Charles K. Abrams - Publications

Albert Einstein College of Medicine, New York, New York, United States 

37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, 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
2018 Papaneophytou CP, Georgiou E, Karaiskos C, Sargiannidou I, Markoullis K, Freidin MM, Abrams CK, Kleopa KA. Regulatory role of oligodendrocyte gap junctions in inflammatory demyelination. Glia. PMID 30325069 DOI: 10.1002/glia.23513  0.32
2018 Alaei SR, Abrams CK, Bulinski JC, Hertzberg EL, Freidin MM. Acetylation of C-terminal lysines modulates protein turnover and stability of Connexin-32. Bmc Cell Biology. 19: 22. PMID 30268116 DOI: 10.1186/s12860-018-0173-0  0.32
2018 Abrams CK, Peinado A, Mahmoud R, Bocarsly M, Zhang H, Chang P, Botello-Smith WM, Freidin MM, Luo Y. Alterations at Arg76 of human connexin 46, a residue associated with cataract formation, cause loss of gap junction formation but preserve hemichannel function. American Journal of Physiology. Cell Physiology. PMID 30044662 DOI: 10.1152/ajpcell.00157.2018  0.32
2018 Flores-Obando RE, Freidin MM, Abrams CK. Rapid and Specific Immunomagnetic Isolation of Mouse Primary Oligodendrocytes. Journal of Visualized Experiments : Jove. PMID 29863670 DOI: 10.3791/57543  0.32
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  0.32
2015 Peinado A, Abrams CK. Patterns of Spontaneous Local Network Activity in Developing Cerebral Cortex: Relationship to Adult Cognitive Function. Plos One. 10: e0131259. PMID 26098958 DOI: 10.1371/journal.pone.0131259  1
2015 Freidin M, Asche-Godin S, Abrams CK. Gene expression profiling studies in regenerating nerves in a mouse model for CMT1X: uninjured Cx32-knockout peripheral nerves display expression profile of injured wild type nerves. Experimental Neurology. 263: 339-49. PMID 25447941 DOI: 10.1016/j.expneurol.2014.10.014  1
2015 Abrams CK, Freidin M. GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems. Cell and Tissue Research. 360: 659-73. PMID 25370202 DOI: 10.1007/s00441-014-2014-6  1
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  1
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  1
2013 Abrams CK, Islam M, Mahmoud R, Kwon T, Bargiello TA, Freidin MM. Functional requirement for a highly conserved charged residue at position 75 in the gap junction protein connexin 32. The Journal of Biological Chemistry. 288: 3609-19. PMID 23209285 DOI: 10.1074/jbc.M112.392670  1
2013 Abrams CK, Orthmann-Murphy J. Connexin Mutations in Pelizaeus-Merzbacher-Like Disease, Oculodentodigital Dysplasia and Related Diseases Gap Junctions in the Brain. 165-187. DOI: 10.1016/B978-0-12-415901-3.00010-4  1
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  1
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  1
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  1
2009 Freidin M, Asche S, Bargiello TA, Bennett MV, Abrams CK. Connexin 32 increases the proliferative response of Schwann cells to neuregulin-1 (Nrg1). Proceedings of the National Academy of Sciences of the United States of America. 106: 3567-72. PMID 19218461 DOI: 10.1073/pnas.0813413106  1
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  1
2009 Abrams CK, Rash JE. Connexins in the nervous system Connexins: a Guide. 323-357. DOI: 10.1007/978-1-59745-489-6_15  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  1
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  1
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  1
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  1
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  1
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  1
2006 Abrams CK, Freidin MM, Verselis VK, Bargiello TA, Kelsell DP, Richard G, Bennett MV, Bukauskas FF. Properties of human connexin 31, which is implicated in hereditary dermatological disease and deafness. Proceedings of the National Academy of Sciences of the United States of America. 103: 5213-8. PMID 16549784 DOI: 10.1073/pnas.0511091103  1
2003 Abrams CK, Freidin M, Bukauskas F, Dobrenis K, Bargiello TA, Verselis VK, Bennett MV, Chen L, Sahenk Z. Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 10548-58. PMID 14627639  1
2002 Abrams CK, Bennett MV, Verselis VK, Bargiello TA. Voltage opens unopposed gap junction hemichannels formed by a connexin 32 mutant associated with X-linked Charcot-Marie-Tooth disease. Proceedings of the National Academy of Sciences of the United States of America. 99: 3980-4. PMID 11891346 DOI: 10.1073/pnas.261713499  1
2001 Abrams CK, Freidin MM, Verselis VK, Bennett MV, Bargiello TA. Functional alterations in gap junction channels formed by mutant forms of connexin 32: evidence for loss of function as a pathogenic mechanism in the X-linked form of Charcot-Marie-Tooth disease. Brain Research. 900: 9-25. PMID 11325342 DOI: 10.1016/S0006-8993(00)03327-8  1
2000 Purnick PE, Oh S, Abrams CK, Verselis VK, Bargiello TA. Reversal of the gating polarity of gap junctions by negative charge substitutions in the N-terminus of connexin 32. Biophysical Journal. 79: 2403-15. PMID 11053119 DOI: 10.1016/S0006-3495(00)76485-X  1
2000 Oh S, Abrams CK, Verselis VK, Bargiello TA. Stoichiometry of transjunctional voltage-gating polarity reversal by a negative charge substitution in the amino terminus of a connexin32 chimera. The Journal of General Physiology. 116: 13-31. PMID 10871637 DOI: 10.1085/jgp.116.1.13  1
2000 Abrams CK, Oh S, Ri Y, Bargiello TA. Mutations in connexin 32: the molecular and biophysical bases for the X-linked form of Charcot-Marie-Tooth disease. Brain Research. Brain Research Reviews. 32: 203-14. PMID 10751671 DOI: 10.1016/S0165-0173(99)00082-X  1
1999 Ri Y, Ballesteros JA, Abrams CK, Oh S, Verselis VK, Weinstein H, Bargiello TA. The role of a conserved proline residue in mediating conformational changes associated with voltage gating of Cx32 gap junctions. Biophysical Journal. 76: 2887-98. PMID 10354417 DOI: 10.1016/S0006-3495(99)77444-8  1
1999 Abrams CK, Bennett MVL. Chapter 20: Hereditary Human Diseases Caused by Connexin Mutations Current Topics in Membranes and Transport. 49: 423-459. DOI: 10.1016/S0070-2161(08)61024-2  1
1991 Abrams CK, Jakes KS, Finkelstein A, Slatin SL. Identification of a translocated gating charge in a voltage-dependent channel. Colicin E1 channels in planar phospholipid bilayer membranes. The Journal of General Physiology. 98: 77-93. PMID 1719126  1
1990 Andrews NW, Abrams CK, Slatin SL, Griffiths G. A T. cruzi-secreted protein immunologically related to the complement component C9: evidence for membrane pore-forming activity at low pH. Cell. 61: 1277-87. PMID 2194668 DOI: 10.1016/0092-8674(90)90692-8  1
1990 Slatin SL, Abrams CK, English L. Delta-endotoxins form cation-selective channels in planar lipid bilayers. Biochemical and Biophysical Research Communications. 169: 765-72. PMID 1694077 DOI: 10.1016/0006-291X(90)90397-6  1
1990 Jakes KS, Abrams CK, Finkelstein A, Slatin SL. Alteration of the pH-dependent ion selectivity of the colicin E1 channel by site-directed mutagenesis. The Journal of Biological Chemistry. 265: 6984-91. PMID 1691183  1
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