Antoine Guerin

Sydney, NSW, Australia

Last Updated: 09/26/2026

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Found 24 publications

Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Journal: medRxiv : the preprint server for health sciences

Published: August 01, 2026

Biologically inspired solutions to micro- and nanoplastic filtration in wastewater treatment plants.

Biologically inspired solutions to micro- and nanoplastic filtration in wastewater treatment plants.

Journal: Bioinspiration & biomimetics

Published: May 22, 2026

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Journal: The Journal of experimental medicine

Published: October 01, 2025

Automatic target volume segmentation for offline adaptive head-and-neck radiotherapy.

Automatic target volume segmentation for offline adaptive head-and-neck radiotherapy.

Journal: Journal of applied clinical medical physics

Published: August 25, 2025

Expanded T cell clones with lymphoma driver somatic mutations accumulate in refractory celiac disease.

Expanded T cell clones with lymphoma driver somatic mutations accumulate in refractory celiac disease.

Journal: Science translational medicine

Published: May 14, 2025

Functional validation of a novel STAT3 'variant of unknown significance' identifies a new case of STAT3 GOF syndrome and reveals broad immune cell defects.

Functional validation of a novel STAT3 'variant of unknown significance' identifies a new case of STAT3 GOF syndrome and reveals broad immune cell defects.

Journal: Clinical and experimental immunology

Published: October 21, 2024

Correction to: A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries.

Correction to: A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries.

Journal: Journal of clinical immunology

Published: September 19, 2024

A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries.

A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries.

Journal: Journal of clinical immunology

Published: March 21, 2024

FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice.

FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice.

Journal: Cell

Published: July 26, 2023

Helper T cell immunity in humans with inherited CD4 deficiency.

Helper T cell immunity in humans with inherited CD4 deficiency.

Journal: The Journal of experimental medicine

Published: June 19, 2023

Guiding Breathing at the Resonance Frequency with Haptic Sensors Potentiates Cardiac Coherence.

Guiding Breathing at the Resonance Frequency with Haptic Sensors Potentiates Cardiac Coherence.

Journal: Sensors (Basel, Switzerland)

Published: March 14, 2023

The ups and downs of STAT3 function: too much, too little and human immune dysregulation.

The ups and downs of STAT3 function: too much, too little and human immune dysregulation.

Journal: Clinical and experimental immunology

Published: October 07, 2022

Showing 1-12 of 24

Last Updated: 09/26/2026