(Q61781514)

English

Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis

scientific article published on 15 May 2007

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17505501%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17505501%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

molecular medicine

0 references

Bryan J Barratt

4

1 reference

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30 December 2019

Karin Cederbrant

8

1 reference

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30 December 2019

author name string

Kindmark A

1

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30 December 2019

Jawaid A

2

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30 December 2019

Harbron CG

3

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30 December 2019

Bengtsson OF

5

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30 December 2019

Andersson TB

6

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30 December 2019

Carlsson S

7

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30 December 2019

Gibson NJ

9

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30 December 2019

Armstrong M

10

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30 December 2019

Lagerström-Fermér ME

11

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30 December 2019

Dellsén A

12

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30 December 2019

Brown EM

13

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30 December 2019

Thornton M

14

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30 December 2019

Dukes C

15

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30 December 2019

Jenkins SC

16

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30 December 2019

Firth MA

17

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30 December 2019

Harrod GO

18

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30 December 2019

Pinel TH

19

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30 December 2019

Billing-Clason SM

20

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30 December 2019

Cardon LR

21

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30 December 2019

March RE

22

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30 December 2019

publication date

15 May 2007

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30 December 2019

The Pharmacogenomics Journal

1 reference

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30 December 2019

8

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30 December 2019

186-195

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30 December 2019

3

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30 December 2019

https://scigraph.springernature.com/pub.10.1038/sj.tpj.6500458

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Hepatic findings in long-term clinical trials of ximelagatran

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Observations of alanine aminotransferase and aspartate aminotransferase in THRIVE studies treated orally with ximelagatran

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Whole-genome patterns of common DNA variation in three human populations

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A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms

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