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BO-LSTM: classifying relations via long short-term memory networks along biomedical ontologies

BMC bioinformatics, 2019-01, Vol.20 (1), p.10-12, Article 10

2019

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Extracting microRNA-gene relations from biomedical literature using distant supervision

PloS one, 2017-03, Vol.12 (3), p.e0171929-e0171929

2017

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What Can RNA-Based Therapy Do for Monogenic Diseases?

Pharmaceutics, 2023-01, Vol.15 (1), p.260

2023

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High-Content siRNA Screen Reveals Global ENaC Regulators and Potential Cystic Fibrosis Therapy Targets

Cell, 2013-09, Vol.154 (6), p.1390-1400

2013

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Transcriptome meta-analysis reveals common differential and global gene expression profiles in cystic fibrosis and other respiratory disorders and identifies CFTR regulators

Genomics (San Diego, Calif.), 2015-11, Vol.106 (5), p.268-277

2015

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Enhanced Expression of Human Epididymis Protein 4 (HE4) Reflecting Pro-Inflammatory Status Is Regulated by CFTR in Cystic Fibrosis Bronchial Epithelial Cells

Frontiers in pharmacology, 2021-05, Vol.12, p.592184-592184

2021

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Integrity and Stability of PTC Bearing CFTR mRNA and Relevance to Future Modulator Therapies in Cystic Fibrosis

Genes, 2021-11, Vol.12 (11), p.1810

2021

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KLF4 Acts as a wt-CFTR Suppressor through an AKT-Mediated Pathway

Cells (Basel, Switzerland), 2020-07, Vol.9 (7), p.1607

2020

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Measurements of Functional Responses in Human Primary Lung Cells as a Basis for Personalized Therapy for Cystic Fibrosis

EBioMedicine, 2015-02, Vol.2 (2), p.147-153

2015

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Transcription-Dependent Spatial Arrangements of CFTR and Adjacent Genes in Human Cell Nuclei

The Journal of cell biology, 2004-09, Vol.166 (6), p.815-825

2004

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GRYFUN: a web application for GO term annotation visualization and analysis in protein sets

PloS one, 2015-03, Vol.10 (3), p.e0119631-e0119631

2015

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Generating a Tolerogenic Cell Therapy Knowledge Graph from Literature

Frontiers in immunology, 2017-11, Vol.8, p.1656-1656

2017

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Correction of a Cystic Fibrosis Splicing Mutation by Antisense Oligonucleotides

Human mutation, 2016-02, Vol.37 (2), p.209-215

2016

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Changes in transcriptome of native nasal epithelium expressing F508del-CFTR and intersecting data from comparable studies

Respiratory research, 2013-03, Vol.14 (1), p.38-38

2013

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The effect of premature termination codon mutations on CFTR mRNA abundance in human nasal epithelium and intestinal organoids: a basis for read‐through therapies in cystic fibrosis

Human mutation, 2019-03, Vol.40 (3), p.326-334, Article humu.23692

2019

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Mutant CFTR Drives TWIST1 mediated epithelial-mesenchymal transition

Cell death & disease, 2020-10, Vol.11 (10), p.920-920, Article 920

2020

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Organoids as a personalized medicine tool for ultra-rare mutations in cystic fibrosis: The case of S955P and 1717-2A>G

Biochimica et biophysica acta. Molecular basis of disease, 2020-11, Vol.1866 (11), p.165905-165905, Article 165905

2020

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Comparative ex vivo , in vitro and in silico analyses of a CFTR splicing mutation: Importance of functional studies to establish disease liability of mutations

Journal of cystic fibrosis, 2016-01, Vol.15 (1), p.21-33

2016

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TMEM16A chloride channel does not drive mucus production

Life science alliance, 2019-12, Vol.2 (6), p.e201900462

2019

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Functional coherence metrics in protein families

Journal of biomedical semantics, 2016-06, Vol.7 (1), p.41-41, Article 41

2016

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Methods for RNA extraction, cDNA preparation and analysis of CFTR transcripts

Journal of cystic fibrosis, 2004-08, Vol.3, p.11-15

2004

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Microarray mRNA expression profiling to study cystic fibrosis

Methods in molecular biology (Clifton, N.J.), 2011, Vol.742, p.193

2011

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Annotation extension through protein family annotation coherence metrics

Frontiers in genetics, 2013, Vol.4, p.201-201

2013

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Detection of cystic fibrosis related DNA targets using AC field focusing of magnetic labels and spin-valve sensors

IEEE transactions on magnetics, 2005-10, Vol.41 (10), p.4140-4142

2005

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BO-LSTM: classifying relations via long short-term memory networks along biomedical ontologies

Extracting microRNA-gene relations from biomedical literature using distant supervision

What Can RNA-Based Therapy Do for Monogenic Diseases?

High-Content siRNA Screen Reveals Global ENaC Regulators and Potential Cystic Fibrosis Therapy Targets

Transcriptome meta-analysis reveals common differential and global gene expression profiles in cystic fibrosis and other respiratory disorders and identifies CFTR regulators

Human Epididymis Protein 4: A Novel Serum Inflammatory Biomarker in Cystic Fibrosis

Enhanced Expression of Human Epididymis Protein 4 (HE4) Reflecting Pro-Inflammatory Status Is Regulated by CFTR in Cystic Fibrosis Bronchial Epithelial Cells

Integrity and Stability of PTC Bearing CFTR mRNA and Relevance to Future Modulator Therapies in Cystic Fibrosis

KLF4 Acts as a wt-CFTR Suppressor through an AKT-Mediated Pathway

Measurements of Functional Responses in Human Primary Lung Cells as a Basis for Personalized Therapy for Cystic Fibrosis

Transcription-Dependent Spatial Arrangements of CFTR and Adjacent Genes in Human Cell Nuclei

GRYFUN: a web application for GO term annotation visualization and analysis in protein sets

Generating a Tolerogenic Cell Therapy Knowledge Graph from Literature

Correction of a Cystic Fibrosis Splicing Mutation by Antisense Oligonucleotides

Changes in transcriptome of native nasal epithelium expressing F508del-CFTR and intersecting data from comparable studies

The effect of premature termination codon mutations on CFTR mRNA abundance in human nasal epithelium and intestinal organoids: a basis for read‐through therapies in cystic fibrosis

Mutant CFTR Drives TWIST1 mediated epithelial-mesenchymal transition

Organoids as a personalized medicine tool for ultra-rare mutations in cystic fibrosis: The case of S955P and 1717-2A>G

Comparative ex vivo , in vitro and in silico analyses of a CFTR splicing mutation: Importance of functional studies to establish disease liability of mutations

TMEM16A chloride channel does not drive mucus production

Functional coherence metrics in protein families

Methods for RNA extraction, cDNA preparation and analysis of CFTR transcripts

Microarray mRNA expression profiling to study cystic fibrosis

Annotation extension through protein family annotation coherence metrics

Detection of cystic fibrosis related DNA targets using AC field focusing of magnetic labels and spin-valve sensors

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