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Evolution of LuxR solos in bacterial communication: receptors and signals

Biotechnology letters, 2020-02, Vol.42 (2), p.181-186

Xu, Gangming

2020

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Independent Evolution of Six Families of Halogenating Enzymes

PloS one, 2016-05, Vol.11 (5), p.e0154619-e0154619

2016

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Autoregulation of antibiotic biosynthesis by binding of the end product to an atypical response regulator

Proceedings of the National Academy of Sciences - PNAS, 2009-05, Vol.106 (21), p.8617-8622

2009

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Evolution of orphan and atypical histidine kinases and response regulators for microbial signaling diversity

International journal of biological macromolecules, 2024-08, Vol.275 (Pt 1), p.133635, Article 133635

2024

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Regulatory and evolutionary roles of pseudo γ-butyrolactone receptors in antibiotic biosynthesis and resistance

Applied microbiology and biotechnology, 2019-12, Vol.103 (23-24), p.9373-9378

2019

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Diverse evolutionary origins of microbial [4 + 2]-cyclases in natural product biosynthesis

International journal of biological macromolecules, 2021-07, Vol.182, p.154-161

2021

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Optimizing production of asperolide A, a potential anti-tumor tetranorditerpenoid originally produced by the algal-derived endophytic fungus Aspergillus wentii EN-48

Chinese journal of oceanology and limnology, 2017-05, Vol.35 (3), p.658-663

2017

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Regulatory and evolutionary roles of pseudo [gamma]-butyrolactone receptors in antibiotic biosynthesis and resistance

Applied microbiology and biotechnology, 2019-12, Vol.103 (23-24), p.9373

2019

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Mineralization of chlorpyrifos by co-culture of Serratia and Trichosporon spp

Biotechnology letters, 2007-10, Vol.29 (10), p.1469-1473

2007

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Molecular cloning and expression of a gene encoding alcohol acyltransferase ( MdAAT2) from apple (cv. Golden Delicious)

Phytochemistry (Oxford), 2006-04, Vol.67 (7), p.658-667

2006

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The plant hormone abscisic acid regulates the growth and metabolism of endophytic fungus Aspergillus nidulans

Scientific reports, 2018-04, Vol.8 (1), p.6504-9, Article 6504

2018

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“Pseudo” γ-Butyrolactone Receptors Respond to Antibiotic Signals to Coordinate Antibiotic Biosynthesis

The Journal of biological chemistry, 2010-08, Vol.285 (35), p.27440-27448

2010

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Therapeutic action against chronic cholestatic liver injury by low-dose fenofibrate involves anti-chemotaxis via JNK–AP1–CCL2/CXCL2 signaling

Pharmacological reports, 2020-08, Vol.72 (4), p.935-944

2020

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Biodegradation of chlorpyrifos and 3,5,6-trichloro-2-pyridinol by a newly isolated Paracoccus sp. strain TRP

International biodeterioration & biodegradation, 2008-07, Vol.62 (1), p.51-56

2008

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Inhibition of JNK signalling mediates PPARα‐dependent protection against intrahepatic cholestasis by fenofibrate

British journal of pharmacology, 2017-09, Vol.174 (18), p.3000-3017

2017

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Inhibition of inflammation by SP600125 in cholestatic liver injury is dependent on the administration‑based exposure profile

International journal of molecular medicine, 2020-12, Vol.46 (6), p.2271-2279

2020

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Targeted Metabolomics Reveals a Protective Role for Basal PPARα in Cholestasis Induced by α‑Naphthylisothiocyanate

Journal of proteome research, 2018-04, Vol.17 (4), p.1500-1508

2018

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Cholestatic models induced by lithocholic acid and α‑naphthylisothiocyanate: Different etiological mechanisms for liver injury but shared JNK/STAT3 signaling

Molecular medicine reports, 2020-08, Vol.22 (2), p.1583-1593

2020

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Basal PPARα inhibits bile acid metabolism adaptation in chronic cholestatic model induced by α-naphthylisothiocyanate

Toxicology letters, 2019-01, Vol.300, p.31-39

2019

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Prokaryotic expression, purification, and sub-cellular localization of a novel alcohol acyltransferase from apple

Biotechnology letters, 2007-09, Vol.29 (9), p.1363-1368

2007

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Cholestatic models induced by lithocholic acid and [alpha]-naphthylisothiocyanate: Different etiological mechanisms for liver injury but shared JNK/STAT3 signaling

Molecular medicine reports, 2020-08, Vol.22 (2), p.1583

2020

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PPARα‐independent action against metabolic syndrome development by fibrates is mediated by inhibition of STAT3 signalling

Journal of pharmacy and pharmacology, 2018-12, Vol.70 (12), p.1630-1642

2018

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Peroxisome Proliferator‐Activated Receptor α Activation Suppresses Cytochrome P450 Induction Potential in Mice Treated with Gemfibrozil

Basic & clinical pharmacology & toxicology, 2017-09, Vol.121 (3), p.169-174

2017

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Peroxisome Proliferator-Activated Receptor [alpha] Activation Suppresses Cytochrome P450 Induction Potential in Mice Treated with Gemfibrozil

Basic & clinical pharmacology & toxicology, 2017-09, Vol.121 (3), p.169

2017

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PPARα Activation Suppresses Cytochrome P450 Induction Potential in Mice Treated with Gemfibrozil

Basic & clinical pharmacology & toxicology, 2017-05, Vol.121 (3), p.169-174

2017

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Evolution of LuxR solos in bacterial communication: receptors and signals

Independent Evolution of Six Families of Halogenating Enzymes

Autoregulation of antibiotic biosynthesis by binding of the end product to an atypical response regulator

Evolution of orphan and atypical histidine kinases and response regulators for microbial signaling diversity

Regulatory and evolutionary roles of pseudo γ-butyrolactone receptors in antibiotic biosynthesis and resistance

Diverse evolutionary origins of microbial [4 + 2]-cyclases in natural product biosynthesis

Optimizing production of asperolide A, a potential anti-tumor tetranorditerpenoid originally produced by the algal-derived endophytic fungus Aspergillus wentii EN-48

Regulatory and evolutionary roles of pseudo [gamma]-butyrolactone receptors in antibiotic biosynthesis and resistance

Mineralization of chlorpyrifos by co-culture of Serratia and Trichosporon spp

Molecular cloning and expression of a gene encoding alcohol acyltransferase ( MdAAT2) from apple (cv. Golden Delicious)

The plant hormone abscisic acid regulates the growth and metabolism of endophytic fungus Aspergillus nidulans

“Pseudo” γ-Butyrolactone Receptors Respond to Antibiotic Signals to Coordinate Antibiotic Biosynthesis

Therapeutic action against chronic cholestatic liver injury by low-dose fenofibrate involves anti-chemotaxis via JNK–AP1–CCL2/CXCL2 signaling

Biodegradation of chlorpyrifos and 3,5,6-trichloro-2-pyridinol by a newly isolated Paracoccus sp. strain TRP

Inhibition of JNK signalling mediates PPARα‐dependent protection against intrahepatic cholestasis by fenofibrate

Inhibition of inflammation by SP600125 in cholestatic liver injury is dependent on the administration‑based exposure profile

Targeted Metabolomics Reveals a Protective Role for Basal PPARα in Cholestasis Induced by α‑Naphthylisothiocyanate

Cholestatic models induced by lithocholic acid and α‑naphthylisothiocyanate: Different etiological mechanisms for liver injury but shared JNK/STAT3 signaling

Basal PPARα inhibits bile acid metabolism adaptation in chronic cholestatic model induced by α-naphthylisothiocyanate

Prokaryotic expression, purification, and sub-cellular localization of a novel alcohol acyltransferase from apple

Cholestatic models induced by lithocholic acid and [alpha]-naphthylisothiocyanate: Different etiological mechanisms for liver injury but shared JNK/STAT3 signaling

PPARα‐independent action against metabolic syndrome development by fibrates is mediated by inhibition of STAT3 signalling

Peroxisome Proliferator‐Activated Receptor α Activation Suppresses Cytochrome P450 Induction Potential in Mice Treated with Gemfibrozil

Peroxisome Proliferator-Activated Receptor [alpha] Activation Suppresses Cytochrome P450 Induction Potential in Mice Treated with Gemfibrozil

PPARα Activation Suppresses Cytochrome P450 Induction Potential in Mice Treated with Gemfibrozil

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