(Q80587522)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15378351%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

title

Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15378351%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference

2

1 reference

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1 January 2020

author name string

Yoshihiro Maruo

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15378351%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Asami Mori

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15378351%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Masaru Iwai

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15378351%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Hiroko Takahashi

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15378351%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Hiroshi Sato

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15378351%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Yoshihiro Takeuchi

7

1 reference

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1 January 2020

publication date

17 September 2004

1 reference

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1 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15378351%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

volume

115

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15378351%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15378351%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

page(s)

525-526

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00439-004-1183-x

1 January 2020

exact match

0 references

cites work

Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism

1 reference

12 December 2020

Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?

1 reference

12 December 2020