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Yalan Liu

Showing results (251-260 of 269) with videos related to

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British Journal of Cancer|July 7, 2021
The genomic architectures of tumour-adjacent tissues, plasma and saliva reveal evolutionary underpinnings of relapse in head and neck squamous cell carcinomaPing Wu, Chubo Xie, Ling Yang, et al.
Journal of Human Genetics|March 22, 2018
A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese familyYuyuan Deng, Zhijie Niu, LiangLiang Fan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 25, 2024
Recombinant neutralizing secretory IgA antibodies for preventing mucosal acquisition and transmission of SARS-CoV-2Kathrin Göritzer, Elisabetta Groppelli, Clemens Grünwald-Gruber, et al.
Gene|April 12, 2019
A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum reviewTaoxi Li, Yong Feng, Yalan Liu, et al.
BMC Biology|January 31, 2026
Paternal genomic history and Y-chromosome phylogeny from the Chengdu Plain reveal multiple Indigenous East Asian farmer contributions to ancient Shu and their descendantsLisiteng Luo, Yanling Liu, Yalan Liu, et al.
Human Genetics|March 13, 2012
Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese populationZhengmao Hu, Zhimin Xiong, Xiaojuan Xu, et al.
Frontiers in Immunology|April 4, 2022
Short-Term Instantaneous Prophylaxis and Efficient Treatment Against SARS-CoV-2 in hACE2 Mice Conferred by an Intranasal Nanobody (Nb22)Xilin Wu, Yaxing Wang, Lin Cheng, et al.
Journal of Translational Medicine|September 1, 2012
Trastuzumab anti-tumor efficacy in patient-derived esophageal squamous cell carcinoma xenograft (PDECX) mouse modelsXianhua Wu, Jingchuan Zhang, Ruheng Zhen, et al.
Human Genetics|May 2, 2018
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing lossWu Li, Jie Sun, Jie Ling, et al.
Journal of Human Genetics|January 16, 2015
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese familyHonghan Wang, Xinwei Wang, Chufeng He, et al.
Pageof 27

Showing results (251-260 of 269) with videos related to

Sort By:
Pageof 27
British Journal of Cancer|July 7, 2021
The genomic architectures of tumour-adjacent tissues, plasma and saliva reveal evolutionary underpinnings of relapse in head and neck squamous cell carcinomaPing Wu, Chubo Xie, Ling Yang, et al.
Journal of Human Genetics|March 22, 2018
A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese familyYuyuan Deng, Zhijie Niu, LiangLiang Fan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 25, 2024
Recombinant neutralizing secretory IgA antibodies for preventing mucosal acquisition and transmission of SARS-CoV-2Kathrin Göritzer, Elisabetta Groppelli, Clemens Grünwald-Gruber, et al.
Gene|April 12, 2019
A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum reviewTaoxi Li, Yong Feng, Yalan Liu, et al.
BMC Biology|January 31, 2026
Paternal genomic history and Y-chromosome phylogeny from the Chengdu Plain reveal multiple Indigenous East Asian farmer contributions to ancient Shu and their descendantsLisiteng Luo, Yanling Liu, Yalan Liu, et al.
Human Genetics|March 13, 2012
Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese populationZhengmao Hu, Zhimin Xiong, Xiaojuan Xu, et al.
Frontiers in Immunology|April 4, 2022
Short-Term Instantaneous Prophylaxis and Efficient Treatment Against SARS-CoV-2 in hACE2 Mice Conferred by an Intranasal Nanobody (Nb22)Xilin Wu, Yaxing Wang, Lin Cheng, et al.
Journal of Translational Medicine|September 1, 2012
Trastuzumab anti-tumor efficacy in patient-derived esophageal squamous cell carcinoma xenograft (PDECX) mouse modelsXianhua Wu, Jingchuan Zhang, Ruheng Zhen, et al.
Human Genetics|May 2, 2018
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing lossWu Li, Jie Sun, Jie Ling, et al.
Journal of Human Genetics|January 16, 2015
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese familyHonghan Wang, Xinwei Wang, Chufeng He, et al.
Pageof 27