Qing Sang

发表

Mutations in TUBB8 and Human Oocyte Meiotic Arrest.

B. Li, E. Nogales, Mohan L Gupta, 2016, The New England journal of medicine.

Common genetic variation in CYP1B1 is associated with concentrations of T4, FT3 and FT4 in the sera of polycystic ovary syndrome patients

Huan Wang, Qiaoli Li, Q. Xing, 2013, Molecular Biology Reports.

A possible new mechanism in the pathophysiology of polycystic ovary syndrome (PCOS): the discovery that leukocyte telomere length is strongly associated with PCOS.

Qiaoli Li, Q. Xing, Ruizhi Feng, 2014, The Journal of clinical endocrinology and metabolism.

Genetic factors as potential molecular markers of human oocyte and embryo quality

Qing Sang, Lei Wang, Zhou Zhou, 2021, Journal of Assisted Reproduction and Genetics.

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.

Ildr1b is essential for semicircular canal development, migration of the posterior lateral line primordium and hearing ability in zebrafish: implications for a role in the recessive hearing impairment DFNB42.

Shan Sun, Dong Liu, R. Chai, 2014, Human molecular genetics.

Ildr 1 b is essential for semicircular canal development , migration of the posterior lateral line primordium and hearing ability in zebrafish : implications for a role in the recessive hearing impairment DFNB 42

Shan Sun, Dong Liu, R. Chai, 2014 .

The role of the TOB1 gene in growth suppression of hepatocellular carcinoma.

Jia Fan, Q. Xing, Qing Sang, 2012, Oncology letters.

Effects of SASH1 on melanoma cell proliferation and apoptosis in vitro.

Q. Xing, Qing Sang, Lin He, 2012, Molecular medicine reports.

Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment.

Lei Wang, Li Jin, Ruizhi Feng, 2016, International journal of pediatric otorhinolaryngology.

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.

The physiological and pathological mechanisms of early embryonic development

Qing Sang, Zhou Zhou, Jian Mu, 2022, Fundamental Research.

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.

Meiotic defects in human oocytes: Potential causes and clinical implications

Qing Sang, Lei Wang, Tianyu Wu, 2022, BioEssays : news and reviews in molecular, cellular and developmental biology.

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.

Angulin proteins ILDR1 and ILDR2 regulate alternative pre-mRNA splicing through binding to splicing factors TRA2A, TRA2B, or SRSF1

C. Liu, D. Shi, Qing Sang, 2017, Scientific Reports.

Identification of microRNAs in human follicular fluid: characterization of microRNAs that govern steroidogenesis in vitro and are associated with polycystic ovary syndrome in vivo.

Li Jin, Xinzhi Zhao, Qinghe Xing, 2013, The Journal of clinical endocrinology and metabolism.

MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro

R. Chai, Ruizhi Feng, Qing Sang, 2015, Scientific Reports.

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.

Screening of miRNAs in human follicular fluid reveals an inverse relationship between microRNA-663b expression and blastocyst formation.

Qing Sang, Ronggui Qu, Lei Wang, 2018, Reproductive biomedicine online.

Quantitative analysis of follistatin (FST) promoter methylation in peripheral blood of patients with polycystic ovary syndrome.

Huan Wang, Qiaoli Li, Q. Xing, 2013, Reproductive biomedicine online.

MOS is a novel genetic marker for human early embryonic arrest and fragmentation

Qing Sang, Lei Wang, 2021, EMBO Molecular Medicine.

Genetic screening in patients with ovarian dysfunction

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

Improving genetic diagnosis of Mendelian disease with RNA sequencing: a narrative review

Qing Sang, Lei Wang, Zhou Zhou, 2021, Journal of Bio-X Research.

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.

Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment

Huawei Li, Ruizhi Feng, Qing Sang, 2015, Molecular Genetics and Genomics.

Lpar2b Controls Lateral Line Tissue Size by Regulating Yap1 Activity in Zebrafish

Ying Cao, Qing Sang, Xueqian Wang, 2018, Front. Mol. Neurosci..

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.

ILDR1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti: a mouse model for human DFNB42

Huawei Li, Ruizhi Feng, Qing Sang, 2015, Biology Open.

ILDR 1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti : a mouse model for human DFNB 42

Huawei Li, Ruizhi Feng, Qing Sang, 2015 .

ADGB variants cause asthenozoospermia and male infertility

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

Polymorphisms of pentanucleotide repeats (tttta)n in the promoter of CYP11A1 and their relationships to polycystic ovary syndrome (PCOS) risk: a meta-analysis

Huan Wang, Ruizhi Feng, Qing Sang, 2014, Molecular Biology Reports.

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility

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

Understanding the genetics of human infertility

P. Ray, Qing Sang, Lei Wang, 2023, Science.

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

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

A common polymorphism in the human aromatase gene alters the risk for polycystic ovary syndrome and modifies aromatase activity in vitro.

Huan Wang, Qiaoli Li, Q. Xing, 2011, Molecular human reproduction.

The association of APOH and NCF1 polymorphisms on susceptibility to recurrent pregnancy loss in women with antiphospholipid syndrome

Qing Sang, Ruixiu Zhang, S. Bao, 2023, Journal of Assisted Reproduction and Genetics.

Common genetic variation in CYP1B1 is associated with concentrations of T4, FT3 and FT4 in the sera of polycystic ovary syndrome patients

Huan Wang, Qiaoli Li, Q. Xing, 2013, Molecular Biology Reports.

Common genetic variation in the 3′-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well as insulin sensitivity in polycystic ovary syndrome patients

Huan Wang, Qiaoli Li, Q. Xing, 2011, Human Genetics.

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.

Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11)

Huan Wang, Duan Ma, Huawei Li, 2013, PloS one.

Angulin proteins ILDR1 and ILDR2 regulate alternative pre-mRNA splicing through binding to splicing factors TRA2A, TRA2B, or SRSF1

D. Shi, Qing Sang, Lei Wang, 2017, Scientific Reports.

The mechanism of acentrosomal spindle assembly in human oocytes

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

Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment

Huawei Li, Ruizhi Feng, Qing Sang, 2015, Molecular Genetics and Genomics.

Quantitative Methylation Level of the EPHX1 Promoter in Peripheral Blood DNA Is Associated with Polycystic Ovary Syndrome

Huan Wang, Qiaoli Li, Q. Xing, 2014, PloS one.

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.

Polymorphisms of pentanucleotide repeats (tttta)n in the promoter of CYP11A1 and their relationships to polycystic ovary syndrome (PCOS) risk: a meta-analysis

Huan Wang, Ruizhi Feng, Qing Sang, 2014, Molecular Biology Reports.

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.