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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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Structure-Activity Predictions From Computational Mining of Protein Databases to Assist Modular Design of Antimicrobial Peptides

Frontiers in microbiology, 2022-04, Vol.13, p.812903-812903

2022

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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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Aspergillus niger as a cell factory for the production of pyomelanin, a molecule with UV-C radiation shielding activity

Frontiers in microbiology, 2023-07, Vol.14, p.1233740-1233740

2023

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Prediction of Chromatin Accessibility in Gene-Regulatory Regions from Transcriptomics Data

Scientific reports, 2017-07, Vol.7 (1), p.4660-10, Article 4660

2017

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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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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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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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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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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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Structure–Function Evaluation of Imidazopyridine Derivatives Selective for δ‑Subunit-Containing γ‑Aminobutyric Acid Type A (GABAA) Receptors

Journal of medicinal chemistry, 2018-03, Vol.61 (5), p.1951-1968

2018

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

Structure-Activity Predictions From Computational Mining of Protein Databases to Assist Modular Design of Antimicrobial Peptides

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?

Aspergillus niger as a cell factory for the production of pyomelanin, a molecule with UV-C radiation shielding activity

Prediction of Chromatin Accessibility in Gene-Regulatory Regions from Transcriptomics Data

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

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

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

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

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

Structure–Function Evaluation of Imidazopyridine Derivatives Selective for δ‑Subunit-Containing γ‑Aminobutyric Acid Type A (GABAA) Receptors

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

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