Prigione Alessandro

Heinrich Heine University Düsseldorf

Germany

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Articles (15)

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2024

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2024

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2024

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2024

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2021

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2021

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2021

Collaborators (9)

Valeria Tiranti

Associate Professor

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Heidi Olzscha

University of Oxford

UNITED KINGDOM

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Vera Zywitza

Max Delbrück Centrum für Molekulare Medizin Berlin Buch

GERMANY

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Andreas Kurtz

Head

GERMANY

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Marie-Thérèse Henke

Charité - Universitätsmedizin Berlin

GERMANY

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Michela Di Virgilio

Professor (W1)

Charité - Universitätsmedizin Berlin

GERMANY

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Christian Hiepen

Substitute Professor for Biology

South Westphalia University of Applied Sciences

GERMANY

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Carlo Viscomi

University of Padova

ITALY

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Andrea Rossi

Group Leader

IUF - Leibniz-Institut für umwelt- medizinische Forschung gGmbH

GERMANY

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Prigione Alessandro

Research Interests

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Articles (15)

A Standardized Nomenclature Design for Systematic Referencing and Identification of Animal Cellular Material

Disease models of Leigh syndrome: From yeast to organoids

Reassessment of marker genes in human induced pluripotent stem cells for enhanced quality control

Mutant huntingtin impairs neurodevelopment in human brain organoids through CHCHD2-mediated neurometabolic failure.

Balancing neuronal activity to fight neurodevelopmental disorders

Modeling mitochondrial DNA diseases: from base editing to pluripotent stem‐cell‐derived organoids

How to mitigate neurological and cardiac decompensation in Leigh syndrome: Can nicotinamide riboside be an answer?

Mitochondria in Neurogenesis: Implications for Mitochondrial Diseases

Corrigendum to: Complete suppression of Htt fibrilization and disaggregation of Htt fibrils by a trimeric chaperone complex (The EMBO Journal, (2018), 37, 2, (282-299), 10.15252/embj.201797212)

Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome

Generation of human brain organoids for mitochondrial disease modeling

Generation of human iPSC-derived neural progenitor cells (NPCs) as drug discovery model for neurological and mitochondrial disorders

Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability

Stem cell research moving forward

TLR4 Associated Signaling Disrupters as a New Means to Overcome HERV-W Envelope-Mediated Myelination Deficits

Collaborators (9)

Valeria Tiranti

Heidi Olzscha

Vera Zywitza

Andreas Kurtz

Marie-Thérèse Henke

Michela Di Virgilio

Christian Hiepen

Carlo Viscomi

Andrea Rossi

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