...
机译:由De Novo PTPN4 PTPN4单核苷酸变异破坏神经元树突脊柱蛋白定位引起的神经发育表型
Department of Medical GeneticsMedical University of WarsawWarsaw Poland;
Laboratory of Molecular Basis of Synaptic PlasticityCentre of New Technologies University of;
Postgraduate School of Molecular Medicine Medical University of WarsawWarsaw Poland;
Department of Medical GeneticsMedical University of WarsawWarsaw Poland;
Department of Child PsychiatryMedical University of WarsawWarsaw Poland;
Department of Pediatric Respiratory Diseases and AllergyMedical University of WarsawWarsaw Poland;
Department of MethodologyCentre for Preclinical Research Medical University of WarsawWarsaw Poland;
Department of Medical GeneticsMedical University of WarsawWarsaw Poland;
Department of Medical GeneticsMedical University of WarsawWarsaw Poland;
Department of Medical GeneticsMedical University of WarsawWarsaw Poland;
Department of Medical GeneticsMedical University of WarsawWarsaw Poland;
Department of MethodologyCentre for Preclinical Research Medical University of WarsawWarsaw Poland;
Laboratory of Molecular Basis of Synaptic PlasticityCentre of New Technologies University of;
Department of Medical GeneticsMedical University of WarsawWarsaw Poland;
Department of ImmunologyCenter of Biostructure Research Medical University of WarsawWarsaw Poland;
Laboratory of Molecular Basis of Synaptic PlasticityCentre of New Technologies University of;
Department of Medical GeneticsMedical University of WarsawWarsaw Poland;
autistic features; dendritic spines; developmental delay; PTPN4;
机译:由De Novo PTPN4 PTPN4单核苷酸变异破坏神经元树突脊柱蛋白定位引起的神经发育表型
机译:在KCNB1基因型和表型中的De Novo变体引起的神经发育障碍
机译:酪氨酸磷酸酶PTPN4 / PTP-MEG1是一种能够使TCR ITAM脱磷酸并调节NF-κB的酶,可用于T细胞发育和/或T细胞效应子功能。
机译:用于指导树突状细胞表型的母题的Sams表面蛋白质的糖修饰分析
机译:T细胞中蛋白酪氨酸磷酸酶PTPN3和PTPN4以及PTPN11在组织重塑中的作用。
机译:具有Rett综合征样表型的双胞胎中的蛋白质酪氨酸磷酸酶非受体4型(PTPN4)的删除
机译:用Rett综合征样表型删除蛋白酪氨酸磷酸酶,非受体型4(PTPN4)的双胞胎中