| Year |
Citation |
Score |
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 2015 |
Scherer SS. Blocking bad. Brain : a Journal of Neurology. 138: 3132-3. PMID 26503937 DOI: 10.1093/brain/awv279 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 2003 |
Suter U, Scherer SS. Disease mechanisms in inherited neuropathies. Nature Reviews. Neuroscience. 4: 714-26. PMID 12951564 DOI: 10.1038/nrn1196 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 1999 |
Scherer SS, Fischbeck KH. Is CMTX an axonopathy? Neurology. 52: 432-3. PMID 9932989 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
|
| 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 |
0.68 |
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