刘洪彬
教授
所属院部: 生殖医学研究中心
访问次数:
基本信息
  • 教师英文名称:
    Hongbin Liu
  • 电子邮箱:
  • 入职时间:
    2011-07
  • 所在单位:
    妇儿与生殖健康研究院
  • 职务:
    研究院(院长助理)、生殖内分泌教育部重点实验室(副主任)
  • 学历:
    研究生(博士)毕业
  • 办公地点:
    山东大学千佛山校区南院10号科研楼
  • 性别:
  • 学位:
    博士生
  • 博士生导师
  • 硕士生导师
教师简介

长寿与男性生殖健康的药物研发


生殖医学与子代健康全国重点实验室

山东大学附属生殖医院

 

教授,博士生导师,省级青年专家,山东大学妇儿与生殖健康研究院院长助理,生殖内分泌教育部重点实验室副主任,山东大学杰出中青年学者,山东大学齐鲁青年学者。主要从事生殖发育分子调控、男性生殖障碍致病机制及中药二次研发等研究。在国家自然科学基金(5项)、国家重点研发计划课题(4项)、山东省重大科技创新工程及自然科学基金(4项)、横向课题(5项)等资助下,在Nature Communications2篇)、EMBO JournalGenome BiologyScience AdvancesCurrent BiologyNucleic Acids Research4篇)、Advanced Science4篇)、Cell Death Differentiation2篇)、National Science ReviewProtein & CellScience Bulletin杂志等发表论文30余篇,申请国家发明专利20件,已授权9件。荣获山东医学科技进步奖一等奖、全国妇幼健康科学技术奖一等奖、中华医学科技奖一等奖。现任生殖医学与子代健康全国重点实验室课题组组长。兼任中国生理学会生殖科学专业委员会委员、中国解剖学会医学发育生物学分会青年委员、中国细胞生物学生殖细胞分会常委、山东省干细胞学会第一届干细胞技术与临床应用研究专业委员会委员等。

 

研究领域:长寿与男性生殖健康

本课题组聚焦长寿调控与男性生殖健康交叉前沿,依托新筛选动物模型、生殖干细胞培养体系与高通量测序平台,紧扣基础科研与临床转化需求,围绕配子发生调控、男性不育机制、睾丸衰老与长寿关联开展创新研究,课题新颖、平台完善、转化前景广阔。现诚招博士后、博士、硕士及本科科研爱好者加入团队。

 

主要研究方向

1. 配子发生与减数分裂调控分子机制

依托实验室特色小鼠表型与多个生殖Cre工具鼠资源,重点研究生殖细胞减数分裂核心机制,聚焦同源重组修复、性染色体沉默等关键过程,挖掘生殖发育稳态的核心调控分子,阐明生殖细胞发育的关键分子机理。

2. 男性不育发病机理与优生遗传标记筛选

以临床男性不育疑难问题为导向,结合临床样本高通量测序与小鼠模型,解析男性不育致病机制,筛选并验证优生遗传分子标志物,为优生优育提供理论依据与潜在靶点。

3. 生殖干细胞中药筛选与睾丸长寿抗衰老研究

依托成熟的精原干细胞体外培养体系,重点研究:精原干细胞增殖分化调控网络、减数分裂启动核心机制;同时筛选药食同源中医药活性成分/复方,并结合动物模型,探究其调控睾丸衰老、关联机体长寿的作用机制,开拓生殖长寿抗衰老新方向。

 

团队培养优势

课题组拥有博士后-博士-硕士-本科完整科研梯队,科研氛围和谐、传承完善。团队提供充足科研资源、系统化实验训练与学术交流平台,全方位培养学生科研思维与创新能力,适配各阶段学生成长发展需求。

热忱欢迎对生殖生物学、衰老、遗传学、中医药转化等研究感兴趣的同学加入,携手深耕前沿科研,共促学术成长

 

招生信息

招生学科(一级和二级学科):

一级学科:临床医学

二级学科:临床检验诊断学

学科方向:细胞生物学与生殖健康

 

荣誉奖励/Honors & Awards

1.      山东大学青年学者未来计划

2.      山东大学齐鲁青年学者

3.      山东大学杰出中青年学者

4.      山东省泰山学者青年专家

5.      山东省杰出青年基金获得者

6.      山东省研究生教育课程思政师范教学团队

7.      山东省医学科技进步奖一等奖

8.      中华医学科技奖青年科技奖

9.      妇幼健康科学技术奖自然科学奖一等奖


代表性论文/Representative publications

  • Li M#, Du Z#, Li H#, Zhang M, Liu Y, Zhang F, Hu L, Gu L, Chen X, Huang T, Lu G, Chan WY, Gao F, Chen Z-J*, Xie W*, Liu H*. Nucleolar migration regulates meiotic sex chromosome inactivation via phase separation during mammalian spermatogenesis. Nat Commun. 2026;17(1):4485.

  •  Cai Y#, Li T#, Fang Q#, Bao Z, Kong F, Qi H, Li H, Zhang M, Wang W, Guan Y, Liu W, Chen X, Chen Z-J, Jiang X*, Wang X*, Liu H*. EIF5A couples translational control with transcriptional reprogramming through chromocenter reorganization during spermiogenesis. Adv Sci (Weinh). 2026;13(9):e17423.

  • Li W#, Liu S#, Fang X#, Zou J#, Jiang Q, Min X, Zhu X, Cao Y, Gao X, Han W, Azhar M, Xing X, Li F, Zhang Y*, Liu H*, Cheng L*, Wang C*, Bao J*. Efficient high-precision transgene knock-in by Recombinases (Red α/β)-enhanced DNA integration-CRISPR-Cas9 (RED-CRISPR). Nat Commun. 2025;17(1):538.

  • Wang M, Li J, Liu B, Shen Z, Chen M, Cui X, Liu H*, Gao F*, Zhao H*. TRAPPC2l participates in male germ cell development by regulating cell division. Cell Prolif. 2025;58(6):e13810.

  • Zhang M, Li M, Li H, Wan Y, Yang S, Ji S, Zhang H, Liu C, Lu G, Jiang X, Liu H*. Dysregulation of N-glycosylation by Rpn1 knockout in spermatocytes induces male infertility via endoplasmic reticulum stress in mice. Int J Biol Sci. 2025;21(5):2360-2379.

  • Meng L, Xu C, Cao Y, Wu L, Zhu Y, Zou J, Uddin I, Zafar I, Muhammad A, Xing X, Jin RT, He L, Liu H*, Li W*, Bao J*. Combinatorial tagging generates a multi-purpose knock-in mouse model revealing phase separation-dependent germ granules in RNA homeostasis and germline development. Cell Death Differ. 2025;32(9):1595-1612.

  • Wang S#, Cai Y#, Li T, Wang Y, Bao Z, Wang R, Qin J, Wang Z, Liu Y, Liu Z, Chan WY, Chen X, Lu G, Chen Z-J*, Huang T*, Liu H*. CWF19L2 is essential for male fertility and spermatogenesis by regulating alternative splicing. Adv Sci (Weinh). 2024;11(32):e2403866.

  • Wan Y#, Yang S#, Li T, Cai Y, Wu X, Zhang M, Muhammad T, Huang T, Lv Y, Chan WY, Lu G, Li J, Sha QQ*, Chen Z-J*, Liu H*. LSM14B is essential for oocyte meiotic maturation by regulating maternal mRNA storage and clearance. Nucleic Acids Res. 2023;51(21):11652-11667.

  • Liu C#, Wang Q#, Gu L#, Wang X#, Yin Y#, Huang T, Xiao S, Zhang S, Wang F, Zhou T, Xu G, Wang L, Dong F, Jiang J, Luo M, Li J, Zhang H, Chen Z-J, Ji W*, Ji B*, Liu H*, Li W*. CCDC176 stabilizes microtubule doublets 1 and 9 to ensure proper sperm movement. Curr Biol. 2023;33(16):3371-3388.e7.

  • Wang M, Kang J, Shen Z, Hu Y, Chen M, Cui X, Liu H*, Gao F*. CCDC189 is involved in sperm flagellum formation by interacting with CABCOCO1. Natl Sci Rev. 2023;10(9):nwad181.

  • Huang T#, Wu X#, Wang S, Bao Z, Wan Y, Wang Z, Li M, Yu X, Lv Y, Liu Z, Chen X, Chan W-Y, Gao F, Lu G*, Chen Z-J*, Liu H*. SPIDR is required for homologous recombination during mammalian meiosis. Nucleic Acids Res. 2023;51(8):3855-3868.

  • Qin J# , Huang T#Wang Z# , Zhang X , Wang J, Dang Q, Cui D, Wang X, Zhai Y, Zhao L, Lu G, Shao C , Li S, Liu H*, Liu Z*. Bud31-mediated alternative splicing is required for spermatogonial stem cell self-renewal and differentiation . Cell Death Differ. 2023;30(1):184-194.

  • Yuan S#, Huang T*#, Bao Z#, Wang S#, Wu X#, Liu J*, Liu H*, Chen Z-J*. The histone modification reader ZCWPW1 promotes double‑strand break repair by regulating cross‑talk of histone modifications and chromatin accessibility at meiotic hotspots. Genome Biol. 2022;23(1):187.

  • Liu C#, Liu H#, Zhang H#, Wang L#, Li M, Cai F, Wang X, Wang L, Zhang R,Yang S, Liu W, Liang Y, Wang L, Song X, Su S, Gao H, Jiang J, Li J, Luo M, Gao F, Chen Q, Li W*, Chen Z-J*. Paternal USP26 mutations raise Klinefelter Syndrome risk in the offspring of mice and humans. EMBO J. 2021;40(13):e106864.

  • Huang T#, Yin Y#, Liu C, Li M, Yu X, Wang X, Zhang H, Muhammad T, Gao F, Li W, Chen Z-J*, Liu H*, Ma J*. Absence of murine CFAP61 causes male infertility due to multiple morphological abnormalities of the flagella. Sci Bull. 2020;65(10):854-864.

 



工作经历
  • 2013-07-至今
    山东大学、山东大学附属生殖医院
  • 2011-07 — 2013-07
    生殖医学研究中心
科研成果
研究方向
论文

1.  . The histone modification reader ZCWPW1 promotes double strand break repair by regulating cross talk of histone modifications and chromatin accessibility at meiotic hotspots.  GENOME BIOLOGY,  187, 2022. 

2.  . The histone modification reader ZCWPW1 links histone methylation to PRDM9-induced double-strand break repair.  Elife,  2020. 

3.  . Absence of murine CFAP61 causes male infertility due to multiple morphological abnormalities of the flagella.  Science bulletin,  854, 2020. 

4.  刘伊宁. MORN2 regulates the morphology and energy metabolism of mitochondria and is required for male fertility in mice.  Journal of Translational Medicine,  2024. 

5.  . UBE2J2 is essential for the progression of meiosis prophase I during spermatogenesis in mice.  ISCIENCE,  2025. 

6.  . UBE2J2 is essential for the progression of meiosis prophase I during spermatogenesis in mice.  ISCIENCE,  2025. 

7.  . Article CCDC176 stabilizes microtubule doublets 1 and 9 to ensure proper sperm movement.  CURRENT BIOLOGY,  33,  3371, 2023. 

8.  . UBE2J2 is essential for the progression of meiosis prophase I during spermatogenesis in mice.  eScience,  28,  2025. 

9.  . UBE2J2 is essential for the progression of meiosis prophase I during spermatogenesis in mice.  ISCIENCE,  2025. 

10.  岑洁. YKT6 Is Essential for Male Fertility by Promoting Meiosis Progression During Spermatogenesis of Mice.  Cell proliferation,  2025. 

11.  . CWF19L2 is Essential for Male Fertility and Spermatogenesis by Regulating Alternative Splicing.  Advanced Science,  2024. 

12.  刘伊宁. MORN2 regulates the morphology and energy metabolism of mitochondria and is required for male fertility in mice.  JOURNAL OF TRANSLATIONAL MEDICINE,  2024. 

13.  王子奇. The deubiquitinase cofactor UAF1 interacts with USP1 and plays an essential role in spermiogenesis.  IScience,  2024. 

14.  王子奇. TTC6-Mediated Stabilization of the Flagellum Annulus Ensures the Rapid and Directed Motion of Sperm.  CELLS,  12,  2023. 

15.  . The histone modification reader ZCWPW1 promotes double-strand break repair by regulating cross-talk of histone modifications and chromatin accessibility at meiotic hotspots.  GENOME BIOLOGY,  23,  187, 2022. 

16.  . Bud31-mediated alternative splicing is required for spermatogonial stem cell self-renewal and differentiation.  Cell Death and Differentiation,  2023. 

17.  . Absence of murine CFAP61 causes male infertility due to multiple morphological abnormalities of the flagella.  Science bulletin,  2020. 

18.  . The histone modification reader ZCWPW1 links histone methylation to PRDM9-induced double-strand break repair.  Elife,  2020. 

19.  . Spliceosome component Usp39 contributes to hepatic lipid homeostasis through the regulation of autophagy.  NATURE COMMUNICATIONS,  14,  2023. 

20.  . TOX3 deficiency mitigates hyperglycemia by suppressing hepatic gluconeogenesis through FoxO1.  METABOLISM-CLINICAL AND EXPERIMENTAL,  152,  2024. 

21.  . THADA inhibition in mice protects against type 2 diabetes mellitus by improving pancreatic β-cell function and preserving β-cell mass.  NATURE COMMUNICATIONS,  14,  2023. 

22.  . MEIOK21: A New Component of Meiotic Recombination Bridges Required for Spermatogenesis.  Nucleic Acid Research,  2020. 

23.  . Deficiency of the Tmem232 Gene Causes Male Infertility with Morphological Abnormalities of the Sperm Flagellum in Mice.  CELLS,  12,  2023. 

24.  . Bud31-mediated alternative splicing is required for spermatogonial stem cell self-renewal and differentiation.  Cell Death and Differentiation,  184, 2023. 

25.  王子翔. Splicing factor BUD31 promotes ovarian cancer progression through sustaining the expression of anti-apoptotic BCL2L12.  NATURE COMMUNICATIONS,  2022. 

26.  Wu, Bingbing. Essential Role of CFAP53 in Sperm Flagellum Biogenesis.  Front. Cell Dev. Biol.,  9,  2021. 

27.  袁慎立. The histone modification reader ZCWPW1 promotes double strand break repair by regulating cross talk of histone modifications and chromatin accessibility at meiotic hotspots.  GENOME BIOLOGY,  2022. 

28.  于小宸. Does ICSI outcome in obstructive azoospermia differ according to the origin of retrieved spermatozoa or the cause of epididymal obstruction? A comparative study.  International urology and nephrology,  2022. 

29.  秦君超. Bud31-mediated alternative splicing is required for spermatogonial stem cell self-renewal and differentiation.  Cell Death and Differentiation,  2022. 

30.  吕跃. RBM46 is essential for gametogenesis and functions in posttranscriptional roles affecting meiotic cohesin subunits.  Protein & Cell,  2022. 

31.  尹莹莹. LRRC46 Accumulates at the Midpiece of Sperm Flagella and Is Essential for Spermiogenesis and Male Fertility in Mouse. International Journal of Molecular Sciences.  INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES ,  2022. 

32.  万彦伶. IGF2 reduces meiotic defects in oocytes from obese mice and improves embryonic developmental competency..  Reproductive Biology and Endocrinology,  20,  101, 2022. 

33.  李婧博. microRNA183在PCOS胰岛素抵抗中的表达及其临床意义.  山东大学学报(医学版),  55,  69, 2016. 

34.  贾月月. 多囊卵巢综合征患者颗粒细胞microRNA200b的表达及影响.  山东大学学报(医学版),  55,  63, 2016. 

35.  石玉华. Comprehensive assessment the expression of core elements related to IGFIR/PI3K pathway in granulosa cells of women with polycystic ovary syndrome.  Eur J Obstet Gynecol Reprod Biol,  233,  134, 2018. 

36.  秦君超. RAD51 is essential for spermatogenesis and male fertility in mice.  CELL DEATH DISCOVERY,  8,  118, 2022. 

37.  游力. Common variant rs9939609 in gene FTO confers risk to polycystic ovary syndrome.  Plos one,  2013. 

38.  曹连宝. Hormone-Like Effects of 4-Vinylcyclohexene Diepoxide on Follicular Development.  Front. Cell Dev. Biol.,  8,  2020. 

39.  zhang xu. Mutational analysis of the GATA4 gene in Chinese men with nonobstructive azoospermia.  Asian Journal of Andrology,  23,  205, 2021. 

40.  曹连宝. Hormone-Like Effects of 4-Vinylcyclohexene Diepoxide on Follicular Development (vol 8, 587, 2020).  Front. Cell Dev. Biol.,  8,  2020. 

41.  曹连宝. Systemic changes in a mouse model of VCD-induced premature ovarian failure.  Life Sciences,  262,  2020. 

42.  赵世刚. Family-based analysis of eight susceptibility loci in polycystic ovary syndrome.  Scientific Reports,  2015. 

43.  吕跃,路钢,蔡玉玲. RBM46 is essential for gametogenesis and functions in post-transcriptional roles affecting meiotic cohesin subunits.  Protein & Cell,  2022. 

44.  秦君超,黄涛,王子翔. Bud31-mediated alternative splicing is required for spermatogonial stem cell self-renewal and differentiation.  Cell Death Differ,  2022. 

45.  黄涛. The histone modification reader ZCWPW1 promotes double‑strand break repair by regulating cross‑talk of histone modifications and chromatin accessibility at meiotic hotspots.  Genome Biology,  23,  2022. 

46.  于小宸. Does ICSI outcome in obstructive azoospermia differ according to the origin of retrieved spermatozoa or the cause of epididymal obstruction? A comparative study.  International Urology and Nephrology,  2022. 

47.  尹莹. LRRC46 Accumulates at the Midpiece of Sperm Flagella and Is Essential for Spermiogenesis and Male Fertility in Mouse.  International Journal of Molecular Sciences,  23,  2022. 

48.  万彦伶  and Muhammad T. IGF2 reduces meiotic defects in oocytes from obese mice and improves embryonic developmental competency.  Reproductive Biology and Endocrinology,  20,  2022. 

49.  Song, Ting. ENKD1 promotes CP110 removal through competing with CEP97 to initiate ciliogenesis.  EMBO Reports,  23,  2022. 

50.  于小宸. A new TEX11 mutation causes azoospermia and testicular meiotic arrest.  Asian Journal of Andrology,  2021. 

51.  Liu, Chao. Paternal USP26 mutations raise Klinefelter syndrome risk in the offspring of mice and humans.  EMBO Journal,  40,  2021. 

52.  刘洪彬. Essential role of CFAP53 in sperm flagellum biogenesis.  Front. Cell Dev. Biol.,  2021. 

53.  Muhammad, Tahir. IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice.  Aging-US,  13,  2118, 2021. 

54.  高雪莹. Role of Androgen Receptor for Reconsidering the "True" Polycystic Ovarian Morphology in PCOS.  Scientific Reports,  10,  2020. 

55.  尚永亮. MEIOK21: a new component of meiotic recombination bridges required for spermatogenesis.  Nucleic Acids Research,  48,  6624, 2020. 

56.  张栩. Mutational analysis of the GATA4 gene in Chinese men with nonobstructive azoospermia.  Asian Journal of Andrology,  2021. 

57.  黄涛. Absence of murine CFAP61 causes male infertility due to multiple morphological abnormalities of the flagella.  Science Bulletin,  65,  854, 2020. 

58.  黄涛. The histone modification reader ZCWPW1 links histone methylation to PRDM9-induced double-strand break repair.  Elife,  9,  2020. 

59.  Muhammad, Tahir. Roles of insulin-like growth factor II in regulating female reproductive physiology.  Science China-life sciences,  63,  849, 2020. 

60.  张亮然 , 刘洪彬 , 陈子江 , 王顺心  and 王顺心. Per-Nucleus Crossover Covariation and Implications for Evolution.  细胞,  2019. 

61.  张亮然 , 刘洪彬 , 陈子江 , 王顺心  and 王顺心. Per-Nucleus Crossover Covariation and Implications for Evolution.  Cell,  177,  326, 2019. 

62.  陈子江 , 刘洪彬 , 马金龙  and 李苗. The histone modification reader ZCWPW1 is required for meiosis prophase I in male but not in female mice.  Science Advances,  5,  2019. 

63.  刘洪彬 , 石玉华  and 贺婷婷. MicroRNA-141 and MicroRNA-200c Are Overexpressed in Granulosa Cells of Polycystic Ovary Syndrome Patients.  FRONTIERS IN MEDICINE,  5,  2018. 

64.  张亮然 , 陈子江 , 刘洪彬  and 刘洪彬. SCRE serves as a unique synaptonemal complex fastener and is essential for progression of meiosis prophase I in mice.  Nucleic Acids Research,  47,  5670, 2019. 

65.  赵世刚 , 陈子江 , 刘洪彬 , 赵涵 , 魏代敏 , 赵跃然 , 颜磊  and 赵世刚. The HMGA2-IMP2 Pathway Promotes Granulosa Cell Proliferation in Polycystic Ovary Syndrome.  J Clin Endocrinol Metab,  2019. 

66.  陈子江 , 刘洪彬 , 赵涵 , 赵世刚  and 赵世刚. RNA-Binding Protein IGF2BP2/IMP2 is a Critical Maternal Activator in Early Zygotic Genome Activation.  Advanced Science,  2019. 

67.  陈子江 , 刘洪彬 , 赵涵 , 赵世刚  and 赵世刚. An association study between USP34 and polycystic ovary syndrome.  JOURNAL OF OVARIAN RESEARCH,  2015. 

68.  高选 , 刘洪彬 , 赵涵 , 刘晓满 , 张玉超 , 赵世刚 , 陈子江  and 赵世刚. STMN1 Promotes Progesterone Production Via StAR Up-regulation in Mouse Granulosa Cells.  Scientific Reports,  2016. 

69.  刘洪彬 , 马金龙 , 赵涵 , 赵世刚  and 赵世刚. Growth Hormone Promotes in vitro Maturation of Human Oocytes.  Frontiers in Endocrinology,  2019. 

70.  马金龙 , 赵涵 , 赵世刚 , 吴克良 , 刘洪彬 , 陈子江  and 赵世刚. Melatonin promotes human oocyte maturation and early embryo development by enhancing clathrin-mediated endocytosis.  JOURNAL OF PINEAL RESEARCH,  2019. 

71.  刘昕 , 刘洪彬 , 石玉华  and 贺婷婷. 多囊卵巢综合征患者颗粒细胞FOXO1 mRNA的表达与意义.  山东大学学报(医学版),  2018. 

72.  窦云德 , 122200160003 , 赵世刚  and 刘洪彬. Integrated microRNA and mRNA signatures in peripheral blood lymphocytes of familial epithelial ovarian cancer.  Biochemical and Biophysical Research Communications,  496,  191, 2018. 

73.  赵世刚 , 李梅 , 赵涵 , 刘洪彬  and 刘美菊. Resveratrol improves in vitro maturation of oocytes in aged mice and humans.  Fertility and Sterility,  109,  900, 2018. 

74.  刘洪彬 , 陈子江 , 赵涵 , 李梅 , 吴克良 , 边月红  and 于梦汝. Mutational analysis of IZUMO1R in women with fertilization failure and polyspermy after in vitro fertilization.  Journal of assisted reproduction and genetics,  35,  539, 2018. 

75.  赵涵 , 陈子江 , 赵世刚 , 吴克良 , 颜磊 , 李梅 , 刘洪彬  and 陈泰来. A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility.  AMERICAN JOURNAL OF HUMAN GENETICS,  101,  459, 2017. 

76.  赵世刚 , 边月红 , 刘洪彬 , 赵涵 , 吕跃  and 马金龙. Association study of HNF1A in women with polycystic ovary syndrome.  Journal of assisted reproduction and genetics,  34,  677, 2017. 

77.  马金龙 , 刘洪彬 , 吕跃  and 赵世刚. Identification of reference genes for qRT-PCR in granulosa cells of healthy women and polycystic ovarian syndrome patients.  Scientific Reports,  7,  2017. 

78.  赵涵 , 刘洪彬  and 刘涛. The role of fructose-1,6-bisphosphatase 1 in abnormal development of ovarian follicles caused by high testosterone concentration.  MOLECULAR MEDICINE REPORTS,  16,  6489, 2017. 

79.  陈子江  and 刘洪彬. STMN1 Promotes Progesterone Production Via StAR Up-regulation in Mouse Granulosa Cells.  SCI REP,  2016. 

80.  刘洪彬 , 游力 , 赵涵 , 陈子江 , 高选  and 陈子江. Family-based analysis of eight susceptibility loci in polycystic ovary syndrome.  SCI REP,  2015. 

81.  赵涵 , 刘洪彬 , 赵世斗 , 陈子江  and 陈子江. High levels of testosterone inhibit ovarian follicle development by repressing the FSH signaling pathway.  J Huazhong Univ Sci Technolog Med Sci,  2015. 

82.  刘洪彬  and 刘洪彬. Association of AQP8 in women with PCOS.  Reprod Biomed online,  2013. 

83.  陈子江 , 刘洪彬  and 刘洪彬. Genome-Wide Association Studies for Polycystic Ovary Syndrome.  Semin Reprod Med,  2016. 

84.  刘洪彬 , 赵涵 , 李梅 , 陈子江  and 陈子江. Hypomethylation of the LH/Choriogonadotropin Receptor Promoter Region Is a Potential Mechanism Underlying Susceptibility to Polycystic Ovary Syndrome.  Endocrinology,  2014. 

85.  赵涵 , 游力 , 崔琳琳 , 刘洪彬 , 陈子江 , 边月红  and 陈子江. Common variant rs9939609 in gene FTO confers risk to polycystic ovary syndrome.  Plos one,  2013. 

86.  赵世刚 , 刘洪彬 , 石玉华  and 贺婷婷. Comprehensive assessment the expression of core elements related to IGFIR/PI3K pathway in granulosa cells of women with polycystic ovary syndrome.  《European Journal of Obstetrics and Gynecology》,  233,  134, 2019. 

87.  刘洪彬 , 马金龙 , 赵涵  and 赵世刚. Growth Hormone Promotes in vitro Maturation of Human Oocytes.  Frontiers in Endocrinology,  2019. 

88.  陈子江 , 高选 , 刘洪彬 , 游力  and 赵涵. Family-based analysis of eight susceptibility loci in polycystic ovary syndrome.  SCI REP,  2015. 

89.  刘洪彬 , 赵世斗 , 陈子江  and 赵涵. High levels of testosterone inhibit ovarian follicle development by repressing the FSH signaling pathway.  J Huazhong Univ Sci Technolog Med Sci,  2015. 

90.  刘洪彬 , 赵涵 , 李梅  and 陈子江. Hypomethylation of the LH/Choriogonadotropin Receptor Promoter Region Is a Potential Mechanism Underlying Susceptibility to Polycystic Ovary Syndrome.  Endocrinology,  2014. 

91.  边月红 , 赵涵 , 游力 , 崔琳琳 , 刘洪彬  and 陈子江. Common variant rs9939609 in gene FTO confers risk to polycystic ovary syndrome.  Plos one,  2013. 

92.  魏代敏 , 赵跃然 , 颜磊 , 赵世刚 , 刘洪彬 , 陈子江  and 赵涵. The HMGA2-IMP2 Pathway Promotes Granulosa Cell Proliferation in Polycystic Ovary Syndrome.  J Clin Endocrinol Metab,  2019. 

93.  陈子江 , 刘洪彬 , 赵涵  and 赵世刚. RNA-Binding Protein IGF2BP2/IMP2 is a Critical Maternal Activator in Early Zygotic Genome Activation.  Advanced Science,  2019. 

94.  陈子江 , 刘洪彬 , 赵涵  and 赵世刚. An association study between USP34 and polycystic ovary syndrome.  JOURNAL OF OVARIAN RESEARCH,  2015. 

95.  高选 , 刘洪彬 , 陈子江 , 赵涵 , 刘晓满 , 张玉超  and 赵世刚. STMN1 Promotes Progesterone Production Via StAR Up-regulation in Mouse Granulosa Cells.  Scientific reports,  2016. 

96.  赵涵 , 陈子江 , 高选 , 刘洪彬 , 游力  and 赵世刚. Family-based analysis of eight susceptibility loci in polycystic ovary syndrome.  Scientific reports,  2016. 

97.  刘洪彬 , 马金龙 , 赵涵  and 赵世刚. Growth Hormone Promotes in vitro Maturation of Human Oocytes.  Frontiers in Endocrinology,  2019. 

98.  吴克良 , 刘洪彬 , 陈子江 , 马金龙 , 赵涵  and 赵世刚. Melatonin promotes human oocyte maturation and early embryo development by enhancing clathrin-mediated endocytosis.  JOURNAL OF PINEAL RESEARCH,  2019. 

99.  刘昕 , 刘洪彬 , 石玉华  and 贺婷婷. 多囊卵巢综合征患者颗粒细胞FOXO1 mRNA的表达与意义.  山东大学学报(医学版),  2018. 

100.  刘洪彬 , 石玉华 , 贺婷婷  and 赵世刚. Comprehensive assessment the expression of core elements related to IGFIR/PI3K pathway in granulosa cells of women with polycystic ovary syndrome.  《European Journal of Obstetrics and Gynecology》,  233,  134, 2019. 

101.  赵世刚 , 马金龙 , 刘洪彬  and 吕跃. Identification of reference genes for qRT-PCR in granulosa cells of healthy women and polycystic ovarian syndrome patients.  scientific reports,  7,  2017. 

102.  刘美菊 , 赵世刚 , 李梅 , 赵涵  and 刘洪彬. Resveratrol improves in vitro maturation of oocytes in aged mice and humans.  Fertility and Sterility,  109,  900, 2018. 

103.  赵涵 , 陈子江 , 赵世刚 , 吴克良 , 颜磊 , 李梅 , 刘洪彬  and 陈泰来. A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility.  AMERICAN JOURNAL OF HUMAN GENETICS,  101,  459, 2017. 

104.  赵涵 , 刘洪彬  and 刘涛. The role of fructose-1,6-bisphosphatase 1 in abnormal development of ovarian follicles caused by high testosterone concentration.  MOLECULAR MEDICINE REPORTS,  16,  6489, 2017. 

105.  赵世刚 , 边月红 , 刘洪彬 , 赵涵 , 吕跃  and 马金龙. Association study of HNF1A in women with polycystic ovary syndrome.  Journal of assisted reproduction and genetics,  34,  677, 2017. 

106.  赵涵 , 李梅 , 刘洪彬  and 陈子江. Hypomethylation of the LH/Choriogonadotropin Receptor Promoter Region Is a Potential Mechanism Underlying Susceptibility to Polycystic Ovary Syndrome.  Endocrinology,  2014. 

107.  游力 , 崔琳琳 , 刘洪彬 , 边月红 , 赵涵  and 陈子江. Common variant rs9939609 in gene FTO confers risk to polycystic ovary syndrome.  Plos one,  2013. 

108.  赵涵 , 刘洪彬 , 赵世斗  and 陈子江. High levels of testosterone inhibit ovarian follicle development by repressing the FSH signaling pathway.  J Huazhong Univ Sci Technolog Med Sci,  2015. 

109.  刘洪彬 , 游力 , 赵涵 , 陈子江  and 高选. Family-based analysis of eight susceptibility loci in polycystic ovary syndrome.  SCI REP,  2015. 

110.  刘洪彬. Association of AQP8 in women with PCOS.  Reprod Biomed online,  2013. 

111.  陈子江  and 刘洪彬. STMN1 Promotes Progesterone Production Via StAR Up-regulation in Mouse Granulosa Cells.  SCI REP,  2016. 

112.  陈子江  and 刘洪彬. Genome-Wide Association Studies for Polycystic Ovary Syndrome.  Semin Reprod Med,  2016. 

113.  刘洪彬 , 陈子江 , 赵涵 , 李梅 , 吴克良 , 边月红  and 于梦汝. Mutational analysis of IZUMO1R in women with fertilization failure and polyspermy after in vitro fertilization.  Journal of assisted reproduction and genetics,  35,  539, 2018. 

114.  窦云德. Integrated microRNA and mRNA signatures in peripheral blood lymphocytes of familial epithelial ovarian cancer.  Biochemical and biophysical research communications,  496,  191, 2018. 

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16. 生殖细胞染色体行为的分子调控, 2018-12-01-2021-12-31

17. 多囊卵巢综合征的发病机制及干预, 2018-04-01-2021-06-30

18. TOX3在多囊卵巢综合征卵泡发育异常中的作用及转化医学研究, 2014-08-15-2019-12-31

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