Adijat A. Adebola, Ph.D. - Publications

Affiliations: 
Columbia University, New York, NY 
Area:
Cytoskeleton

6 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
2015 Adebola AA, Di Castri T, He CZ, Salvatierra LA, Zhao J, Brown K, Lin CS, Worman HJ, Liem RK. Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype. Human Molecular Genetics. 24: 2163-74. PMID 25552649 DOI: 10.1093/hmg/ddu736  0.6
2015 Saporta MA, Dang V, Volfson D, Zou B, Xie XS, Adebola A, Liem RK, Shy M, Dimos JT. Axonal Charcot-Marie-Tooth disease patient-derived motor neurons demonstrate disease-specific phenotypes including abnormal electrophysiological properties. Experimental Neurology. 263: 190-9. PMID 25448007 DOI: 10.1016/j.expneurol.2014.10.005  0.6
2014 Poliakova K, Adebola A, Leung CL, Favre B, Liem RK, Schepens I, Borradori L. BPAG1a and b associate with EB1 and EB3 and modulate vesicular transport, Golgi apparatus structure, and cell migration in C2.7 myoblasts. Plos One. 9: e107535. PMID 25244344 DOI: 10.1371/journal.pone.0107535  0.6
2010 Steiner-Champliaud MF, Schneider Y, Favre B, Paulhe F, Praetzel-Wunder S, Faulkner G, Konieczny P, Raith M, Wiche G, Adebola A, Liem RK, Langbein L, Sonnenberg A, Fontao L, Borradori L. BPAG1 isoform-b: complex distribution pattern in striated and heart muscle and association with plectin and alpha-actinin. Experimental Cell Research. 316: 297-313. PMID 19932097 DOI: 10.1016/j.yexcr.2009.11.010  0.6
2010 Adebola A, Liem RKH. Cytoskeletal Interactions in the Neuron Encyclopedia of Neuroscience. 301-309. DOI: 10.1016/B978-008045046-9.00719-1  0.6
2007 Goryunov D, Adebola A, Jefferson JJ, Leung CL, Messer A, Liem RK. Molecular characterization of the genetic lesion in Dystonia musculorum (dt-Alb) mice. Brain Research. 1140: 179-87. PMID 16725123 DOI: 10.1016/j.brainres.2006.04.068  0.6
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