Murine fumarylacetoacetate hydrolase (Fah) gene is disrupted by a neonatally lethal albino deletion that defines the hepatocyte-specific developmental regulation 1 (hsdr-1) locus
about
Type 1 hereditary tyrosinemia. Evidence for molecular heterogeneity and identification of a causal mutation in a French Canadian patientComplete rescue of lethal albino c14CoS mice by null mutation of 4-hydroxyphenylpyruvate dioxygenase and induction of apoptosis of hepatocytes in these mice by in vivo retrieval of the tyrosine catabolic pathwayPoint mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1Mouse fzd4 maps within a region of chromosome 7 important for thymus and cardiac developmentMouse homologues of human hereditary disease.Fungal metabolic model for human type I hereditary tyrosinaemia.Molecular analysis of radiation-induced albino (c)-locus mutations that cause death at preimplantation stages of developmentDeletion mapping of four loci defined by N-ethyl-N-nitrosourea-induced postimplantation-lethal mutations within the pid-Hbb region of mouse chromosome 7.Molecular genetics of the brown (b)-locus region of mouse chromosome 4. II. Complementation analyses of lethal brown deletions.Hereditary tyrosinaemia type I: from basics to progress in treatment.Pleiotropy in microdeletion syndromes: neurologic and spermatogenic abnormalities in mice homozygous for the p6H deletion are likely due to dysfunction of a single geneHepatocyte injury in tyrosinemia type 1 is induced by fumarylacetoacetate and is inhibited by caspase inhibitors.Molecular characterization of four induced alleles at the Ednrb locusSelective loss of a DNase I hypersensitive site upstream of the tyrosine aminotransferase gene in mice homozygous for lethal albino deletions.Validation of a multi-omics strategy for prioritizing personalized candidate driver genesFah Knockout Animals as Models for Therapeutic Liver Repopulation.Transcriptional regulation of genes for ornithine cycle enzymes.
P2860
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P2860
Murine fumarylacetoacetate hydrolase (Fah) gene is disrupted by a neonatally lethal albino deletion that defines the hepatocyte-specific developmental regulation 1 (hsdr-1) locus
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Murine fumarylacetoacetate hyd ...... al regulation 1 (hsdr-1) locus
@en
type
label
Murine fumarylacetoacetate hyd ...... al regulation 1 (hsdr-1) locus
@en
prefLabel
Murine fumarylacetoacetate hyd ...... al regulation 1 (hsdr-1) locus
@en
P2093
P2860
P356
P1476
Murine fumarylacetoacetate hyd ...... al regulation 1 (hsdr-1) locus
@en
P2093
P2860
P304
P356
10.1073/PNAS.89.4.1363
P407
P577
1992-02-01T00:00:00Z