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High-throughput co-culture system for analysis of spatiotemporal cell-cell signaling

Biosensors & bioelectronics, 2023-04, Vol.225, p.115089-115089, Article 115089

2023

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NF-κB memory coordinates transcriptional responses to dynamic inflammatory stimuli

Cell reports (Cambridge), 2022-08, Vol.40 (7), p.111159-111159, Article 111159

2022

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Development of Masitinib Derivatives with Enhanced M[sup.pro] Ligand Efficiency and Reduced Cytotoxicity

Molecules (Basel, Switzerland), 2023-09, Vol.28 (18)

2023

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Development of Masitinib Derivatives with Enhanced M pro Ligand Efficiency and Reduced Cytotoxicity

Molecules (Basel, Switzerland), 2023-09, Vol.28 (18)

2023

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Discovery of New States of Immunomodulation for Vaccine Adjuvants via High Throughput Screening: Expanding Innate Responses to PRRs

ACS central science, 2023-03, Vol.9 (3), p.427-439

2023

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High-Throughput Co-Culture System for Analysis of Spatiotemporal Cell-Cell Signaling

SSRN Electronic Journal

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Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia

PLoS genetics, 2011-03, Vol.7 (3), p.e1002027-e1002027

2011

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Panel-Based Population Next-Generation Sequencing for Inherited Retinal Degenerations

Scientific reports, 2016-09, Vol.6 (1), p.33248-33248, Article 33248

2016

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Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS

Neuron (Cambridge, Mass.), 2014-10, Vol.84 (2), p.324-331

2014

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Detailed analysis of an enriched deep intronic ABCA4 variant in Irish Stargardt disease patients

Scientific reports, 2023-06, Vol.13 (1), p.9380-9380, Article 9380

2023

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Usher Syndrome on the Island of Ireland: A Genotype-Phenotype Review

Investigative ophthalmology & visual science, 2023-07, Vol.64 (10), p.23-23

2023

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Target 5000: a standardized all-Ireland pathway for the diagnosis and management of inherited retinal degenerations

Orphanet journal of rare diseases, 2021-05, Vol.16 (1), p.200-200, Article 200

2021

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Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasia

Journal of medical genetics, 2016-07, Vol.53 (7), p.457-464

2016

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Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases

Npj genomic medicine, 2021-11, Vol.6 (1), p.97-97, Article 97

2021

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A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration

British journal of ophthalmology, 2016-04, Vol.100 (4), p.495-500

2016

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Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

Science (American Association for the Advancement of Science), 2015-03, Vol.347 (6229), p.1436-1441

2015

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Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis

Science translational medicine, 2017-05, Vol.9 (388)

2017

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Audiologic Phenotype and Progression in Pediatric STRC‐Related Autosomal Recessive Hearing Loss

The Laryngoscope, 2021-12, Vol.131 (12), p.E2897-E2903

2021

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595 Unremitting Pro-inflammatory Cell Phenotypes and Macrophage Activity, Following Paediatric Burn Injury

Journal of burn care & research, 2024-04, Vol.45 (Supplement_1), p.180-181

2024

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Unremitting pro-inflammatory T-cell phenotypes, and macrophage activity, following paediatric burn injury

Clinical & translational immunology, 2024-01, Vol.13 (3), p.e1496-e1496

2024

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Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

Genetics in medicine, 2021-11, Vol.23 (11), p.2208-2212

2021

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Ophthalmic Manifestations of Vitamin A and D Deficiency in Two Autistic Teenagers: Case Reports and a Review of the Literature

Case reports in ophthalmology, 2015-01, Vol.6 (1), p.24-29

2015

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Identification of the thiophene ring of methapyrilene as a novel bioactivation-dependent hepatic toxicophore

The Journal of pharmacology and experimental therapeutics, 2008-08, Vol.326 (2), p.657-671

2008

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The Efficacy and Safety of Treating Acquired MET Resistance Through Combinations of Parent and MET Tyrosine Kinase Inhibitors in Patients With Metastatic Oncogene-Driven NSCLC

JTO clinical and research reports, 2024-02, Vol.5 (2), p.100637-100637, Article 100637

2024

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High-throughput co-culture system for analysis of spatiotemporal cell-cell signaling

NF-κB memory coordinates transcriptional responses to dynamic inflammatory stimuli

Development of Masitinib Derivatives with Enhanced M[sup.pro] Ligand Efficiency and Reduced Cytotoxicity

Development of Masitinib Derivatives with Enhanced M pro Ligand Efficiency and Reduced Cytotoxicity

Discovery of New States of Immunomodulation for Vaccine Adjuvants via High Throughput Screening: Expanding Innate Responses to PRRs

High-Throughput Co-Culture System for Analysis of Spatiotemporal Cell-Cell Signaling

Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia

Panel-Based Population Next-Generation Sequencing for Inherited Retinal Degenerations

Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS

Detailed analysis of an enriched deep intronic ABCA4 variant in Irish Stargardt disease patients

Usher Syndrome on the Island of Ireland: A Genotype-Phenotype Review

Target 5000: a standardized all-Ireland pathway for the diagnosis and management of inherited retinal degenerations

Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasia

Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases

A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis

Audiologic Phenotype and Progression in Pediatric STRC‐Related Autosomal Recessive Hearing Loss

595 Unremitting Pro-inflammatory Cell Phenotypes and Macrophage Activity, Following Paediatric Burn Injury

Unremitting pro-inflammatory T-cell phenotypes, and macrophage activity, following paediatric burn injury

Innate αβ T Cells Mediate Antitumor Immunity by Orchestrating Immunogenic Macrophage Programming

Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

Ophthalmic Manifestations of Vitamin A and D Deficiency in Two Autistic Teenagers: Case Reports and a Review of the Literature

Identification of the thiophene ring of methapyrilene as a novel bioactivation-dependent hepatic toxicophore

The Efficacy and Safety of Treating Acquired MET Resistance Through Combinations of Parent and MET Tyrosine Kinase Inhibitors in Patients With Metastatic Oncogene-Driven NSCLC

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