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FunRes: resolving tissue-specific functional cell states based on a cell–cell communication network model

Briefings in bioinformatics, 2021-07, Vol.22 (4)

2021

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A 3D system to model human pancreas development and its reference single-cell transcriptome atlas identify signaling pathways required for progenitor expansion

Nature communications, 2021-05, Vol.12 (1), p.3144-3144, Article 3144

2021

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VSFlow: an open-source ligand-based virtual screening tool

Journal of cheminformatics, 2023-03, Vol.15 (1), p.40-40, Article 40

2023

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Antifungal Peptides of the AFP Family Revisited: Are These Cannibal Toxins?

Microorganisms (Basel), 2018-06, Vol.6 (2), p.50

2018

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Breaking down barriers: comprehensive functional analysis of the Aspergillus niger chitin synthase repertoire

Fungal biology and biotechnology, 2024-03, Vol.11 (1), p.3-3, Article 3

2024

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Mechanical, physical and thermal properties of composite materials produced with the basidiomycete Fomes fomentarius

Fungal biology and biotechnology, 2023-12, Vol.10 (1), p.1-22, Article 22

2023

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Species-Specific Differences in the Susceptibility of Fungi to the Antifungal Protein AFP Depend on C-3 Saturation of Glycosylceramides

mSphere, 2019-12, Vol.4 (6)

2019

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The Importance of Computational Modeling in Stem Cell Research

Trends in biotechnology (Regular ed.), 2021-02, Vol.39 (2), p.126-136

2021

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Corrigendum to: FunRes: resolving tissue-specific functional cell states based on a cell-cell communication network model

Briefings in bioinformatics, 2021-09, Vol.22 (5)

2021

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Synthesis and Pharmacological Evaluation of [11C]4-Methoxy‑N‑[2-(thiophen-2-yl)imidazo[1,2‑a]pyridin-3-yl]benzamide as a Brain Penetrant PET Ligand Selective for the δ‑Subunit-Containing γ‑Aminobutyric Acid Type A Receptors

ACS omega, 2019-05, Vol.4 (5), p.8846-8851

2019

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New peptidomimetic rhodesain inhibitors with improved selectivity towards human cathepsins

European journal of medicinal chemistry, 2022-08, Vol.238, p.114460-114460, Article 114460

2022

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Fluorovinylsulfones and -Sulfonates as Potent Covalent Reversible Inhibitors of the Trypanosomal Cysteine Protease Rhodesain: Structure–Activity Relationship, Inhibition Mechanism, Metabolism, and In Vivo Studies

Journal of medicinal chemistry, 2021-08, Vol.64 (16), p.12322-12358

2021

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Quantum Chemical-Based Protocol for the Rational Design of Covalent Inhibitors

Journal of the American Chemical Society, 2016-07, Vol.138 (27), p.8332-8335

2016

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Multiomics data integration unveils core transcriptional regulatory networks governing cell-type identity

NPJ systems biology and applications, 2020-08, Vol.6 (1), p.26-26, Article 26

2020

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Picomolar FKBP inhibitors enabled by a single water-displacing methyl group in bicyclic [4.3.1] aza-amides

Chemical science (Cambridge), 2021-11, Vol.12 (44), p.14758-14765

2021

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Author Correction: Senescence atlas reveals an aged-like inflamed niche that blunts muscle regeneration

Nature (London), 2023-02, Vol.614 (7949), p.E45-E45

2023

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Warhead Reactivity Limits the Speed of Inhibition of the Cysteine Protease Rhodesain

ACS chemical biology, 2021-04, Vol.16 (4), p.661-670

2021

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Structural Determinants for the Mode of Action of Imidazopyridine DS2 at δ‑Containing γ‑Aminobutyric Acid Type A Receptors

Journal of medicinal chemistry, 2021-04, Vol.64 (8), p.4730-4743

2021

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Abstract 3005: Comprehensive profile of platelet derived growth factor receptor alpha (PDGFRA) mutations in gastrointestinal stromal tumors

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.3005-3005

2020

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Predictive factors for the IOP reduction in phacocanaloplasty with suprachoroidal drainage

International ophthalmology, 2020-08, Vol.40 (8), p.1897-1903

2020

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Dipeptidyl Nitroalkenes as Potent Reversible Inhibitors of Cysteine Proteases Rhodesain and Cruzain

ACS medicinal chemistry letters, 2016-12, Vol.7 (12), p.1073-1076

2016

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mTNF reverse signalling induced by TNF[alpha] antagonists involves a GDF-1 dependent pathway: implications for Crohn's disease

Gut, 2013-03, Vol.62 (3), p.376

2013

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A Computational Modeling Approach Predicts Interaction of the Antifungal Protein AFP from italic toggle="yes">Aspergillus giganteus /italic> with Fungal Membranes via Its γ-Core Motif

mSphere, 2018-10, Vol.3 (5)

2018

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Characterization and Function of the First Antibiotic Isolated from a Vent Organism: The Extremophile Metazoan Alvinella pompejana: e95737

PloS one, 2014-04, Vol.9 (4)

2014

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A novel horse {alpha}-defensin: gene transcription, recombinant expression and characterisation of the structure and function

Biochemical journal, 2007-07, Vol.407 (2), p.267-276

2007

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FunRes: resolving tissue-specific functional cell states based on a cell–cell communication network model

A 3D system to model human pancreas development and its reference single-cell transcriptome atlas identify signaling pathways required for progenitor expansion

VSFlow: an open-source ligand-based virtual screening tool

Antifungal Peptides of the AFP Family Revisited: Are These Cannibal Toxins?

Breaking down barriers: comprehensive functional analysis of the Aspergillus niger chitin synthase repertoire

Mechanical, physical and thermal properties of composite materials produced with the basidiomycete Fomes fomentarius

Species-Specific Differences in the Susceptibility of Fungi to the Antifungal Protein AFP Depend on C-3 Saturation of Glycosylceramides

The Importance of Computational Modeling in Stem Cell Research

Corrigendum to: FunRes: resolving tissue-specific functional cell states based on a cell-cell communication network model

Synthesis and Pharmacological Evaluation of [11C]4-Methoxy‑N‑[2-(thiophen-2-yl)imidazo[1,2‑a]pyridin-3-yl]benzamide as a Brain Penetrant PET Ligand Selective for the δ‑Subunit-Containing γ‑Aminobutyric Acid Type A Receptors

New peptidomimetic rhodesain inhibitors with improved selectivity towards human cathepsins

Fluorovinylsulfones and -Sulfonates as Potent Covalent Reversible Inhibitors of the Trypanosomal Cysteine Protease Rhodesain: Structure–Activity Relationship, Inhibition Mechanism, Metabolism, and In Vivo Studies

Quantum Chemical-Based Protocol for the Rational Design of Covalent Inhibitors

Multiomics data integration unveils core transcriptional regulatory networks governing cell-type identity

Picomolar FKBP inhibitors enabled by a single water-displacing methyl group in bicyclic [4.3.1] aza-amides

Author Correction: Senescence atlas reveals an aged-like inflamed niche that blunts muscle regeneration

Warhead Reactivity Limits the Speed of Inhibition of the Cysteine Protease Rhodesain

Structural Determinants for the Mode of Action of Imidazopyridine DS2 at δ‑Containing γ‑Aminobutyric Acid Type A Receptors

Abstract 3005: Comprehensive profile of platelet derived growth factor receptor alpha (PDGFRA) mutations in gastrointestinal stromal tumors

Predictive factors for the IOP reduction in phacocanaloplasty with suprachoroidal drainage

Dipeptidyl Nitroalkenes as Potent Reversible Inhibitors of Cysteine Proteases Rhodesain and Cruzain

mTNF reverse signalling induced by TNF[alpha] antagonists involves a GDF-1 dependent pathway: implications for Crohn's disease

A Computational Modeling Approach Predicts Interaction of the Antifungal Protein AFP from italic toggle="yes">Aspergillus giganteus /italic> with Fungal Membranes via Its γ-Core Motif

Characterization and Function of the First Antibiotic Isolated from a Vent Organism: The Extremophile Metazoan Alvinella pompejana: e95737

A novel horse {alpha}-defensin: gene transcription, recombinant expression and characterisation of the structure and function

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