Cuize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

Prevention and control of thalassemia in Guangdong Province, Southern China: insights from an 11-year retrospective study

中国南方广东省地中海贫血症的预防和控制：一项为期11年的回顾性研究的启示

doi:10.1080/07853890.2025.2548970

Qin, Danqing; He, Wei; Wang, Jicheng; Zhu, Juan; Yao, Cuize; Bao, Xiuqin; Liang, Jie; Wang, Yixia; Liang, Kailing; Luo, Mingyong; Du, Li; Wu, Jing

发表日期：2025

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High positive predictive value of CNVs detected by clinical exome sequencing in suspected genetic diseases

临床外显子组测序检测到的拷贝数变异在疑似遗传疾病中具有较高的阳性预测值

期刊:Journal of Translational Medicine

影响因子:7.5

doi:10.1186/s12967-024-05468-1

Zeng, Yimo; Ding, Hongke; Wang, Xingwang; Huang, Yanlin; Liu, Ling; Du, Li; Lu, Jian; Wu, Jing; Zeng, Yukun; Mai, Mingqin; Zhu, Juan; Yu, Lihua; He, Wei; Guo, Fangfang; Peng, Haishan; Yao, Cuize; Qi, Yiming; Liu, Yuan; Li, Fake; Yang, Jiexia; Hu, Rong; Liang, Jie; Wang, Jicheng; Wang, Wei; Zhang, Yan; Yin, Aihua

发表日期：2024

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Abnormal hemoglobin anti-Lepore Hong Kong compound with β(0)-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia

异常血红蛋白抗Lepore香港复合物与β(0)-地中海贫血同时遗传时，可减轻地中海贫血的严重程度。

期刊:Scientific Reports

影响因子:3.9

doi:10.1038/s41598-024-56921-6

Bao, Xiuqin; Wang, Jicheng; Qin, Danqing; Yao, Cuize; Liang, Jie; Liang, Kailing; Du, Li

发表日期：2024

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Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population

在中国人群中鉴定出α-珠蛋白基因座的四个新的大片段缺失和复杂变异

期刊:Human Genomics

影响因子:4.3

doi:10.1186/s40246-023-00486-4

Bao, Xiuqin; Wang, Jicheng; Qin, Danqing; Yao, Cuize; Liang, Jie; Liang, Kailing; Zeng, Yukun; Du, Li

发表日期：2023

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Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families

两个中国家族中，β-珠蛋白基因的两个新的缺失突变导致β-地中海贫血性状。

期刊:Human Genomics

影响因子:4.3

doi:10.1186/s40246-023-00559-4

Bao, Xiuqin; Qin, Danqing; Wang, Jicheng; Chen, Jing; Yao, Cuize; Liang, Jie; Liang, Kailing; Wang, Yixia; Wang, Yousheng; Du, Li; Yin, Aihua

发表日期：2023

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Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C)

与 Hb Zurich-Albisrieden (HBA2:c.178G>C) 和 Hb Quong Sze (HBA2:c.377T>C) 复合杂合子相关的严重胎儿贫血和胎儿水肿

期刊:Journal of International Medical Research

影响因子:1.5

doi:10.1177/03000605211031429

Du, Li; Bao, Xiuqin; He, Wei; Qin, Danqing; Wang, Jicheng; Xiong, Ying; Shi, Xiaomei; Ding, Hongke; Yao, Cuize; Wu, Jing

发表日期：2021

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Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients

携带血红蛋白变异体Hb-Broomhill和东南亚α-地中海贫血缺失的复合杂合子不会恶化预后：两例无关患者的病例报告

期刊:Journal of International Medical Research

影响因子:1.5

doi:10.1177/0300060520967825

Qin, Danqing; Du, Li; Wang, Jicheng; Yao, Cuize; Guo, Hao; Yuan, Tenglong; Liang, Jie; Yin, Aihua

发表日期：2020

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Rough surface Au@Ag core-shell nanoparticles to fabricating high sensitivity SERS immunochromatographic sensors

粗糙表面 Au@Ag 核壳纳米粒子制备高灵敏度 SERS 免疫色谱传感器

期刊:Journal of Nanobiotechnology

影响因子:10.6

doi:10.1186/s12951-015-0142-0

Qiangqiang Fu, Hongwu Liu Liu, Ze Wu, An Liu, Cuize Yao, Xiuqing Li, Wei Xiao, Shiting Yu, Zhi Luo, Yong Tang1

发表日期：2015

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