Ming-Yu Han相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

Correlation between Disc Imaging Observations and Clinical Efficacy after Percutaneous Endoscopic Lumbar Discectomy: A 1-Year Follow-up Study

经皮内镜腰椎间盘切除术后椎间盘影像学观察结果与临床疗效的相关性：一项为期1年的随访研究

期刊:Orthopaedic Surgery

影响因子:2.1

doi:10.1111/os.14013

Li, Bing; Wang, Tian-Hao; Huang, Yi; Fan, Yi-Ming; Yu, Han; Li, Ao-Qiong; Qi, Deng-Bin; Wang, Qi; Xue, Chao; Wang, Ze; Zheng, Guo-Quan; Wang, Yan

发表日期：2024

文献求助收藏

Diagnostic utility of serum IgG4 level in IgG4-related diseases: a comprehensive systematic review and meta-analysis

血清IgG4水平在IgG4相关疾病诊断中的应用价值：一项全面的系统评价和荟萃分析

期刊:PLoS One

影响因子:2.6

doi:10.1371/journal.pone.0296180

Kanaparthy, Naga Sasidhar; Loza, Andrew J; Hauser, Ronald George; Chang, Che-Tzu; Chan, Tien-Ming; Yu, Han-Hua; Yu, Kuang-Hui

发表日期：2023

文献求助收藏

Recent Progress in Double-Layer Honeycomb Structure: A New Type of Two-Dimensional Material

双层蜂窝结构研究的最新进展：一种新型二维材料

期刊:Materials

影响因子:3.2

doi:10.3390/ma15217715

Ma, Ming-Yu; Han, Dong; Chen, Nian-Ke; Wang, Dan; Li, Xian-Bin

发表日期：2022

文献求助收藏

Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2

以一名患有 DDOD 综合征的 10 个月大女性患者为样本，建立人类诱导性多能干细胞系 (CPGHi002-A)，该患者携带 ATP6V1B2 杂合 c.1516 C > T 突变

期刊:Stem Cell Research

影响因子:0.8

doi:10.1016/j.scr.2020.101986

Xue Gao, Shi-Wei Qiu, Meng-Long Feng, Sha-Sha Huang, Dong-Yang Kang, Ming-Yu Han, Pu Dai, Yong-Yi Yuan

发育与干细胞

发表日期：2020

文献求助收藏

Notch1-ADAM8 positive feed-back loop regulates the degradation of chondrogenic extracellular matrix and osteoarthritis progression

Notch1-ADAM8正反馈环路调节软骨细胞外基质的降解和骨关节炎的进展。

期刊:Cell Communication and Signaling

影响因子:8.9

doi:10.1186/s12964-019-0443-2

Duan, Biao; Liu, Yan; Hu, He; Shi, Fu-Guo; Liu, Ya-Long; Xue, Hao; Yun, Xin-Yu; Yan, Ming-Yu; Han, Xi-Rui; Chen, An-Fu; Wang, Yong; Li, Zhe-Hai

细胞生物学

发表日期：2019

文献求助收藏

Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

干扰素λ受体1（IFNLR1）的突变与常染色体显性遗传性非综合征性听力损失相关。

期刊:Journal of Medical Genetics

影响因子:3.5

doi:10.1136/jmedgenet-2017-104954

Xue Gao #,Yong-Yi Yuan #,Qiong-Fen Lin #,Jin-Cao Xu,Wei-Qian Wang,Yue-Hua Qiao,Dong-Yang Kang,Dan Bai,Feng Xin,Sha-Sha Huang,Shi-Wei Qiu,Li-Ping Guan,Yu Su,Guo-Jian Wang,Ming-Yu Han,Yi Jiang,Han-Kui Liu,Pu Dai

发表日期：2018

文献求助收藏

A regulatory mutant on TRIM26 conferring the risk of nasopharyngeal carcinoma by inducing low immune response

TRIM26 的调控突变通过诱导低免疫反应而带来罹患鼻咽癌的风险

期刊:Cancer Medicine

影响因子:2.9

doi:10.1002/cam4.1537

Xiao-Ming Lyu, Xiao-Wei Zhu, Manli Zhao, Xian-Bo Zuo, Zhong-Xi Huang, Xiao Liu, Tao Jiang, Xue-Xi Yang, Xin Li, Xiao-Bing Long, Jian-Guo Wang, Jin-Bang Li, Ming-Yu Han, Shuang Wang, Teng-Fei Liu, Bo Zhang, Tao Sun, Zhi Cheng, Mo-Chang Qiu, Lei Dong, Lu Zheng, Long-Cheng Zhang, Jia-Hong Wang, Gan-Gua

发表日期：2018

文献求助收藏