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Retrieved differentially expressed genes in Liver Disease (from [38–41]).

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https://figshare.com/articles/dataset/Retrieved_differentially_expressed_genes_in_Liver_Disease_from_38_41_/4786888
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When possible, names or abbreviations as well as OMIM accession number were added (in italic). The number sign # is used because α1-antitrypsin deficiency is caused by mutation in the SERPINA1 gene (OMIM: 107400). “?” is used when no result was obtained in our OMIM search for the corresponding gene name or when several results could be retrieved. The lower list is retrieved from [21] shows the Solute Carrier Family (SLC, sodium/potassium/chloride transporter family) with differential gene expression in NASH.

若可行,将为相关条目添加名称、缩写以及OMIM(Online Mendelian Inheritance in Man,在线人类孟德尔遗传)登录号,格式为斜体。使用井号(#)标注的原因在于,α1-抗胰蛋白酶缺乏症是由SERPINA1基因突变所导致(OMIM登录号:107400)。当针对对应基因名称的OMIM检索未获得有效结果,或可检索到多条匹配结果时,使用问号(?)进行标注。下方的列表源自文献[21],呈现了在非酒精性脂肪性肝炎(NASH, Non-Alcoholic Steatohepatitis)中存在差异基因表达的溶质载体家族(SLC, sodium/potassium/chloride transporter family,钠/钾/氯转运蛋白家族)。
创建时间:
2017-03-25
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