Maria B. Lioi

Potenza, Italy

Last Updated: 09/26/2026

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Found 22 publications

A case of Incontinentia Pigmenti associated with concurrent IKBKG/NEMO and MED13L mutations.

A case of Incontinentia Pigmenti associated with concurrent IKBKG/NEMO and MED13L mutations.

Journal: Frontiers in medicine

Published: February 27, 2026

GADD45β inhibits RIPK3-mediated NF-κB activation by interfering with NEMO-RIPK1-RIPK3 interactions.

GADD45β inhibits RIPK3-mediated NF-κB activation by interfering with NEMO-RIPK1-RIPK3 interactions.

Journal: Cell death discovery

Published: May 26, 2025

Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability.

Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability.

Journal: International journal of molecular sciences

Published: February 17, 2022

Radiofrequency Electromagnetic Field Exposure and Apoptosis: A Scoping Review of In Vitro Studies on Mammalian Cells.

Radiofrequency Electromagnetic Field Exposure and Apoptosis: A Scoping Review of In Vitro Studies on Mammalian Cells.

Journal: International journal of molecular sciences

Published: January 04, 2022

Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male.

Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male.

Journal: International journal of molecular sciences

Published: December 20, 2021

Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy.

Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy.

Journal: Human molecular genetics

Published: October 30, 2021

Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures.

Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures.

Journal: Genes

Published: June 18, 2021

Histone demethylase KDM5C is a SAHA-sensitive central hub at the crossroads of transcriptional axes involved in multiple neurodevelopmental disorders.

Histone demethylase KDM5C is a SAHA-sensitive central hub at the crossroads of transcriptional axes involved in multiple neurodevelopmental disorders.

Journal: Human molecular genetics

Published: August 19, 2019

Treatment with 3-Aminobenzamide Negates the Radiofrequency-Induced Adaptive Response in Two Cell Models.

Treatment with 3-Aminobenzamide Negates the Radiofrequency-Induced Adaptive Response in Two Cell Models.

Journal: International journal of environmental research and public health

Published: July 17, 2019

Clinical utility gene card: for incontinentia pigmenti.

Clinical utility gene card: for incontinentia pigmenti.

Journal: European journal of human genetics : EJHG

Published: February 05, 2019

The Incontinentia Pigmenti Genetic Biobank: study design and cohort profile to facilitate research into a rare disease worldwide.

The Incontinentia Pigmenti Genetic Biobank: study design and cohort profile to facilitate research into a rare disease worldwide.

Journal: European journal of human genetics : EJHG

Published: November 07, 2018

EDA-ID and IP, two faces of the same coin: how the same IKBKG/NEMO mutation affecting the NF-κB pathway can cause immunodeficiency and/or inflammation.

EDA-ID and IP, two faces of the same coin: how the same IKBKG/NEMO mutation affecting the NF-κB pathway can cause immunodeficiency and/or inflammation.

Journal: International reviews of immunology

Published: August 14, 2015

Showing 1-12 of 22

Last Updated: 09/26/2026