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List of works by Adrián González-Quintana

25th Annual Computational Neuroscience Meeting: CNS-2016

scientific article

Different mitochondrial genetic defects exhibit the same protein signature of metabolism in skeletal muscle of PEO and MELAS patients: A role for oxidative stress

scientific article published on 20 August 2018

Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 update.

scientific article

In vivo evidence of mitochondrial dysfunction and altered redox homeostasis in a genetic mouse model of propionic acidemia: Implications for the pathophysiology of this disorder.

scientific article

Inhibition of c-jun N terminal kinase (JNK) improves functional beta cell mass in human islets and leads to AKT and glycogen synthase kinase-3 (GSK-3) phosphorylation

scientific article published on 08 December 2007

Missense mutations have unexpected consequences: The McArdle disease paradigm

scientific article published on 26 July 2018

NetPyNE, a tool for data-driven multiscale modeling of brain circuits

scientific article published on 26 April 2019

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

scientific article published on 26 July 2020

Rapamycin impairs beta-cell proliferation in vivo.

scientific article published in March 2008

Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders.

scientific article published on 30 June 2016

Taking advantage of an old concept, "illegitimate transcription", for a proposed novel method of genetic diagnosis of McArdle disease.

scientific article published on 25 February 2016

[Modal failure analysis and effects in the detection of errors in the transport of samples to the clinical laboratory]

scientific article published on 13 April 2014

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