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Stem cell research moving forward

Stem cell research, 2021-08, Vol.55, p.102503-102503, Article 102503

Prigione, Alessandro

2021

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Mitochondria and the dynamic control of stem cell homeostasis

EMBO reports, 2018-05, Vol.19 (5), p.n/a

2018

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The Senescence‐Related Mitochondrial/Oxidative Stress Pathway is Repressed in Human Induced Pluripotent Stem Cells

Stem cells (Dayton, Ohio), 2010-04, Vol.28 (4), p.721-733

2010

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Human Stromal (Mesenchymal) Stem Cells from Bone Marrow, Adipose Tissue and Skin Exhibit Differences in Molecular Phenotype and Differentiation Potential

Stem cell reviews, 2013-02, Vol.9 (1), p.32-43

2013

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Brain energy rescue: an emerging therapeutic concept for neurodegenerative disorders of ageing

Nature reviews. Drug discovery, 2020-09, Vol.19 (9), p.609-633

2020

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The return of metabolism: biochemistry and physiology of the pentose phosphate pathway

Biological reviews of the Cambridge Philosophical Society, 2015-08, Vol.90 (3), p.927-963

2015

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Primate-specific endogenous retrovirus-driven transcription defines naive-like stem cells

Nature (London), 2014-12, Vol.516 (7531), p.405-409

2014

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Complete suppression of Htt fibrilization and disaggregation of Htt fibrils by a trimeric chaperone complex

The EMBO journal, 2018-01, Vol.37 (2), p.282-299

2018

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Mitochondrial Function in Pluripotent Stem Cells and Cellular Reprogramming

Gerontology (Basel), 2014-01, Vol.60 (2), p.174-182

2014

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

Clinical and translational discovery, 2022-09, Vol.2 (3), p.n/a

2022

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Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies

Pharmaceutics, 2020-11, Vol.12 (11), p.1083

2020

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Concise Review: Induced Pluripotent Stem Cell‐Based Drug Discovery for Mitochondrial Disease

Stem cells (Dayton, Ohio), 2017-07, Vol.35 (7), p.1655-1662

2017

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Isolation and cultivation of naive-like human pluripotent stem cells based on HERVH expression

Nature protocols, 2016-02, Vol.11 (2), p.327-346

2016

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Generation of two mother–child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations

Stem cell research, 2023-03, Vol.67, p.103030-103030, Article 103030

2023

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Comparative analysis of human embryonic stem cell and induced pluripotent stem cell-derived hepatocyte-like cells reveals current drawbacks and possible strategies for improved differentiation

Stem cells and development, 2011-07, Vol.20 (7), p.1259

2011

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Human Induced Pluripotent Stem Cells Harbor Homoplasmic and Heteroplasmic Mitochondrial DNA Mutations While Maintaining Human Embryonic Stem Cell–like Metabolic Reprogramming

Stem cells (Dayton, Ohio), 2011-09, Vol.29 (9), p.1338-1348

2011

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Activated microglia and neuroinflammation as a pathogenic mechanism in Leigh syndrome

Frontiers in neuroscience, 2023-01, Vol.16, p.1068498-1068498

2023

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Teriflunomide as a therapeutic means for myelin repair

Journal of neuroinflammation, 2023-01, Vol.20 (1), p.7-7, Article 7

2023

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Generation of an induced pluripotent stem cell line from a Huntington’s disease patient with a long HTT-PolyQ sequence

Stem cell research, 2023-04, Vol.68, p.103056-103056, Article 103056

2023

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The LARGE principle of cellular reprogramming: lost, acquired and retained gene expression in foreskin and amniotic fluid-derived human iPS cells

PloS one, 2010-10, Vol.5 (10), p.e13703-e13703

2010

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

Frontiers in cellular neuroscience, 2021-11, Vol.15, p.777542-777542

2021

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RNA-based generation of iPSCs from a boy carrying the mutation m.9185 T>C in the mitochondrial gene MT-ATP6 and from his healthy mother

Stem cell research, 2022-10, Vol.64, p.102920-102920, Article 102920

2022

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DRUG DISCOVERY OF MITOCHONDRIAL DISEASES USING PATIENT‑SPECIFIC BRAIN ORGANOIDS

Acta neurobiologiae experimentalis, 2022-01, Vol.82, p.XXI

Prigione, Alessandro

2022

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Stem cell research moving forward

Mitochondria and the dynamic control of stem cell homeostasis

The Senescence‐Related Mitochondrial/Oxidative Stress Pathway is Repressed in Human Induced Pluripotent Stem Cells

Human Stromal (Mesenchymal) Stem Cells from Bone Marrow, Adipose Tissue and Skin Exhibit Differences in Molecular Phenotype and Differentiation Potential

Brain energy rescue: an emerging therapeutic concept for neurodegenerative disorders of ageing

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

The return of metabolism: biochemistry and physiology of the pentose phosphate pathway

Primate-specific endogenous retrovirus-driven transcription defines naive-like stem cells

Complete suppression of Htt fibrilization and disaggregation of Htt fibrils by a trimeric chaperone complex

Mitochondrial Function in Pluripotent Stem Cells and Cellular Reprogramming

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

Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies

Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders

Concise Review: Induced Pluripotent Stem Cell‐Based Drug Discovery for Mitochondrial Disease

Isolation and cultivation of naive-like human pluripotent stem cells based on HERVH expression

Generation of two mother–child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations

Comparative analysis of human embryonic stem cell and induced pluripotent stem cell-derived hepatocyte-like cells reveals current drawbacks and possible strategies for improved differentiation

Human Induced Pluripotent Stem Cells Harbor Homoplasmic and Heteroplasmic Mitochondrial DNA Mutations While Maintaining Human Embryonic Stem Cell–like Metabolic Reprogramming

Activated microglia and neuroinflammation as a pathogenic mechanism in Leigh syndrome

Teriflunomide as a therapeutic means for myelin repair

Generation of an induced pluripotent stem cell line from a Huntington’s disease patient with a long HTT-PolyQ sequence

The LARGE principle of cellular reprogramming: lost, acquired and retained gene expression in foreskin and amniotic fluid-derived human iPS cells

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

RNA-based generation of iPSCs from a boy carrying the mutation m.9185 T>C in the mitochondrial gene MT-ATP6 and from his healthy mother

DRUG DISCOVERY OF MITOCHONDRIAL DISEASES USING PATIENT‑SPECIFIC BRAIN ORGANOIDS

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