Works by He, Chufeng

Results: 30

Functional Analysis of Pendrin (SLC26A4) and its Pathogenic Mutations in cos-7 cells.

Published in:

Journal of International Advanced Otology, 2012, v. 8, n. 2, p. 195

By:

Hailin Zhanga;
Yong Feng;
Kun Xia;
Lu Jiang;
Chufeng He;
Lingyun Mei

Publication type:

Article

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 3, p. 119, doi. 10.1038/jhg.2014.114

By:

Wang, Honghan;
Wang, Xinwei;
He, Chufeng;
Li, Haibo;
Qing, Jie;
Grati, M'hamed;
Hu, Zhengmao;
Li, Jiada;
Hu, Yiqiao;
Xia, Kun;
Mei, Lingyun;
Wang, Xingwei;
Yu, Jianjun;
Chen, Hongsheng;
Jiang, Lu;
Liu, Yalan;
Men, Meichao;
Zhang, Hailin;
Guan, Liping;
Xiao, Jingjing

Publication type:

Article

Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta‐analysis.

Published in:

Clinical Genetics, 2021, v. 100, n. 1, p. 3, doi. 10.1111/cge.13949

By:

Chen, Anhai;
Song, Jian;
Acke, Frederic R. E.;
Mei, Lingyun;
Cai, Xinzhang;
Feng, Yong;
He, Chufeng

Publication type:

Article

Identification and functional analysis of a novel missense mutation of PAX3 associated with Waardenburg syndrome type I.

Published in:

European Archives of Oto-Rhino-Laryngology, 2021, v. 278, n. 8, p. 2807, doi. 10.1007/s00405-020-06361-5

By:

Niu, Zhijie;
Mei, Lingyun;
Tang, Fen;
Li, Jiada;
Wang, Xueping;
Sun, Jie;
He, Chufeng;
Cheng, Hongsheng;
Liu, Yalan;
Cai, Xinzhang;
Song, Jian;
Feng, Yong;
Jiang, Lu

Publication type:

Article

Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families.

Published in:

European Archives of Oto-Rhino-Laryngology, 2020, v. 277, n. 12, p. 3331, doi. 10.1007/s00405-020-06050-3

By:

Liu, Yalan;
Wen, Jie;
Sang, Shushan;
Mei, Lingyun;
He, Chufeng;
Jiang, Lu;
Huang, Sida;
Feng, Yong

Publication type:

Article

Multivariate analysis of prognostic factors for idiopathic sudden sensorineural hearing loss treated with adjuvant hyperbaric oxygen therapy.

Published in:

European Archives of Oto-Rhino-Laryngology, 2018, v. 275, n. 1, p. 47, doi. 10.1007/s00405-017-4784-4

By:

Xie, Shaobing;
Qiang, Qingfen;
Mei, Lingyun;
He, Chufeng;
Feng, Yong;
Sun, Hong;
Wu, Xuewen

Publication type:

Article

A non-coding variant in 5' untranslated region drove up-regulation of pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humans.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 5, p. 720, doi. 10.1093/hmg/ddac223

By:

Huang, Sida;
Ma, Lu;
Liu, Xuezhong;
He, Chufeng;
Li, Jiada;
Hu, Zhengmao;
Jiang, Lu;
Liu, Yalan;
Liu, Xianlin;
Feng, Yong;
Cai, Xinzhang

Publication type:

Article

Downregulation of p66Shc can reduce oxidative stress and apoptosis in oxidative stress model of marginal cells of stria vascularis in Sprague Dawley rats.

Published in:

Drug Design, Development & Therapy, 2019, v. 13, p. 3199, doi. 10.2147/DDDT.S214918

By:

Hao, Cong;
Wu, Xuewen;
Zhou, Ruoyu;
Zhang, Hao;
Zhou, Yulai;
Wang, Xinxing;
Feng, Yong;
Mei, Lingyun;
He, Chufeng;
Cai, Xinzhang;
Wu, Lisha

Publication type:

Article

A Study of Community Group Purchasing Vehicle Routing Problems Considering Service Time Windows.

Published in:

Sustainability (2071-1050), 2022, v. 14, n. 12, p. N.PAG, doi. 10.3390/su14126968

By:

Song, Wei;
Yuan, Shuailei;
Yang, Yun;
He, Chufeng

Publication type:

Article

A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing.

Published in:

PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0168508

By:

Liu, Yalan;
Wang, Lili;
Feng, Yong;
He, Chufeng;
Liu, Deyuan;
Cai, Xinzhang;
Jiang, Lu;
Chen, Hongsheng;
Liu, Chang;
Wu, Hong;
Mei, Lingyun

Publication type:

Article

Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China.

Published in:

PLoS ONE, 2016, v. 11, n. 3, p. 1, doi. 10.1371/journal.pone.0151909

By:

Wu, Hong;
Feng, Yong;
Jiang, Lu;
Pan, Qian;
Liu, Yalan;
Liu, Chang;
He, Chufeng;
Chen, Hongsheng;
Liu, Xueming;
Hu, Chang;
Hu, Yiqiao;
Mei, Lingyun

Publication type:

Article

A comprehensive genotype–phenotype evaluation of eight Chinese probands with Waardenburg syndrome.

Published in:

BMC Medical Genomics, 2022, v. 13, n. 1, p. 1, doi. 10.1186/s12920-022-01379-6

By:

Li, Sijun;
Qin, Mengyao;
Mao, Shuang;
Mei, Lingyun;
Cai, Xinzhang;
Feng, Yong;
He, Chufeng;
Song, Jian

Publication type:

Article

The Distribution and Therapeutic Effectiveness of Clinical Unilateral Ménière's Disease Phenotypes.

Published in:

Clinical Otolaryngology, 2025, v. 50, n. 2, p. 336, doi. 10.1111/coa.14264

By:

Chen, Yongjia;
Cai, Xinzhang;
Zhang, Yulu;
He, Chufeng;
Wu, Xuewen;
Jiang, Lu;
Chen, Hongsheng;
Liu, Jing;
Pang, Bo;
Zhang, Shuai;
Chen, Anhai;
Jiang, Mengzhu;
Huang, Huping;
Bai, Yijiang;
Nie, Zequn;
Mei, Lingyun

Publication type:

Article

A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family.

Published in:

PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0178384

By:

Niu, Zhijie;
Feng, Yong;
Mei, Lingyun;
Sun, Jie;
Wang, Xueping;
Wang, Juncheng;
Hu, Zhengmao;
Dong, Yunpeng;
Chen, Hongsheng;
He, Chufeng;
Liu, Yalan;
Cai, Xinzhang;
Liu, Xuezhong;
Jiang, Lu

Publication type:

Article

Modeling of pigmentation disorders associated with MITF mutation in Waardenburg syndrome revealed an impaired melanogenesis pathway in iPS‐derived melanocytes.

Published in:

Pigment Cell & Melanoma Research, 2024, v. 37, n. 1, p. 21, doi. 10.1111/pcmr.13118

By:

Wen, Jie;
Song, Jian;
Chen, Jiale;
Feng, Zhili;
Jing, Qiancheng;
Gong, Wei;
Kang, Xiaoming;
Mei, Lingyun;
He, Chufeng;
Ma, Lu;
Feng, Yong

Publication type:

Article

Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2

Published in:

FEBS Letters, 2012, v. 586, n. 23, p. 4126, doi. 10.1016/j.febslet.2012.10.006

By:

Zhang, Hua;
Luo, Hunjin;
Chen, Hongsheng;
Mei, Lingyun;
He, Chufeng;
Jiang, Lu;
Li, Jia-Da;
Feng, Yong

Publication type:

Article

Short-term effects of intravenous batroxobin in treatment of sudden sensorineural hearing loss: a propensity score-matched study.

Published in:

Frontiers in Neurology, 2023, p. 1, doi. 10.3389/fneur.2023.1102297

By:

Mengzhu Jiang;
Huping Huang;
Lingyun Mei;
Chufeng He;
Xinzhang Cai;
Lu Jiang;
Hong Wu;
Xin Wang;
Xuewen Wu

Publication type:

Article

Houttuynia cordata Thunb. Extracts Alleviate Atherosclerosis and Modulate Gut Microbiota in Male Hypercholesterolemic Hamsters.

Published in:

Nutrients, 2024, v. 16, n. 19, p. 3290, doi. 10.3390/nu16193290

By:

Lin, Yuhong;
He, Chufeng;
Liu, Jianhui;
Chung, Hau-Yin;
Chen, Zhen-Yu;
Wong, Wing-Tak

Publication type:

Article

Licorice Extract Isoliquiritigenin Protects Endothelial Function in Type 2 Diabetic Mice.

Published in:

Nutrients, 2024, v. 16, n. 18, p. 3160, doi. 10.3390/nu16183160

By:

Wang, Lin;
Zhu, Ruiwen;
He, Chufeng;
Li, Huixian;
Zhang, Qile;
Cheung, Yiu Ming;
Leung, Fung Ping;
Wong, Wing Tak

Publication type:

Article

Nutritional Assessment of Plant-Based Meat Products Available on Hong Kong Market: A Cross-Sectional Survey.

Published in:

Nutrients, 2023, v. 15, n. 17, p. 3684, doi. 10.3390/nu15173684

By:

Zhang, Qile;
Liu, Yilin;
He, Chufeng;
Zhu, Ruiwen;
Li, Minghui;
Lam, Hon-Ming;
Wong, Wing-Tak

Publication type:

Article

A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss.

Published in:

PLoS ONE, 2019, v. 14, n. 4, p. 1, doi. 10.1371/journal.pone.0215212

By:

Liu, Yalan;
Hu, Chang;
Liu, Chang;
Liu, Deyuan;
Mei, Lingyun;
He, Chufeng;
Jiang, Lu;
Wu, Hong;
Chen, Hongsheng;
Feng, Yong

Publication type:

Article

<italic>ELMOD3</italic>, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss.

Published in:

Human Genetics, 2018, v. 137, n. 4, p. 329, doi. 10.1007/s00439-018-1885-0

By:

Li, Wu;
Sun, Jie;
Ling, Jie;
Li, Jiada;
He, Chufeng;
Liu, Yalan;
Chen, Hongsheng;
Men, Meichao;
Niu, Zhijie;
Deng, Yuyuan;
Li, Meng;
Li, Taoxi;
Wen, Jie;
Sang, Shushan;
Li, Haibo;
Wan, Zhengqing;
Richard, Elodie M.;
Chapagain, Prem;
Yan, Denise;
Liu, Xue Zhong

Publication type:

Article

Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 491, doi. 10.1007/s00439-011-1098-2

By:

Zhang, Hua;
Chen, Hongsheng;
Luo, Hunjin;
An, Jing;
Sun, Lin;
Mei, Lingyun;
He, Chufeng;
Jiang, Lu;
Jiang, Wen;
Xia, Kun;
Li, Jia-Da;
Feng, Yong

Publication type:

Article

Gene localization in a Chinese family with autosomal dominant non-syndromic deafness.

Published in:

Acta Oto-Laryngologica, 2011, v. 131, n. 10, p. 1061, doi. 10.3109/00016489.2011.591822

By:

Jiang, Lu;
Liu, Yalan;
Feng, Yong;
Hu, Zhengmao;
Mei, Lingyun;
Long, Liwei;
Chen, Hongsheng;
Xue, Jingjie;
Xia, Kun;
He, Chufeng

Publication type:

Article

Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation.

Published in:

Acta Oto-Laryngologica, 2011, v. 131, n. 9, p. 970, doi. 10.3109/00016489.2011.575794

By:

Men, Meichao;
Jiang, Lu;
Wang, Honghan;
Liu, Yalan;
Hu, Zhengmao;
He, Chufeng;
Feng, Yong

Publication type:

Article

Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing loss.

Published in:

PLoS ONE, 2023, v. 18, n. 9, p. 1, doi. 10.1371/journal.pone.0288640

By:

Liu, Xianlin;
Wen, Jie;
Liu, Xuezhong;
Chen, Anhai;
Li, Sijun;
Liu, Jing;
Sun, Jie;
Gong, Wei;
Kang, Xiaoming;
Feng, Zhili;
He, Chufeng;
Mei, Lingyun;
Ling, Jie;
Feng, Yong

Publication type:

Article

A Combined Fuzzy Optimization Model for the Location of an Intelligent Energy-Efficient Manufacturing Industrial Park.

Published in:

Energies (19961073), 2022, v. 15, n. 24, p. 9346, doi. 10.3390/en15249346

By:

He, Chufeng;
Liu, Aijun;
Xu, Lei;
Yuan, Shuailei;
Cheng, Mingbao;
Wang, Huan;
Wang, Fang;
Lu, Hui;
Liu, Xiaoxue

Publication type:

Article

LEF-1 Regulates Tyrosinase Gene Transcription In Vitro.

Published in:

PLoS ONE, 2015, v. 10, n. 11, p. 1, doi. 10.1371/journal.pone.0143142

By:

Wang, Xueping;
Liu, Yalan;
Chen, Hongsheng;
Mei, Lingyun;
He, Chufeng;
Jiang, Lu;
Niu, Zhijie;
Sun, Jie;
Luo, Hunjin;
Li, Jiada;
Feng, Yong

Publication type:

Article

Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families.

Published in:

Frontiers in Genetics, 2019, p. 1, doi. 10.3389/fgene.2019.00639

By:

Sang, Shushan;
Ling, Jie;
Liu, Xuezhong;
Mei, Lingyun;
Cai, Xinzhang;
Li, Taoxi;
Li, Wu;
Li, Meng;
Wen, Jie;
Liu, Xianlin;
Liu, Jing;
Liu, Yalan;
Chen, Hongsheng;
He, Chufeng;
Feng, Yong

Publication type:

Article

Identification of a family with van der Hoeve's syndrome harboring a novel COL1A1 mutation and generation of patient-derived iPSC lines and CRISPR/Cas9-corrected isogenic iPSCs.

Published in:

Human Cell, 2024, v. 37, n. 3, p. 817, doi. 10.1007/s13577-024-01028-3

By:

Li, SiJun;
Mei, Lingyun;
He, Chufeng;
Cai, Xinzhang;
Wu, Hong;
Wu, XueWen;
Liu, Yalan;
Feng, Yong;
Song, Jian

Publication type:

Article