Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians

Detalhes bibliográficos
Autor(a) principal: Bezerra, Rosângela M. N
Data de Publicação: 2004
Outros Autores: Chadid, Thiago T, Altemani, Cláudia M, Sales, Teresa S. I, Menezes, Raimundo, Soares, Manoel do Carmo Pereira, Saad, Sara T. O, Saad, Mario J. A
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Digital do Instituto Evandro Chagas (Patuá)
Texto Completo: https://patua.iec.gov.br/handle/iec/458
Resumo: Several polymorphisms in the insulin receptor substrate-I (IRS I) gene have been reported in the last years. The most common IRSI variant, a Gly -cArg substitution at codon 972 (Arg972 IRS I). is more prevalent among subjects who have features of insulin resistance syndrome associated, or not, with type 2 diabetes in European populations. To determine whether the absence of IRS I polymorphism is a more general characteristic of Paleo-Indian-derived populations, we examined the Arg972 IRSI polymorphism in Parakan5t Indians and found a lack of this polymorphism in the Parakana population.
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spelling Bezerra, Rosângela M. NChadid, Thiago TAltemani, Cláudia MSales, Teresa S. IMenezes, RaimundoSoares, Manoel do Carmo PereiraSaad, Sara T. OSaad, Mario J. A2016-01-26T11:28:53Z2016-01-26T11:28:53Z2004BEZERRA, Rosângela M. N. et al. Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians. Human Biology, v. 76, n. 1, p. 147-151, Feb. 2004.0018-7143https://patua.iec.gov.br/handle/iec/458Several polymorphisms in the insulin receptor substrate-I (IRS I) gene have been reported in the last years. The most common IRSI variant, a Gly -cArg substitution at codon 972 (Arg972 IRS I). is more prevalent among subjects who have features of insulin resistance syndrome associated, or not, with type 2 diabetes in European populations. To determine whether the absence of IRS I polymorphism is a more general characteristic of Paleo-Indian-derived populations, we examined the Arg972 IRSI polymorphism in Parakan5t Indians and found a lack of this polymorphism in the Parakana population.Universidade Estadual de Campinas. Faculdade de Ciêncas Médicas. Departamento de Clínica Médica. Campinas, SP, Brasil.Universidade Estadual de Campinas. Faculdade de Ciências Médicas. Departamento de Clínica Médica. Campinas, SP, Brasil.Universidade Estadual de Campinas. Faculdade de Ciências Médicas. Departamento de Clínica Médica. Campinas, SP, Brasil.Universidade Estadual de Campinas. Faculdade de Ciências Médicas. Departamento de Clínica Médica. Campinas, SP, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Belém, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Belém, PA, Brasil.Universidade Estadual de Campinas. Faculdade de Ciências Médicas. Departamento de Clínica Médica. Campinas, SP, Brasil.Universidade Estadual de Campinas. Faculdade de Ciêncas Médicas. Departamento de Clínica Médica. 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dc.title.pt_BR.fl_str_mv Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians
title Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians
spellingShingle Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians
Bezerra, Rosângela M. N
Polimorfismo Genético
Receptor de Insulina
Resistência à Insulina
title_short Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians
title_full Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians
title_fullStr Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians
title_full_unstemmed Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians
title_sort Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians
author Bezerra, Rosângela M. N
author_facet Bezerra, Rosângela M. N
Chadid, Thiago T
Altemani, Cláudia M
Sales, Teresa S. I
Menezes, Raimundo
Soares, Manoel do Carmo Pereira
Saad, Sara T. O
Saad, Mario J. A
author_role author
author2 Chadid, Thiago T
Altemani, Cláudia M
Sales, Teresa S. I
Menezes, Raimundo
Soares, Manoel do Carmo Pereira
Saad, Sara T. O
Saad, Mario J. A
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Bezerra, Rosângela M. N
Chadid, Thiago T
Altemani, Cláudia M
Sales, Teresa S. I
Menezes, Raimundo
Soares, Manoel do Carmo Pereira
Saad, Sara T. O
Saad, Mario J. A
dc.subject.decsPrimary.pt_BR.fl_str_mv Polimorfismo Genético
Receptor de Insulina
Resistência à Insulina
topic Polimorfismo Genético
Receptor de Insulina
Resistência à Insulina
description Several polymorphisms in the insulin receptor substrate-I (IRS I) gene have been reported in the last years. The most common IRSI variant, a Gly -cArg substitution at codon 972 (Arg972 IRS I). is more prevalent among subjects who have features of insulin resistance syndrome associated, or not, with type 2 diabetes in European populations. To determine whether the absence of IRS I polymorphism is a more general characteristic of Paleo-Indian-derived populations, we examined the Arg972 IRSI polymorphism in Parakan5t Indians and found a lack of this polymorphism in the Parakana population.
publishDate 2004
dc.date.issued.fl_str_mv 2004
dc.date.accessioned.fl_str_mv 2016-01-26T11:28:53Z
dc.date.available.fl_str_mv 2016-01-26T11:28:53Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.citation.fl_str_mv BEZERRA, Rosângela M. N. et al. Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians. Human Biology, v. 76, n. 1, p. 147-151, Feb. 2004.
dc.identifier.uri.fl_str_mv https://patua.iec.gov.br/handle/iec/458
dc.identifier.issn.-.fl_str_mv 0018-7143
identifier_str_mv BEZERRA, Rosângela M. N. et al. Lack of Arg972 polymorphism in the IRS1 gene in Parakanã brazilian indians. Human Biology, v. 76, n. 1, p. 147-151, Feb. 2004.
0018-7143
url https://patua.iec.gov.br/handle/iec/458
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dc.publisher.none.fl_str_mv Wayne State University Press
publisher.none.fl_str_mv Wayne State University Press
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