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Association among lifestyle, clinical examination, polymorphisms in CDH1 gene and Traditional Chinese Medicine syndrome differentiation of gastric cancer 被引量:4
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作者 Junfeng Zhang Zhen Zhan +6 位作者 Juan Wu Chunbing Zhang Yaping Yang Shujuan Tong Ruiping Wang Xuewen Yang Wei Dong 《Journal of Traditional Chinese Medicine》 SCIE CAS CSCD 2013年第5期572-579,共8页
OBJECTIVE:To explore the association among lifestyle,clinical examination,polymorphisms in CDH1 gene and Traditional Chinese Medicine(TCM)syndrome differentiation of gastric cancer(GC). METHODS:A hospital-based popula... OBJECTIVE:To explore the association among lifestyle,clinical examination,polymorphisms in CDH1 gene and Traditional Chinese Medicine(TCM)syndrome differentiation of gastric cancer(GC). METHODS:A hospital-based population of 387 GC patients was investigated in Jiangsu province.Relevant information regarding lifestyle and clinical examination were collected by a standard questionnaire.Four known single nucleotide polymorphisms(SNPs)in CDH1 were investigated by polymerase chain reaction-ligation detection reaction methods.Statistical analysis was conducted by SPSS 16.0 software.RESULTS:The results showed that meal duration and the status of glutamic pyruvic transaminase were significantly associated with TCM syndrome differentiation of GC(both P<0.05).None of the four SNPs in the E-cadherin(CDH1)gene achieved significant differences in their distributions among the nine syndrome types of GC(both P>0.05).However,significant differences were observed in rs13689 genotype distributions between several pairs of syndrome types of GC,suggesting that rs13689 is correlated with the syndrome differentiation of GC.CONCLUSION:Integrated analysis of lifestyle,clinical examination and CDH1 gene polymorphisms can contribute to a better understanding of the GC syndrome types and may improve the efficacy of interventions by stratifying disease according to TCM criteria. 展开更多
关键词 Cadherins Stomach neoplasms Polymorphism single nucleotide syndrome differentiation Clinical examination
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A novel arg616Cys mutation in the DNA-binding domain of complete androgen insensitivity syndrome in a Chinese family
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作者 Zhou Lu Wang Chen-hong 《Chinese Medical Journal》 SCIE CAS CSCD 2013年第21期4192-4193,共2页
Awide spectrum of Androgen insensitivity syndrome (AIS) occur due to mutations in the androgen receptor(AR). The clinical presentation of AIS ranges from a typically male phenotype with decreased body hair and/ or... Awide spectrum of Androgen insensitivity syndrome (AIS) occur due to mutations in the androgen receptor(AR). The clinical presentation of AIS ranges from a typically male phenotype with decreased body hair and/ or oligospermia to a typically female phenotype with primary amenorrhea and without pubic and axillary hair; 展开更多
关键词 androgen insensitivity syndrome androgen receptor DNA-binding domain single aminoacid substitution
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