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1. X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes

2. Nonvesicular lipid transfer drives myelin growth in the central nervous system

3. Phosphorylation of PFKL regulates metabolic reprogramming in macrophages following pattern recognition receptor activation

4. Rational correction of pathogenic conformational defects in HTRA1

5. PARK7/DJ-1 deficiency impairs microglial activation in response to LPS-induced inflammation

6. Correction to 'The thymocyte-specific RNA-binding protein Arpp21 provides TCR repertoire diversity by binding to the 3’-UTR and promoting Rag1 mRNA expression'

8. The thymocyte-specific RNA-binding protein Arpp21 provides TCR repertoire diversity by binding to the 3’-UTR and promoting Rag1 mRNA expression

9. Engrailed 1 deficiency induces changes in ciliogenesis during human neuronal differentiation

10. A reversible state of hypometabolism in a human cellular model of sporadic Parkinson’s disease

11. Toxicity of extracellular alpha-synuclein is independent of intracellular alpha-synuclein

12. Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice

13. Primary cilia and SHH signaling impairments in human and mouse models of Parkinson’s disease

14. Parkinson's disease motor symptoms rescue by CRISPRa‐reprogramming astrocytes into GABAergic neurons

15. Characterising a homozygous two‐exon deletion in UQCRH: comparing human and mouse phenotypes

16. Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome

17. The Alzheimer’s disease-associated protective Plcγ2-P522R variant promotes immune functions

18. The Deep Genome Project

19. Human and mouse essentiality screens as a resource for disease gene discovery

20. Concept of the Munich/Augsburg Consortium Precision in Mental Health for the German Center of Mental Health

21. Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk

22. iPS Cell-Based Model for MAPT Haplotype as a Risk Factor for Human Tauopathies Identifies No Major Differences in TAU Expression

23. Comprehensive miRNome-Wide Profiling in a Neuronal Cell Model of Synucleinopathy Implies Involvement of Cell Cycle Genes

24. Mutant non-coding RNA resource in mouse embryonic stem cells

25. Diabetes type 2 risk gene Dusp8 is associated with altered sucrose reward behavior in mice and humans

26. Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.

27. Dose-Dependent and Subset-Specific Regulation of Midbrain Dopaminergic Neuron Differentiation by LEF1-Mediated WNT1/b-Catenin Signaling

28. The FTLD Risk Factor TMEM106B Regulates the Transport of Lysosomes at the Axon Initial Segment of Motoneurons

29. Innate Immune Pathways Promote Oligodendrocyte Progenitor Cell Recruitment to the Injury Site in Adult Zebrafish Brain

30. The Trem2 R47H Alzheimer’s risk variant impairs splicing and reduces Trem2 mRNA and protein in mice but not in humans

31. Epigenome-wide DNA methylation profiling in Progressive Supranuclear Palsy reveals major changes at DLX1

32. Zebrafish and medaka offer insights into the neurobehavioral correlates of vertebrate magnetoreception

33. Identification of genetic elements in metabolism by high-throughput mouse phenotyping

34. ENCoRE: an efficient software for CRISPR screens identifies new players in extrinsic apoptosis

35. A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction

36. Meis1: effects on motor phenotypes and the sensorimotor system in mice

37. Every-other-day feeding extends lifespan but fails to delay many symptoms of aging in mice

38. The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations

39. The Aryl Hydrocarbon Receptor Pathway Defines the Time Frame for Restorative Neurogenesis

40. Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data.

41. Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts

42. A WNT1-regulated developmental gene cascade prevents dopaminergic neurodegeneration in adult En1+/− mice

43. Creation of targeted genomic deletions using TALEN or CRISPR/Cas nuclease pairs in one‐cell mouse embryos

44. Uncoupling Malt1 Threshold Function from Paracaspase Activity Results in Destructive Autoimmune Inflammation

45. Products of the Parkinson's disease-related glyoxalase DJ-1, D-lactate and glycolate, support mitochondrial membrane potential and neuronal survival

47. Sphingomyelin Synthase 1 Is Essential for Male Fertility in Mice.

48. The REST remodeling complex protects genomic integrity during embryonic neurogenesis

49. Forebrain CRHR1 deficiency attenuates chronic stress-induced cognitive deficits and dendritic remodeling

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