30 results on '"Linda, Katrin"'
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2. Navigating Human Astrocyte Differentiation: Direct and Rapid one-step Differentiation of Induced Pluripotent Stem Cells to Functional Astrocytes Supporting Neuronal Network development
3. Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder
4. The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant
5. Revisiting multi-level governance theory: Politics and innovation in the urban climate transition in Rizhao, China
6. The (In-)Visible Hand: A Governance Perspective on Low-Carbon Transitions in the PRC
7. The promise of induced pluripotent stem cells for neurodevelopmental disorders
8. Epigenetic regulation of autophagy-related genes: Implications for neurodevelopmental disorders.
9. Epigenetic regulation of autophagy-relatedgenes: Implications for neurodevelopmental disorders
10. Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling
11. Human neuronal networks on micro-electrode arrays are a highly robust tool to study disease-specific genotype-phenotype correlations in vitro
12. Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders
13. Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks
14. Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders.
15. KANSL1 Deficiency Causes Neuronal Dysfunction by Oxidative Stress-Induced Autophagy
16. Cadherin-13 is a critical regulator of GABAergic modulation in human stem cell derived neuronal networks
17. m.3243A > G-Induced Mitochondrial Dysfunction Impairs Human Neuronal Development and Reduces Neuronal Network Activity and Synchronicity
18. Emerging dynamics of public participation in climate governance: A case study of solar energy application in Shenzhen, China
19. Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype
20. Neuronal network dysfunction in a human model for Kleefstra syndrome mediated by enhanced NMDAR signaling
21. Biallelic variants in TMEM222cause a new autosomal recessive neurodevelopmental disorder
22. Distinct pathogenic genes causing intellectual disability and autism exhibit overlapping effects on neuronal network development
23. Cell-type specific contribution to neuronal network (dys)function in neurodevelopmental disorders.
24. Neurons derived from induced pluripotent stem cells on microelectrode arrays: a human model for neurodevelopmental disorders
25. Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition
26. Rapid Neuronal Differentiation of Induced Pluripotent Stem Cells for Measuring Network Activity on Micro-electrode Arrays
27. The Koolen-de Vries syndrome : A phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant
28. The Koolen-de Vries syndrome: A phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant
29. Added effects of dexamethasone and mesenchymal stem cells on early Natural Killer cell activation
30. Trivsel i dei Seine Barneåra: Ei empirisk Undersøking av Stabilitet i Livstilfredsheitsrapportar, og Prediksjon av Livs- og Skuletilfredsheit frå Separate Kjelder til Sosial Støtte Kontrollert for Sosioøkonomisk Status
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