A seven-base-pair deletion in an intron of the albumin gene of analbuminemic rats.
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Analbuminemia: three cases resulting from different point mutations in the albumin geneMolecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). RNA and DNA analysis.A nucleotide insertion and frameshift cause analbuminemia in an Italian familyMessenger RNA coding for argininosuccinate synthetase in citrullinemia.Exon skipping by mutation of an authentic splice site of c-kit gene in W/W mouseDNA insertion in the first intron of maize Adh1 affects message levels: cloning of progenitor and mutant Adh1 allelesHigh-frequency illegitimate integration of transfected DNA at preintegrated target sites in a mammalian genomeVirus deletion mutants that affect a 3' splice site in the E3 transcription unit of adenovirus 2Loss of a consensus splice signal in a mutant immunoglobulin gene eliminates the CH1 domain exon from the mRNA.Phenotypic reversion in analbuminemic rats due to an altered splicing mechanism.Marked increases of two kinds of two-exon-skipped albumin mRNAs with aging and their further increase by treatment with 3'-methyl-4-dimethylaminoazobenzene in Nagase analbuminemic rats.Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia.Exon skipping during splicing of albumin mRNA precursors in Nagase analbuminemic rats.Chemical carcinogenesis in analbuminemic rats.Differentiation of the normal and mutant rat albumin genes on hepatic tissue sections by in situ PCR.The 5' splice site: phylogenetic evolution and variable geometry of association with U1RNA.Albumin is not an irreplaceable carrier for amphipathic mediators of thermoregulatory responses to LPS: compensatory role of alpha1-acid glycoprotein.High susceptibility of analbuminemic rats to neurogenic tumor induction by transplacental administration of N-ethyl-N-nitrosourea.Uptake and degradation of filamentous actin and vitamin D-binding protein in the rat.Functional polymorphisms in inbred rat strains and their allele frequencies in commercially available outbred stocks.Quantitative comparison of initiation and mutation phenotypes in hepatocytes of the analbuminemic rat.Genotypic differentiation of intrahepatically transplanted hyperplastic nodule cells of analbuminemic and normal rat origin by polymerase chain reaction.
P2860
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P2860
A seven-base-pair deletion in an intron of the albumin gene of analbuminemic rats.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on January 1983
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A seven-base-pair deletion in an intron of the albumin gene of analbuminemic rats.
@en
A seven-base-pair deletion in an intron of the albumin gene of analbuminemic rats.
@nl
type
label
A seven-base-pair deletion in an intron of the albumin gene of analbuminemic rats.
@en
A seven-base-pair deletion in an intron of the albumin gene of analbuminemic rats.
@nl
prefLabel
A seven-base-pair deletion in an intron of the albumin gene of analbuminemic rats.
@en
A seven-base-pair deletion in an intron of the albumin gene of analbuminemic rats.
@nl
P2093
P2860
P356
P1476
A seven-base-pair deletion in an intron of the albumin gene of analbuminemic rats.
@en
P2093
P2860
P356
10.1073/PNAS.80.1.95
P407
P577
1983-01-01T00:00:00Z