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Corrigendum to"SEMA4D acts as a novel oligogenic pathogenic gene of idiopathic hypogonadotropic hypogonadism through the PlexinB1/MET/RND1/RHOA/RAF1/MAPK signaling axis"[Genes&Diseases 10(2023)65-68]
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作者 Daoqi Wang Yonghua Niu +8 位作者 Jiahong Tan Jiaxin Wang Le Ling Yinwei Chen Jianan Gong Hao Xu Qing Ling jianhe liu Jihong liu 《Genes & Diseases》 SCIE CSCD 2024年第4期428-429,共2页
The authors regret to correct the error in the order of the institute of the first author,which should go as the following.
关键词 Cor DISEASES pogon
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Metformin suppresses calcium oxalate crystal-induced kidney injury by promoting Sirt1 and M2 macrophage-mediated anti-inflammatory activation 被引量:3
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作者 Haoran liu Chen Duan +7 位作者 Xiaoqi Yang jianhe liu Yaoliang Deng Hans-Göran Tiselius Zhangqun Ye Tao Wang Jinchun Xing Hua Xu 《Signal Transduction and Targeted Therapy》 SCIE CSCD 2023年第2期373-376,共4页
Dear Editor,Kidney stones are one of the most common clinical diseases in urology.Approximately 80%of renal calculi are composed of calcium oxalate(CaOx)crystals,which are gradually deposited in the medullary collecti... Dear Editor,Kidney stones are one of the most common clinical diseases in urology.Approximately 80%of renal calculi are composed of calcium oxalate(CaOx)crystals,which are gradually deposited in the medullary collecting duct or in the renal interstitium,causing nephrocalcinosis.1 Although CaOx nephrocalcinosis is usually asymptomatic. 展开更多
关键词 KIDNEY clinical DISEASES
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SEMA4D acts as a novel oligogenic pathogenic gene of idiopathic hypogonadotropic hypogonadism through thePlexinB1/MET/RND1/RHOA/RAF1/MAPK signaling axis
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作者 Daoqi Wang Yonghua Niu +8 位作者 Jiahong Tan Jiaxin Wang Le Ling Yinwei Chen Jjianan Gong Hao Xu Qing Ling jianhe liu Jihong liu 《Genes & Diseases》 SCIE CSCD 2023年第1期65-68,共4页
Idiopathic hypogonadotropic hypogonadism(IHH)is a rare genetic disease with clinical and genetic heterogeneity.This study aimed to investigate a novel causal gene of IHH and a homozygous mutation(p.Ala515Val)in SEMA4D... Idiopathic hypogonadotropic hypogonadism(IHH)is a rare genetic disease with clinical and genetic heterogeneity.This study aimed to investigate a novel causal gene of IHH and a homozygous mutation(p.Ala515Val)in SEMA4D,and sought to determine the mechanism of SEMA4D promoting GnRH neurons migration. 展开更多
关键词 heterogeneity. clinical IDIOPATHIC
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