C. Vives-Bauzá

发表

PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome: A Genome-Wide Meta-Analysis

X. Estivill, S. Kittner, Carlos Cruchaga, 2019, Circulation research.

Edinburgh Research Explorer PATJ Low Frequency Variants Are Associated with Worse Ischemic Stroke Functional Outcome: A Genome-Wide Meta-Analysis

S. Kittner, A. Lindgren, J. Martí-Fàbregas, 2018 .

Edinburgh Research Explorer PATJ Low Frequency Variants Are Associated with Worse Ischemic Stroke Functional Outcome: A Genome-Wide Meta-Analysis

S. Kittner, A. Lindgren, J. Martí-Fàbregas, 2018 .

Assay of mitochondrial ATP synthesis in animal cells and tissues.

Lichuan Yang, G. Manfredi, C. Vives-Bauza, 2007, Methods in cell biology.

Stroke genetics informs drug discovery and risk prediction across ancestries

Sebastian M. Armasu, Laurent F. Thomas, J. Danesh, 2022, Nature.

Exercise intolerance resulting: from a muscle-restricted mutation in the mitochondrial tRNALeu(CUN) gene

J. Montoya, A. Solano, P. Briones, 2001, Annals of medicine.

Sequence analysis of the entire mitochondrial genome in Parkinson's disease.

M. Beal, Michael T. Lin, A. Andreu, 2002, Biochemical and biophysical research communications.

Validation of a clinical-genetics score to predict hemorrhagic transformations after rtPA.

Carlos Cruchaga, J. Arenillas, C. Molina, 2019, Neurology.

Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 Genes

K. Strauch, D. Heine-Suñer, G. Olmos, 2021, Frontiers in Genetics.

Novel Role of ATPase Subunit C Targeting Peptides Beyond Mitochondrial Protein Import

A. Andreu, G. Manfredi, C. Vives-Bauza, 2010, Molecular biology of the cell.

Mitophagy: the latest problem for Parkinson's disease.

S. Przedborski, C. Vives-Bauza, C. Vives-Bauzá, 2011, Trends in molecular medicine.

Is there a pathogenic role for mitochondria in Parkinson's disease?

S. Przedborski, R. D. de Vries, C. Vives-Bauza, 2009, Parkinsonism & related disorders.

PINK1-dependent recruitment of Parkin to mitochondria in mitophagy

Ted M. Dawson, Valina L. Dawson, T. Dawson, 2009, Proceedings of the National Academy of Sciences.

The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain

K. Strauch, D. Heine-Suñer, G. Olmos, 2021, Scientific Reports.

Role of PATJ in stroke prognosis by modulating endothelial to mesenchymal transition through the Hippo/Notch/PI3K axis

C. Carrera, A. Rosell, R. Rabionet, 2024, Cell death discovery.

Genome-Wide Association Study of VKORC1 and CYP2C9 on acenocoumarol dose, stroke recurrence and intracranial haemorrhage in Spain

J. Arenillas, J. Montaner, J. Martí-Fàbregas, 2020, Scientific Reports.

A Polygenic Risk Score Based on a Cardioembolic Stroke Multitrait Analysis Improves a Clinical Prediction Model for This Stroke Subtype

Carlos Cruchaga, J. Arenillas, C. Molina, 2022, Frontiers in Cardiovascular Medicine.

Control of mitochondrial integrity in Parkinson's disease.

S. Przedborski, V. Jackson-Lewis, C. Vives-Bauza, 2010, Progress in brain research.

The Age Lipid A2E and Mitochondrial Dysfunction Synergistically Impair Phagocytosis by Retinal Pigment Epithelial Cells*

Junping Gao, G. Manfredi, M. Anand, 2008, Journal of Biological Chemistry.

Relapsing–Remitting Multiple Sclerosis Is Characterized by a T Follicular Cell Pro-Inflammatory Shift, Reverted by Dimethyl Fumarate Treatment

Vanessa Núñez, J. Ferrer, M. Massot, 2018, Front. Immunol..

Whole exome sequencing analysis reveals TRPV3 as a risk factor for cardioembolic stroke/subtitle

Carlos Cruchaga, J. Montaner, S. Beltran, 2016, Thrombosis and Haemostasis.

Multi-ancestry GWAS reveals excitotoxicity associated with outcome after ischaemic stroke.

Í. Lopes-Cendes, M. Barboza, J. Budde, 2022, Brain : a journal of neurology.

Exploring the genetic basis of stroke. Spanish stroke genetics consortium

J. Montaner, I. Férnandez-Cadenas, C. Carrera, 2014 .

Exploring the genetic basis of stroke. Spanish stroke genetics consortium.

C. Carrera, C. Vives-Bauza, Eva Giralt-Steinhauer, 2014, Neurologia.

PINK1 points Parkin to mitochondria

S. Przedborski, C. Vives-Bauza, C. Vives-Bauzá, 2010, Autophagy.

PINK1 Defect Causes Mitochondrial Dysfunction, Proteasomal Deficit and α-Synuclein Aggregation in Cell Culture Models of Parkinson's Disease

M. Beal, M. Kaplitt, Xin-Yun Huang, 2009, PloS one.

Anti-NMDAR antibodies in new-onset psychosis. Positive results in an HIV-infected patient

J. Haro, F. Canellas, C. Vives-Bauza, 2016, Brain, Behavior, and Immunity.

CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis

E. Génin, P. Yu-Wai-Man, J. Ricci, 2015, EMBO molecular medicine.

Mitochondrial DNA background modifies the bioenergetics of NARP/MILS ATP6 mutant cells.

G. Manfredi, C. Vives-Bauza, M. Davidson, 2010, Human molecular genetics.

MULTI-ANCESTRY GENETIC STUDY IN 5,876 PATIENTS IDENTIFIES AN ASSOCIATION BETWEEN EXCITOTOXIC GENES AND EARLY OUTCOMES AFTER ACUTE ISCHEMIC STROKE.

Í. Lopes-Cendes, M. Barboza, C. Cruchaga, 2020, medRxiv.

Enhanced ROS production and antioxidant defenses in cybrids harbouring mutations in mtDNA

E. García-Arumí, A. Andreu, G. Manfredi, 2006, Neuroscience Letters.

PINK1/Parkin direct mitochondria to autophagy

S. Przedborski, R. D. de Vries, C. Vives-Bauza, 2010, Autophagy.

Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene

J. Montoya, A. Solano, M. López-Pérez, 2003, Annals of neurology.

Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies

S. Dimauro, M. Mancuso, M. Filosto, 2003, Annals of neurology.

Measurements of the antioxidant enzyme activities of superoxide dismutase, catalase, and glutathione peroxidase.

E. García-Arumí, A. Starkov, C. Vives-Bauza, 2007, Methods in cell biology.