| Year |
Citation |
Score |
| 2023 |
Abrams CK. Mechanisms of Diseases Associated with Mutation in GJC2/Connexin 47. Biomolecules. 13. PMID 37189458 DOI: 10.3390/biom13040712 |
0.469 |
|
| 2022 |
Flores-Obando RE, Freidin MM, Hernández AI, Abrams CK. Activation of the unfolded protein response by Connexin47 mutations associated with Pelizaeus-Merzbacher-like disease. Molecular and Cellular Neurosciences. 103716. PMID 35276347 DOI: 10.1016/j.mcn.2022.103716 |
0.72 |
|
| 2021 |
Abrams CK, Flores-Obando RE, Dungan GD, Cherepanova E, Freidin MM. Investigating oligodendrocyte connexins: Heteromeric interactions between Cx32 and mutant or wild-type forms of Cx47 do not contribute to or modulate gap junction function. Glia. PMID 33835612 DOI: 10.1002/glia.23999 |
0.739 |
|
| 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 |
0.363 |
|
| 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 |
0.483 |
|
| 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 |
0.547 |
|
| 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 |
0.667 |
|
| 2017 |
Abrams CK. Diseases of connexins expressed in myelinating glia. Neuroscience Letters. PMID 28545922 DOI: 10.1016/J.Neulet.2017.05.037 |
0.438 |
|
| 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 |
0.436 |
|
| 2016 |
Olympiou M, Sargiannidou I, Markoullis K, Karaiskos C, Kagiava A, Kyriakoudi S, Abrams CK, Kleopa KA. Systemic inflammation disrupts oligodendrocyte gap junctions and induces ER stress in a model of CNS manifestations of X-linked Charcot-Marie-Tooth disease. Acta Neuropathologica Communications. 4: 95. PMID 27585976 DOI: 10.1186/S40478-016-0369-5 |
0.369 |
|
| 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 |
0.311 |
|
| 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 |
0.74 |
|
| 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 |
|
| 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 |
0.509 |
|
| 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 |
0.415 |
|
| 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 |
0.42 |
|
| 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 |
0.451 |
|
| 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 |
0.369 |
|
| 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 |
0.576 |
|
| 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 |
0.471 |
|
| 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 |
0.456 |
|
| 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 |
0.433 |
|
| 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 |
0.516 |
|
| 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 |
0.462 |
|
| 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 |
0.446 |
|
| 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 DOI: 10.1523/Jneurosci.23-33-10548.2003 |
0.415 |
|
| 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: 10.1046/J.1529-8027.2002.02026_14.X |
0.43 |
|
| 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 |
0.399 |
|
| 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 |
0.391 |
|
| 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 |
0.481 |
|
| 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 |
0.37 |
|
| 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 DOI: 10.1085/Jgp.98.1.77 |
0.717 |
|
| 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 |
0.652 |
|
| 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 |
0.7 |
|
| 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 |
0.724 |
|
| Show low-probability matches. |