Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia (Q36637770)

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scientific article published on October 1997

Language	Label	Description	Also known as
English	Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia	scientific article published on October 1997

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

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

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

glucose-6-phosphate dehydrogenase deficiency

0 references

bilirubin metabolic disorder

1 reference

based on heuristic

inferred from title

Gilbert syndrome

1 reference

based on heuristic

inferred from title

author name string

M Kaplan

1

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

P Renbaum

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

E Levy-Lahad

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

C Hammerman

4

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

A Lahad

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

E Beutler

6

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

language of work or name

0 references

publication date

1 October 1997

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

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

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Europe PubMed Central

PMC publication ID

15 August 2017

94

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

22

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

12128-12132

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Neonatal Jaundice Associated with Familial G6PD Deficiency in Israel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

Drug reactions enzymes, and biochemical genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

Neonatal screening for glucose-6-phosphate dehydrogenase deficiency: sex distribution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

G6PD deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

Severe neonatal jaundice associated with glucose-6-phosphate dehydrogenase deficiency: pathogenesis and global epidemiology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

Hepatic Bilirubin UDP-Glucuronyl Transferase Activity in Liver Disease and Gilbert's Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

Alternative splicing of human glucose-6-phosphate dehydrogenase messenger RNA in different tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

Molecular genetics of the glucose-6-phosphate dehydrogenase (G6PD) Mediterranean variant and description of a new G6PD mutant, G6PD Andalus1361A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

30 September 2017

Hidden risks: early discharge and bilirubin toxicity due to glucose 6-phosphate dehydrogenase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

28 June 2018

Incidence and mechanism of neonatal jaundice related to glucose-6-phosphate dehydrogenase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

28 June 2018

Gilbert's syndrome: diagnosis by typical serum bilirubin pattern

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

28 June 2018

Neonatal hyperbilirubinemia associated with glucose-6-phosphate dehydrogenase deficiency in Sephardic-Jewish neonates: incidence, severity, and the effect of phototherapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

28 June 2018

Genetically determined deficiency of glucose 6-phosphate dehydrogenase (type-A-) is expressed in the liver

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

28 June 2018

Glucose-6-phosphate dehydrogenase deficiency and carboxyhemoglobin concentrations associated with bilirubin-related morbidity and death in Nigerian infants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23725

20 September 2018

Management of irritable hip: a review of hospital admission policy

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.22.12128

21 January 2018

Interactions of glucose-6-phosphate dehydrogenase deficiency with drug acetylation and hydroxylation reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tissue enzyme levels in erythrocyte glucose-6-phosphate dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Henna: a potential cause of oxidative hemolysis and neonatal hyperbilirubinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[New contributions on the subject of the bio-enzymology of ictero-hemoglobinuric favism. Note 3. Glucose-6-phosphate dehydrogenase activity of the hepatic parenchyma.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The hemolytic effect of primaquine. V. Primaquine sensitivity as a manifestation of a multiple drug sensitivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationships between serum bilirubins and production and conjugation of bilirubin. Studies in Gilbert's syndrome, Crigler-Najjar disease, hemolytic disorders, and rat models

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiologic surveys of deleterious genes in different population groups in Israel

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haptoglobin, hemopexin, hemoglobin and hematocrit in newborns with erythrocyte glucose-6-phosphate dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/9342374

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.94.22.12128

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

1997PNAS...9412128K

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

0 references

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