Lista de obras - Petr Pecina - Dominio Público Uruguay

A suggested role for mitochondria in Noonan syndrome.

artículo científico publicado en 2009

Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6.

artículo científico publicado en 2016

Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations

artículo científico publicado en 2012

COX7AR is a Stress-inducible Mitochondrial COX Subunit that Promotes Breast Cancer Malignancy

artículo científico publicado en 2016

Cytochrome C is tyrosine 97 phosphorylated by neuroprotective insulin treatment

artículo científico publicado en 2013

Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathology

artículo científico publicado en 2012

Data on cytochrome c oxidase assembly in mice and human fibroblasts or tissues induced by SURF1 defect

artículo científico publicado en 2016

Decreased affinity for oxygen of cytochrome-c oxidase in Leigh syndrome caused by SURF1 mutations

artículo científico publicado en 2004

Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206.

artículo científico publicado en 2004

Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains

artículo científico publicado en 2007

Evaluation of basic mitochondrial functions using rat tissue homogenates

scientific article published on 02 June 2011

Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome

artículo científico publicado en 2003

High molecular weight forms of mammalian respiratory chain complex II

artículo científico publicado en 2013

Impaired mitochondrial energetic in patients harbouring SURF1 mutations is caused by uncoupling of cytochrome c oxidase

Inhibition of cytochrome c oxidase subunit 4 precursor processing by the hypoxia mimic cobalt chloride.

artículo científico publicado en 2006

Isolation of regulatory-competent, phosphorylated cytochrome C oxidase.

artículo científico publicado en 2009

Loss of COX4I1 Leads to Combined Respiratory Chain Deficiency and Impaired Mitochondrial Protein Synthesis

artículo científico publicado en 2021

Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy.

artículo científico publicado en 2011

Mitochondrial ATP synthasome: Expression and structural interaction of its components.

artículo científico publicado en 2015

Mitochondrial diseases and genetic defects of ATP synthase.

artículo científico publicado en 2006

Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry

artículo científico publicado en 2014

Phosphomimetic substitution of cytochrome C tyrosine 48 decreases respiration and binding to cardiolipin and abolishes ability to trigger downstream caspase activation

artículo científico publicado en 2010

Pleiotropic Effects of Biguanides on Mitochondrial Reactive Oxygen Species Production.

artículo científico publicado en 2017

Polyunsaturated fatty acids of marine origin upregulate mitochondrial biogenesis and induce beta-oxidation in white fat.

artículo científico publicado en 2005

Regulation of oxidative phosphorylation, the mitochondrial membrane potential, and their role in human disease.

artículo científico publicado en 2008

The multiple functions of cytochrome c and their regulation in life and death decisions of the mammalian cell: from respiration to apoptosis

artículo científico publicado en 2011

Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects.

artículo científico publicado en 2016

Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1

artículo científico publicado en 2005

Two components in pathogenic mechanism of mitochondrial ATPase deficiency: energy deprivation and ROS production.

artículo científico publicado en 2006

Lista de obras de Petr Pecina

A suggested role for mitochondria in Noonan syndrome.

Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6.

Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations

COX7AR is a Stress-inducible Mitochondrial COX Subunit that Promotes Breast Cancer Malignancy

Cytochrome C is tyrosine 97 phosphorylated by neuroprotective insulin treatment

Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathology

Data on cytochrome c oxidase assembly in mice and human fibroblasts or tissues induced by SURF1 defect

Decreased affinity for oxygen of cytochrome-c oxidase in Leigh syndrome caused by SURF1 mutations

Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206.

Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains

Evaluation of basic mitochondrial functions using rat tissue homogenates

Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome

High molecular weight forms of mammalian respiratory chain complex II

Impaired mitochondrial energetic in patients harbouring SURF1 mutations is caused by uncoupling of cytochrome c oxidase

Inhibition of cytochrome c oxidase subunit 4 precursor processing by the hypoxia mimic cobalt chloride.

Isolation of regulatory-competent, phosphorylated cytochrome C oxidase.

Loss of COX4I1 Leads to Combined Respiratory Chain Deficiency and Impaired Mitochondrial Protein Synthesis

Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy.

Mitochondrial ATP synthasome: Expression and structural interaction of its components.

Mitochondrial diseases and genetic defects of ATP synthase.

Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry

Phosphomimetic substitution of cytochrome C tyrosine 48 decreases respiration and binding to cardiolipin and abolishes ability to trigger downstream caspase activation

Pleiotropic Effects of Biguanides on Mitochondrial Reactive Oxygen Species Production.

Polyunsaturated fatty acids of marine origin upregulate mitochondrial biogenesis and induce beta-oxidation in white fat.

Regulation of oxidative phosphorylation, the mitochondrial membrane potential, and their role in human disease.

The multiple functions of cytochrome c and their regulation in life and death decisions of the mammalian cell: from respiration to apoptosis

Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects.

Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1

Two components in pathogenic mechanism of mitochondrial ATPase deficiency: energy deprivation and ROS production.