Charles K. Abrams

Albert Einstein College of Medicine, New York, New York, United States 
"Charles Abrams"
Mean distance: 15.21 (cluster 32)
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Peinado A, Abrams CK. (2015) Patterns of Spontaneous Local Network Activity in Developing Cerebral Cortex: Relationship to Adult Cognitive Function. Plos One. 10: e0131259
Freidin M, Asche-Godin S, Abrams CK. (2015) 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
Abrams CK, Freidin M. (2015) GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems. Cell and Tissue Research. 360: 659-73
Abrams CK, Scherer SS, Flores-Obando R, et al. (2014) A new mutation in GJC2 associated with subclinical leukodystrophy. Journal of Neurology. 261: 1929-38
Caramins M, Colebatch JG, Bainbridge MN, et al. (2013) Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1). Human Molecular Genetics. 22: 4329-38
Abrams CK, Islam M, Mahmoud R, et al. (2013) 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
Abrams CK, Orthmann-Murphy J. (2013) Connexin Mutations in Pelizaeus-Merzbacher-Like Disease, Oculodentodigital Dysplasia and Related Diseases Gap Junctions in the Brain. 165-187
Kleopa KA, Abrams CK, Scherer SS. (2012) How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease? Brain Research. 1487: 198-205
Abrams CK, Scherer SS. (2012) Gap junctions in inherited human disorders of the central nervous system. Biochimica Et Biophysica Acta. 1818: 2030-47
Wasseff S, Abrams CK, Scherer SS. (2010) A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes. Neuron Glia Biology. 6: 213-23
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