(Q24670527)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

Bilirubin is an antioxidant of possible physiological importance

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

Growth of human hepatoma cells lines with differentiated functions in chemically defined medium

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

Studies on the neonatal development of the glucuronide conjugating system

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

Is bilirubin good for you?

28 September 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

28 September 2017

https://api.crossref.org/works/10.1073/PNAS.95.14.8170

7 January 2021

inferred from DOI database lookup

Variation of initial serum bilirubin rise in newborn infants with type of illness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

Sequence of exons and the flanking regions of human bilirubin-UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

Population studies on Gilbert's syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

NADH-methemoglobin reductase (cytochrome b5 reductase) levels in two groups of American blacks and whites

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

Comparison of bilirubin production in Japanese and Caucasian infants

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

The Non-lron-deficiency-related Difference in Hemoglobin Concentration Distribution between Blacks and Whites and between Men and Women

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

Hemoglobin concentration in white, black, and Oriental children: is there a need for separate criteria in screening for anemia?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

[Prevalence of Gilbert's syndrome in Germany]

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=20948

Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.

19 June 2018

1 reference

https://api.crossref.org/works/10.1073/PNAS.95.14.8170

Serum bilirubin distribution and its relation to cardiovascular risk in children and young adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1073/PNAS.95.14.8170

Hemoglobin comparisons between African American and European American males with hemoglobin values in the normal range.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073/PNAS.95.14.8170

Ethnic differences in neonatal jaundice: Comparison of Japanese and Caucasian newborn infants

21 January 2018

1 reference

12 December 2020

Sex- and race-related differences in liver-associated serum chemistry tests in young adults in the CARDIA study

1 reference

12 December 2020

Transcutaneous bilirubinometry in normal Japanese infants

1 reference

12 December 2020

The total free radical trapping ability of cord blood plasma in preterm and term babies

1 reference

12 December 2020

Efficacy of phototherapy in prevention and management of neonatal hyperbilirubinemia

1 reference

12 December 2020

The protective role of bilirubin in oxygen-radical diseases of the preterm infant

1 reference

12 December 2020

Hemoglobin difference between black and white women with comparable iron status: justification for race-specific anemia criteria

1 reference

12 December 2020

[Bilirubin in the early neonatal period. Is there a positive aspect of hyperbilirubinemia?--A medical hypothesis]

1 reference

12 December 2020

Association of low serum concentration of bilirubin with increased risk of coronary artery disease

2 references

12 December 2020

https://api.crossref.org/works/10.1073/PNAS.95.14.8170

7 January 2021

inferred from DOI database lookup

Hyperbilirubinaemia in heterozygous β‐thalassaemia is related to co‐inherited Gilbert's syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias

1 reference

12 December 2020

UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.95.14.8170

1 reference

ADS bibcode

1998PNAS...95.8170B

0 references

1 reference

1 reference

PubMed publication ID

9653159

1 reference