ALDH1L1 and ALDH1L2 folate regulatory enzymes in cancer
SA Krupenko, NI Krupenko - Alcohol and Cancer: Proceedings of the Third …, 2018 - Springer
Epidemiological studies implicate excess ethanol ingestion as a risk factor for several
cancers and support the concept of a synergistic effect of chronic alcohol consumption and …
cancers and support the concept of a synergistic effect of chronic alcohol consumption and …
[HTML][HTML] Combined Water Extracts from Oxidation-Treated Leaves and Branches of Hovenia dulcis Has Anti-Hangover and Liver Protective Effects in Binge Alcohol …
J Je, M Song, JH Baek, JS Kang, HJ Chung, K Lee… - Nutrients, 2021 - mdpi.com
Hovenia dulcis, known as the oriental raisin tree, is used for food supplements and
traditional medicine for the liver after alcohol-related symptoms. However, little information …
traditional medicine for the liver after alcohol-related symptoms. However, little information …
[HTML][HTML] Phenotype Prediction of Pathogenic Nonsynonymous Single Nucleotide Polymorphisms in WFS1
X Qian, L Qin, G Xing, X Cao - Scientific reports, 2015 - nature.com
Wolfram syndrome (WS) is a rare, progressive, neurodegenerative disorder that has an
autosomal recessive pattern of inheritance. The gene for WS, wolfram syndrome 1 gene …
autosomal recessive pattern of inheritance. The gene for WS, wolfram syndrome 1 gene …
人肌球蛋白7A 基因非同义单核苷酸多态性位点潜在致聋突变的预测分析
王全， 鲁雅洁， 曹新 - 生物技术通讯, 2016 - cqvip.com
目的: 人肌球蛋白7A (MYO7A) 基因是遗传性耳聋分子筛查的候选基因之一. 从已知的MYO7A
非同义单核苷酸多态性(ns SNPs) 位点数据库中筛选可能与致病表型相关的ns SNPs 位点 …
非同义单核苷酸多态性(ns SNPs) 位点数据库中筛选可能与致病表型相关的ns SNPs 位点 …
Brain atrophy in alcoholics
E González-Reimers… - Handbook of Behavior …, 2011 - Springer
Chronic alcoholics are at risk of developing several neurological alterations, such as the
Wernicke–Korsakoff syndrome, the so-called alcoholic dementia, related to brain atrophy …
Wernicke–Korsakoff syndrome, the so-called alcoholic dementia, related to brain atrophy …
In Silico survey of functional coding variants in human AEG-1 gene
Background and aims: Non-synonymous (ns) SNPs represent typical genetic variations that
may potentially affect the structure or function of expressed proteins and therefore could …
may potentially affect the structure or function of expressed proteins and therefore could …
耳聋相关基因COCH 的非同义单核苷酸多态性致聋表型预测
钱旭丽， 曹新 - 遗传, 2015 - chinagene.cn
群体凝血因子C 同源物基因(Coagulation factor C homology, COCH) 是人类发现的第一个伴
前庭功能障碍的耳聋基因, 位于人类染色体14q12-q13 上. 迄今, 在COCH 基因上发现16 …
前庭功能障碍的耳聋基因, 位于人类染色体14q12-q13 上. 迄今, 在COCH 基因上发现16 …
[HTML][HTML] Prioritization of Deleterious Variations in the Human Hypoxanthine-Guanine Phosphoribosyltransferase Gene
S Kheiri, M Safarzad, M Shariati… - Medical Laboratory Journal, 2018 - goums.ac.ir
ABSTRACT Background and Objectives: Non-synonymous single nucleotide
polymorphisms are typical genetic variations that may potentially affect the structure or …
polymorphisms are typical genetic variations that may potentially affect the structure or …