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Home › Dataset Library › Transcription profiling of mouse cerebellum cells containing expanded or normal CAG trinucleotide repeats in the coding region for TATA-...

Dataset: Transcription profiling of mouse cerebellum cells containing expanded or normal CAG trinucleotide repeats in the coding region for TATA-binding protein (TBP)

[u'Transcription profiles were obtained for 2-month old mice containing an expanded or normal CAG trinucleotide repeat in the coding...

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[u'Transcription profiles were obtained for 2-month old mice containing an expanded or normal CAG trinucleotide repeat in the coding region for TATA-binding protein (TBP). Three different genotypes were used : TBP-13Q (normal), TBP-71Q (71 repeats), and TBP-105Q (105 repeats). Two lines of TBP-71Q (lines 16 and 27) were used in these experiments. ', {u'br': None}, {u'br': None}, u' The 71Q and 105Q mice express a mutant version of the protein (TBP) and faithfully model the disease SCA17 (spinocerebellar ataxia-17, huntington disease-like 4, HDL4). ', {u'br': None}, {u'br': None}, u' The constructs containing mixed CAG/CAA trinucleotide repeats (and encoding polyglutamine tracts) of variable length were made using a previously described method (Michalik A et al., Biotechniques, 2001). Briefly, synthetic CAG/CAA oligonucleotides were subcloned into a cDNA construct of the normal mouse (13 CAG/CAA) TBP gene. Because of the mixed nature of the repeat, its length is stable in mitotic and meiotic transmission.']

Species:
mouse

Samples:
9

Source:
E-MEXP-1313

PubMed:
17994014

Updated:
Dec.12, 2014

Registered:
Nov.21, 2014


Factors: (via ArrayExpress)
Sample disease state strain genotype
TBP-13Q-12_2 normal TBP-13Q-12 TBP-13Q
TBP-13Q-12_2 normal TBP-13Q-12 TBP-13Q
TBP-13Q-12_2 normal TBP-13Q-12 TBP-13Q
TBP-71Q-16_735 SCA17 TBP-71Q-16 TBP-71Q
TBP-71Q-16_735 SCA17 TBP-71Q-16 TBP-71Q
TBP-71Q-16_735 SCA17 TBP-71Q-16 TBP-71Q
TBP-71Q-27_686 SCA17 TBP-71Q-27 TBP-71Q
TBP-71Q-27_686 SCA17 TBP-71Q-27 TBP-71Q
TBP-71Q-27_686 SCA17 TBP-71Q-27 TBP-71Q

Tags

  • disease
  • huntington disease
  • protein
  • spinocerebellar ataxia

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