Glucose-6-phosphate dehydrogenase deficiency (Q28263721)

Glucose-6-phosphate dehydrogenase

Europe PubMed Central

title

Glucose-6-phosphate dehydrogenase deficiency (English)

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main subject

glycobiology

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glucose-6-phosphate dehydrogenase deficiency

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glucose

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author name string

M D Cappellini

series ordinal

1

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G Fiorelli

series ordinal

2

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language of work or name

English

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publication date

5 January 2008

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published in

The Lancet

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volume

371

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issue

9606

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page(s)

64-74

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cites work

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Enzymatic Deficiency in Primaquine-Sensitive Erythrocytes

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[Hemolysis and absence of glucose-6-phosphate dehydrogenase in erythrocytes; an enzyme abnormality of erythrocytes]

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7 January 2021

Impaired production of nitric oxide, superoxide, and hydrogen peroxide in glucose 6-phosphate-dehydrogenase-deficient granulocytes

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7 January 2021

Human glucose-6-phosphate dehydrogenase: the crystal structure reveals a structural NADP(+) molecule and provides insights into enzyme deficiency

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7 January 2021

Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3' end of the gene

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Intracellular restraint: a new basis for the limitation in response to oxidative stress in human erythrocytes containing low-activity variants of glucose-6-phosphate dehydrogenase

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The normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker

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An Ashkenazi Jewish woman presenting with favism

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Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site

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7 January 2021

Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non-coding region

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Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome.

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HMG CoA reductase: a negatively regulated gene with unusual promoter and 5' untranslated regions

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7 January 2021

The CpG island in the 5' region of the G6PD gene of man and mouse

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Hematologically important mutations: glucose-6-phosphate dehydrogenase

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Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotype

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7 January 2021

A single mutation 202G>A in the human glucose-6-phosphate dehydrogenase gene (G6PD) can cause acute hemolysis by itself

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Molecular anatomy of the human glucose 6-phosphate dehydrogenase core promoter

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Promoter function of the human glucose-6-phosphate dehydrogenase gene depends on two GC boxes that are cell specifically controlled

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7 January 2021

Identification of the binding domain for NADP+ of human glucose-6-phosphate dehydrogenase by sequence analysis of mutants

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Amino acid substitutions at the dimer interface of human glucose-6-phosphate dehydrogenase that increase thermostability and reduce the stabilising effect of NADP

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Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia

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Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-.

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Severe malaria and glucose-6-phosphate-dehydrogenase deficiency: a reappraisal of the malaria/G-6-P.D. hypothesis

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Natural selection of hemi- and heterozygotes for G6PD deficiency in Africa by resistance to severe malaria

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Glucose-6-phosphate dehydrogenase deficiency inhibits in vitro growth of Plasmodium falciparum

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Plasmodium falciparum: thiol status and growth in normal and glucose-6-phosphate dehydrogenase deficient human erythrocytes

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Hexose-monophosphate shunt activity in intact Plasmodium falciparum-infected erythrocytes and in free parasites

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Glucose-6-Phosphate Dehydrogenase Deficient Red Cells: Resistance to Infection by Malarial Parasites

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G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype

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7 January 2021

G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish Jews

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Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Al-Ain District, United Arab Emirates

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7 January 2021

Different polymorphic variants of glucose-6-phosphate dehydrogenase (G6PD) in Italy

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Human enzyme polymorphism in the Canary Islands. VII. G6PD Seattle in Canarians and North African Berbers

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7 January 2021

A novel C to T substitution at nucleotide 1360 of cDNA which abolishes a natural Hha I site accounts for a new G6PD deficiency gene in Chinese

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7 January 2021

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Brilliant cresyl blue screening test for demonstrating glucose-6-phosphate dehydrogenase deficiency in red cells.

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Sickle cell trait and glucose-6-phosphate dehydrogenase deficiency. Effects on health and military performance in black Navy enlistees

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7 January 2021

Diabetic ketoacidosis does not precipitate haemolysis in patients with the Mediterranean variant of glucose-6-phosphate dehydrogenase deficiency

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7 January 2021

Acute hemolytic anemia precipitated by myocardial infarction and pericardial tamponade in G6PD deficiency

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7 January 2021

Muscle glucose 6-phosphate dehydrogenase (G6PD) deficiency and oxidant stress during physical exercise

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7 January 2021

Anemia and the liver. Hepatobiliary manifestations of anemia

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7 January 2021

Hepatitis A and cytomegalovirus infection precipitating acute hemolysis in glucose-6-phosphate dehydrogenase deficiency

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7 January 2021

Glucose-6-phosphate-dehydrogenase deficiency in Nigerians with jaundice associated with lobar pneumonia.

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7 January 2021

Chloramphenicol-Induced Hemolysis in Caucasian Glucose-6-Phosphate Dehydrogenase Deficiency

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7 January 2021

Viral hepatitis in G.-6-P.D. deficiency

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7 January 2021

Reversible renal failure and G.-6-P.D. deficiency

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7 January 2021

Glucose-6-phosphate dehydrogenase deficiency and acute renal failure

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7 January 2021

Favism: clinical and biochemical data

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7 January 2021

Favism and hemolytic anemia in glucose-6-phosphate dehydrogenase-deficient subjects in North Sardinia

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https://api.crossref.org/works/10.1016%2FS0140-6736%2808%2960073-2

7 January 2021

Glucose-6-phosphate dehydrogenase deficiency in Sicily. Incidence, biochemical characteristics and clinical implications

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7 January 2021

Membrane cross bonding in red cells in favic crisis: a missing link in the mechanism of extravascular haemolysis

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7 January 2021

Marked decline of favism after neonatal glucose-6-phosphate dehydrogenase screening and health education: the northern Sardinian experience

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7 January 2021

Acute hemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes

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7 January 2021

Favism in a female newborn infant whose mother ingested fava beans before delivery

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7 January 2021

Kernicterus and G6PD Deficiency—a Case Series from Oman

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7 January 2021

System-based approach to management of neonatal jaundice and prevention of kernicterus

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7 January 2021

Incidence and causes of severe neonatal hyperbilirubinemia in Canada

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7 January 2021

Contribution of haemolysis to jaundice in Sephardic Jewish glucose-6-phosphate dehydrogenase deficient neonates

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7 January 2021

Role of hemolysis in neonatal jaundice associated with glucose-6 phosphate dehydrogenase deficiency

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7 January 2021

Hydrops fetalis and stillbirth in a male glucose-6-phosphate dehydrogenase-deficient fetus possibly due to maternal ingestion of sulfisoxazole

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7 January 2021

ACUTE HEMOLYSIS DUE TO NAPHTHALENE INHALATION

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7 January 2021

Conjugated bilirubin in neonates with glucose-6-phosphate dehydrogenase deficiency

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7 January 2021

Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia

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7 January 2021

Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation

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7 January 2021

Pyruvate kinase deficiency. Association with G6PD deficiency

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7 January 2021

Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child

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7 January 2021

Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia

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7 January 2021

The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2808%2960073-2

7 January 2021

The interaction between Gilbert's syndrome and G6PD deficiency influences bilirubin levels.

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7 January 2021

Improved erythrocyte survival with combined vitamin E and selenium therapy in children with glucose-6-phosphate dehydrogenase deficiency and mild chronic hemolysis

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7 January 2021

Prenatal Diagnosis of Glucose-6-Phosphate-Dehydrogenase Deficiency

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7 January 2021

10.1016/S0140-6736(08)60073-2

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

18177777

1 reference

Consolidated OpenCitations Corpus – April 2017