(Q54559255)

31 May 2018

title

SLCO1B1 haplotypes are not associated with atorvastatin-induced myalgia in Brazilian patients with familial hypercholesterolemia. (English)

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31 May 2018

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6

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author name string

Paulo Caleb Junior Lima Santos

1

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31 May 2018

Ana Carolina Moron Gagliardi

2

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31 May 2018

Márcio Hiroshi Miname

3

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31 May 2018

Ana Paula Chacra

4

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31 May 2018

Raul Dias Santos

5

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Alexandre Costa Pereira

7

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31 May 2018

publication date

18 September 2011

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31 May 2018

European Journal of Clinical Pharmacology

published in

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31 May 2018

volume

68

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31 May 2018

issue

3

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31 May 2018

page(s)

273-279

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31 May 2018

https://scigraph.springernature.com/pub.10.1007/s00228-011-1125-1

exact match

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cites work

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The SLCO1B1*5 genetic variant is associated with statin-induced side effects

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The effect of SLCO1B1*15 on the disposition of pravastatin and pitavastatin is substrate dependent: the contribution of transporting activity changes by SLCO1B1*15.

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Functional characterization of SLCO1B1 (OATP-C) variants, SLCO1B1*5, SLCO1B1*15 and SLCO1B1*15+C1007G, by using transient expression systems of HeLa and HEK293 cells

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Characterization of hepatobiliary transport systems of a novel alpha4beta1/alpha4beta7 dual antagonist, TR-14035.

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Documented need for more effective diagnosis and treatment of familial hypercholesterolemia according to data from 502 heterozygotes in Utah

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APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population

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CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population

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Ethnicity and arterial stiffness in Brazil

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Different Effects of SLCO1B1 Polymorphism on the Pharmacokinetics of Atorvastatin and Rosuvastatin

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SLCO1B1 polymorphism markedly affects the pharmacokinetics of simvastatin acid

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12 December 2020

Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin.

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Genetic involvement in statins induced myopathy. Preliminary data from an observational case-control study

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Frequency of the SLCO1B1 388A>G and the 521T>C polymorphism in Tanzania genotyped by a new LightCycler®-based method

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Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients

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12 December 2020

10.1007/S00228-011-1125-1

Identifiers

DOI

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31 May 2018

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31 May 2018