Molecular characterization of seven beta-thalassemia mutations in Asian Indians.
about
Customizing the genome as therapy for the β-hemoglobinopathiesAnalysis of four diverse population groups indicates that a subset of cystic fibrosis mutations occur in common among CaucasiansProfiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmesPrenatal diagnosis of the common haemoglobin disorders.The spectrum of beta thalassaemia mutations in the UAE national populationHigh frequency of beta thalassaemia in a small island population in Melanesia.Prenatal diagnosis of beta thalassaemia by oligonucleotide analysis in Mediterranean populationsBeta thalassaemia mutations in Turkish Cypriots.Human beta-globin mRNAs that harbor a nonsense codon are degraded in murine erythroid tissues to intermediates lacking regions of exon I or exons I and II that have a cap-like structure at the 5' termini.Homology requirements for unequal crossing over in humans.Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes.Alpha 1-antitrypsin deficiency caused by the alpha 1-antitrypsin Nullmattawa gene. An insertion mutation rendering the alpha 1-antitrypsin gene incapable of producing alpha 1-antitrypsinHereditary thrombophilia: identification of nonsense and missense mutations in the protein C geneBeta-thalassemia mutations in Indonesia and their linkage to beta haplotypes.The molecular basis of beta-thalassemia in Thailand: application to prenatal diagnosisDistribution of beta-thalassemia mutations in south China and their association with haplotypes.Evidence supporting a single origin of the beta(C)-globin gene in blacksCharacterization of a spontaneous mutation to a beta-thalassemia allele.Past, present & future scenario of thalassaemic care & control in India.A novel beta thalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3' end of IVS 2beta-Thalassemia in Chinese: use of in vivo RNA analysis and oligonucleotide hybridization in systematic characterization of molecular defects.Recombination hot spot in the human beta-globin gene cluster: meiotic recombination of human DNA fragments in Saccharomyces cerevisiae.The evolutionarily conserved repetitive sequence d(TG.AC)n promotes reciprocal exchange and generates unusual recombinant tetrads during yeast meiosisOn the origin and spread of beta-thalassemia: recurrent observation of four mutations in different ethnic groups.Innumerable studies on single nucleotide polymorphisms: What could be its utility?Diversity of beta-globin mutations in Israeli ethnic groups reflects recent historic eventsHb Baden: structural and functional characterization.Using 5'-PTMs to repair mutant beta-globin transcripts.The 5' splice site: phylogenetic evolution and variable geometry of association with U1RNA.Genotype-phenotype correlation of β-thalassemia spectrum of mutations in an Indian population.Allan Award Lecture: on jumping fields and "jumping genes".High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh.
P2860
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P2860
Molecular characterization of seven beta-thalassemia mutations in Asian Indians.
description
1984 nî lūn-bûn
@nan
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
1984年论文
@zh
1984年论文
@zh-cn
name
Molecular characterization of seven beta-thalassemia mutations in Asian Indians.
@en
type
label
Molecular characterization of seven beta-thalassemia mutations in Asian Indians.
@en
prefLabel
Molecular characterization of seven beta-thalassemia mutations in Asian Indians.
@en
P2093
P2860
P1433
P1476
Molecular characterization of seven beta-thalassemia mutations in Asian Indians
@en
P2093
Antonarakis SE
Kazazian HH Jr
P2860
P304
P356
10.1002/J.1460-2075.1984.TB01853.X
P407
P577
1984-03-01T00:00:00Z