http://rdf.ncbi.nlm.nih.gov/pubmed/12897163

http://rdf.ncbi.nlm.nih.gov/pubmed/12897163

Megan. Maxwell, et.al., Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype., Molecular and cellular biology, 2003, 23

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

トランスクリプトームデータ

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

• CD19528
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD19528

表現型アノテーション

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

• abnormal cell morphology_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0000358I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• abnormal cerebral cortex morphology_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0000788I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• decreased body weight_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0001262I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• aphagia_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0001438I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• respiratory distress_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0001954I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• hepatic steatosis_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0002628I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
他11件を見る
• neuron degeneration_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0003224I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• hypotonia_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0004144I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• bradykinesia_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0005156I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• abnormal renal glomerulus morphology_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0005325I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• abnormal cell physiology_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0005621I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• abnormal mitochondrion morphology_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0006035I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• thin cerebral cortex_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0006254I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• abnormal podocyte foot process morphology_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0008059I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• abnormal adrenocortical cell morphology_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0008291I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• neonatal lethality, complete penetrance_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0011087I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne
• abnormal mitochondrial crista morphology_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>
  http://metadb.riken.jp/0011635I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne