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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
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142 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 Pipis M, Feely SME, Polke JM, Skorupinska M, Perez L, Shy RR, Laura M, Morrow JM, Moroni I, Pisciotta C, Taroni F, Vujovic D, Lloyd TE, Acsadi G, Yum SW, ... ... Scherer SS, et al. Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study. Brain : a Journal of Neurology. PMID 33415332 DOI: 10.1093/brain/awaa323  0.76
2020 Bray P, Cornett KMD, Estilow T, Pareyson D, Zuccarino R, Skorupinska M, Pipis M, Sowden JE, Scherer S, Reilly MM, Shy ME, Herrmann DN, Burns J, Eichinger KJ. Reliability of the Charcot-Marie-Tooth functional outcome measure. Journal of the Peripheral Nervous System : Jpns. 25: 288-291. PMID 32844461 DOI: 10.1111/jns.12406  0.76
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. Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. Nature Genetics. PMID 32457452 DOI: 10.1038/s41588-020-0649-7  0.76
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  0.76
2020 Fridman V, Sillau S, Acsadi G, Bacon C, Dooley K, Burns J, Day J, Feely S, Finkel RS, Grider T, Gutmann L, Herrmann DN, Kirk CA, Knause SA, Laurá M, ... ... Scherer SS, et al. A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores. Neurology. PMID 32047073 DOI: 10.1212/WNL.0000000000009035  0.76
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  0.76
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  0.76
2019 Tao F, Beecham GW, Rebelo AP, Blanton SH, Moran JJ, Lopez-Anido C, Svaren J, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, Herrmann DN, ... ... Scherer SS, et al. Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Journal of Neuromuscular Diseases. PMID 30958311 DOI: 10.3233/JND-190377  0.76
2019 Tao F, Beecham GW, Rebelo AP, Blanton SH, Moran JJ, Lopez-Anido C, Svaren J, Morrow JM, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, ... ... Scherer SS, et al. Variation in SIPA1L2 is Correlated with Phenotype Modification in CMT Type 1A. Annals of Neurology. PMID 30706531 DOI: 10.1002/ana.25426  0.76
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  0.76
2018 Saghira C, Bis DM, Stanek D, Strickland A, Herrmann DN, Reilly MM, Scherer SS, Shy ME, Züchner S. Variantpathogenicity evaluationin the community-driven Inherited Neuropathy Variant Browser. Human Mutation. PMID 29473246 DOI: 10.1002/humu.23412  0.76
2017 Rossor AM, Carr AS, Devine H, Chandrashekar H, Pelayo-Negro AL, Pareyson D, Shy ME, Scherer SS, Reilly MM. Peripheral neuropathy in complex inherited diseases: an approach to diagnosis. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 28794150 DOI: 10.1136/jnnp-2016-313960  0.76
2017 Panosyan FB, Laura M, Rossor AM, Pisciotta C, Piscosquito G, Burns J, Li J, Yum SW, Lewis RA, Day J, Horvath R, Herrmann DN, Shy ME, Pareyson D, Reilly MM, ... Scherer SS, et al. Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1). Neurology. PMID 28768847 DOI: 10.1212/WNL.0000000000004296  0.76
2017 Panosyan FB, Kirk CA, Marking D, Reilly MM, Scherer SS, Shy ME, Herrmann DN. Carpal Tunnel Syndrome in Inherited Neuropathies: A Retrospective Survey. Muscle & Nerve. PMID 28692128 DOI: 10.1002/mus.25742  0.76
2017 Laurá M, Singh D, Ramdharry G, Morrow J, Skorupinska M, Pareyson D, Burns J, Lewis RA, Scherer S, Herrmann DN, Cullen N, Bradish C, Gaiani L, Martinelli N, Gibbons P, et al. Prevalence and orthopedic management of foot and ankle deformities in Charcot Marie Tooth disease. Muscle & Nerve. PMID 28632967 DOI: 10.1002/mus.25724  0.76
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  0.6
2015 Scherer SS. Blocking bad. Brain : a Journal of Neurology. 138: 3132-3. PMID 26503937 DOI: 10.1093/brain/awv279  0.76
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  0.76
2015 Wasseff SK, Scherer SS. Activated immune response in an inherited leukodystrophy disease caused by the loss of oligodendrocyte gap junctions. Neurobiology of Disease. 82: 86-98. PMID 26051537 DOI: 10.1016/j.nbd.2015.05.018  0.76
2015 Motley WW, Griffin LB, Mademan I, Baets J, De Vriendt E, De Jonghe P, Antonellis A, Jordanova A, Scherer SS. A novel AARS mutation in a family with dominant myeloneuropathy. Neurology. 84: 2040-7. PMID 25904691 DOI: 10.1212/WNL.0000000000001583  0.76
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  0.76
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  0.76
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  0.76
2014 Willison H, Scherer SS. Ranvier revisited: novel nodal antigens stimulate interest in GBS pathogenesis. Neurology. 83: 106-8. PMID 24920859 DOI: 10.1212/WNL.0000000000000581  0.76
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  0.76
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  0.76
2014 Scherer SS, Arroyo EJ. Myelin: Molecular Architecture of CNS and PNS Myelin Sheath Reference Module in Biomedical Research. DOI: 10.1016/B978-0-12-801238-3.04676-6  0.76
2014 Scherer SS, Kleopa KA, Benson MD. Peripheral Neuropathies Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease: Fifth Edition. 1051-1074. DOI: 10.1016/B978-0-12-410529-4.00088-7  0.76
2013 Niu J, Ding L, Li JJ, Kim H, Liu J, Li H, Moberly A, Badea TC, Duncan ID, Son YJ, Scherer SS, Luo W. Modality-based organization of ascending somatosensory axons in the direct dorsal column pathway. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 17691-709. PMID 24198362 DOI: 10.1523/JNEUROSCI.3429-13.2013  0.76
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  0.76
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  0.76
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  0.8
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  0.76
2011 Holzbaur EL, Scherer SS. Microtubules, axonal transport, and neuropathy. The New England Journal of Medicine. 365: 2330-2. PMID 22168648 DOI: 10.1056/NEJMcibr1112481  0.76
2011 Murphy SM, Herrmann DN, McDermott MP, Scherer SS, Shy ME, Reilly MM, Pareyson D. Reliability of the CMT neuropathy score (second version) in Charcot-Marie-Tooth disease. Journal of the Peripheral Nervous System : Jpns. 16: 191-8. PMID 22003934 DOI: 10.1111/j.1529-8027.2011.00350.x  0.76
2011 Zhai J, Zhou W, Li J, Hayworth CR, Zhang L, Misawa H, Klein R, Scherer SS, Balice-Gordon RJ, Kalb RG. The in vivo contribution of motor neuron TrkB receptors to mutant SOD1 motor neuron disease. Human Molecular Genetics. 20: 4116-31. PMID 21816949 DOI: 10.1093/hmg/ddr335  0.76
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  0.76
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  0.76
2011 Wasseff SK, Scherer SS. Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling. Neurobiology of Disease. 42: 506-13. PMID 21396451 DOI: 10.1016/j.nbd.2011.03.003  0.01
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
2008 Scherer SS, Wrabetz L. Molecular mechanisms of inherited demyelinating neuropathies. Glia. 56: 1578-89. PMID 18803325 DOI: 10.1002/glia.20751  1
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
2006 Atanasoski S, Scherer SS, Sirkowski E, Leone D, Garratt AN, Birchmeier C, Suter U. ErbB2 signaling in Schwann cells is mostly dispensable for maintenance of myelinated peripheral nerves and proliferation of adult Schwann cells after injury. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 2124-31. PMID 16481445 DOI: 10.1523/JNEUROSCI.4594-05.2006  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
2004 Berger P, Sirkowski EE, Scherer SS, Suter U. Expression analysis of the N-Myc downstream-regulated gene 1 indicates that myelinating Schwann cells are the primary disease target in hereditary motor and sensory neuropathy-Lom. Neurobiology of Disease. 17: 290-9. PMID 15474366 DOI: 10.1016/j.nbd.2004.07.014  0.76
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  0.76
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  0.76
2003 Suter U, Scherer SS. Disease mechanisms in inherited neuropathies. Nature Reviews. Neuroscience. 4: 714-26. PMID 12951564 DOI: 10.1038/nrn1196  0.76
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  0.76
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  0.76
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  0.76
2003 Scherer SS, Arroyo EJ, Peles E. Functional Organization of the Nodes of Ranvier Myelin Biology and Disorders. 1: 89-116. DOI: 10.1016/B978-012439510-7/50057-7  0.76
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  0.76
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  0.76
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  0.76
2002 Genoud S, Lappe-Siefke C, Goebbels S, Radtke F, Aguet M, Scherer SS, Suter U, Nave KA, Mantei N. Notch1 control of oligodendrocyte differentiation in the spinal cord. The Journal of Cell Biology. 158: 709-18. PMID 12186854 DOI: 10.1083/jcb.200202002  0.76
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  0.76
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  0.76
2002 Awatramani R, Shumas S, Kamholz J, Scherer SS. TGFbeta1 modulates the phenotype of Schwann cells at the transcriptional level. Molecular and Cellular Neurosciences. 19: 307-19. PMID 11906205 DOI: 10.1006/mcne.2001.1094  0.76
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  0.76
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  0.76
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  0.76
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  0.76
2001 Weiner JA, Fukushima N, Contos JJ, Scherer SS, Chun J. Regulation of Schwann cell morphology and adhesion by receptor-mediated lysophosphatidic acid signaling. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 7069-78. PMID 11549717  0.76
2001 Vogelezang MG, Liu Z, Relvas JB, Raivich G, Scherer SS, ffrench-Constant C. Alpha4 integrin is expressed during peripheral nerve regeneration and enhances neurite outgrowth. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 6732-44. PMID 11517262  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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: 481-4. PMID 10586279  0.76
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  0.76
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  0.76
1999 Vogelezang MG, Scherer SS, Fawcett JW, ffrench-Constant C. Regulation of fibronectin alternative splicing during peripheral nerve repair. Journal of Neuroscience Research. 56: 323-33. PMID 10340741 DOI: 10.1002/(SICI)1097-4547(19990515)56:4<323::AID-JNR1>3.0.CO;2-6  0.76
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  0.76
1999 Scherer SS, Fischbeck KH. Is CMTX an axonopathy? Neurology. 52: 432-3. PMID 9932989  0.76
1998 Burstyn-Cohen T, Frumkin A, Xu YT, Scherer SS, Klar A. Accumulation of F-spondin in injured peripheral nerve promotes the outgrowth of sensory axons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 18: 8875-85. PMID 9786993  0.44
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  0.76
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  0.76
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  0.44
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  0.76
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  0.44
1997 Marchionni MA, Grinspan JB, Canoll PD, Mahanthappa NK, Salzer JL, Scherer SS. Neuregulins as potential neuroprotective agents. Annals of the New York Academy of Sciences. 825: 348-65. PMID 9370000  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  1
1996 Fischbeck KH, Deschênes SM, Bone LJ, Scherer SS. Connexin32 and X-linked Charcot-Marie-Tooth disease. Cold Spring Harbor Symposia On Quantitative Biology. 61: 673-7. PMID 9246493  0.76
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  0.36
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  0.76
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 8918830 DOI: 10.1006/mcne.1996.0052  0.36
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  0.76
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  0.76
1996 Bird SJ, Brown MJ, Shy ME, Scherer SS. Chronic inflammatory demyelinating polyneuropathy associated with malignant melanoma. Neurology. 46: 822-4. PMID 8618691 DOI: 10.1212/WNL.46.3.822  0.76
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  0.76
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  0.76
1995 Scherer SS, Xu YT, Bannerman PG, Sherman DL, Brophy PJ. Periaxin expression in myelinating Schwann cells: modulation by axon-glial interactions and polarized localization during development. Development (Cambridge, England). 121: 4265-73. PMID 8575326  0.44
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  0.76
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  0.76
1994 Kamholz J, Shy M, Scherer S, Yoshikawa H, Nishimura T, Sakoda S, Yanagihara T. Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A [5] Annals of Neurology. 36: 451-452. PMID 8080259 DOI: 10.1002/ana.410360326  0.76
1994 Feltri ML, Scherer SS, Nemni R, Kamholz J, Vogelbacker H, Scott MO, Canal N, Quaranta V, Wrabetz L. Beta 4 integrin expression in myelinating Schwann cells is polarized, developmentally regulated and axonally dependent. Development (Cambridge, England). 120: 1287-301. PMID 8026337  0.76
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  0.76
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  0.76
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  0.76
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  0.76
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  0.76
1993 Griot C, Pekosz A, Lukac D, Scherer SS, Stillmock K, Schmeidler D, Endres MJ, Gonzalez-Scarano F, Nathanson N. Polygenic control of neuroinvasiveness in California serogroup bunyaviruses. Journal of Virology. 67: 3861-7. PMID 8510208  0.76
1993 Scherer SS, Kamholz J, Jakowlew SB. Axons modulate the expression of transforming growth factor-betas in Schwann cells. Glia. 8: 265-76. PMID 8406683 DOI: 10.1002/glia.440080407  0.76
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  0.76
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  0.76
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  0.76
1992 Cohen JA, Yachnis AT, Arai M, Davis JG, Scherer SS. Expression of the neu proto-oncogene by Schwann cells during peripheral nerve development and Wallerian degeneration. Journal of Neuroscience Research. 31: 622-34. PMID 1374476 DOI: 10.1002/jnr.490310406  0.76
1992 Feltri ML, Scherer SS, Wrabetz L, Kamholz J, Shy ME. Mitogen-expanded Schwann cells retain the capacity to myelinate regenerating axons after transplantation into rat sciatic nerve. Proceedings of the National Academy of Sciences of the United States of America. 89: 8827-31. PMID 1326765 DOI: 10.1073/PNAS.89.18.8827  0.76
1984 Scherer SS, Easter SS. Degenerative and regenerative changes in the trochlear nerve of goldfish. Journal of Neurocytology. 13: 519-65. PMID 6481411 DOI: 10.1007/BF01148079  0.76
1984 Easter SS, Bratton B, Scherer SS. Growth-related order of the retinal fiber layer in goldfish. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 4: 2173-90. PMID 6470771  0.76
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