Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia.
about
Phosphoglucomutase 1: a gene with two promoters and a duplicated first exonA detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination ratesLinkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locusLoss of constitutional heterozygosity on chromosome 5q in hepatocellular carcinoma without cirrhosis.Splicing mutation in human hereditary analbuminemia.Molecular genetics of human chromosome 4.Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma.Oxidative modification of albumin in the parenchymal lung tissue of current smokers with chronic obstructive pulmonary diseaseImmunoreactive apolipoprotein E is a widely distributed cellular protein. Immunohistochemical localization of apolipoprotein E in baboon tissues.An intragenic deletion of the factor IX gene in a family with hemophilia B.Dentin phosphoprotein gene locus is not associated with dentinogenesis imperfecta types II and III.A revised estimate of the amount of genetic variation in human proteins: implications for the distribution of DNA polymorphisms.Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuriaChromosome 13 homozygosity in osteosarcoma without retinoblastoma.The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4.Pairwise linkage analysis of 11 loci on human chromosome 4.Factor IXPortland: a nonsense mutation (CGA to TGA) resulting in hemophilia BA colorimetric method for DNA hybridization.Low frequency of p53 mutations observed in a diverse collection of primary hepatocellular carcinomas2013 Presidential Address: Just another president's speech (but it's all about you).Optimizing selection of restriction enzymes in the search for DNA variants.Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27.Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosome.Alpha 1-antitrypsin and serum albumin mRNA accumulation in normal, acute phase and ZZ human liver.
P2860
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P2860
Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 1983
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Molecular genetics of human se ...... lymorphisms and analbuminemia.
@en
Molecular genetics of human se ...... lymorphisms and analbuminemia.
@nl
type
label
Molecular genetics of human se ...... lymorphisms and analbuminemia.
@en
Molecular genetics of human se ...... lymorphisms and analbuminemia.
@nl
prefLabel
Molecular genetics of human se ...... lymorphisms and analbuminemia.
@en
Molecular genetics of human se ...... lymorphisms and analbuminemia.
@nl
P2093
P2860
P356
P1476
Molecular genetics of human se ...... lymorphisms and analbuminemia.
@en
P2093
A G Motulsky
C M Demopulos
J C Murray
P2860
P304
P356
10.1073/PNAS.80.19.5951
P407
P577
1983-10-01T00:00:00Z