(Q84571475)

English

Genetic polymorphism of CYP2C19 in a Jordanian population: influence of allele frequencies of CYP2C191 and CYP2C192 on the pharmacokinetic profile of lansoprazole

scientific article published on 17 July 2011

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21769476%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Genetic polymorphism of CYP2C19 in a Jordanian population: influence of allele frequencies of CYP2C19*1 and CYP2C19*2 on the pharmacokinetic profile of lansoprazole (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21769476%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

pharmacokinetics

1 reference

based on heuristic

inferred from title

author name string

Imad Zalloum

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21769476%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Nancy Hakooz

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21769476%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Tawfiq Arafat

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21769476%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

publication date

17 July 2011

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21769476%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Molecular Biology Reports

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21769476%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

39

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21769476%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21769476%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

4195-4200

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21769476%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

CYP2C19 genotypes in a population of healthy volunteers and in children with hematological malignancies in Gaza Strip.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bioequivalence evaluation of lansoprazole 30-mg capsules (Lanfast and Lanzor) in healthy volunteers

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pharmacogenetics of CYP2C19: functional and clinical implications of a new variant CYP2C19*17

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proton pump inhibitors and acid-related diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of CYP2C19 polymorphisms in the Lebanese population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influences of CYP2C19 polymorphism on recurrence of reflux esophagitis during proton pump inhibitor maintenance therapy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequencies of the defective CYP2C19 alleles responsible for the mephenytoin poor metabolizer phenotype in various Oriental, Caucasian, Saudi Arabian and American black populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lansoprazole quantification in human plasma by liquid chromatography-electrospray tandem mass spectrometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pharmacokinetics/genotype associations for major cytochrome P450 enzymes in native and first- and third-generation Japanese populations: comparison with Korean, Chinese, and Caucasian populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotyping polymorphic drug metabolism in the French Caucasian population

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allele and genotype frequencies of polymorphic cytochromes P450 (CYP2C9, CYP2C19, CYP2E1) and dihydropyrimidine dehydrogenase (DPYD) in the Egyptian population

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CYP2C19-guided design of a proton pump inhibitor dose regimen to avoid the need for pharmacogenetic individualisation in H. pylori eradication

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphism of CYP2C19 in Maharashtrian population

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pharmacogenetics of the proton pump inhibitors: a systematic review.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphic hydroxylation of S-mephenytoin and omeprazole metabolism in Caucasian and Chinese subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Different contribution of CYP2C19 in the in vitro metabolism of three proton pump inhibitors

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CYP2C19 genotype status and intragastric pH during dosing with lansoprazole or rabeprazole

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of cytochrome P4502C19 genotypic differences on cure rates for gastroesophageal reflux disease by lansoprazole

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pharmacology of the gastric acid pump: the H+,K+ ATPase

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotyping of S-mephenytoin 4'-hydroxylation in an extended Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Individual and ethnic differences in CYP2C19 activity in Chinese populations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of lansoprazole and five metabolites in plasma by high-performance liquid chromatography

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/21769476

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q84571475&oldid=2221616821"