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http://purl.uniprot.org/citations/22067082http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22067082http://www.w3.org/2000/01/rdf-schema#comment"The Japanese Fancy Mouse 1 (JF1) has a characteristic coat color similar to a very old mutant, piebald. The mutation in JF1 and the classic piebald was previously thought to be the same recessive allele in the endothelin B receptor gene (Ednrb) according to the haplotype pattern, which is insufficient for this conclusion. In this study, we identified the same insertion of a retroposon-like element in intron 1 of the Ednrb gene in JF1 as in the classic piebald mutation by PCR. Further, we investigated whether the intestine shows neuronal intestinal malformations such as hypoganglionosis and immaturity of ganglion cells by histochemical staining. Though it has been assumed that the defect of neural crest-derived lineages is restricted to melanocytes in JF1, we found that the enteric innervation and neuronal density were impaired throughout the whole colon in JF1 mice."xsd:string
http://purl.uniprot.org/citations/22067082http://purl.org/dc/terms/identifier"doi:10.1292/jvms.11-0447"xsd:string
http://purl.uniprot.org/citations/22067082http://purl.uniprot.org/core/author"Sasaki N."xsd:string
http://purl.uniprot.org/citations/22067082http://purl.uniprot.org/core/author"Dang R."xsd:string
http://purl.uniprot.org/citations/22067082http://purl.uniprot.org/core/author"Agui T."xsd:string
http://purl.uniprot.org/citations/22067082http://purl.uniprot.org/core/author"Torigoe D."xsd:string
http://purl.uniprot.org/citations/22067082http://purl.uniprot.org/core/date"2012"xsd:gYear
http://purl.uniprot.org/citations/22067082http://purl.uniprot.org/core/name"J Vet Med Sci"xsd:string
http://purl.uniprot.org/citations/22067082http://purl.uniprot.org/core/pages"391-394"xsd:string
http://purl.uniprot.org/citations/22067082http://purl.uniprot.org/core/title"Anatomic modifications in the enteric nervous system of JF1 mice with the classic piebald mutation."xsd:string
http://purl.uniprot.org/citations/22067082http://purl.uniprot.org/core/volume"74"xsd:string
http://purl.uniprot.org/citations/22067082http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/22067082
http://purl.uniprot.org/citations/22067082http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/22067082
http://purl.uniprot.org/uniprot/#_P48302-mappedCitation-22067082http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22067082
http://purl.uniprot.org/uniprot/#_Q8BJE1-mappedCitation-22067082http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22067082
http://purl.uniprot.org/uniprot/P48302http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22067082
http://purl.uniprot.org/uniprot/Q8BJE1http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22067082