Assignment of the structural gene for the third component of human complement to chromosome 19.
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Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expressionHuman DNA ligase I cDNA: cloning and functional expression in Saccharomyces cerevisiaeThe chromosomal location of T-cell receptor genes and a T cell rearranging gene: possible correlation with specific translocations in human T cell leukaemiaHuman complement component C3: cDNA coding sequence and derived primary structureIsolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CIIAssignment of the human gene for the low density lipoprotein receptor to chromosome 19: synteny of a receptor, a ligand, and a genetic diseaseHuman genes involved in cholesterol metabolism: chromosomal mapping of the loci for the low density lipoprotein receptor and 3-hydroxy-3-methylglutaryl-coenzyme A reductase with cDNA probesIsolation of cDNA clones for the human complement protein factor B, a class III major histocompatibility complex gene productMolecular cloning of a human genomic region containing the H blood group alpha(1,2)fucosyltransferase gene and two H locus-related DNA restriction fragments. Isolation of a candidate for the human Secretor blood group locusThe human chromosome 19 linkage group FUT1 (H), FUT2 (SE), LE, LU, PEPD, C3, APOC2, D19S7 and D19S9Mapping of the gene coding for the human liver/bone/kidney isozyme of alkaline phosphatase to chromosome 1Assignment of eight human genomic DNA sequences detecting high frequency restriction fragment length polymorphisms.The human genes for complement components 6 (C6) and 9 (C9) are closely linked on chromosome 5.Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.Gene mapping and chromosome 19.Conservation of structural and functional domains in complement component C3 of Xenopus and mammals.The gene for human muscle specific carbonic anhydrase (CAIII) is assigned to chromosome 8.Molecular basis of hereditary C3 deficiency.Assignment of the human gene for uridine 5'-monophosphate phosphohydrolase (UMPH2) to the long arm of chromosome 17.A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locusNucleotide sequence of cDNA encoding human alpha 2-macroglobulin and assignment of the chromosomal locus.De novo myotonic dystrophy mutation in a Nigerian kindred.Chromosomal localization of the human c-fms oncogeneSegregation distortion of the CTG repeats at the myotonic dystrophy locus.Lengths of chromosomal segments conserved since divergence of man and mouseDecay-accelerating factor. Genetic polymorphism and linkage to the RCA (regulator of complement activation) gene cluster in humansChromosomal assignment of seven human genomic DNA sequences associated with restriction fragment length polymorphisms.Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy.A genetic map of chromosome 19 based on family linkage data.The human Thy-1 gene: structure and chromosomal location.Insulin-gene flanking sequences, diabetes mellitus and atherosclerosis: a review.Myotonic dystrophy and gene mapping on human chromosome 19.Hereditary deficiency of C3 in animals and humans.A human T-cell antigen receptor beta chain gene maps to chromosome 7Cis- and trans-acting elements required for constitutive and cytokine-regulated expression of the mouse complement C3 geneIsolation of a cDNA probe for the human intestinal dipeptidylpeptidase IV and assignment of the gene locus DPP4 to chromosome 2.A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.MHC Class III products: an electron microscopic study of the C3 convertases of human complement.rs2230201 polymorphism may dictate complement C3 levels and response to treatment in chronic hepatitis C patients.The use of chromosomal translocations to study human immunoglobulin gene organization: mapping DH segments within 35 kb of the C mu gene and identification of a new DH locus.
P2860
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P2860
Assignment of the structural gene for the third component of human complement to chromosome 19.
description
1982 nî lūn-bûn
@nan
1982年の論文
@ja
1982年学术文章
@wuu
1982年学术文章
@zh-cn
1982年学术文章
@zh-hans
1982年学术文章
@zh-my
1982年学术文章
@zh-sg
1982年學術文章
@yue
1982年學術文章
@zh
1982年學術文章
@zh-hant
name
Assignment of the structural g ...... n complement to chromosome 19.
@ast
Assignment of the structural g ...... n complement to chromosome 19.
@en
type
label
Assignment of the structural g ...... n complement to chromosome 19.
@ast
Assignment of the structural g ...... n complement to chromosome 19.
@en
prefLabel
Assignment of the structural g ...... n complement to chromosome 19.
@ast
Assignment of the structural g ...... n complement to chromosome 19.
@en
P2093
P2860
P356
P1476
Assignment of the structural g ...... n complement to chromosome 19.
@en
P2093
P2860
P304
P356
10.1073/PNAS.79.16.5021
P407
P577
1982-08-01T00:00:00Z