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1. STRESS IN A DISH: MODELING THE IMPACT OF COMMON GENETIC VARIATION ON STRESS RESPONSE IN HIPSC-DERIVED NEURONS IN PTSD

3. A Semi-Automated Pipeline for Quantifying Drusen-Like Deposits in Human Induced Pluripotent Stem Cell-Derived Retinal Pigmented Epithelial Cells

5. T73. MODELING GENE BY ENVIRONMENT INTERACTIONS IN POST-TRAUMATIC STRESS DISORDER USING HIPSC-DERIVED NEURONS

7. A human iPSC-array-based GWAS identifies a virus susceptibility locus in the NDUFA4 gene and functional variants

10. Reactive Astrocytes Derived From Human Induced Pluripotent Stem Cells Suppress Oligodendrocyte Precursor Cell Differentiation

11. A dual SHOX2:GFP; MYH6:mCherry knockin hESC reporter line for derivation of human SAN-like cells

12. Stem cell-derived neurons reflect features of protein networks, neuropathology, and cognitive outcome of their aged human donors

13. MODELING GENE X ENVIRONMENT INTERACTIONS IN PTSD USING GLUCOCORTICOID-INDUCED TRANSCRIPTOMICS IN HUMAN NEURONS

16. List of Contributors

17. Modeling gene x environment interactions in PTSD using glucocorticoid-induced transcriptomics in human neurons

18. Lipid Deprivation Induces a Stable, Naive-to-Primed Intermediate State of Pluripotency in Human PSCs

25. CRISPR/Cas9-Correctable mutation-related molecular and physiological phenotypes in iPSC-derived Alzheimer’s PSEN2 N141I neurons

27. Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome

28. Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS

29. P4-278: Characterization of Basal Forebrain Cholinergic Neurons From Induced Pluripotent Stem Cells Harboring Familial Alzheimer’S MUTATION PSEN2 N141I

30. Genetic Drift Can Compromise Mitochondrial Replacement by Nuclear Transfer in Human Oocytes

33. Automated, high-throughput derivation, characterization and differentiation of induced pluripotent stem cells

34. iPSC-Derived Dopamine Neurons Reveal Differences between Monozygotic Twins Discordant for Parkinson’s Disease

35. Comparable Frequencies of Coding Mutations and Loss of Imprinting in Human Pluripotent Cells Derived by Nuclear Transfer and Defined Factors

36. Pathways Disrupted in Human ALS Motor Neurons Identified through Genetic Correction of Mutant SOD1

37. Pathways Disrupted in Human ALS Motor Neurons Identified through Genetic Correction of Mutant SOD1

38. Human oocytes reprogram adult somatic nuclei of a type 1 diabetic to diploid pluripotent stem cells

44. Improved Methods for Reprogramming Human Dermal Fibroblasts Using Fluorescence Activated Cell Sorting

47. Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants

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