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Repressive translational control in germ cells

Molecular reproduction and development, 2013-08, Vol.80 (8), p.665-676

2013

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Secreted HSP90α-LRP1 Signaling Promotes Tumor Metastasis and Chemoresistance in Pancreatic Cancer

International journal of molecular sciences, 2022-05, Vol.23 (10), p.5532

2022

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Validating a Selective S1P1 Receptor Modulator Syl930 for Psoriasis Treatment

Biological and Pharmaceutical Bulletin, 2018/04/01, Vol.41(4), pp.592-596

2018

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Design and Synthesis of Indoleamine 2,3-Dioxygenase 1 Inhibitors and Evaluation of Their Use as Anti-Tumor Agents

Molecules (Basel, Switzerland), 2019-06, Vol.24 (11), p.2124

2019

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The effect of rapid and delayed insemination on reproductive outcome in conventional insemination and intracytoplasmic sperm injection in vitro fertilization cycles

Journal of assisted reproduction and genetics, 2021-10, Vol.38 (10), p.2697-2706

2021

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Rutaecarpine suppresses atherosclerosis in ApoE−/− mice through upregulating ABCA1 and SR-BI within RCT[S]

Journal of lipid research, 2014-08, Vol.55 (8), p.1634-1647

2014

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Repression of zygotic gene expression in the Xenopus germline

Development (Cambridge), 2010-02, Vol.137 (4), p.651-660

2010

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Development of 3-alkyl-6-methoxy-7-hydroxy-chromones (AMHCs) from natural isoflavones, a new class of fluorescent scaffolds for biological imaging

Chemical communications (Cambridge, England), 2015-01, Vol.51 (5), p.881-884

2015

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Associations between serum total bilirubin, obesity and type 2 diabetes

Diabetology and metabolic syndrome, 2021-12, Vol.13 (1), p.143-143, Article 143

2021

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Association between intrahepatic triglyceride content in subjects with metabolically healthy abdominal obesity and risks of pre-diabetes plus diabetes: an observational study

BMJ open, 2022-02, Vol.12 (2), p.e057820-e057820

2022

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YPD-30, a prodrug of YPD-29B, is an oral small-molecule inhibitor targeting PD-L1 for the treatment of human cancer

Acta pharmaceutica Sinica. B, 2022-06, Vol.12 (6), p.2845-2858

2022

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Quantitative Evaluation of in Vivo Target Efficacy of Anti-tumor Agents via an Immunofluorescence and EdU Labeling Strategy

Frontiers in pharmacology, 2018-07, Vol.9, p.812-812

2018

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Author correction to “YPD-30, a prodrug of YPD-29B, is an oral small-molecule inhibitor targeting PD-L1 for the treatment of human cancer” [Acta Pharmaceutica Sinica B 12 (2022) 2845–2858]

Acta pharmaceutica Sinica. B, 2023-07, Vol.13 (7), p.3178-3179

2023

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S1PR1 serves as a viable drug target against pulmonary fibrosis by increasing the integrity of the endothelial barrier of the lung

Acta pharmaceutica Sinica. B, 2023-03, Vol.13 (3), p.1110-1127

2023

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Sphingosine-1-Phosphate Receptor Subtype 1 (S1P1) Modulator IMMH001 Regulates Adjuvant- and Collagen-Induced Arthritis

Frontiers in pharmacology, 2019-09, Vol.10, p.1085-1085

2019

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A novel S1P1 modulator IMMH002 ameliorates psoriasis in multiple animal models

Acta pharmaceutica Sinica. B, 2020-02, Vol.10 (2), p.276-288

2020

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Joint associations of metabolically healthy abdominal obesity and non-alcoholic fatty liver disease with prediabetes and diabetes in Chinese adults

BMJ open diabetes research & care, 2021-08, Vol.9 (1), p.e002362

2021

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Discovery and druggability evaluation of pyrrolamide-type GyrB/ParE inhibitor against drug-resistant bacterial infection

Acta pharmaceutica Sinica. B, 2023-12, Vol.13 (12), p.4945-4962

2023

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Profiling of mismatch discrimination in RNAi enabled rational design of allele-specific siRNAs

Nucleic acids research, 2009-12, Vol.37 (22), p.7560

2009

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Design, synthesis and biological evaluation of indole-2-carboxylic acid derivatives as IDO1/TDO dual inhibitors

European journal of medicinal chemistry, 2020-02, Vol.188, p.111985, Article 111985

2020

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Xenopus Nanos1 is required to prevent endoderm gene expression and apoptosis in primordial germ cells

Development (Cambridge), 2012-04, Vol.139 (8), p.1476-1486

2012

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Bioevaluation of a dual PI3K/HDAC inhibitor for the treatment of diffuse large B-cell lymphoma

Bioorganic & medicinal chemistry letters, 2022-09, Vol.71, p.128825-128825, Article 128825

2022

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Identification of potential indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitors by an FBG-based 3D QSAR pharmacophore model

Journal of molecular graphics & modelling, 2020-09, Vol.99, p.107628-107628, Article 107628

2020

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Design, Synthesis, and Biological Evaluation of 4‑Methyl Quinazoline Derivatives as Anticancer Agents Simultaneously Targeting Phosphoinositide 3‑Kinases and Histone Deacetylases

Journal of medicinal chemistry, 2019-08, Vol.62 (15), p.6992-7014

2019

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Long non‐coding RNA SNHG6 increases JAK2 expression by targeting the miR‐181 family to promote colorectal cancer cell proliferation

The journal of gene medicine, 2020-12, Vol.22 (12), p.e3262-n/a

2020

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Repressive translational control in germ cells

Secreted HSP90α-LRP1 Signaling Promotes Tumor Metastasis and Chemoresistance in Pancreatic Cancer

Validating a Selective S1P1 Receptor Modulator Syl930 for Psoriasis Treatment

Design and Synthesis of Indoleamine 2,3-Dioxygenase 1 Inhibitors and Evaluation of Their Use as Anti-Tumor Agents

The effect of rapid and delayed insemination on reproductive outcome in conventional insemination and intracytoplasmic sperm injection in vitro fertilization cycles

Rutaecarpine suppresses atherosclerosis in ApoE−/− mice through upregulating ABCA1 and SR-BI within RCT[S]

Repression of zygotic gene expression in the Xenopus germline

Development of 3-alkyl-6-methoxy-7-hydroxy-chromones (AMHCs) from natural isoflavones, a new class of fluorescent scaffolds for biological imaging

Associations between serum total bilirubin, obesity and type 2 diabetes

Association between intrahepatic triglyceride content in subjects with metabolically healthy abdominal obesity and risks of pre-diabetes plus diabetes: an observational study

YPD-30, a prodrug of YPD-29B, is an oral small-molecule inhibitor targeting PD-L1 for the treatment of human cancer

Quantitative Evaluation of in Vivo Target Efficacy of Anti-tumor Agents via an Immunofluorescence and EdU Labeling Strategy

Author correction to “YPD-30, a prodrug of YPD-29B, is an oral small-molecule inhibitor targeting PD-L1 for the treatment of human cancer” [Acta Pharmaceutica Sinica B 12 (2022) 2845–2858]

S1PR1 serves as a viable drug target against pulmonary fibrosis by increasing the integrity of the endothelial barrier of the lung

Sphingosine-1-Phosphate Receptor Subtype 1 (S1P1) Modulator IMMH001 Regulates Adjuvant- and Collagen-Induced Arthritis

A novel S1P1 modulator IMMH002 ameliorates psoriasis in multiple animal models

Joint associations of metabolically healthy abdominal obesity and non-alcoholic fatty liver disease with prediabetes and diabetes in Chinese adults

Discovery and druggability evaluation of pyrrolamide-type GyrB/ParE inhibitor against drug-resistant bacterial infection

Profiling of mismatch discrimination in RNAi enabled rational design of allele-specific siRNAs

Design, synthesis and biological evaluation of indole-2-carboxylic acid derivatives as IDO1/TDO dual inhibitors

Xenopus Nanos1 is required to prevent endoderm gene expression and apoptosis in primordial germ cells

Bioevaluation of a dual PI3K/HDAC inhibitor for the treatment of diffuse large B-cell lymphoma

Identification of potential indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitors by an FBG-based 3D QSAR pharmacophore model

Design, Synthesis, and Biological Evaluation of 4‑Methyl Quinazoline Derivatives as Anticancer Agents Simultaneously Targeting Phosphoinositide 3‑Kinases and Histone Deacetylases

Long non‐coding RNA SNHG6 increases JAK2 expression by targeting the miR‐181 family to promote colorectal cancer cell proliferation

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