Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase.
about
Sequences of members of the human gene family for the c subunit of mitochondrial ATP synthaseA "housekeeping" gene on the X chromosome encodes a protein similar to ubiquitinStructure of the human sialophorin (CD43) gene. Identification of features atypical of genes encoding integral membrane proteinsStructure of the gene for human uroporphyrinogen decarboxylaseThe scanning model for translation: an updateGlucose-6-Phosphate Dehydrogenase: Update and Analysis of New Mutations around the WorldMolecular Analysis of Glucose-6-Phosphate Dehydrogenase Gene Mutations in Bangladeshi Individuals.Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferaseMolecular cloning and nucleotide sequence of cDNA for human glucose-6-phosphate dehydrogenase variant A(-).Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.Molecular diversity of glucose-6-phosphate dehydrogenase: rat enzyme structure identifies NH2-terminal segment, shows initiation from sites nonequivalent in different organisms, and establishes otherwise extensive sequence conservation.X-inactivation normalizes O-GlcNAc transferase levels and generates an O-GlcNAc-depleted Barr body.Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA.Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.Structure of the rat ornithine carbamoyltransferase gene, a large, X chromosome-linked gene with an atypical promoter.DNA methylation stabilizes X chromosome inactivation in eutherians but not in marsupials: evidence for multistep maintenance of mammalian X dosage compensation.Epstein-Barr virus genomes in lymphoid cells: activation in mitosis and chromosomal locationHuman Xq24-Xq28: approaches to mapping with yeast artificial chromosomes.Alternative splicing of human glucose-6-phosphate dehydrogenase messenger RNA in different tissuesDetailed ordering of markers localizing to the Xq26-Xqter region of the human X chromosome by the use of an interspecific Mus spretus mouse cross.Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation.Molecular abnormalities of a human glucose-6-phosphate dehydrogenase variant associated with undetectable enzyme activity and immunologically cross-reacting material.A contiguous, 3-Mb physical map of Xq28 extending from the colorblindness locus to DXS15.The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia.An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequencePulse-field linkage of the P3, G6pd and Cf-8 genes on the mouse X chromosome: demonstration of synteny at the physical levelNuclear factors specifically bind to upstream sequences of a Xenopus laevis ribosomal protein gene promoter.Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNAPharmGKB summary: very important pharmacogene information for G6PD.Activity of the adenosine deaminase promoter in transgenic mice.Molecular Characterization of Glucose-6-phosphate Dehydrogenase Deficiency in Families from the Republic of Macedonia and Genotype-phenotype Correlation.Influence of the Inherited Glucose-6-phosphate Dehydrogenase Deficiency on the Appearance of Neonatal Hyperbilirubinemia in Southern CroatiaPrevalence of G6PD deficiency in selected populations from two previously high malaria endemic areas of Sri Lanka.Molecular epidemiological investigation of G6PD deficiency by a gene chip among Chinese Hakka of southern Jiangxi province.Chromatin loop structure of the human X chromosome: relevance to X inactivation and CpG clusters.Isolation and characterization of the human diacylglycerol kinase gene.Structural and functional analysis of the rat malic enzyme gene promoterNuclease sensitivity of the mouse HPRT gene promoter region: differential sensitivity on the active and inactive X chromosomes.Glucose-6-phosphate dehydrogenase deficiency and malaria: cytochemical detection of heterozygous G6PD deficiency in women.Stable integration and expression in mouse cells of yeast artificial chromosomes harboring human genes
P2860
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P2860
Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase.
description
1986 nî lūn-bûn
@nan
1986 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
Structural analysis of the X-l ...... ose 6-phosphate dehydrogenase.
@ast
Structural analysis of the X-l ...... ose 6-phosphate dehydrogenase.
@en
type
label
Structural analysis of the X-l ...... ose 6-phosphate dehydrogenase.
@ast
Structural analysis of the X-l ...... ose 6-phosphate dehydrogenase.
@en
prefLabel
Structural analysis of the X-l ...... ose 6-phosphate dehydrogenase.
@ast
Structural analysis of the X-l ...... ose 6-phosphate dehydrogenase.
@en
P2093
P2860
P1433
P1476
Structural analysis of the X-l ...... ose 6-phosphate dehydrogenase.
@en
P2093
Luzzatto L
Paonessa G
Persico MG
Viglietto G
Vulliamy T
P2860
P304
P407
P577
1986-08-01T00:00:00Z