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Klaus, J.* et al.: Altered neuronal migratory trajectories in human cerebral organoids derived from individuals with neuronal heterotopia. Nat. Med. 25, 561–568 (2019)
O'Neill, A.C. et al.: Mob2 insufficiency disrupts neuronal migration in the developing cortex. Front. Cell. Neurosci. 12:57 (2018)
O'Neill, A.C. et al.: A primate-specific isoform of PLEKHG6 regulates neurogenesis and neuronal migration. Cell Rep. 25, 2729-2741.e6 (2018)
Gascón, S. et al.: Identification and successful negotiation of a metabolic checkpoint in direct neuronal repogramming. Cell Stem Cell 18, 396-409 (2016)
Wade, E.M.* et al.: Mutations in MAP3K7 that alter the activity of the TAK1 signaling complex cause frontometaphyseal dysplasia. Am. J. Hum. Genet. 99, 392-406 (2016)
Cappello, S. et al.: Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development. Nat. Genet. 45, 1300-1308 (2013)