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| Acquired renal glucosuria in an undifferentiated connective tissue disease patient with a SLC5A2 heterozygous mutation: A case report 期刊论文
Medicine, 2018, 卷号: 97, 页码: e13664
作者: Gu Xiangchen[1]; Chen Min[2]; Xu Yanqiu[3]; Wang Yi[4]
  收藏 | 浏览/下载：4/0 | 提交时间：2019/04/22 |
| Novel Mutations in the PKD1 and PKD2 Genes of Chinese Patients with Autosomal Dominant Polycystic Kidney Disease 期刊论文
Kidney & blood pressure research, 2018, 卷号: 43, 页码: 297-309
作者: Xu Dechao[1]; Ma Yiyi[2]; Gu Xiangchen[3]; Bian Rongrong[4]; Lu Yunhui[5]
收藏 | 浏览/下载：2/0 | 提交时间：2019/04/24
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| The loss of Krüppel-like factor 15 in Foxd1+ stromal cells exacerbates kidney fibrosis 期刊论文
Kidney international, 2017, 卷号: 92, 页码: 1178-1193
作者: Gu Xiangchen[1]; Mallipattu Sandeep K[2]; Guo Yiqing[3]; Revelo Monica P[4]; Pace Jesse[5]
收藏 | 浏览/下载：9/0 | 提交时间：2019/04/26
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| Acquired Gitelman syndrome in a primary Sjögren syndrome patient with a SLC12A3 heterozygous mutation: A case report and literature review 期刊论文
Nephrology (Carlton, Vic.), 2017, 卷号: 22, 页码: 652-655
作者: Gu Xiangchen[1]; Su Zheling[2]; Chen Min[3]; Xu Yanqiu[4]; Wang Yi[5]
收藏 | 浏览/下载：6/0 | 提交时间：2019/04/26
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| KLF 15 Works as an Early Anti-Fibrotic Transcriptional Regulator in Ang II-Induced Renal Fibrosis via Down-Regulation of CTGF Expression 期刊论文
Kidney & blood pressure research, 2017, 卷号: 42, 页码: 999-1012
作者: Gu Xiangchen[1]; Xu Dechao[2]; Fu Lili[3]; Wang Yi[4]; Mei Changlin[5]
收藏 | 浏览/下载：4/0 | 提交时间：2019/04/26
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