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Vershkov, D.; Benvenisty, N. Human pluripotent stem cells in modeling human disorders: the case of fragile X syndrome 2017 Regenerative Medicine 12 53-68 details   doi
Smith, John; Smith, Jane Some very captivating research 2017 details   openurl
Polex-Wolf, J.; Yeo, G.S.H.; O'Rahilly, S. Impaired prohormone processing: a grand unified theory for features of Prader-Willi syndrome? 2017 The Journal of Clinical Investigation 127 98-99 details   doi
Li, M.; Zhao, H.; Ananiev, G.E.; Musser, M.T.; Ness, K.H.; Maglaque, D.L.; Saha, K.; Bhattacharyya, A.; Zhao, X. Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells 2017 Stem Cells (Dayton, Ohio) 35 158-169 details   doi
Lacovich, V.; Espindola, S.L.; Alloatti, M.; Pozo Devoto, V.; Cromberg, L.E.; Carna, M.E.; Forte, G.; Gallo, J.-M.; Bruno, L.; Stokin, G.B.; Avale, M.E.; Falzone, T.L. Tau Isoforms Imbalance Impairs the Axonal Transport of the Amyloid Precursor Protein in Human Neurons 2017 The Journal of Neuroscience : the Official Journal of the Society for Neuroscience 37 58-69 details   doi
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