Identification of rs11615992 as a novel regulatory SNP for human P2RX7 by allele-specific expression.

Peng, Tao; Zhong, Li; Gao, Jing; Wan, Zhu; Fu, Wei-Ping; Sun, Chang

Peng, Tao; Zhong, Li; Gao, Jing; Wan, Zhu; Fu, Wei-Ping; Sun, Chang.

Afiliação

Peng T; National Engineering Laboratory for Resource Development of Endangered Crude Drugs in Northwest China, Key Laboratory of the Ministry of Education for Medicinal Resources and Natural Pharmaceutical Chemistry, College of Life Sciences, Shaanxi Normal University, Xi'an, 710119, Shaanxi, People's Repub
Zhong L; National Engineering Laboratory for Resource Development of Endangered Crude Drugs in Northwest China, Key Laboratory of the Ministry of Education for Medicinal Resources and Natural Pharmaceutical Chemistry, College of Life Sciences, Shaanxi Normal University, Xi'an, 710119, Shaanxi, People's Repub
Gao J; National Engineering Laboratory for Resource Development of Endangered Crude Drugs in Northwest China, Key Laboratory of the Ministry of Education for Medicinal Resources and Natural Pharmaceutical Chemistry, College of Life Sciences, Shaanxi Normal University, Xi'an, 710119, Shaanxi, People's Repub
Wan Z; Department of Respiratory Critical Care Medicine, The First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, People's Republic of China.
Fu WP; Department of Respiratory Critical Care Medicine, The First Affiliated Hospital of Kunming Medical University, Kunming, 650032, Yunnan, People's Republic of China. fuweiping2@163.com.
Sun C; National Engineering Laboratory for Resource Development of Endangered Crude Drugs in Northwest China, Key Laboratory of the Ministry of Education for Medicinal Resources and Natural Pharmaceutical Chemistry, College of Life Sciences, Shaanxi Normal University, Xi'an, 710119, Shaanxi, People's Repub

Mol Genet Genomics ; 295(1): 23-30, 2020 Jan.

Article em En | MEDLINE | ID: mdl-31410611

Assuntos

Polimorfismo de Nucleotídeo Único/genética; Receptores Purinérgicos P2X7/genética; Alelos; Frequência do Gene/genética; Predisposição Genética para Doença/genética; Genoma Humano/genética; Haplótipos/genética; Humanos; Desequilíbrio de Ligação/genética; Regiões Promotoras Genéticas/genética

Palavras-chave

Allele-specific expression (ASE); Enhancer; Expression regulation; P2RX7; rs11615992; rs3751143

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Receptores Purinérgicos P2X7 Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Mol Genet Genomics Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2020 Tipo de documento: Article País de publicação: Alemanha

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google