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The following properties are used in the wiki.


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  1. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  2. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  3. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  4. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  5. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  6. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  7. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  8. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  9. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  10. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  11. ADH with or without polyadenylation signals were constructed. Placed under the control of the strong CMV promoter, these constructs induced intense ADH substrate staining and phleomycin resistance, whatever the position of the ADH gene, in avian or mammal of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  12. ADH, or ADH of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  13. Abstract of type Text (0 uses) This property is hardly used within the wiki!
  14. Allows valueThis property is a special property in this wiki. (0)
  15. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  16. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  17. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  18. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  19. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  20. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  21. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  22. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  23. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  24. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  25. Bicaudal-D (Bic-D) is essential for the establishment of oocyte fate and subsequently for polarity formation within the developing Drosophila oocyte. To find out where in the germ cells Bic-D performs its various functions we made transgenic flies express of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  26. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  27. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  28. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  29. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  30. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  31. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  32. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  33. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  34. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  35. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  36. Brother and Big brother were isolated as Runt-interacting proteins and are homologous to CBF(beta), which interacts with the mammalian CBF(alpha) Runt-domain proteins. In vitro experiments indicate that Brother family proteins regulate the DNA binding act of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  37. Bulk flow constitutes a substantial part of the slow transport of soluble proteins in axons. Though the underlying mechanism is unclear, evidences indicate that intermittent, kinesin-based movement of large protein-aggregates aids this process. Choline ac of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  38. Bulk flow constitutes a substantial part of the slow transport of soluble proteins in axons. Though the underlying mechanism is unclear, evidences indicate that intermittent, kinesin-based movement of large protein-aggregates aids this process. Choline ac of type Page (1 use)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  39. ChAT directly bind to the KLP64D tail, which is essential for the GFP of type Page (1 use)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  40. ChAT), in Drosophila axons, lacks particulate features. It occurs for a brief period during the larval stages. In addition, both the endogenous ChAT and GFP of type Page (1 use)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  41. Corresponds toThis property is a special property in this wiki. (0)
  42. Creation dateThis property is a special property in this wiki. of type Date (0 uses)
  43. Display unitsThis property is a special property in this wiki. (0)
  44. Equivalent URIThis property is a special property in this wiki. (0)
  45. GAD into MARCM, which we call dual-expression-control MARCM, permits the induction of distinct transgenes in different patterns among GAL80-minus cells in mosaic tissues. Lineage analysis with dual-expression-control MARCM suggested the presence of neurog of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  46. GAD into MARCM, which we call dual-expression-control MARCM, permits the induction of distinct transgenes in different patterns among GAL80-minus cells in mosaic tissues. Lineage analysis with dual-expression-control MARCM suggested the presence of neurog of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  47. GAD into MARCM, which we call dual-expression-control MARCM, permits the induction of distinct transgenes in different patterns among GAL80-minus cells in mosaic tissues. Lineage analysis with dual-expression-control MARCM suggested the presence of neurog of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  48. GAD into MARCM, which we call dual-expression-control MARCM, permits the induction of distinct transgenes in different patterns among GAL80-minus cells in mosaic tissues. Lineage analysis with dual-expression-control MARCM suggested the presence of neurog of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  49. GAD into MARCM, which we call dual-expression-control MARCM, permits the induction of distinct transgenes in different patterns among GAL80-minus cells in mosaic tissues. Lineage analysis with dual-expression-control MARCM suggested the presence of neurog of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!
  50. GAD into MARCM, which we call dual-expression-control MARCM, permits the induction of distinct transgenes in different patterns among GAL80-minus cells in mosaic tissues. Lineage analysis with dual-expression-control MARCM suggested the presence of neurog of type Page (0 uses)
    • This property is hardly used within the wiki!
    • All properties should be described by a page!

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