Robyn L. Kosinsky, et.al., Usp22 deficiency impairs intestinal epithelial lineage specification in vivo., Oncotarget, 2015, 6

http://rdf.ncbi.nlm.nih.gov/pubmed/26431380

Robyn L. Kosinsky, et.al., Usp22 deficiency impairs intestinal epithelial lineage specification in vivo., Oncotarget, 2015, 6

pubmed

表現型アノテーション

http://purl.org/net/cito/citesAsAuthority

• abnormal cell differentiation_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0005076C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• abnormal intestinal villus goblet cell morphology_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0013794C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• postnatal growth retardation_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0001732C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• abnormal cerebral cortex morphology_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0000788C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• abnormal intestinal epithelium morphology_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0000488C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• abnormal small intestine morphology_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0000496C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• decreased body weight_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0001262C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• abnormal cortical plate morphology_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0008439C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• abnormal intestinal enteroendocrine cell morphology_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0010802C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• abnormal stratification in cerebral cortex_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0000790C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• impaired neuron differentiation_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0011827C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi
• increased Paneth cell number_Usp22<tm1a(KOMP)Wtsi>/Usp22<tm1a(KOMP)Wtsi>
  http://metadb.riken.jp/0013485C57BL6Usp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsiUsp22tm1aKOMPWtsi