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Huadie Liu

University of South China

H指数:10

被引数:304

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荣誉奖项

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Establishing the role of ZBTB20 mutations in GnRH deficiency and impaired neurogenesis in the subventricular zone: a human cohort and animal model study

建立ZBTB20基因突变在GnRH缺乏和侧脑室下区神经发生受损中的作用：一项人类队列和动物模型研究

IF10.8

2026-08-040

OAAI

Reciprocal regulation between autism risk gene POGZ and circadian clock

自闭症风险基因POGZ与时钟基因的互惠调控

IF6.1

2026-05-080

OA

Loss of Necdin causes social deficit and aberrant synaptic function through destabilization of SynGAP

Necdin蛋白的丢失通过破坏SynGAP的稳定性导致社交缺陷和异常突触功能。

Molecular Psychiatry

IF10.1

2025-08-300

PRE

H3K9me3 loss and ERVs activation as hallmarks for osteoarthritis progression and knee joint aging

OSTEOARTHRITIS AND CARTILAGE

IF9

2025-01-010

PRE

The histone demethylase KDM5C controls female bone mass by promoting energy metabolism in osteoclasts

SCIENCE ADVANCES

IF12.5

2023-04-0717

OAAI

TRIM28 secures skeletal stem cell fate during skeletogenesis by silencing neural gene expression and repressing GREM1/AKT/mTOR signaling axis

IF6.9

2023-01-014

OAAI

SUMOylation in Skeletal Development, Homeostasis, and Disease

IF5.2

2022-08-313

OAAI

RNF216 Regulates the Migration o Immortalized GnRH Neurons by Suppressing Beclin1-Mediated Autophagy

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2019-01-2438

OAAI

LRP1 Suppresses Bone Resorption in Mice by Inhibiting the RANKL-Stimulated NF-B and p38 Pathways During Osteoclastogenesis

JOURNAL OF BONE AND MINERAL RESEARCH

IF5.9

2018-05-1124

OAAI

Desumoylase SENP6 maintains osteochondroprogenitor homeostasis by suppressing the p53 pathway (vol 9, 2018)

NATURE COMMUNICATIONS

IF15.7

2018-02-084

OAAI

Ginkgolic acid, a sumoylation inhibitor, promotes adipocyte commitment but suppresses adipocyte terminal differentiation of mouse bone marrow stromal cells

SCIENTIFIC REPORTS

IF3.9

2018-02-0720

OAAI

Desumoylase SENP6 maintains osteochondroprogenitor homeostasis by suppressing the p53 pathway

NATURE COMMUNICATIONS

IF15.7

2018-01-1026

OAAI

Sclt1 deficiency causes cystic kidney by activating ERK and STAT3 signaling

HUMAN MOLECULAR GENETICS

IF3.2

2017-05-0929

OAAI

Functional Rescue of Kallmann Syndrome-associated Prokineticin Receptor 2 (PKR2) Mutants Deficient in Trafficking

Kallmann综合征相关的前动力蛋白受体2 (PKR2) 缺乏贩运的突变体的功能拯救

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2014-05-0120

OAAI

Mechanisms that underlie the internalization and extracellular signal regulated kinase 1/2 activation by PKR2 receptor

CELLULAR SIGNALLING

IF3.7

2014-05-0120

PREAI