Publications - iGeneTech Bioscience Co., Ltd.

A new TEX11 mutation causes azoospermia and testicular meiotic arrest

2024

Xiao-Chen Yu; Meng-Jing Li; Fei-Fei Cai; Si-Jie Yang; Hong-Bin Liu; Hao-Bo Zhang

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Landscape of pathogenic mutations in premature ovarian insufficiency

2023

Ke H, Tang S, Guo T, Hou D, Jiao X, Li S, Luo W, Xu B, Zhao S, Li G, Zhang X, Xu S, Wang L, Wu Y, Wang J, Zhang F, Qin Y, Jin L, Chen ZJ.

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An Efficient and User-Friendly Software for PCR Primer Design for Detection of Highly Variable Bacteria

2023

Dongzheng Hu; Wubin Qu; Fan Tong; Xiangwen Zheng; Jiangyu Li; Dongsheng Zhao

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HTLV-1 infection of donor-derived T cells might promote acute graft-versus-host disease following liver transplantation

2022

Chuan Shen; Yiyang Li; Boqian Wang; Zhipeng Zong; Tianfei Lu; Nokuzola Maboyi; Yuxiao Deng; Yongbing Qian; Jianjun Zhang; Xianting Ding; Qiang Xia

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Ancient plastid genomes solve the tree species mystery of the imperial wood

2022

Lichao Jiao; Yang Lu; Ming Zhang; Yongping Chen; Zhaoshan Wang; Yu Guo; Chao Xu; Juan Guo; Tuo He; Lingyu Ma; Wenqiang Gao; Jie Wang; Shiliang Zhou; Yonggang Zhang; Xiaomei Jiang; Pieter Baas; Yafang Yin

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A novel mutation located in the intermembrane space domain of AFG3L2 causes dominant optic atrophy through decreasing the stability of the encoded protein

2022

Lin Yang; Xiuxiu Jin; Ya Li; Qingge Guo; Mingzhu Yang; Ya You; Shun Yao; Xiaoli Zhang; Zhongfeng Wang; Bo Lei

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CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family

2022

MahdiehDaliri Ghouchanatigh; Ranjha Khan; Majid Mojarrad; Uzma Hameed; Muhammad Zubair; Ahmed Waqas; Mohsen Jalali; Mahmoudreza Kalantari; Ali Shamsa; Huan Zhang; Qing-Hua Shi

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Four Novel PAX9 Variants and the PAX9-Related Non-Syndromic Tooth Agenesis Patterns

2022

Haochen Liu; Hangbo Liu; Lanxin Su; Jinglei Zheng; Hailan Feng; Yang Liu; Miao Yu; Dong Han

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Identification of clinical implications and potential prognostic models of chromatin regulator mutations in multiple myeloma

2022

Lina Zhang; Run Zhang; Jing Wang; Ying Chen; Chun Qiao; Qinglin Shi; Yuanyuan Jin; Xuxing Shen; Jianyong Li; Lijuan Chen

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Genetic evidence of tri-genealogy hypothesis on the origin of ethnic minorities in Yunnan

2022

Zhaoqing Yang; Hao Chen; Yan Lu; Yang Gao; Hao Sun; Jiucun Wang; Li Jin; Jiayou Chu; Shuhua Xu