M Melia - Concepedia

Author

M Melia

Also Known As

M J. Melia, M Jesús Melià, M Melia, M. J. Melià, M.J. Melia, Ma Jesús Melià, Maria J. Melià, Maria Jesús Melià, María Jesús Melià, Marı́a J. Meliá

Publications

642

Citations

H-Index

Concepts

All Affiliations

Vall d'Hebron Institut de Recerca Centre for Biomedical Network Research on Rare Diseases Universitat Autònoma de Barcelona Biomedical Research Networking Center on Neurodegenerative Diseases Instituto de Salud Carlos III

About

M Melia is an author at Vall d'Hebron Institut de Recerca specializing in medicine, genetics, and mitochondrial function.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	234
2	Cell Biology	3	3	104
3	Natural Sciences	2	2	49
4	Engineering	1	1	11
5	Cellular Physiology	1	1	70

M Melia

Publications

606

Citations

H-Index

Page 1

	Year	Citations
Prevalence of atherosclerotic renal artery stenosis in patients with atherosclerosis elsewhere. Jeffrey W. Olin, M Melia, Jess R. Young, PubMed	1990	331
Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanisms Céline Perier, Andreas Bender, Elena García‐Arumí, Brain Mitochondrial BiogenesisMitochondrial FunctionDopaminergic NeuronsGeneticsMitochondrial Medicine	2013	73
Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene M Melia, Akatsuki Kubota, Saida Ortolano, Brain Mutant GeneMendelian DisorderSkeletal MuscleGenetic DisorderGenetics	2013	70
Identification of Androgen-Regulated Genes in Mouse Kidney by Representational Difference Analysis and Random Arbitrarily Primed Polymerase Chain Reaction<sup>1</sup> M Melia, Nuria Bofill, Anna Meseguer Endocrinology	1998	41
Identification and biochemical characterization of the novel mutation m.<scp>8839G</scp>>C in the mitochondrial <i><scp>ATP6</scp></i> gene associated with <scp>NARP</scp> syndrome Albert Blanco‐Grau, I. Bonaventura‐Ibars, J Coll, Genes Brain & Behavior Mitochondrial BiogenesisMitochondrial FunctionGenetic DisorderGeneticsPhysiology	2013	31
Severe TK2 enzyme activity deficiency in patients with mild forms of myopathy Yolanda Cámara, Lidia Carreño‐Gago, Miguel A. Martı́n, Neurology GeneticsPathologyMolecular BiologyMitochondrial BiologyMitochondrial Myopathy	2015	26
Asymmetric Binding of Histone H1 Stabilizes MMTV Nucleosomes and the Interaction of Progesterone Receptor with the Exposed HRE Guillermo P. Vicent, M Melia, Miguel Beato Journal of Molecular Biology ChromatinSignal TransductionChromatin StructureProgesterone ReceptorChromatin Remodeling	2002	23
Identification of Androgen-Regulated Genes in Mouse Kidney by Representational Difference Analysis and Random Arbitrarily Primed Polymerase Chain Reaction M Melia Endocrinology EngineeringGeneticsRenal PathologyTranscriptomics TechnologyGene Characterization	1998	11

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