Lista de obras - Luisa Iommarini - Dominio Público Uruguay

A Humanized Bone Niche Model Reveals Bone Tissue Preservation Upon Targeting Mitochondrial Complex I in Pseudo-Orthotopic Osteosarcoma

scientific article published on 11 December 2019

A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16.

artículo científico publicado en 2011

A comprehensive characterization of mitochondrial DNA mutations in glioblastoma multiforme

artículo científico publicado en 2015

A mutation threshold distinguishes the antitumorigenic effects of the mitochondrial gene MTND1, an oncojanus function.

artículo científico publicado en 2011

A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance

artículo científico publicado en 2014

A unique combination of rare mitochondrial ribosomal RNA variants affects the kinetics of complex I assembly

artículo científico publicado en 2016

An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells

artículo científico publicado en 2009

Analysis of the mitochondrial proteome of cybrid cells harbouring a truncative mitochondrial DNA mutation in respiratory complex I.

artículo científico publicado en 2014

Association of optic disc size with development and prognosis of Leber's hereditary optic neuropathy.

artículo científico publicado en 2008

Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways

artículo científico publicado en 2015

Complex I impairment in mitochondrial diseases and cancer: parallel roads leading to different outcomes

artículo científico publicado en 2012

Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions

scientific article published on 14 December 2012

Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment

artículo científico publicado en 2013

Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.

artículo científico publicado en 2007

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy

artículo científico publicado en 2013

Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α.

artículo científico publicado en 2013

Genome-wide expression profiling and functional characterization of SCA28 lymphoblastoid cell lines reveal impairment in cell growth and activation of apoptotic pathways

artículo científico publicado en 2013

Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases.

artículo científico publicado en 2018

Inducing cancer indolence by targeting mitochondrial Complex I is potentiated by blocking macrophage-mediated adaptive responses

article

Mild phenotypes and proper supercomplex assembly in human cells carrying the homoplasmic m.15557G > A mutation in cytochrome b gene

artículo científico publicado en 2017

Mitochondrial Diseases Part I: mouse models of OXPHOS deficiencies caused by defects in respiratory complex subunits or assembly factors

artículo científico publicado en 2015

Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function

artículo científico publicado en 2015

Mitochondrial Diseases Part III: Therapeutic interventions in mouse models of OXPHOS deficiencies

artículo científico publicado en 2015

Mitochondrial complex I and cell death: a semi-automatic shotgun model ⬇️

artículo científico publicado el 27 de octubre de 2011

Mitochondrial metabolism and energy sensing in tumor progression

artículo científico publicado en 2017

Mitochondrial optic neuropathies: how two genomes may kill the same cell type?

artículo científico publicado en 2007

Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer

artículo científico publicado en 2017

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

artículo científico publicado en 2008

PGC-1alpha/beta induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders.

artículo científico publicado en 2009

Packaging and transfer of mitochondrial DNA via exosomes regulate escape from dormancy in hormonal therapy-resistant breast cancer

artículo científico publicado en 2017

Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy

artículo científico publicado en 2018

Platinum-induced mitochondrial DNA mutations confer lower sensitivity to paclitaxel by impairing tubulin cytoskeletal organization.

artículo científico publicado en 2017

Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus.

artículo científico publicado en 2008

Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy

artículo científico publicado en 2012

Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies

Syndromic parkinsonism and dementia associated with OPA1 missense mutations

artículo científico publicado en 2015

Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy.

artículo científico publicado en 2015

Targeting respiratory complex I to prevent the Warburg effect

artículo científico publicado en 2015

The Oncojanus Paradigm of Respiratory Complex I.

artículo científico publicado en 2018

The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I.

artículo científico publicado en 2008

The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity

artículo científico publicado en 2009

The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes

artículo científico publicado en 2013

Tuning Cysteine Reactivity and Sulfenic Acid Stability by Protein Microenvironment in Glyceraldehyde-3-Phosphate Dehydrogenases of Arabidopsis thaliana

scientific article published on 01 February 2016

Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization

artículo científico publicado en 2018

Lista de obras de Luisa Iommarini

A Humanized Bone Niche Model Reveals Bone Tissue Preservation Upon Targeting Mitochondrial Complex I in Pseudo-Orthotopic Osteosarcoma

A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16.

A comprehensive characterization of mitochondrial DNA mutations in glioblastoma multiforme

A mutation threshold distinguishes the antitumorigenic effects of the mitochondrial gene MTND1, an oncojanus function.

A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance

A unique combination of rare mitochondrial ribosomal RNA variants affects the kinetics of complex I assembly

An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells

Analysis of the mitochondrial proteome of cybrid cells harbouring a truncative mitochondrial DNA mutation in respiratory complex I.

Association of optic disc size with development and prognosis of Leber's hereditary optic neuropathy.

Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways

Complex I impairment in mitochondrial diseases and cancer: parallel roads leading to different outcomes

Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions

Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment

Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy

Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α.

Genome-wide expression profiling and functional characterization of SCA28 lymphoblastoid cell lines reveal impairment in cell growth and activation of apoptotic pathways

Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases.

Inducing cancer indolence by targeting mitochondrial Complex I is potentiated by blocking macrophage-mediated adaptive responses

Mild phenotypes and proper supercomplex assembly in human cells carrying the homoplasmic m.15557G > A mutation in cytochrome b gene

Mitochondrial Diseases Part I: mouse models of OXPHOS deficiencies caused by defects in respiratory complex subunits or assembly factors

Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function

Mitochondrial Diseases Part III: Therapeutic interventions in mouse models of OXPHOS deficiencies

Mitochondrial complex I and cell death: a semi-automatic shotgun model ⬇️

Mitochondrial metabolism and energy sensing in tumor progression

Mitochondrial optic neuropathies: how two genomes may kill the same cell type?

Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

PGC-1alpha/beta induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders.

Packaging and transfer of mitochondrial DNA via exosomes regulate escape from dormancy in hormonal therapy-resistant breast cancer

Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy

Platinum-induced mitochondrial DNA mutations confer lower sensitivity to paclitaxel by impairing tubulin cytoskeletal organization.

Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus.

Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy

Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies

Syndromic parkinsonism and dementia associated with OPA1 missense mutations

Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy.

Targeting respiratory complex I to prevent the Warburg effect

The Oncojanus Paradigm of Respiratory Complex I.

The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I.

The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity

The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes

Tuning Cysteine Reactivity and Sulfenic Acid Stability by Protein Microenvironment in Glyceraldehyde-3-Phosphate Dehydrogenases of Arabidopsis thaliana

Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization