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  • 閱讀 更多 【光鼎x環球生技 檢測科學實驗計畫】系列一 : 酒精不耐症(ALDH2)

    【光鼎x環球生技 檢測科學實驗計畫】系列一 : 酒精不耐症(ALDH2)

    2020-06-22

    由日本科學家 Harada 博士於 1981 年發現,人體若缺乏乙醛去氫酶(Aldehyde Dehydrogenase, ALDH2),喝酒就會臉紅,此現象稱為酒精不耐症(Alcohol Intolerance)。據統計,全球有五億六仟萬東亞人有酒精不耐症的潛在可能,台灣有高達一半的人口有酒精不耐症潛質,為全世界罹患該症比例最高的國家,其次為中國和新加坡各為 40%。

  • 閱讀 更多 【行動檢測實驗室-實現隨時隨地進行檢測】

    【行動檢測實驗室-實現隨時隨地進行檢測】

    2020-05-20

    你聽過「行動檢測實驗室」嗎? 顧名思義,就是可移動的實驗室。有時是否常常覺得要將檢體帶到具有某些特定儀器的實驗室,才有辦法做實驗很麻煩?那你有想過隨時帶著實驗室一堆大型儀器到處移動做檢測嗎?

  • 閱讀 更多 High MTHFR promoter methylation levels in men confer protection against ischemic stroke

    High MTHFR promoter methylation levels in men confer protection against ischemic stroke

    2020-04-29

    The MTHFR gene encodes methylenetetrahydrofolate reductase required for the metabolism of homocysteine (Hcy) – a previously reported independent risk factor for ischemic stroke (IS). In this study, we first aimed to clarify the association between DNA methylation leve

  • 閱讀 更多 Simultaneous Identification of 6 Pathogens Causing Porcine Reproductive Failure by Using Multiplex

    Simultaneous Identification of 6 Pathogens Causing Porcine Reproductive Failure by Using Multiplex

    2020-04-18

  • 閱讀 更多 Oxygen-glucose deprivation and reoxygenation on human cerebral organoids alters expression related

    Oxygen-glucose deprivation and reoxygenation on human cerebral organoids alters expression related

    2020-04-01

    Ischemic stroke is one of the most common neurological disease. However, the impact of ischemic stroke on human cerebral tissue remains largely unknown; due to a lack of ischemic human brain samples. In this study, we used cerebral organoids derived from human induced pluripotent stem cells to eva

  • 閱讀 更多 Genome-wide association study and fine mapping reveals candidate genes for birth weight

    Genome-wide association study and fine mapping reveals candidate genes for birth weight

    2020-03-27

    Birth weight of pigs is an important economic factor in the livestock industry. The identification of the genes and variants that underlie birth weight is of great importance. In this study, we integrated two genotyping methods, single nucleotide polymorphism (SNP) chip analysis and restriction site associated DNA sequencing (RAD-seq) to genotype genome-wide SNPs. In total, 45,175 and 139,634 SNPs were detected with the SNP chip and RAD-seq, respectively. The genome-wide association study (GWAS) of the combined SNP panels identified two significant loci located at chr1: 97,745,041 and chr4: 112,031,589, that explained 6.36% and 4.25% of the phenotypic variance respect