Konu "PATHWAYS" için Fen Edebiyat Fakültesi / Faculty of Letters and Science listeleme
Toplam kayıt 2, listelenen: 1-2
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Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation
(2018)PURPOSE Congenital mirror movement disorder (CMMD) is characterized by unintended, nonsuppressible, homologous mirroring activity contralateral to the movement on the intended side of the body. healthy controls, unilateral ... -
Transcriptomic profile of Pea3 family members reveal regulatory codes for axon outgrowth and neuronal connection specificity
(2020)PEA3 transcription factor subfamily is present in a variety of tissues with branching morphogenesis, and play a particularly significant role in neural circuit formation and specificity. Many target genes in axon guidance ...