Search Results - "Xu, Hongen" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Genome‐wide analysis of somatic copy number alterations and chromosomal breakages in osteosarcoma

Genome‐wide analysis of somatic copy number alterations and chromosomal breakages in osteosarcoma

by Smida, Jan, Xu, Hongen, Zhang, Yanping, Baumhoer, Daniel, Ribi, Sebastian, Kovac, Michal, von Luettichau, Irene, Bielack, Stefan, O'Leary, Valerie B., Leib‐Mösch, Christine, Frishman, Dmitrij, Nathrath, Michaela
Published in International journal of cancer (15.08.2017)

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Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma

Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma

by Cao, Wei, Lee, Hayan, Wu, Wei, Zaman, Aubhishek, McCorkle, Sean, Yan, Ming, Chen, Justin, Xing, Qinghe, Sinnott-Armstrong, Nasa, Xu, Hongen, Sailani, M Reza, Tang, Wenxue, Cui, Yuanbo, Liu, Jia, Guan, Hongyan, Lv, Pengju, Sun, Xiaoyan, Sun, Lei, Han, Pengli, Lou, Yanan, Chang, Jing, Wang, Jinwu, Gao, Yuchi, Guo, Jiancheng, Schenk, Gundolf, Shain, Alan Hunter, Biddle, Fred G, Collisson, Eric, Snyder, Michael, Bivona, Trever G
Published in Nature communications (22.07.2020)

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Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms

Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms

by Zhang, Hui, Gao, Jian, Wang, Hanjun, Liu, Mengli, Lu, Shuangshuang, Xu, Hongen, Tang, Wenxue, Zheng, Guoxi
Published in BMC medical genomics (16.04.2024)

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Novel compound heterozygous pathogenic variants in the SLC3A1 gene in a Chinese family with cystinuria

Novel compound heterozygous pathogenic variants in the SLC3A1 gene in a Chinese family with cystinuria

by Liu, Danhua, Zhao, Yongli, Xue, Xia, Hou, Xinyue, Xu, Hongen, Zhao, Xinghua, Tian, Yongan, Tang, Wenxue, Guo, Jiancheng, Xu, Changbao
Published in BMC medical genomics (19.12.2023)

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Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto Syndrome

Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto Syndrome

by Feng, Haifeng, Xu, Hongen, Chen, Bei, Sun, Shuping, Zhai, Rongqun, Zeng, Beiping, Tang, Wenxue, Lu, Wei
Published in Frontiers in genetics (15.11.2021)

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Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant

Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant

by Dou, Qian, Xu, HongEn, Ma, LiYing, Tan, Li, Tang, WenXue
Published in BMC medical genomics (30.10.2023)

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Establishment of an induced pluripotent stem cell line (ZZUPMCi001-A) derived from peripheral blood mononuclear cells in a patient with type 1 Waardenburg syndrome

Establishment of an induced pluripotent stem cell line (ZZUPMCi001-A) derived from peripheral blood mononuclear cells in a patient with type 1 Waardenburg syndrome

by Wang, Xiaoxuan, Zhang, Sen, Hu, Sang, Xu, Hongen, Zhang, Qi, Tang, Wenxue
Published in Stem cell research (01.12.2021)

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Early prediction of growth patterns after pediatric kidney transplantation based on height-related single-nucleotide polymorphisms

Early prediction of growth patterns after pediatric kidney transplantation based on height-related single-nucleotide polymorphisms

by Feng, Yi, Feng, Yonghua, Hu, Mingyao, Xu, Hongen, Wang, Zhigang, Xu, Shicheng, Yan, Yongchuang, Feng, Chenghao, Li, Zhou, Feng, Guiwen, Shang, Wenjun
Published in Chinese medical journal (20.05.2024)

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A likely pathogenic POLD1 variant associated with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome in a Chinese patient

A likely pathogenic POLD1 variant associated with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome in a Chinese patient

by Zuo, Bin, Xu, Hongen, Pan, Zhaoyu, Mao, Lu, Feng, Haifeng, Zeng, Beiping, Tang, Wenxue, Lu, Wei
Published in BMC medical genomics (21.10.2022)

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Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants

Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants

by Mao, Lu, Wang, Yueqiang, An, Lei, Zeng, Beiping, Wang, Yanyan, Frishman, Dmitrij, Liu, Mengli, Chen, Yanyu, Tang, Wenxue, Xu, Hongen
Published in Biology (Basel, Switzerland) (27.03.2023)

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Dynamics of binding ability prediction between spike protein and human ACE2 reveals the adaptive strategy of SARS-CoV-2 in humans

Dynamics of binding ability prediction between spike protein and human ACE2 reveals the adaptive strategy of SARS-CoV-2 in humans

by Xue, Xia, Shi, Jianxiang, Xu, Hongen, Qin, Yaping, Yang, Zengguang, Feng, Shuaisheng, Liu, Danhua, Jian, Liguo, Hua, Linlin, Wang, Yaohe, Zhang, Qi, Huang, Xueyong, Zhang, Xiaoju, Li, Xinxin, Chen, Chunguang, Guo, Jiancheng, Tang, Wenxue, Liu, Jianbo
Published in Scientific reports (04.02.2021)

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Case report: Clinical and genetic analysis of a family with nonsyndromic auditory neuropathy

Case report: Clinical and genetic analysis of a family with nonsyndromic auditory neuropathy

by Jiang, Lan, Xu, Hongen, Liu, Danhua, Zhang, Sen, Xu, Ying
Published in Frontiers in pediatrics (15.11.2022)

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A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family

A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family

by Zeng, Beiping, Xu, Hongen, Tian, Yongan, Lin, Qianyu, Feng, Haifeng, Zhang, Zhifeng, Li, Siqi, Tang, Wenxue
Published in Chinese medical journal (05.11.2022)

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Increased diagnostic yield in a cohort of hearing loss families using a comprehensive stepwise strategy of molecular testing

Increased diagnostic yield in a cohort of hearing loss families using a comprehensive stepwise strategy of molecular testing

by Zeng, Beiping, Xu, Hongen, Yu, Yanan, Li, Siqi, Tian, Yongan, Li, Tiandong, Yang, Zengguang, Wang, Haili, Wang, Guangke, Chang, Mingxiu, Tang, Wenxue
Published in Frontiers in genetics (07.12.2022)

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Association of pre-surgery to pre-radiotherapy lymphocyte counts ratio with disease-free survival in rectal cancer patients receiving neoadjuvant concurrent chemoradiotherapy

Association of pre-surgery to pre-radiotherapy lymphocyte counts ratio with disease-free survival in rectal cancer patients receiving neoadjuvant concurrent chemoradiotherapy

by Xu, Hongen, You, Guangxian, Zhang, Minjun, Song, Tao, Zhang, Haibo, Yang, Jia, Jia, Yongshi, Tang, Jianming, Liang, Xiaodong
Published in World journal of surgical oncology (30.11.2019)

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High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing

High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing

by Zhang, Sen, Xu, Hongen, Tian, Yongan, Liu, Danhua, Hou, Xinyue, Zeng, Beiping, Chen, Bei, Liu, Huanfei, Li, Ruijun, Li, Xiaohua, Zuo, Bin, Tang, Ryan, Tang, Wenxue
Published in Frontiers in genetics (04.06.2021)

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Genetic Epidemiology of Medication Safety and Efficacy Related Variants in the Central Han Chinese Population With Whole Genome Sequencing

Genetic Epidemiology of Medication Safety and Efficacy Related Variants in the Central Han Chinese Population With Whole Genome Sequencing

by Tian, Junbo, Zhang, Jing, Yang, Zengguang, Feng, Shuaisheng, Li, Shujuan, Ren, Shiqi, Shi, Jianxiang, Hou, Xinyue, Xue, Xia, Yang, Bei, Xu, Hongen, Guo, Jiancheng
Published in Frontiers in pharmacology (23.02.2022)

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Porcine familial adenomatous polyposis model enables systematic analysis of early events in adenoma progression

Porcine familial adenomatous polyposis model enables systematic analysis of early events in adenoma progression

by Flisikowska, Tatiana, Stachowiak, Monika, Xu, Hongen, Wagner, Alexandra, Hernandez-Caceres, Alejandra, Wurmser, Christine, Perleberg, Carolin, Pausch, Hubert, Perkowska, Anna, Fischer, Konrad, Frishman, Dmitrij, Fries, Ruedi, Switonski, Marek, Kind, Alexander, Saur, Dieter, Schnieke, Angelika, Flisikowski, Krzysztof
Published in Scientific reports (26.07.2017)

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Perrault syndrome: Clinical report and retrospective analysis

Perrault syndrome: Clinical report and retrospective analysis

by Pan, Zhaoyu, Xu, Hongen, Tian, Yongan, Liu, Danhua, Liu, Huanfei, Li, Ruijun, Dou, Qian, Zuo, Bin, Zhai, Rongqun, Tang, Wenxue, Lu, Wei
Published in Molecular genetics & genomic medicine (01.10.2020)

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COVID-19 Resulting in Potential Hearing Damage of Rodents

COVID-19 Resulting in Potential Hearing Damage of Rodents

by Miao, Jinxin, Xu, Hongen, Tian, Yongan, Wang, Jianyao, Tang, Wenxue, Wang, Yaohe, Miao, Mingsan, Liu, Jianbo, Xue, Xia, Guo, Yongjun
Published in Chinese Medicine and Natural Products (01.03.2022)

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