R. Viana

发表

A novel EPM2A mutation yields a slow progression form of Lafora disease

Matthew S. Gentry, M. Garcia-Gimeno, P. Sanz, 2018, Epilepsy Research.

Role of AMP-activated protein kinase in autophagy and proteasome function.

B. Viollet, E. Knecht, P. Sanz, 2008, Biochemical and biophysical research communications.

Ubiquitin conjugating enzyme E2-N and sequestosome-1 (p62) are components of the ubiquitination process mediated by the malin-laforin E3-ubiquitin ligase complex.

C. Romá-Mateo, P. Sanz, R. Viana, 2015, The international journal of biochemistry & cell biology.

Enzyme I and HPr from Lactobacillus casei: their role in sugar transport, carbon catabolite repression and inducer exclusion

V. Monedero, J. Deutscher, G. Pérez-Martínez, 2000, Molecular microbiology.

Two-hybrid analysis identifies PSMD11, a non-ATPase subunit of the proteasome, as a novel interaction partner of AMP-activated protein kinase.

P. Sanz, R. Viana, Daniel Moreno, 2009, The international journal of biochemistry & cell biology.

Homeostasis of the astrocytic glutamate transporter GLT-1 is altered in mouse models of Lafora disease.

A. Berthier, C. Muñoz-Ballester, P. Sanz, 2016, Biochimica et biophysica acta.

Endocytosis of the glutamate transporter 1 is regulated by laforin and malin: Implications in Lafora disease

C. Muñoz-Ballester, M. Garcia-Gimeno, P. Sanz, 2020, Glia.

Regulation of the autophagic PI3KC3 complex by laforin/malin E3-ubiquitin ligase, two proteins involved in Lafora disease.

E. Knecht, P. Sanz, R. Viana, 2019, Biochimica et biophysica acta. Molecular cell research.

Inflammation in Lafora Disease: Evolution with Disease Progression in Laforin and Malin Knock-out Mouse Models

I. Ferrer, P. Sanz, R. Viana, 2017, Molecular Neurobiology.

SARS-CoV-2 accessory proteins ORF3a and ORF7a modulate autophagic flux and Ca2+ homeostasis in yeast

M. Proft, Josep Fita-Torró, R. Viana, 2022, bioRxiv.

In vivo glutamate clearance defects in a mouse model of Lafora disease

F. Artigas, C. Muñoz-Ballester, R. Viana, 2019, Experimental Neurology.

Astrocytes: new players in progressive myoclonus epilepsy of Lafora type

Jose Bonet, M. Garcia-Gimeno, M. Heredia, 2018, Human molecular genetics.

The laforin/malin E3-ubiquitin ligase complex ubiquitinates pyruvate kinase M1/M2

P. Luján, P. Sanz, R. Viana, 2015, BMC Biochemistry.

TNF and IL6/Jak2 signaling pathways are the main contributors of the glia-derived neuroinflammation present in Lafora disease, a fatal form of progressive myoclonus epilepsy

T. Rubio, P. Sanz, R. Viana, 2023, Neurobiology of Disease.

An empirical pipeline for personalized diagnosis of Lafora disease mutations

J. Serratosa, C. V. Vander Kooi, Matthew S. Gentry, 2021, bioRxiv.

Tumor suppressor p27Kip1 undergoes endolysosomal degradation through its interaction with sorting nexin 6

P. Boya, V. Andrés, J. Fuster, 2010, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

The FASEB JournalResearch Communication Tumor suppressor p27 Kip1 undergoes endolysosomal degradation through its interaction with sorting nexin 6

P. Boya, V. Andrés, J. Cervera, 2010 .

Sorting Nexin 6 Enhances Lamin A Synthesis and Incorporation into the Nuclear Envelope

V. Andrés, Jaime Font de Mora, P. Molina-Sánchez, 2014, PloS one.

AMPK in Yeast: The SNF1 (Sucrose Non-fermenting 1) Protein Kinase Complex.

M. Garcia-Gimeno, P. Sanz, Pascual Sanz, 2016, Experientia supplementum.

Pleiotropic effects of lactate dehydrogenase inactivation in Lactobacillus casei.

V. Monedero, G. Pérez-Martínez, M. J. Yebra, 2005, Research in microbiology.

TOR kinase pathway and 14‐3‐3 proteins regulate glucose‐induced expression of HXT1, a yeast low‐affinity glucose transporter

P. Sanz, L. Tomás-Cobos, R. Viana, 2005, Yeast.

An Esterase Gene from Lactobacillus casei Cotranscribed with Genes Encoding a Phosphoenolpyruvate:Sugar Phosphotransferase System and Regulated by a LevR-Like Activator and σ54 Factor

V. Monedero, J. Deutscher, G. Pérez-Martínez, 2005, Journal of Molecular Microbiology and Biotechnology.

Inflammation in Lafora Disease: Evolution with Disease Progression in Laforin and Malin Knock-out Mouse Models

I. Ferrer, P. Sanz, R. Viana, 2016, Molecular Neurobiology.

Genetic Variants in CCNB1 Associated With Differential Gene Transcription and Risk of Coronary In-Stent Restenosis

G. Condorelli, R. D. de Winter, F. Chaves, 2014, Circulation. Cardiovascular genetics.

Abstracts of the 10th International Conference on Cachexia, Sarcopenia and Muscle Wasting, Rome, Italy, 8–10 December 2017 (Part 1)

J. Duarte, F. Voltarelli, A. Jordão, 2017, Journal of Cachexia, Sarcopenia and Muscle.

The glycolytic genes pfk and pyk from Lactobacillus casei are induced by sugars transported by the phosphoenolpyruvate:sugar phosphotransferase system and repressed by CcpA

V. Monedero, J. Deutscher, G. Pérez-Martínez, 2005, Archives of Microbiology.

A Conserved Sequence Immediately N-terminal to the Bateman Domains in AMP-activated Protein Kinase γ Subunits Is Required for the Interaction with the β Subunits*

B. Viollet, D. Hardie, D. Carling, 2007, Journal of Biological Chemistry.

AMPK Protein Interaction Analyses by Yeast Two-Hybrid.

M. Garcia-Gimeno, P. Sanz, R. Viana, 2018, Methods in molecular biology.

Oral immunization of mice with Lactococcus lactis expressing the rotavirus VP8* protein

V. Monedero, G. Pérez-Martínez, J. Buesa, 2011, Biotechnology Letters.

Selection of Single-Chain Antibodies against the VP8* Subunit of Rotavirus VP4 Outer Capsid Protein and Their Expression in Lactobacillus casei

V. Monedero, G. Pérez-Martínez, J. Buesa, 2004, Applied and Environmental Microbiology.