Frequency of the mdr-1 C>;T gene polymorphism in patients with COPD
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/18490 |
Resumo: | BACKGROUND AND AIM: The multi-drug resistant-1 (MDR-1) gene is located on human chromosome 7 and encodes a glycosylated membrane protein that is a member of the ATP-binding cassette transporters superfamily. The aim of the study was to reveal the role of the C3435T MDR-1 gene polymorphism in chronic obstructive pulmonary disease. METHOD: DNA samples from 41 patients with chronic obstructive pulmonary disease and 50 healthy control participants were used to compare MDR-1 gene profiles. Genotyping assays were performed using the StripAssay technique that is based on reverse-hybridization. RESULTS: The T allele polymorphism in the MDR-1 gene located at position 3435 in exon 26 was shown to correlate with chronic obstructive pulmonary disease. CONCLUSION: These preliminary results suggest that the T allele polymorphism of the MDR-1 gene is associated with chronic obstructive pulmonary disease. |
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oai:revistas.usp.br:article/18490 |
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USP-19 |
network_name_str |
Clinics |
repository_id_str |
|
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Frequency of the mdr-1 C>;T gene polymorphism in patients with COPD COPDMDR-1 geneT allele frequencyTransporter glycoproteinReverse-hybridization BACKGROUND AND AIM: The multi-drug resistant-1 (MDR-1) gene is located on human chromosome 7 and encodes a glycosylated membrane protein that is a member of the ATP-binding cassette transporters superfamily. The aim of the study was to reveal the role of the C3435T MDR-1 gene polymorphism in chronic obstructive pulmonary disease. METHOD: DNA samples from 41 patients with chronic obstructive pulmonary disease and 50 healthy control participants were used to compare MDR-1 gene profiles. Genotyping assays were performed using the StripAssay technique that is based on reverse-hybridization. RESULTS: The T allele polymorphism in the MDR-1 gene located at position 3435 in exon 26 was shown to correlate with chronic obstructive pulmonary disease. CONCLUSION: These preliminary results suggest that the T allele polymorphism of the MDR-1 gene is associated with chronic obstructive pulmonary disease. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1849010.1590/S1807-59322010001100010Clinics; Vol. 65 No. 11 (2010); 1115-1117 Clinics; v. 65 n. 11 (2010); 1115-1117 Clinics; Vol. 65 Núm. 11 (2010); 1115-1117 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/18490/20553Dogan, Ömer TamerKatrancioglu, NurkayKarahan, OuzSanli, Gülizar CananZorlu, AliManduz, Şinasiinfo:eu-repo/semantics/openAccess2012-05-23T11:27:10Zoai:revistas.usp.br:article/18490Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-23T11:27:10Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Frequency of the mdr-1 C>;T gene polymorphism in patients with COPD |
title |
Frequency of the mdr-1 C>;T gene polymorphism in patients with COPD |
spellingShingle |
Frequency of the mdr-1 C>;T gene polymorphism in patients with COPD Dogan, Ömer Tamer COPD MDR-1 gene T allele frequency Transporter glycoprotein Reverse-hybridization |
title_short |
Frequency of the mdr-1 C>;T gene polymorphism in patients with COPD |
title_full |
Frequency of the mdr-1 C>;T gene polymorphism in patients with COPD |
title_fullStr |
Frequency of the mdr-1 C>;T gene polymorphism in patients with COPD |
title_full_unstemmed |
Frequency of the mdr-1 C>;T gene polymorphism in patients with COPD |
title_sort |
Frequency of the mdr-1 C>;T gene polymorphism in patients with COPD |
author |
Dogan, Ömer Tamer |
author_facet |
Dogan, Ömer Tamer Katrancioglu, Nurkay Karahan, Ouz Sanli, Gülizar Canan Zorlu, Ali Manduz, Şinasi |
author_role |
author |
author2 |
Katrancioglu, Nurkay Karahan, Ouz Sanli, Gülizar Canan Zorlu, Ali Manduz, Şinasi |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Dogan, Ömer Tamer Katrancioglu, Nurkay Karahan, Ouz Sanli, Gülizar Canan Zorlu, Ali Manduz, Şinasi |
dc.subject.por.fl_str_mv |
COPD MDR-1 gene T allele frequency Transporter glycoprotein Reverse-hybridization |
topic |
COPD MDR-1 gene T allele frequency Transporter glycoprotein Reverse-hybridization |
description |
BACKGROUND AND AIM: The multi-drug resistant-1 (MDR-1) gene is located on human chromosome 7 and encodes a glycosylated membrane protein that is a member of the ATP-binding cassette transporters superfamily. The aim of the study was to reveal the role of the C3435T MDR-1 gene polymorphism in chronic obstructive pulmonary disease. METHOD: DNA samples from 41 patients with chronic obstructive pulmonary disease and 50 healthy control participants were used to compare MDR-1 gene profiles. Genotyping assays were performed using the StripAssay technique that is based on reverse-hybridization. RESULTS: The T allele polymorphism in the MDR-1 gene located at position 3435 in exon 26 was shown to correlate with chronic obstructive pulmonary disease. CONCLUSION: These preliminary results suggest that the T allele polymorphism of the MDR-1 gene is associated with chronic obstructive pulmonary disease. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/18490 10.1590/S1807-59322010001100010 |
url |
https://www.revistas.usp.br/clinics/article/view/18490 |
identifier_str_mv |
10.1590/S1807-59322010001100010 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/18490/20553 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 65 No. 11 (2010); 1115-1117 Clinics; v. 65 n. 11 (2010); 1115-1117 Clinics; Vol. 65 Núm. 11 (2010); 1115-1117 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222755668361216 |