Angelique Quartier

Illkirch-graffenstaden, France

Last Updated: 09/26/2026

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Found 15 publications

Correction: DYRK1A roles in human neural progenitors.

Correction: DYRK1A roles in human neural progenitors.

Journal: Frontiers in neuroscience

Published: January 12, 2026

Proteomic Signatures and Blood Adenosine Triphosphate Levels as Markers of Empagliflozin Efficacy in Type 2 Diabetes Mellitus and Heart Failure.

Proteomic Signatures and Blood Adenosine Triphosphate Levels as Markers of Empagliflozin Efficacy in Type 2 Diabetes Mellitus and Heart Failure.

Journal: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme

Published: November 17, 2025

Molecular Resonance Quantification and Label-Free Interactome Characterization of Total Proteome of Tumor Specimens Decipher Responder and Success Predictors in Colorectal Cancer Patients Treated With Panitumumab.

Molecular Resonance Quantification and Label-Free Interactome Characterization of Total Proteome of Tumor Specimens Decipher Responder and Success Predictors in Colorectal Cancer Patients Treated With Panitumumab.

Journal: Cancer medicine

Published: June 04, 2025

DYRK1A roles in human neural progenitors.

DYRK1A roles in human neural progenitors.

Journal: Frontiers in neuroscience

Published: November 23, 2024

Drug upgrade: A complete methodology from old drug to new chemical entities using Nematic Protein Organization Technique.

Drug upgrade: A complete methodology from old drug to new chemical entities using Nematic Protein Organization Technique.

Journal: Drug development research

Published: August 25, 2023

Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome.

Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome.

Journal: Molecular psychiatry

Published: January 12, 2023

Vutiglabridin Modulates Paraoxonase 1 and Ameliorates Diet-Induced Obesity in Hyperlipidemic Mice.

Vutiglabridin Modulates Paraoxonase 1 and Ameliorates Diet-Induced Obesity in Hyperlipidemic Mice.

Journal: Biomolecules

Published: December 01, 2022

De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder.

De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder.

Journal: American journal of human genetics

Published: December 30, 2019

Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment.

Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment.

Journal: Human mutation

Published: January 08, 2019

Sex-specific impact of prenatal androgens on social brain default mode subsystems.

Sex-specific impact of prenatal androgens on social brain default mode subsystems.

Journal: Molecular psychiatry

Published: March 08, 2018

Genes and Pathways Regulated by Androgens in Human Neural Cells, Potential Candidates for the Male Excess in Autism Spectrum Disorder.

Genes and Pathways Regulated by Androgens in Human Neural Cells, Potential Candidates for the Male Excess in Autism Spectrum Disorder.

Journal: Biological psychiatry

Published: July 14, 2017

Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome.

Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome.

Journal: European journal of human genetics : EJHG

Published: September 21, 2016

Showing 1-12 of 15

Last Updated: 09/26/2026