/S1740925X11000019  0.372
2010 Kennerson ML, Nicholson GA, Kaler SG, Kowalski B, Mercer JF, Tang J, Llanos RM, Chu S, Takata RI, Speck-Martins CE, Baets J, Almeida-Souza L, Fischer D, Timmerman V, Taylor PE, ... Scherer SS, et al. Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy. American Journal of Human Genetics. 86: 343-52. PMID 20170900 DOI: 10.1016/J.Ajhg.2010.01.027  0.345
2010 Yum SW, Zhang J, Scherer SS. Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30. Neurobiology of Disease. 38: 226-36. PMID 20096356 DOI: 10.1016/J.Nbd.2010.01.010  0.36
2009 Yum SW, Zhang J, Mo K, Li J, Scherer SS. A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy. Annals of Neurology. 66: 759-70. PMID 20039262 DOI: 10.1002/Ana.21728  0.428
2009 Orthmann-Murphy JL, Salsano E, Abrams CK, Bizzi A, Uziel G, Freidin MM, Lamantea E, Zeviani M, Scherer SS, Pareyson D. Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations. Brain : a Journal of Neurology. 132: 426-38. PMID 19056803 DOI: 10.1093/Brain/Awn328  0.77
2008 Scherer SS, Wrabetz L. Molecular mechanisms of inherited demyelinating neuropathies. Glia. 56: 1578-89. PMID 18803325 DOI: 10.1002/Glia.20751  0.344
2008 Sargiannidou I, Ahn M, Enriquez AD, Peinado A, Reynolds R, Abrams C, Scherer SS, Kleopa KA. Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants. Neurobiology of Disease. 30: 221-33. PMID 18353664 DOI: 10.1016/J.Nbd.2008.01.009  0.428
2008 Orthmann-Murphy JL, Abrams CK, Scherer SS. Gap junctions couple astrocytes and oligodendrocytes. Journal of Molecular Neuroscience : Mn. 35: 101-16. PMID 18236012 DOI: 10.1007/S12031-007-9027-5  0.768
2008 Ahn M, Lee J, Gustafsson A, Enriquez A, Lancaster E, Sul JY, Haydon PG, Paul DL, Huang Y, Abrams CK, Scherer SS. Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct. Journal of Neuroscience Research. 86: 992-1006. PMID 17972320 DOI: 10.1002/Jnr.21561  0.383
2007 Orthmann-Murphy JL, Freidin M, Fischer E, Scherer SS, Abrams CK. Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 13949-57. PMID 18094232 DOI: 10.1523/Jneurosci.3395-07.2007  0.751
2007 Maurel P, Einheber S, Galinska J, Thaker P, Lam I, Rubin MB, Scherer SS, Murakami Y, Gutmann DH, Salzer JL. Nectin-like proteins mediate axon Schwann cell interactions along the internode and are essential for myelination. The Journal of Cell Biology. 178: 861-74. PMID 17724124 DOI: 10.1083/Jcb.200705132  0.391
2007 Yum SW, Zhang J, Valiunas V, Kanaporis G, Brink PR, White TW, Scherer SS. Human connexin26 and connexin30 form functional heteromeric and heterotypic channels. American Journal of Physiology. Cell Physiology. 293: C1032-48. PMID 17615163 DOI: 10.1152/Ajpcell.00011.2007  0.379
2007 Spiegel I, Adamsky K, Eshed Y, Milo R, Sabanay H, Sarig-Nadir O, Horresh I, Scherer SS, Rasband MN, Peles E. A central role for Necl4 (SynCAM4) in Schwann cell-axon interaction and myelination. Nature Neuroscience. 10: 861-9. PMID 17558405 DOI: 10.1038/Nn1915  0.388
2007 Shy ME, Siskind C, Swan ER, Krajewski KM, Doherty T, Fuerst DR, Ainsworth PJ, Lewis RA, Scherer SS, Hahn AF. CMT1X phenotypes represent loss of GJB1 gene function. Neurology. 68: 849-55. PMID 17353473 DOI: 10.1212/01.Wnl.0000256709.08271.4D  0.369
2007 Orthmann-Murphy JL, Enriquez AD, Abrams CK, Scherer SS. Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease. Molecular and Cellular Neurosciences. 34: 629-41. PMID 17344063 DOI: 10.1016/J.Mcn.2007.01.010  0.772
2007 Huang Y, Grinspan JB, Abrams CK, Scherer SS. Pannexin1 is expressed by neurons and glia but does not form functional gap junctions. Glia. 55: 46-56. PMID 17009242 DOI: 10.1002/Glia.20435  0.381
2006 Menichella DM, Majdan M, Awatramani R, Goodenough DA, Sirkowski E, Scherer SS, Paul DL. Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 10984-91. PMID 17065440 DOI: 10.1523/Jneurosci.0304-06.2006  0.39
2006 Jeng LJ, Balice-Gordon RJ, Messing A, Fischbeck KH, Scherer SS. The effects of a dominant connexin32 mutant in myelinating Schwann cells. Molecular and Cellular Neurosciences. 32: 283-98. PMID 16790356 DOI: 10.1016/J.Mcn.2006.05.001  0.459
2006 Spiegel I, Adamsky K, Eisenbach M, Eshed Y, Spiegel A, Mirsky R, Scherer SS, Peles E. Identification of novel cell-adhesion molecules in peripheral nerves using a signal-sequence trap. Neuron Glia Biology. 2: 27-38. PMID 16721426 DOI: 10.1017/S1740925X0600007X  0.399
2006 Kleopa KA, Elman LB, Lang B, Vincent A, Scherer SS. Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations. Brain : a Journal of Neurology. 129: 1570-84. PMID 16613892 DOI: 10.1093/Brain/Awl084  0.358
2006 Pan Z, Kao T, Horvath Z, Lemos J, Sul JY, Cranstoun SD, Bennett V, Scherer SS, Cooper EC. A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 2599-613. PMID 16525039 DOI: 10.1523/Jneurosci.4314-05.2006  0.354
2006 Shy ME, Scavina MT, Clark A, Krajewski KM, Li J, Kamholz J, Kolodny E, Szigeti K, Fischer RA, Saifi GM, Scherer SS, Lupski JR. T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy. Annals of Neurology. 59: 358-64. PMID 16437560 DOI: 10.1002/Ana.20777  0.35
2005 Occhi S, Zambroni D, Del Carro U, Amadio S, Sirkowski EE, Scherer SS, Campbell KP, Moore SA, Chen ZL, Strickland S, Di Muzio A, Uncini A, Wrabetz L, Feltri ML. Both laminin and Schwann cell dystroglycan are necessary for proper clustering of sodium channels at nodes of Ranvier. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 9418-27. PMID 16221851 DOI: 10.1523/Jneurosci.2068-05.2005  0.618
2005 Huang Y, Sirkowski EE, Stickney JT, Scherer SS. Prenylation-defective human connexin32 mutants are normally localized and function equivalently to wild-type connexin32 in myelinating Schwann cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 7111-20. PMID 16079393 DOI: 10.1523/Jneurosci.1319-05.2005  0.411
2005 Liang GS, de Miguel M, Gómez-Hernández JM, Glass JD, Scherer SS, Mintz M, Barrio LC, Fischbeck KH. Severe neuropathy with leaky connexin32 hemichannels. Annals of Neurology. 57: 749-54. PMID 15852376 DOI: 10.1002/Ana.20459  0.383
2005 Scherer SS, Xu YT, Messing A, Willecke K, Fischbeck KH, Jeng LJ. Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 1550-9. PMID 15703409 DOI: 10.1523/Jneurosci.3082-04.2005  0.414
2004 Kleopa KA, Orthmann JL, Enriquez A, Paul DL, Scherer SS. Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes. Glia. 47: 346-57. PMID 15293232 DOI: 10.1002/Glia.20043  0.401
2004 Devaux JJ, Kleopa KA, Cooper EC, Scherer SS. KCNQ2 is a nodal K+ channel. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 1236-44. PMID 14762142 DOI: 10.1523/Jneurosci.4512-03.2004  0.367
2003 Taylor RA, Simon EM, Marks HG, Scherer SS. The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem. Neurology. 61: 1475-8. PMID 14663027 DOI: 10.1212/01.Wnl.0000095960.48964.25  0.444
2003 Scarlato M, Ara J, Bannerman P, Scherer S, Pleasure D. Induction of neuropilins-1 and -2 and their ligands, Sema3A, Sema3F, and VEGF, during Wallerian degeneration in the peripheral nervous system. Experimental Neurology. 183: 489-98. PMID 14552889 DOI: 10.1016/S0014-4886(03)00046-3  0.302
2003 Menichella DM, Goodenough DA, Sirkowski E, Scherer SS, Paul DL. Connexins are critical for normal myelination in the CNS. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 5963-73. PMID 12843301 DOI: 10.1523/Jneurosci.23-13-05963.2003  0.438
2003 Devaux J, Alcaraz G, Grinspan J, Bennett V, Joho R, Crest M, Scherer SS. Kv3.1b is a novel component of CNS nodes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 4509-18. PMID 12805291 DOI: 10.1523/Jneurosci.23-11-04509.2003  0.333
2003 Street VA, Bennett CL, Goldy JD, Shirk AJ, Kleopa KA, Tempel BL, Lipe HP, Scherer SS, Bird TD, Chance PF. Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C. Neurology. 60: 22-6. PMID 12525712 DOI: 10.1212/Wnl.60.1.22  0.346
2002 Yum SW, Kleopa KA, Shumas S, Scherer SS. Diverse trafficking abnormalities of connexin32 mutants causing CMTX. Neurobiology of Disease. 11: 43-52. PMID 12460545 DOI: 10.1006/Nbdi.2002.0545  0.386
2002 Bermingham JR, Shumas S, Whisenhunt T, Sirkowski EE, O'Connell S, Scherer SS, Rosenfeld MG. Identification of genes that are downregulated in the absence of the POU domain transcription factor pou3f1 (Oct-6, Tst-1, SCIP) in sciatic nerve. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 10217-31. PMID 12451123 DOI: 10.1523/Jneurosci.22-23-10217.2002  0.389
2002 Poliak S, Matlis S, Ullmer C, Scherer SS, Peles E. Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells. The Journal of Cell Biology. 159: 361-72. PMID 12403818 DOI: 10.1083/Jcb.200207050  0.389
2002 Altevogt BM, Kleopa KA, Postma FR, Scherer SS, Paul DL. Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 6458-70. PMID 12151525 DOI: 10.1523/Jneurosci.22-15-06458.2002  0.44
2002 Kleopa KA, Yum SW, Scherer SS. Cellular mechanisms of connexin32 mutations associated with CNS manifestations. Journal of Neuroscience Research. 68: 522-34. PMID 12111842 DOI: 10.1002/Jnr.10255  0.44
2002 Mikol DD, Scherer SS, Duckett SJ, Hong HL, Feldman EL. Schwann cell caveolin-1 expression increases during myelination and decreases after axotomy. Glia. 38: 191-9. PMID 11968057 DOI: 10.1002/Glia.10063  0.406
2002 Arroyo EJ, Xu T, Grinspan J, Lambert S, Levinson SR, Brophy PJ, Peles E, Scherer SS. Genetic dysmyelination alters the molecular architecture of the nodal region. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 1726-37. PMID 11880502 DOI: 10.1523/Jneurosci.22-05-01726.2002  0.372
2002 Atanasoski S, Scherer SS, Nave KA, Suter U. Proliferation of Schwann cells and regulation of cyclin D1 expression in an animal model of Charcot-Marie-Tooth disease type 1A. Journal of Neuroscience Research. 67: 443-9. PMID 11835311 DOI: 10.1002/Jnr.10133  0.356
2001 Menichella DM, Arroyo EJ, Awatramani R, Xu T, Baron P, Vallat JM, Balsamo J, Lilien J, Scarlato G, Kamholz J, Scherer SS, Shy ME. Protein zero is necessary for E-cadherin-mediated adherens junction formation in Schwann cells. Molecular and Cellular Neurosciences. 18: 606-18. PMID 11749037 DOI: 10.1006/Mcne.2001.1041  0.37
2001 Atanasoski S, Shumas S, Dickson C, Scherer SS, Suter U. Differential cyclin D1 requirements of proliferating Schwann cells during development and after injury. Molecular and Cellular Neurosciences. 18: 581-92. PMID 11749035 DOI: 10.1006/Mcne.2001.1055  0.326
2001 Arroyo EJ, Xu T, Poliak S, Watson M, Peles E, Scherer SS. Internodal specializations of myelinated axons in the central nervous system. Cell and Tissue Research. 305: 53-66. PMID 11512672 DOI: 10.1007/S004410100403  0.384
2001 Scherer SS, Xu T, Crino P, Arroyo EJ, Gutmann DH. Ezrin, radixin, and moesin are components of Schwann cell microvilli. Journal of Neuroscience Research. 65: 150-64. PMID 11438984 DOI: 10.1002/Jnr.1138  0.359
2001 Brown AA, Xu T, Arroyo EJ, Levinson SR, Brophy PJ, Peles E, Scherer SS. Molecular organization of the nodal region is not altered in spontaneously diabetic BB-Wistar rats. Journal of Neuroscience Research. 65: 139-49. PMID 11438983 DOI: 10.1002/Jnr.1137  0.324
2001 Sperber BR, Boyle-Walsh EA, Engleka MJ, Gadue P, Peterson AC, Stein PL, Scherer SS, McMorris FA. A unique role for Fyn in CNS myelination. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 2039-47. PMID 11245687 DOI: 10.1523/Jneurosci.21-06-02039.2001  0.375
2001 Bermingham JR, Shumas S, Whisenhunt T, Rosenfeld MG, Scherer SS. Modification of representational difference analysis applied to the isolation of forskolin-regulated genes from Schwann cells. Journal of Neuroscience Research. 63: 516-24. PMID 11241587 DOI: 10.1002/Jnr.1046  0.333
2001 Weiner JA, Fukushima N, Contos JJA, Scherer SS, Chun J. Regulation of Schwann Cell Morphology and Adhesion by Receptor-Mediated Lysophosphatidic Acid Signaling The Journal of Neuroscience. 21: 7069-7078. DOI: 10.1523/Jneurosci.21-18-07069.2001  0.337
2000 Jiang H, Duchala CS, Awatramani R, Shumas S, Carlock L, Kamholz J, Garbern J, Scherer SS, Shy ME, Macklin WB. Proteolipid protein mRNA stability is regulated by axonal contact in the rodent peripheral nervous system. Journal of Neurobiology. 44: 7-19. PMID 10880128 DOI: 10.1002/1097-4695(200007)44:1<7::Aid-Neu2>3.0.Co;2-A  0.378
2000 Kamholz J, Menichella D, Jani A, Garbern J, Lewis RA, Krajewski KM, Lilien J, Scherer SS, Shy ME. Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapy. Brain : a Journal of Neurology. 123: 222-33. PMID 10648431 DOI: 10.1093/Brain/123.2.222  0.399
1999 Lin GS, Glass JD, Shumas S, Scherer SS, Fischbeck KH. A Unique Mutation in Connexin32 Associated with Severe, Early Onset CMTX in a Heterozygous Female. Annals of the New York Academy of Sciences. 883: 481-484. PMID 29086962 DOI: 10.1111/J.1749-6632.1999.Tb08616.X  0.308
1999 Fischbeck KH, Abel A, Lin GS, Scherer SS. X-linked Charcot-Marie-Tooth Disease and Connexin32. Annals of the New York Academy of Sciences. 883: 36-41. PMID 29086942 DOI: 10.1111/J.1749-6632.1999.Tb08564.X  0.464
1999 Arroyo EJ, Xu YT, Zhou L, Messing A, Peles E, Chiu SY, Scherer SS. Myelinating Schwann cells determine the internodal localization of Kv1.1, Kv1.2, Kvbeta2, and Caspr. Journal of Neurocytology. 28: 333-47. PMID 10739575 DOI: 10.1023/A:1007009613484  0.403
1999 Fischbeck KH, Abel A, Lin GS, Scherer SS. X-linked Charcot-Marie-Tooth disease and connexin32. Annals of the New York Academy of Sciences. 883: 36-41. PMID 10586227  0.36
1999 Abel A, Bone LJ, Messing A, Scherer SS, Fischbeck KH. Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-Tooth disease. Journal of Neuropathology and Experimental Neurology. 58: 702-10. PMID 10411340 DOI: 10.1097/00005072-199907000-00004  0.398
1999 Scherer SS, Bone LJ, Deschênes SM, Abel A, Balice-Gordon RJ, Fischbeck KH. The role of the gap junction protein connexin32 in the pathogenesis of X-linked Charcot-Marie-Tooth disease. Novartis Foundation Symposium. 219: 175-85; discussion 1. PMID 10207904 DOI: 10.1002/9780470515587.Ch11  0.412
1999 Scherer SS, Fischbeck KH. Is CMTX an axonopathy? Neurology. 52: 432-3. PMID 9932989 DOI: 10.1212/Wnl.52.2.432-A  0.412
1998 Arroyo EJ, Bermingham JR, Rosenfeld MG, Scherer SS. Promyelinating Schwann cells express Tst-1/SCIP/Oct-6. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 18: 7891-902. PMID 9742157 DOI: 10.1523/Jneurosci.18-19-07891.1998  0.359
1998 Balice-Gordon RJ, Bone LJ, Scherer SS. Functional gap junctions in the schwann cell myelin sheath. The Journal of Cell Biology. 142: 1095-104. PMID 9722620 DOI: 10.1083/Jcb.142.4.1095  0.396
1998 Scherer SS, Xu YT, Nelles E, Fischbeck K, Willecke K, Bone LJ. Connexin32-null mice develop demyelinating peripheral neuropathy. Glia. 24: 8-20. PMID 9700485 DOI: 10.1002/(Sici)1098-1136(199809)24:1<8::Aid-Glia2>3.0.Co;2-3  0.417
1998 Wrabetz L, Taveggia C, Feltri ML, Quattrini A, Awatramani R, Scherer SS, Messing A, Kamholz J. A minimal human MBP promoter-lacZ transgene is appropriately regulated in developing brain and after optic enucleation, but not in shiverer mutant mice. Journal of Neurobiology. 34: 10-26. PMID 9469615 DOI: 10.1002/(Sici)1097-4695(199801)34:1<10::Aid-Neu2>3.0.Co;2-F  0.36
1997 Bermingham-McDonogh O, Xu YT, Marchionni MA, Scherer SS. Neuregulin expression in PNS neurons: isoforms and regulation by target interactions. Molecular and Cellular Neurosciences. 10: 184-95. PMID 9532580 DOI: 10.1006/Mcne.1997.0654  0.334
1997 Einheber S, Zanazzi G, Ching W, Scherer S, Milner TA, Peles E, Salzer JL. The axonal membrane protein Caspr, a homologue of neurexin IV, is a component of the septate-like paranodal junctions that assemble during myelination. The Journal of Cell Biology. 139: 1495-506. PMID 9396755 DOI: 10.1083/Jcb.139.6.1495  0.403
1997 Deschênes SM, Walcott JL, Wexler TL, Scherer SS, Fischbeck KH. Altered trafficking of mutant connexin32. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 9077-84. PMID 9364054 DOI: 10.1523/Jneurosci.17-23-09077.1997  0.403
1997 Bone LJ, Deschênes SM, Balice-Gordon RJ, Fischbeck KH, Scherer SS. Connexin32 and X-linked Charcot-Marie-Tooth disease. Neurobiology of Disease. 4: 221-30. PMID 9361298 DOI: 10.1006/Nbdi.1997.0152  0.455
1997 Lynch DR, Hara H, Yum SW, Chance PF, Scherer SS, Bird SJ, Fischbeck KH. Autosomal dominant transmission of Dejerine-Sottas disease (HMSN III). Neurology. 49: 601-3. PMID 9270606 DOI: 10.1212/Wnl.49.2.601  0.313
1997 Shy ME, Arroyo E, Sladky J, Menichella D, Jiang H, Xu W, Kamholz J, Scherer SS. Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP). Journal of Neuropathology and Experimental Neurology. 56: 811-21. PMID 9210878 DOI: 10.1097/00005072-199756070-00008  0.374
1997 Feltri ML, Arona M, Scherer SS, Wrabetz L. Cloning and sequence of the cDNA encoding the beta 4 integrin subunit in rat peripheral nerve. Gene. 186: 299-304. PMID 9074510 DOI: 10.1016/S0378-1119(96)00725-1  0.585
1997 Awatramani R, Scherer S, Grinspan J, Collarini E, Skoff R, O’Hagan D, Garbern J, Kamholz J. Evidence That the Homeodomain Protein Gtx Is Involved in the Regulation of Oligodendrocyte Myelination The Journal of Neuroscience. 17: 6657-6668. DOI: 10.1523/Jneurosci.17-17-06657.1997  0.343
1996 Zorick TS, Syroid DE, Arroyo E, Scherer SS, Lemke G. The Transcription Factors SCIP and Krox-20 Mark Distinct Stages and Cell Fates in Schwann Cell Differentiation Molecular and Cellular Neurosciences. 8: 129-45. PMID 8954628 DOI: 10.1006/Mcne.1996.0052  0.409
1996 Scherer SS, Gutmann DH. Expression of the neurofibromatosis 2 tumor suppressor gene product, merlin, in Schwann cells. Journal of Neuroscience Research. 46: 595-605. PMID 8951671 DOI: 10.1002/(Sici)1097-4547(19961201)46:5<595::Aid-Jnr8>3.0.Co;2-E  0.352
1996 Shy ME, Shi Y, Wrabetz L, Kamholz J, Scherer SS. Axon-Schwann cell interactions regulate the expression of c-jun in Schwann cells. Journal of Neuroscience Research. 43: 511-25. PMID 8833086 DOI: 10.1002/(Sici)1097-4547(19960301)43:5<511::Aid-Jnr1>3.0.Co;2-L  0.401
1996 Bermingham JR, Scherer SS, O'Connell S, Arroyo E, Kalla KA, Powell FL, Rosenfeld MG. Tst-1/Oct-6/SCIP regulates a unique step in peripheral myelination and is required for normal respiration. Genes & Development. 10: 1751-62. PMID 8698235 DOI: 10.1101/Gad.10.14.1751  0.414
1995 Wrabetz L, Feltri ML, Kim H, Daston M, Kamholz J, Scherer SS, Ratner N. Regulation of neurofibromin expression in rat sciatic nerve and cultured Schwann cells. Glia. 15: 22-32. PMID 8847098 DOI: 10.1002/Glia.440150104  0.363
1995 Scherer SS, Deschênes SM, Xu YT, Grinspan JB, Fischbeck KH, Paul DL. Connexin32 is a myelin-related protein in the PNS and CNS. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 15: 8281-94. PMID 8613761 DOI: 10.1523/Jneurosci.15-12-08281.1995  0.421
1995 Shy ME, Tani M, Shi YJ, Whyatt SA, Chbihi T, Scherer SS, Kamholz J. An adenoviral vector can transfer lacZ expression into Schwann cells in culture and in sciatic nerve. Annals of Neurology. 38: 429-36. PMID 7668829 DOI: 10.1002/Ana.410380313  0.387
1994 Scherer SS, Wang DY, Kuhn R, Lemke G, Wrabetz L, Kamholz J. Axons regulate Schwann cell expression of the POU transcription factor SCIP. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 14: 1930-42. PMID 8158248 DOI: 10.1523/Jneurosci.14-04-01930.1994  0.394
1994 Scherer SS, Braun PE, Grinspan J, Collarini E, Wang DY, Kamholz J. Differential regulation of the 2',3'-cyclic nucleotide 3'-phosphodiesterase gene during oligodendrocyte development. Neuron. 12: 1363-75. PMID 8011341 DOI: 10.1016/0896-6273(94)90451-0  0.325
1994 Bruzzone R, White TW, Scherer SS, Fischbeck KH, Paul DL. Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease. Neuron. 13: 1253-60. PMID 7946361 DOI: 10.1016/0896-6273(94)90063-9  0.405
1994 Chiu SY, Scherer SS, Blonski M, Kang SS, Messing A. Axons regulate the expression of Shaker-like potassium channel genes in Schwann cells in peripheral nerve. Glia. 12: 1-11. PMID 7843783 DOI: 10.1002/Glia.440120102  0.408
1994 Scherer SS, Xu YT, Roling D, Wrabetz L, Feltri ML, Kamholz J. Expression of growth-associated protein-43 kD in Schwann cells is regulated by axon-Schwann cell interactions and cAMP. Journal of Neuroscience Research. 38: 575-89. PMID 7815473 DOI: 10.1002/Jnr.490380510  0.396
1994 Curtis R, Scherer SS, Somogyi R, Adryan KM, Ip NY, Zhu Y, Lindsay RM, DiStefano PS. Retrograde axonal transport of LIF is increased by peripheral nerve injury: correlation with increased LIF expression in distal nerve. Neuron. 12: 191-204. PMID 7507340 DOI: 10.1016/0896-6273(94)90163-5  0.536
1993 Bergoffen J, Scherer SS, Wang S, Scott MO, Bone LJ, Paul DL, Chen K, Lensch MW, Chance PF, Fischbeck KH. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science (New York, N.Y.). 262: 2039-42. PMID 8266101 DOI: 10.1126/Science.8266101  0.401
1993 Davis S, Aldrich TH, Ip NY, Stahl N, Scherer S, Farruggella T, DiStefano PS, Curtis R, Panayotatos N, Gascan H. Released form of CNTF receptor alpha component as a soluble mediator of CNTF responses. Science (New York, N.Y.). 259: 1736-9. PMID 7681218 DOI: 10.1126/Science.7681218  0.472
1992 Friedman B, Scherer SS, Rudge JS, Helgren M, Morrisey D, McClain J, Wang DY, Wiegand SJ, Furth ME, Lindsay RM. Regulation of ciliary neurotrophic factor expression in myelin-related Schwann cells in vivo. Neuron. 9: 295-305. PMID 1497895 DOI: 10.1016/0896-6273(92)90168-D  0.4
1992 Scherer SS, Vogelbacker HH, Kamholz J. Axons modulate the expression of proteolipid protein in the CNS. Journal of Neuroscience Research. 32: 138-48. PMID 1383558 DOI: 10.1002/Jnr.490320203  0.371
1992 Kamholz J, Sessa M, Scherer S, Vogelbacker H, Mokuno K, Baron P, Wrabetz L, Shy M, Pleasure D. Structure and expression of proteolipid protein in the peripheral nervous system Journal of Neuroscience Research. 31: 231-244. PMID 1374129 DOI: 10.1002/Jnr.490310204  0.386
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