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1. Contribution of the hexosamine biosynthetic pathway in the hyperglycemia-dependent and -independent breakdown of the retinal neurovascular unit

2. Multiparametric Longitudinal Profiling of RCAS-tva-Induced PDGFB-Driven Experimental Glioma

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3. AAV-Mediated Gene Supplementation Therapy in Achromatopsia Type 2: Preclinical Data on Therapeutic Time Window and Long-Term Effects

4. Multiparametric Longitudinal Profiling of RCAS-tva-Induced PDGFB-Driven Experimental Glioma

5. TAMI-34. TARGETING CSF1R AND PD1 IN EXPERIMENTAL GLIOMA

6. Targeting CSF1R Alone or in Combination with PD1 in Experimental Glioma

7. Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel–associated retinopathy

8. Novel rodent models for macular research.

9. Gene Therapy Successfully Delays Degeneration in a Mouse Model ofPDE6A-Linked Retinitis Pigmentosa (RP43)

10. Retinitis pigmentosa: impact of differentPde6apoint mutations on the disease phenotype

11. A retinal model of cerebral malaria

12. Alterations of the tunica vasculosa lentis in the rat model of retinopathy of prematurity

13. Endothelial SRF/MRTF ablation causes vascular disease phenotypes in murine retinae

14. Murine Autoimmune Optic Neuritis Is Not Phenotypically Altered by the Retinal Degeneration 8 Mutation

15. Gene therapy restores missing cone-mediated vision in the CNGA3-/- mouse model of achromatopsia

16. PALS1 is essential for retinal pigment epithelium structure and neural retina stratification

17. Retina-specific activation of a sustained hypoxia-like response leads to severe retinal degeneration and loss of vision

18. Restoration of Cone Vision in the CNGA3−/− Mouse Model of Congenital Complete Lack of Cone Photoreceptor Function

19. Cone loss is delayed relative to rod loss during induced retinal degeneration in the diurnal cone-rich rodent Arvicanthis ansorgei

20. Cooperative Phagocytes

21. Noninvasive, In Vivo Assessment of Mouse Retinal Structure Using Optical Coherence Tomography

22. Retinal degenerative and hypoxic ischemic disease

23. Influence of the β2-Subunit of L-Type Voltage-Gated Cav Channels on the Structural and Functional Development of Photoreceptor Ribbon Synapses

24. Scale Adjustments to Facilitate Two-Dimensional Measurements in OCT Images

25. Targeted Ablation of the Pde6h Gene in Mice Reveals Cross-species Differences in Cone and Rod Phototransduction Protein Isoform Inventory*

26. A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy

27. Mpp4 recruits Psd95 and Veli3 towards the photoreceptor synapse

28. Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia

29. VEGF Mediates ApoE4-Induced Neovascularization and Synaptic Pathology in the Choroid and Retina

30. Targeted ablation of Crb2 in photoreceptor cells induces retinitis pigmentosa

31. Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosa

32. Mitogenic and adhesive effects of tenascin-C on human hematopoietic cells are mediated by various functional domains

33. Towards a quantitative OCT image analysis

34. Gene Therapy Restores Vision and Delays Degeneration in the CNGB1−/− Mouse Model of Retinitis Pigmentosa

35. Targeted ablation of Crb1 and Crb2 in retinal progenitor cells mimics Leber Congenital Amaurosis

36. Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene

37. Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosa

38. Mice lacking Period 1 and Period 2 circadian clock genes exhibit blue cone photoreceptor defects

39. Relevance of exocytotic glutamate release from retinal glia

40. PGC-1α determines light damage susceptibility of the murine retina

41. Gene therapy restores missing cone-mediated vision in the CNGA3-/- mouse model of achromatopsia

42. A key role for cyclic nucleotide gated (CNG) channels in cGMP-related retinitis pigmentosa

43. Implantation of ultrathin, biofunctionalized polyimide membranes into the subretinal space of rats

44. Vax2 regulates retinoic acid distribution and cone opsin expression in the vertebrate eye

45. Degeneration of the mouse retina upon dysregulated activity of serum response factor

46. In vivo assessment of retinal vascular wall dimensions

47. Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophies

48. Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice

49. Spectral domain optical coherence tomography in mouse models of retinal degeneration

50. Study of gene-targeted mouse models of splicing factor gene Prpf31 implicated in human autosomal dominant retinitis pigmentosa (RP)