57 results on '"Willecke, Klaus"'
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2. Ceramide synthase 2 facilitates S1P‐dependent egress of thymocytes into the circulation in mice
3. Defective ceramide synthases in mice cause reduced amplitudes in electroretinograms and altered sphingolipid composition in retina and cornea
4. Quantified CSF antibody reactivity against myelin in multiple sclerosis
5. Altered epidermal lipid processing and calcium distribution in the KID syndrome mouse model Cx26S17F
6. Exacerbation of experimental autoimmune encephalomyelitis in ceramide synthase 6 knockout mice is associated with enhanced activation/migration of neutrophils
7. The Clouston syndrome mutation connexin30 A88V leads to hyperproliferation of sebaceous glands and hearing impairments in mice
8. Dual reporter approaches for identification of Cre efficacy and astrocyte heterogeneity
9. Subcellular distribution of connexin45 in OFF bipolar cells of the mouse retina
10. Role of astroglial connexin30 in hippocampal gap junction coupling
11. Connexin hemichannel-mediated CO2-dependent release of ATP in the medulla oblongata contributes to central respiratory chemosensitivity
12. Dynamic expression of Cx47 in mouse brain development and in the cuprizone model of myelin plasticity
13. Oligodendrocytes in mouse corpus callosum are coupled via gap junction channels formed by connexin47 and connexin32
14. Connexin 26 is responsible for ATP release underlying central CO2 chemosensitivity
15. A novel type of interplexiform amacrine cell in the mouse retina
16. Gating, permselectivity and pH‐dependent modulation of channels formed by connexin57, a major connexin of horizontal cells in the mouse retina
17. Quality control of astrocyte-directed Cre transgenic mice: The benefits of a direct link between loss of gene expression and reporter activation
18. Connexin57 is expressed in dendro‐dendritic and axo‐axonal gap junctions of mouse horizontal cells and its distribution is modulated by light
19. Analysis of connexin subunits required for the survival of vestibular hair cells
20. Injury of skeletal muscle and specific cytokines induce the expression of gap junction channels in mouse dendritic cells
21. Analysis of connexin expression during mouse Schwann cell development identifies Connexin29 as a novel marker for the transition of neural crest to precursor cells
22. Localization of heterotypic gap junctions composed of connexin45 and connexin36 in the rod pathway of the mouse retina
23. Horizontal cell receptive fields are reduced in connexin57‐deficient mice
24. Spatiotemporal distribution of Connexin45 in the olivocerebellar system
25. Expression pattern and functional characterization of connexin29 in transgenic mice
26. Connexin36 mediates gap junctional coupling of alpha‐ganglion cells in mouse retina
27. Connexin45 mediates gap junctional coupling of bistratified ganglion cells in the mouse retina
28. Distinct types of astroglial cells in the hippocampus differ in gap junction coupling
29. Functional expression of connexin57 in horizontal cells of the mouse retina
30. Expression pattern of lacZ reporter gene representing connexin36 in transgenic mice
31. Spontaneous ectopic recombination in cell‐type‐specific Cre mice removes loxP‐flanked marker cassettes in vivo
32. Astrocyte cultures from conditional connexin43‐deficient mice
33. Pharmacological sensitivity of ATP release triggered by photoliberation of inositol-1,4,5-trisphosphate and zero extracellular calcium in brain endothelial cells
34. Connexin43 is not expressed in principal cells of mouse cortex and hippocampus
35. Reduction of high‐frequency network oscillations (ripples) and pathological network discharges in hippocampal slices from connexin 36‐deficient mice
36. Segment-specific expression ofconnexin31 in the embryonic hindbrain is regulated byKrox20
37. hGFAP‐cre transgenic mice for manipulation of glial and neuronal function in vivo
38. Strongly decreased gap junctional permeability to inositol 1,4,5-trisphosphate in connexin32 deficient hepatocytes
39. Endothelium-specific replacement of the connexin43 coding region by a lacZ reporter gene
40. Expression patterns of connexin genes in mouse retina
41. Cardiac Conduction Abnormalities in Mice Lacking the Gap Junction Protein Connexin40
42. Characterization of Targeted Connexin32‐Deficient Mice: A Model for the Human Charcot‐Marie‐Tooth (X‐Type) Inherited Disease
43. Biophysical properties of mouse connexin30 gap junction channels studied in transfected human HeLa cells
44. Doubly mutant mice, deficient in connexin32 and -43, show normal prenatal development of organs where the two gap junction proteins are expressed in the same cells
45. Connexin32-null mice develop demyelinating peripheral neuropathy
46. The murine gap junction gene connexin36 is highly expressed in mouse retina and regulated during brain development
47. Developmental regulation of connexin 40 gene expression in mouse heart correlates with the differentiation of the conduction system
48. A DNA-Binding Zinc-Protein Increases the Immortalizing Activity of an Extrachromosomal DNA Sequence from Mouse L929 Cells
49. Expression of Cx26, Cx32 AND Cx43 gap junction proteins in normal and neoplastic human tissues
50. Bakterien-, Phagen- und Molekulargenetik. VonU. Winkler, R. Rüger undW. Wackernagel. Springer Verlag, Berlin—Heidelberg—New York 1972. 1. Aufl., XI, 285 S., 15 Abb., geh. DM 14.80
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