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

Journal of Proteomics

Volumn 113, Issue , 2015, Pages 38-56

  Marín Buera, Lorena ^a,b   García Bartolomé, Alberto ^a,b   Morán, María ^a,b   López Bernardo, Elia ^c,d   Cadenas, Susana ^c,d   Hidalgo, Beatriz ^a   Sánchez, Ricardo ^a   Seneca, Sara ^e   Arenas, Joaquín ^a,b   Martín, Miguel A ^a,b   Ugalde, Cristina ^a,b  

^a HOSPITAL UNIVERSITARIO 12 DE OCTUBRE   (Spain)

^b CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

^c UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

^d Instituto de Investigación Sanitaria del Hospital Universitario de La Princesa   (Spain)

^e Center of Medical Genetics and Primary Health Care   (Armenia)

Author keywords

2D DIGE; BCS1L; Complex III deficiency; Mitochondria; OXPHOS system; Respiratory chain

Indexed keywords

ARGININE; CYSTEINE; DJ 1 PROTEIN; GLUTAMINE; GLYCERALDEHYDE 3 PHOSPHATE DEHYDROGENASE; HISTIDINE; LYSINE; METHIONINE; PHENYLALANINE; SERINE; THREONINE; TRYPTOPHAN; TYROSINE; BCS1L PROTEIN, HUMAN; MITOCHONDRIAL PROTEIN; UBIQUINOL CYTOCHROME C REDUCTASE;

AMINO ACID SEQUENCE; ARTICLE; BCS1L GENE; CELLULAR DISTRIBUTION; CLINICAL ARTICLE; COMPLEX III DEFICIENCY; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; ENZYME ACTIVITY; GENE; GENE MUTATION; HUMAN; HUMAN CELL; ISOELECTRIC FOCUSING; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; NUCLEOTIDE SEQUENCE; OXYGEN CONSUMPTION; PROTEIN ANALYSIS; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN SYNTHESIS; PROTEIN TARGETING; PROTEOMICS; RESPIRATORY CHAIN; SIGNAL TRANSDUCTION; SKIN FIBROBLAST; TWO DIMENSIONAL DIFFERENCE GEL ELECTROPHORESIS; UPREGULATION; CELL CULTURE; CYTOSKELETON; DEFICIENCY; ENERGY METABOLISM; FEMALE; FIBROBLAST; GENE EXPRESSION REGULATION; GENETIC DISORDER; GENETICS; MALE; METABOLISM; MITOCHONDRION; PATHOLOGY;

CELLS, CULTURED; CYTOSKELETON; ELECTRON TRANSPORT COMPLEX III; ENERGY METABOLISM; FEMALE; FIBROBLASTS; GENE EXPRESSION REGULATION; GENETIC DISEASES, INBORN; HUMANS; MALE; MITOCHONDRIA; MITOCHONDRIAL PROTEINS; PROTEOMICS; SIGNAL TRANSDUCTION;

EID: 84907964806     PISSN: 18743919     EISSN: 18767737     Source Type: Journal    
DOI: 10.1016/j.jprot.2014.09.007     Document Type: Article

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