List of works - Cristina Ugalde

Abeta accumulation in choroid plexus is associated with mitochondrial-induced apoptosis.

scientific article published on 5 October 2008

Altered Expression Ratio of Actin-Binding Gelsolin Isoforms Is a Novel Hallmark of Mitochondrial OXPHOS Dysfunction

scientific article published on 19 August 2020

Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency.

scientific article published on 31 May 2006

Bulk autophagy, but not mitophagy, is increased in cellular model of mitochondrial disease

scientific article published on 02 April 2014

COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation.

scientific article published on 17 August 2016

Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency.

scientific article published in August 2010

Complex I assembly: a puzzling problem.

scientific article published on April 2004

Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene.

scientific article

Cytoplasmic gelsolin increases mitochondrial activity and reduces Abeta burden in a mouse model of Alzheimer's disease.

scientific article published on 14 July 2009

Differential proteomic profiling unveils new molecular mechanisms associated with mitochondrial complex III deficiency.

scientific article

Gelsolin restores A beta-induced alterations in choroid plexus epithelium.

scientific article

Human COX7A2L Regulates Complex III Biogenesis and Promotes Supercomplex Organization Remodeling without Affecting Mitochondrial Bioenergetics

scientific article published on 01 November 2018

Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies.

scientific article published on 18 August 2004

Human mitochondrial complex I assembly is mediated by NDUFAF1.

scientific article

Identification of a proximal promoter region critical for the expression of the beta-F1-ATPase gene during Drosophila melanogaster development.

scientific article published in October 2001

Impact of the mitochondrial genetic background in complex III deficiency

scientific article

Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene ⬇️

scientific article published on November 1, 2003

Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch.

scientific article published on 19 March 2010

Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease.

scientific article published on 19 September 2008

Mitochondrial disorders due to nuclear OXPHOS gene defects.

scientific article published on January 2009

Mitochondrial respiratory chain dysfunction: implications in neurodegeneration.

scientific article published on 14 May 2012

Multiple pathways coordinate assembly of human mitochondrial complex IV and stabilization of respiratory supercomplexes

scientific article published on 08 June 2020

Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.

scientific article published on 22 September 2006

New perspectives on the assembly process of mitochondrial respiratory chain complex cytochrome c oxidase.

scientific article published in November 2002

Novel ATAD3A recessive mutation associated to fatal cerebellar hypoplasia with multiorgan involvement and mitochondrial structural abnormalities

scientific article published on 06 November 2019

Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report

scientific article published on 26 July 2020

Pathogenic mutations in the 5' untranslated region of BCS1L mRNA in mitochondrial complex III deficiency.

scientific article published on 21 April 2009

Respiratory chain enzyme deficiency induces mitochondrial location of actin-binding gelsolin to modulate the oligomerization of VDAC complexes and cell survival.

scientific article published on 18 April 2017

Respiratory chain supercomplexes: Structures, function and biogenesis.

scientific article

Respiratory supercomplexes act as a platform for complex III-mediated maturation of human mitochondrial complexes I and IV

scientific article published on 08 January 2020

X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy.

scientific article

List of works by Cristina Ugalde

Abeta accumulation in choroid plexus is associated with mitochondrial-induced apoptosis.

Altered Expression Ratio of Actin-Binding Gelsolin Isoforms Is a Novel Hallmark of Mitochondrial OXPHOS Dysfunction

Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency.

Bulk autophagy, but not mitophagy, is increased in cellular model of mitochondrial disease

COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation.

Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency.

Complex I assembly: a puzzling problem.

Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene.

Cytoplasmic gelsolin increases mitochondrial activity and reduces Abeta burden in a mouse model of Alzheimer's disease.

Differential proteomic profiling unveils new molecular mechanisms associated with mitochondrial complex III deficiency.

Gelsolin restores A beta-induced alterations in choroid plexus epithelium.

Human COX7A2L Regulates Complex III Biogenesis and Promotes Supercomplex Organization Remodeling without Affecting Mitochondrial Bioenergetics

Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies.

Human mitochondrial complex I assembly is mediated by NDUFAF1.

Identification of a proximal promoter region critical for the expression of the beta-F1-ATPase gene during Drosophila melanogaster development.

Impact of the mitochondrial genetic background in complex III deficiency

Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene ⬇️

Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch.

Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease.

Mitochondrial disorders due to nuclear OXPHOS gene defects.

Mitochondrial respiratory chain dysfunction: implications in neurodegeneration.

Multiple pathways coordinate assembly of human mitochondrial complex IV and stabilization of respiratory supercomplexes

Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.

New perspectives on the assembly process of mitochondrial respiratory chain complex cytochrome c oxidase.

Novel ATAD3A recessive mutation associated to fatal cerebellar hypoplasia with multiorgan involvement and mitochondrial structural abnormalities

Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report

Pathogenic mutations in the 5' untranslated region of BCS1L mRNA in mitochondrial complex III deficiency.

Respiratory chain enzyme deficiency induces mitochondrial location of actin-binding gelsolin to modulate the oligomerization of VDAC complexes and cell survival.

Respiratory chain supercomplexes: Structures, function and biogenesis.

Respiratory supercomplexes act as a platform for complex III-mediated maturation of human mitochondrial complexes I and IV

X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy.