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No Gastrointestinal Dysmotility in Transgenic Mouse Models of Migraine.

Adam S Sprouse BlumBrigitte LavoieMelody HaagSeamus M MaweElse A TolnerArn M J M van den MaagdenbergShih-Pin ChenKatharina Eikermann-HaerterLouis PtáčekGary M MaweRobert E Shapiro
Published in: Headache (2019)
We detected no evidence of upper gastrointestinal dysmotility in mice that express mutations in genes linked to monogenic migraine-relevant phenotypes. Future studies seeking to understand why humans with migraine experience delayed gastric emptying may benefit from pursuing other modifiers of gastrointestinal motility, such as epigenetic or microbiome-related factors.
Keyphrases
  • mouse model
  • dna methylation
  • gene expression
  • mental health
  • genome wide
  • current status
  • high fat diet induced
  • type diabetes
  • metabolic syndrome
  • insulin resistance
  • bioinformatics analysis
  • wild type