A de novo ANK1 mutation associated to hereditary spherocytosis: a case report by Ti-Long Huang, Bao-Hua Sang, Qing-Ling Lei, Chun-Yan Song, Yun-Bi Lin, Yu Lv, Chun-Hui Yang, Na Li, Yue-Huang Yang, Xian-Wen Zhang, Xin Tian

Subjects: “…Hereditary spherocytosis- ANK1- frameshift mutation…”
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Clinical and genetic characteristics of Chinese pediatric and adult patients with hereditary spherocytosis by Chongjun Wu, Yixin Yan, Ting Xiong, Wen Jiang, Jing Xu, Yanfei Rao, Jianyun Ao, Chun Xu, Xuehong Li, Longwang Qi, Wenhong Zheng, Wenjin Li, Zhongjin Xu, Yu Yang, Zhenjiang Li

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Preliminary Study on the Clinical and Genetic Characteristics of Hereditary Spherocytosis in 15 Chinese Children by Chongjun Wu, Chongjun Wu, Ting Xiong, Zhongjin Xu, Chunlei Zhan, Feng Chen, Yao Ye, Hong Wang, Yu Yang, Yu Yang

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Clinical manifestations of 17 Chinese children with hereditary spherocytosis caused by novel mutations of the ANK1 gene and phenotypic analysis by Meiyun Kang, Meiyun Kang, Huimin Li, Huimin Li, Jun Zhu, Jun Zhu, Liwen Zhu, Liwen Zhu, Yue Hong, Yue Hong, Yongjun Fang, Yongjun Fang

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A de novo ANK1 mutation in a childhood hereditary spherocytosis: a case report by Yafeng Wang, Linlin Liu, Dandan Liu, Wei Liu

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ANK1 inhibits malignant progression of osteosarcoma by promoting ferroptosis by Fei Zhang, Junming Wan, Jinghua Zhong, Jianwen Mo

Subjects: “…ANK1…”
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Genetic and Clinical Characteristics of Patients With Hereditary Spherocytosis in Hubei Province of China by Xiong Wang, Ai Zhang, Ming Huang, Li Chen, Qun Hu, Yanjun Lu, Liming Cheng

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Identification and functional analysis of novel SPTB and ANK1 mutations in hereditary spherocytosis patients by Charuwan Panarach, Chaiwat Netsawang, Issarang Nuchprayoon, Kamonlak Leecharoenkiat

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Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature by Dong Wang, Li Song, Li Shen, Kaihui Zhang, Yuqiang Lv, Min Gao, Jian Ma, Ya Wan, Zhongtao Gai, Yi Liu

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Small ankyrin 1 (sANK1) promotes docetaxel resistance in castration‐resistant prostate cancer cells by enhancing oxidative phosphorylation by Yang Yang, Haixiang Qin, Meng Ding, Changwei Ji, Wei Chen, Wenli Diao, Haoli Yin, Mengxia Chen, Weidong Gan, Hongqian Guo

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De novo variations of ANK1 gene caused hereditary spherocytosis in two Chinese children by affecting pre-mRNA splicing by Yang Wang, Lan Huang, Yao Zhu, Xizhou An, Jiacheng Li, Jiangwei Zhen, Jie Yu

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The histone modification H3K4me3 is altered at the ANK1 locus in Alzheimer's disease brain by Adam R Smith, Rebecca G Smith, Ruby Macdonald, Sarah J Marzi, Joe Burrage, Claire Troakes, Safa Al-Sarraj, Jonathan Mill, Katie Lunnon

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Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis by Fei Xie, Lei Lei, Bin Cai, Lu Gan, Yu Gao, Xiaoying Liu, Lin Zhou, Jinjin Jiang

Subjects: “…ANK1…”
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Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the liter... by Lichun Xie, Zhihao Xing, Changgang Li, Si-xi Liu, Fei-qiu Wen

Subjects: “…ANK1 gene…”
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Identification of a novel ANK1 gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis by Ting Xiong, Zhongjin Xu, Qian Wan, Feng Chen, Yao Ye, Hong Wang, Chongjun Wu

Subjects: “…ANK1…”
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Case of Congenital Hemolytic Anemia with <i>ATP11C</i> and <i>ANK1</i> Variants by Wei Xu, Mengmeng Ma, Sai Zhao, Yufang Yuan, Zhaofang Tian

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MicroRNA-486-3p functions as a tumor suppressor in oral cancer by targeting DDR1 by Sung-Tau Chou, Hsuan-Yu Peng, Kuan-Chi Mo, Yuan-Ming Hsu, Guan-Hsun Wu, Jenn-Ren Hsiao, Su-Fang Lin, Horng-Dar Wang, Shine-Gwo Shiah

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Next-Generation Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Combined Features of Spherocytosis and Antley-Bixler Syndrome With Genital Anomalies and... by Fuying Song, Shunqiao Feng, Xiang Shen, Mu Du, Hui Yin, Rong Liu, Xiaobo Chen

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Неспецифічний виразковий коліт, спадковий сфероцитоз та гемохроматоз у дитини: інтегрований підхід до керування клінічним випадком... by O.I. Dorosh, V.B. Voloshchuk, M.I. Dushar, I.P. Melko, V.I. Zhelоv, B.S. Romanishyn, A.S. Kuzyk, O.A. Petronchak, R.V. Hulei, A.P. Dudash, N.M. Skaletska

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Structural basis of diverse membrane target recognitions by ankyrins by Chao Wang, Zhiyi Wei, Keyu Chen, Fei Ye, Cong Yu, Vann Bennett, Mingjie Zhang

Subjects: “…ANK1/ANK2/ANK3…”
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