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 |
0.616 |
|
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 |
0.559 |
|
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 |
0.529 |
|
2012 |
Saporta M, Volfson D, Adebola A, Shy M, Liem R, Dimos J. Abnormal Mitochondrial Trafficking and Cytoskeletal Organization in a Human Induced Pluripotent Stem Cell and a Mouse Model of Charcot-Marie-Tooth Disease Type 2E (IN7-2.001) Neurology. 78: IN7-2.001-IN7-2.001. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In7-2.001 |
0.572 |
|
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 |
0.538 |
|
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 |
0.531 |
|
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