Chromosomal localization of human beta globin gene on human chromosome 11 in somatic cell hybrids. - Wikidata - awgldk - TriplyDB

Chromosomal localization of human beta globin gene on human chromosome 11 in somatic cell hybrids.

Chromosomal localization of human beta globin gene on human chromosome 11 in somatic cell hybrids.

http://www.wikidata.org/entity/Q33968747

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Human collagen genes encoding basement membrane alpha 1 (IV) and alpha 2 (IV) chains map to the distal long arm of chromosome 13 Human alpha 1(III) and alpha 2(V) procollagen genes are located on the long arm of chromosome 2 Cloning and complete nucleotide sequence of human 5'-alpha-globin gene Human immune interferon gene is located on chromosome 12 β-thalassemias: paradigmatic diseases for scientific discoveries and development of innovative therapies Genetic engineering of a mouse: Dr. Frank Ruddle and somatic cell genetics Partial deletion of chromosome 11p in breast cancer correlates with size of primary tumour and oestrogen receptor level.G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C.Hemolytic disease of the newborn caused by a new deletion of the entire beta-globin cluster Synergistic enhancement of globin gene expression by activator protein-1-like proteins.DNA restriction endonuclease analysis for localization of human beta- and delta-globin genes on chromosome 11.Assignment of human beta-, gamma-, and delta-globin genes to the short arm of chromosome 11 by chromosome sorting and DNA restriction enzyme analysis.Precise localization of human beta-globin gene complex on chromosome 11 Human beta-globin gene expression in transgenic mice is enhanced by a distant DNase I hypersensitive site A chromosome 11-linked determinant controls fetal globin expression and the fetal-to-adult globin switch Renal medullary carcinoma: clinical and therapeutic aspects of a newly described tumor.Compensatory increase in alpha 1-globin gene expression in individuals heterozygous for the alpha-thalassemia-2 deletion.Somatic cell gene mutations in humans: biomarkers for genotoxicity.Human placental and intestinal alkaline phosphatase genes map to 2q34-q37 The occurrence of the alpha G-Philadelphia-globin allele on a double-locus chromosome.Localization of the beta-globin gene by chromosomal in situ hybridization.The William Allan Memorial Award address: Reverse genetics and beyond Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridization Localization of a unique gene by direct hybridization in situ.Isolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome.Restriction endonuclease mapping of the human gamma globin gene loci.Localization of the casein gene family to a single mouse chromosome.Assignment of the genes for the alpha and beta subunits of thyrotropin to different mouse chromosomes.DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22.Regional gene assignment of human porphobilinogen deaminase and esterase A4 to chromosome 11q23 leads to 11qter.Activation of human beta-globin genes from nonerythroid cells by fusion with murine erythroleukemia cells Cloning and direct examination of a structurally abnormal human beta 0-thalassemia globin gene Cloning and characterization of DNA sequences surrounding the human gamma-, delta-, and beta-globin genes Isolation and characterization of cloned human fetal globin genes.Human alpha-globin genes demonstrate autonomous developmental regulation in transgenic mice.Gene localization by chromosome fractionation: globin genes are on at least two chromosomes and three estrogen-inducible genes are on three chromosomes.Activation of phenotypic expression of human globin genes from nonerythroid cells by chromosome-dependent transfer to tetraploid mouse erythroleukemia cells Chromosomal assignment of the mouse kappa light chain genes.Linkage map of the short arm of human chromosome 11: location of the genes for catalase, calcitonin, and insulin-like growth factor II.

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P2860

Chromosomal localization of human beta globin gene on human chromosome 11 in somatic cell hybrids.

http://www.wikidata.org/entity/Q33968747

description

1978 nî lūn-bûn

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1978 թուականի Մարտին հրատարակուած գիտական յօդուած

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1978 թվականի մարտին հրատարակված գիտական հոդված

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1978年の論文

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1978年論文

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1978年論文

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1978年論文

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1978年論文

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1978年論文

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1978年论文

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Chromosomal localization of hu ...... me 11 in somatic cell hybrids.

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Chromosomal localization of hu ...... me 11 in somatic cell hybrids.

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Chromosomal localization of hu ...... me 11 in somatic cell hybrids.

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Chromosomal localization of hu ...... me 11 in somatic cell hybrids.

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Chromosomal localization of hu ...... me 11 in somatic cell hybrids.

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Chromosomal localization of hu ...... me 11 in somatic cell hybrids.

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P2093

Deisseroth A

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Giles R

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Lawrence J

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Nienhuis A

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Ruddle FH

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Turner P

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P2860

In situ hybridization of chromosome loci.

Assignment of three human genes to chromosomes (LDH-A to 11, TK to 17, and IDH to 20) and evidence for translocation between human and mouse chromosomes in somatic cell hybrids (thymidine kinase-lactate dehydrogenase A-isocitrate dehydrogenase-C-11,

Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia.

Studies on nucleic acid reassociation kinetics: empirical equations describing DNA reassociation

A sequential staining technique for the chromosomal analysis of the interspecific mouse/hamster and mouse/human somatic cell hybrids.

beta2-microglobulin locus on human chromosome 15.

A review of enzyme polymorphism, linkage and electrophoretic conditions for mouse and somatic cell hybrids in starch gels.

Gene mapping by fluorescent in situ hybridization.

The status of the gene map of the human chromosomes.

Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9.

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411491

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