(Q44497858)

3 December 2017

title

A novel TPMT missense mutation associated with TPMT deficiency in a 5-year-old boy with ALL. (English)

1 reference

3 December 2017

Schaeffeler E

1

1 reference

3 December 2017

Stanulla M

2

1 reference

3 December 2017

Greil J

3

1 reference

3 December 2017

Schrappe M

4

1 reference

3 December 2017

Eichelbaum M

5

1 reference

3 December 2017

Zanger UM

6

1 reference

3 December 2017

Schwab M

7

1 reference

3 December 2017

publication date

1 July 2003

1 reference

3 December 2017

1 reference

3 December 2017

volume

17

1 reference

3 December 2017

issue

7

1 reference

3 December 2017

page(s)

1422-1424

1 reference

https://scigraph.springernature.com/pub.10.1038/sj.leu.2402981

3 December 2017

exact match

0 references

cites work

Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2402981

Azathioprine therapy and adverse drug reactions in patients with inflammatory bowel disease: impact of thiopurine S-methyltransferase polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2402981

Preponderance of thiopurine S-methyltransferase deficiency and heterozygosity among patients intolerant to mercaptopurine or azathioprine

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2402981

Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2402981

Human thiopurine methyltransferase pharmacogenetics: gene sequence polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2402981

Human erythrocyte thiopurine methyltransferase: radiochemical microassay and biochemical properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2402981

Enhanced proteolysis of thiopurine S-methyltransferase (TPMT) encoded by mutant alleles in humans (TPMT*3A, TPMT*2): mechanisms for the genetic polymorphism of TPMT activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2402981

Acute lymphoblastic leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2402981

inferred from DOI database lookup

7 January 2021

based on heuristic

Thiopurine methyltransferase phenotype and genotype in relation to azathioprine therapy in autoimmune hepatitis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2402981

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.LEU.2402981

1 reference

release_km2xkqmerbagxmswbagqzso2ri

3 December 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/km2xkqmerbagxmswbagqzso2ri

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference