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Primary ciliary dyskinesia (PCD) is a rare phenotypically and genetically heterogeneous disorder resulting from abnormal cilia… Expand Disabled-1 (Dab1) is an essential intracellular protein in the Reelin pathway. It has a nuclear localization signal (NLS… Expand OBJECTIVES
To replicate previous Rasch analysis (RA) that yielded the 7-item Physical Function Short Form of the Knee Injury and… Expand Primary ciliary dyskinesia most often arises from loss of the dynein motors that power ciliary beating. Here we show that DNAAF3… Expand The genetic disorder primary ciliary dyskinesia (PCD) arises from dysmotility of cilia in the respiratory tract, brain ventricles… Expand Starting from the recent UNICEF publications on child poverty in the developed countries, which received a wide audience in the… Expand The study of mice with spontaneous and targeted mutations has uncovered a signaling pathway that controls neuronal positioning… Expand The reelin and dab1 genes are necessary for appropriate neuronal migration and lamination during brain development. Since these… Expand