Louiza Potamiti - Genetic Mutations

Author Information

Louiza Potamiti is affiliated with the Department of Electron Microscopy/Molecular Pathology at The Cyprus Institute of Neurology and Genetics, located in Agios Dometios, Nicosia, Cyprus. Her research spans various aspects of molecular pathology and genetics, contributing to a better understanding of complex biological mechanisms and potential therapeutic interventions.

Research Contributions

Louiza Potamiti has made significant contributions to the field of genetics, particularly in the areas of environmental applications of nanoparticles, genetic diagnosis of diseases, and neuroinflammation. Key highlights of her work include elucidating the mechanisms of silver nanoparticle-induced inhibition of Escherichia coli, implementing multigene panel NGS diagnosis for primary ciliary dyskinesia in Cyprus, and investigating mitochondrial dynamics in a novel mouse model of CMT2A. Her research also delves into the neuroprotective effects of omega-3 fatty acids in optic atrophy, the role of Stbd1 in glycogen clustering during ER stress, and early molecular pathway alterations in Alport syndrome.

Aliases

Louiza Potamiti is also known by the aliases L. Potamiti and Louiza Potamiti.

Publication and Citation Metrics

Metric	Value
Number of Papers	25
Citation Count	91
h-index	6

Publications:

Immobilized Ag-nanoparticles (iNPs) for environmental applications: Elucidation of immobilized silver-induced inhibition mechanism of Escherichia coli

DOI: 10.1016/J.JECE.2021.106001

Year: 2021

Implementation of multigene panel NGS diagnosis in the national primary ciliary dyskinesia cohort of Cyprus: An island with a high disease prevalence

DOI: 10.1002/humu.24196

Year: 2021

Aberrant Mitochondrial Dynamics and Exacerbated Response to Neuroinflammation in a Novel Mouse Model of CMT2A

DOI: 10.3390/ijms222111569

Year: 2021

Omega-3 fatty acids promote neuroprotection, decreased apoptosis and reduced glial cell activation in the retina of a mouse model of OPA1-related autosomal dominant optic atrophy.

DOI: 10.1016/j.exer.2021.108901

Year: 2021

Stbd1 promotes glycogen clustering during endoplasmic reticulum stress and supports survival of mouse myoblasts.

DOI: 10.1242/jcs.244855

Year: 2020

Stbd1 promotes glycogen clustering during endoplasmic reticulum stress and supports survival of mouse myoblasts

DOI: 10.1242/jcs.244855

Year: 2020

Alport syndrome: Proteomic analysis identifies early molecular pathway alterations in Col4a3 knock out mice

DOI: 10.1111/nep.13764

Year: 2020

Case 4 cilia motility assessment

DOI: 10.21037/ASVIDE.2019.140

Year: 2019

Case 2 cilia motility assessment

DOI: 10.21037/ASVIDE.2019.138

Year: 2019

Case 1 cilia motility assessment

DOI: 10.21037/ASVIDE.2019.137

Year: 2019

What are the Implications for Family Planning?

How are Inherited Mutations Detected?

What are the Applications of Induced Mutations in Agriculture?

What are Techniques Used in Molecular Genetics?

What is Asbestos?

What is Polyploidy?

Are There Potential Treatments Targeting Genetic Mutations?

What are Genetic Disorders?

What is Heart Disease?

What Are the Treatment Options?

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