Biaobang Chen

发表

Sequence Analysis of pKF3-70 in Klebsiella pneumoniae: Probable Origin from R100-Like Plasmid of Escherichia coli

Qiyu Bao, Jinyu Wu, Huan Wang, 2010, PloS one.

Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation

B. Li, Ling Wu, Y. Kuang, 2019, Human Genetics.

Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest.

Y. Kuang, Zheng Yan, Ruizhi Feng, 2016, American journal of human genetics.

Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrest.

Ling Wu, Qiaoli Li, Y. Kuang, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos

Zhaogui Sun, Y. Kuang, Zheng Yan, 2016, Journal of Medical Genetics.

A novel splicing variant in DNAH8 causes asthenozoospermia

Ling Wu, Qiaoli Li, Y. Kuang, 2021, Journal of Assisted Reproduction and Genetics.

Homozygous Mutations in BTG4 Cause Zygotic Cleavage Failure and Female Infertility.

G. Lin, Xiangli Niu, Juan-zi Shi, 2020, American journal of human genetics.

Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility.

Ling Wu, Qiaoli Li, Y. Kuang, 2018, American journal of human genetics.

The identification of novel mutations in PLCZ1 responsible for human fertilization failure and a therapeutic intervention by artificial oocyte activation.

Ling Wu, Y. Kuang, Zheng Yan, 2020, Molecular human reproduction.

Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest

Ling Wu, Qiaoli Li, Y. Kuang, 2019, Journal of Medical Genetics.

Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest.

Zhaogui Sun, Qiaoli Li, Suying Liu, 2018, Reproductive biomedicine online.

A pannexin 1 channelopathy causes human oocyte death

Ling Wu, Qiang Sun, Qiaoli Li, 2019, Science Translational Medicine.

Novel biallelic mutations in PADI6 in patients with early embryonic arrest

Zheng Yan, Qing Sang, Lei Wang, 2022, Journal of Human Genetics.

Identification of piggyBac-mediated insertions in Plasmodium berghei by next generation sequencing

Dongmei Zhang, Weiqing Pan, Biaobang Chen, 2013, Malaria Journal.

Identification of Novel Mutations in CDC20: Expanding the Mutational Spectrum for Female Infertility

Ling Wu, Qiaoli Li, Y. Kuang, 2021, Frontiers in Cell and Developmental Biology.

A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility

Congjian Xu, Qing Sang, Xiaoxi Sun, 2021, Journal of Assisted Reproduction and Genetics.

Homozygous variants in PANX1 cause human oocyte death and female infertility

Qiaoli Li, Qing Sang, Ronggui Qu, 2021, European Journal of Human Genetics.

Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development

Ling Wu, Qiaoli Li, Juan-zi Shi, 2020, Protein & Cell.

Bi-allelic Missense Pathogenic Variants in TRIP13Cause Female Infertility Characterized by Oocyte Maturation Arrest.

Ling Wu, Y. Kuang, Zheng Yan, 2020, American journal of human genetics.

Expanding the genetic and phenotypic spectrum of female infertility caused by TLE6 mutations

Qing Sang, Xiaoxi Sun, Lei Wang, 2020, Journal of Assisted Reproduction and Genetics.

Novel mutations in WEE2: Expanding the spectrum of mutations responsible for human fertilization failure

Ling Wu, Y. Kuang, Zheng Yan, 2019, Clinical genetics.

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility

Ling Wu, Qiaoli Li, Da Li, 2018, European Journal of Human Genetics.

Novel mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development

Qiaoli Li, Da Li, Y. Kuang, 2017, Human reproduction.

Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure.

Ling Wu, Qiaoli Li, Da Li, 2021, Human reproduction.

Homozygous mutations in REC114 cause female infertility characterised by multiple pronuclei formation and early embryonic arrest

Ling Wu, Qiaoli Li, Y. Kuang, 2019, Journal of Medical Genetics.

Identification novel mutations in TUBB8 in female infertility and a novel phenotype of large polar body in oocytes with TUBB8 mutations

Ling Wu, Qiaoli Li, Juan-zi Shi, 2020, Journal of Assisted Reproduction and Genetics.

Novel mutations in PATL2: expanding the mutational spectrum and corresponding phenotypic variability associated with female infertility

Ling Wu, Da Li, Y. Kuang, 2019, Journal of Human Genetics.

Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest.

Qiaoli Li, Y. Kuang, Zheng Yan, 2017, American journal of human genetics.

Genetic screening in patients with ovarian dysfunction

K. Choy, Ling Wu, Qingyuan Li, 2022, Clinical genetics.

A homozygous mutation in CMAS causes autosomal recessive intellectual disability in a Kazakh family

Qing Sang, Yao Xu, Ronggui Qu, 2020, Annals of human genetics.

Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome

Ling Wu, Y. Kuang, Zheng Yan, 2020, Journal of Assisted Reproduction and Genetics.

Bioinformatic analysis of the Acinetobacter baumannii phage AB1 genome.

Qiyu Bao, Shouguang Jin, Hongjiang Yang, 2012, Gene.

Identification of a novel homozygous mutation in the MYO15A gene in a Kazakh family with non-syndromic hearing loss.

Biaobang Chen, Zhou Zhou, Jian Mu, 2019, International journal of pediatric otorhinolaryngology.

Proteomic analysis and qRT-PCR verification of Arthrospira platensis strain YZ under dark stress

Qiyu Bao, Xuedong Wang, Aibing Zeng, 2013 .

Transcription of the var genes from a freshly-obtained field isolate of Plasmodium falciparum shows more variable switching patterns than long laboratory-adapted isolates

Shengyue Wang, Dongmei Zhang, Yilong Zhang, 2015, Malaria Journal.

Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects

Ling Wu, Qiaoli Li, Juan-zi Shi, 2023, Genome Biology.

ADGB variants cause asthenozoospermia and male infertility

Ling Wu, Qiaoli Li, Y. Kuang, 2023, Human Genetics.

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility

Ling Wu, Qiaoli Li, Da Li, 2018, European Journal of Human Genetics.

FBXO43 variants in patients with female infertility characterized by early embryonic arrest.

Qiaoli Li, Juan-zi Shi, Qing Sang, 2021, Human reproduction.

Codon usage patterns and adaptive evolution of marine unicellular cyanobacteria Synechococcus and Prochlorococcus.

Fangqing Zhao, Yang Yang, Qiyu Bao, 2012, Molecular phylogenetics and evolution.

Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation

Ling Wu, Y. Kuang, Zheng Yan, 2019, Human Genetics.

A novel homozygous missense variant in BTG4 causes zygotic cleavage failure and female infertility

Qiaoli Li, Yifan Zhou, Qing Sang, 2021, Journal of Assisted Reproduction and Genetics.

The mechanism of acentrosomal spindle assembly in human oocytes

Y. Kuang, Qing Sang, Xiaoxi Sun, 2022, Science.

Transcription of the var genes from a freshly-obtained field isolate of Plasmodium falciparum shows more variable switching patterns than long laboratory-adapted isolates

Shengyue Wang, Dongmei Zhang, Yilong Zhang, 2015, Malaria Journal.

Karyopherin α deficiency contributes to human preimplantation embryo arrest

Ling Wu, Y. Miyamoto, Qiaoli Li, 2023, The Journal of clinical investigation.

Bi‐allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility

Qiaoli Li, Juan-zi Shi, Qing Sang, 2023, EMBO molecular medicine.

Novel mutations in PATL2: expanding the mutational spectrum and corresponding phenotypic variability associated with female infertility

Ling Wu, Da Li, Y. Kuang, 2019, Journal of Human Genetics.

CCDC28A deficiency causes sperm head defects, reduced sperm motility and male infertility in mice

Qing Sang, Ronggui Qu, Biaobang Chen, 2024, Cellular and molecular life sciences : CMLS.