Molecular cloning and nucleotide sequence of cDNA for human glucose-6-phosphate dehydrogenase variant A(-).
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The extent of linkage disequilibrium caused by selection on G6PD in humansRapid screening for glucose-6-phosphate dehydrogenase deficiency and haemoglobin polymorphisms in Africa by a simple high-throughput SSOP-ELISA methodReappraisal of known malaria resistance loci in a large multicenter studyGlucose-6-phosphate dehydrogenase deficiency and the risk of malaria and other diseases in children in Kenya: a case-control and a cohort study.Long term outcome of severe anaemia in Malawian childrenImpact of the method of G6PD deficiency assessment on genetic association studies of malaria susceptibility.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.Molecular genetics of X chromosome-linked color vision among populations of African and Japanese ancestry: high frequency of a shortened red pigment gene among Afro-AmericansAssociation of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia.Glucose-6-phosphate dehydrogenase status and risk of hemolysis in Plasmodium falciparum-infected African children receiving single-dose primaquine.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.Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility.Genetic determinants of glucose-6-phosphate dehydrogenase activity in KenyaAlternative splicing of human glucose-6-phosphate dehydrogenase messenger RNA in different tissuesNucleotide variability at G6pd and the signature of malarial selection in humans.Clinically relevant genetic variations in drug metabolizing enzymes.Case Report: Paroxysmal nocturnal hemoglobinuria in a woman heterozygous for G6PD A-.Inability to maintain GSH pool in G6PD-deficient red cells causes futile AMPK activation and irreversible metabolic disturbanceFrequency of glucose-6-phosphate dehydrogenase deficiency in malaria patients from six African countries enrolled in two randomized anti-malarial clinical trialsGlucose-6-phosphate dehydrogenase deficiency among malaria patients of Honduras: a descriptive study of archival blood samples.PharmGKB summary: very important pharmacogene information for G6PD.Prevalence and molecular characterization of G6PD deficiency in two Plasmodium vivax endemic areas in Venezuela: predominance of the African A-(202A/376G) variant.Glucose-6-phosphate dehydrogenase--from oxidative stress to cellular functions and degenerative diseases.PCR-based allelic discrimination for glucose-6-phosphate dehydrogenase (G6PD) deficiency in Ugandan umbilical cord blood.Pharmacogenetics and human genetic polymorphisms.Glucose-6-phosphate dehydrogenase--beyond the realm of red cell biology.Detailed functional analysis of two clinical glucose-6-phosphate dehydrogenase (G6PD) variants, G6PDViangchan and G6PDViangchan+Mahidol: Decreased stability and catalytic efficiency contribute to the clinical phenotype.Validation of the rapid test Carestart(tm) G6PD among malaria vivax-infected subjects in the Brazilian Amazon.The polymerase chain reaction. Applications in dermatology.A new glucose-6-phosphate dehydrogenase variant, G6PD Orissa (44 Ala-->Gly), is the major polymorphic variant in tribal populations in India.A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil.The origin of glucose-6-phosphate-dehydrogenase (G6PD) polymorphisms in African-Americans.Molecular genetics of the glucose-6-phosphate dehydrogenase (G6PD) Mediterranean variant and description of a new G6PD mutant, G6PD Andalus1361A.Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.Two point mutations are responsible for G6PD polymorphism in Sardinia.Glucose-6-phosphate dehydrogenase deficiency in India.Structural defects underlying protein dysfunction in human glucose-6-phosphate dehydrogenase A(-) deficiency.Severe anemia in Malawian childrenRole of genetic factors and ethnicity on the multiplicity of infection in children with asymptomatic malaria in Yaoundé, Cameroon
P2860
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P2860
Molecular cloning and nucleotide sequence of cDNA for human glucose-6-phosphate dehydrogenase variant A(-).
description
1988 nî lūn-bûn
@nan
1988 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Molecular cloning and nucleoti ...... sphate dehydrogenase variant A
@nl
Molecular cloning and nucleoti ...... te dehydrogenase variant A(-).
@ast
Molecular cloning and nucleoti ...... te dehydrogenase variant A(-).
@en
type
label
Molecular cloning and nucleoti ...... sphate dehydrogenase variant A
@nl
Molecular cloning and nucleoti ...... te dehydrogenase variant A(-).
@ast
Molecular cloning and nucleoti ...... te dehydrogenase variant A(-).
@en
prefLabel
Molecular cloning and nucleoti ...... sphate dehydrogenase variant A
@nl
Molecular cloning and nucleoti ...... te dehydrogenase variant A(-).
@ast
Molecular cloning and nucleoti ...... te dehydrogenase variant A(-).
@en
P2860
P356
P1476
Molecular cloning and nucleoti ...... te dehydrogenase variant A(-).
@en
P2093
P2860
P304
P356
10.1073/PNAS.85.11.3951
P407
P577
1988-06-01T00:00:00Z