Susanna Bodoy Salvans

Adjunct part-time

Scopus Author ID: 12806511400

Researcher ID: H-6883-2015

Knowledge area: Bioquímica i Biologia Molecular

Contact Information
Department of Biochemistry and Molecular Biomedicine
C/Baldiri Reixac, 10
934034700
sbodoy(a)ub.edu

Academic Training

Química . Universitat de Barcelona . 2002 . (Diploma / Degree / Activities)

Bioquímica . Universitat de Barcelona . 2002 . (Diploma / Degree / Activities)

Biomedicina . Universitat de Barcelona . 27/06/2008 . (Ph.D.)

Projects

Transportadores heteroméricos de aminoácidos: Estructura, genomica funcional y fisiopatologia (cistinuria y lisinuria con intolerancia a proteinas) . 2006 - 2009 . Ref.MEC. BFU2006-14600-C02-01 . Ministerio de Educación y Ciencia . PI: Manuel Palacín Prieto

Transportadores heteroméricos de aminoácidos: estructura, genómica funcional y fisiopatología . 2003 - 2006 . Ref.SAF2003-08940-C20-01 . Ministerio de Ciencia y Tecnología . PI: Manuel Palacín Prieto

Transportadores heteroméricos de aminoácidos: estructura, genómica funcional y fisiopatología . 2004 - 2007 . Ref.EC.LSH2002-2.1.1-7. . Unió Europea . PI: Manuel Palacín Prieto

Transportadores heteroméricos de aminoácidos:estudios estructurales . 2006 - 2009 . Ref.BFU2006-14600-C02-01/BMC . Ministerio de Educación y Ciencia . PI: Manuel Palacin Prieto

Mecanismos de patología de los transportadores de aminoácidos HAT: modelos in vivo, celulares y estructurales (HAT-DISEASE) . 2019 - 2021 . Ministerio de Ciencia, Innovación y Universidades . PI: Manuel Palacin

Journal Publications

Bodoy, S.; Martín, L.; Zorzano, A.; Palacín, M.; Estévez, R.; Bertran, J. (2005). Identification of LAT4, a novel amino acid transporter with system L activity. Journal of Biological Chemistry, 280(12), pp. 12002 - 12011 . Institutional Repository . ISSN: 0021-9258

Bodoy S, Sotillo F, Espino-Guarch M, Sperandeo MP, Ormazabal A, Zorzano A, Sebastio G, Artuch R, Palacín M. (2019). Inducible Slc7a7 Knockout Mouse Model Recapitulates Lysinuric Protein Intolerance Disease. International Journal of Molecular Sciences, 20(21), pp. 1 - 15 . Institutional Repository . ISSN: 1661-6596

Espino Gaurch, M.; Font-Llitjós, M.; Murillo-Cuesta, S.; Errasti-Murugarren, E.; Celaya, AM.; Girotto, G.; Vuckovic, D.; Mezzavilla, M.; Vilches, C.; Bodoy, S.; Sahún, I.; González, L.; Prat, E.; Zorzano, A.; Dierssen, M.; Varela-Nieto, I.; Gasparini, P.; Palacín, M.; Nunes, V. (2018). Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in Age-Related Hearing Loss. eLife(7), p. e3151 . Institutional Repository . ISSN: 2050-084X

Vilches, C.; Boiadjieva-Knöpfel, E.; Bodoy, S.; Camargo, S.; López de Heredia, M.; Prat, E.; Ormazabal, A.; Artuch, R.; Zorzano, A.; Verrey, F*.; Nunes, V*.; Palacín, M* (corresponding authors, leadership). (2018). Cooperation of antiporter LAT2/CD98hc with uniporter TAT1 for renal reabsorption of neutral amino acids. Journal of the American Society of Nephrology . https://doi.org/10.1681/ASN.2017111205 . ISSN: 1046-6673

Nagamori, S.; Wiriyasermkul, P.; Guarch, ME.; Okuyama, H.; Nakagomi, S.; Tadagaki,K.; Nishinaka, Y.; Bodoy, S.; Takafuji, K.; Okuda, S.; Kurokawa, J.; Ohgaki, R.; Nunes, V.; Palacín, M.; Kanai, Y. (2016). Novel cystine transporter in renal proximal tubule identified as a missing partner of cystinuria-related plasma membrane protein rBAT/SLC3A1. Proceedings of the National Academy of Sciences of the United States of America - PNAS, 113(3), pp. 775 - 780 . https://doi.org/10.1073/pnas.1519959113 . ISSN: 0027-8424

Ristic, Z.; Camargo, S. M.; Romeo, E.; Bodoy, S.; Bertran, J.; Palacin, M.; Makrides, V.; Furrer, E. M.; Verrey, F. (2006). Neutral amino acid transport mediated by ortholog of imino acid transporter SIT1/SLC6A20 in opossum kidney cells. American Journal of Physiology, 290(4), pp. F880 - F887 . ISSN: 0002-9513

García Cazorla, A.; Oyarzabal, A.; Fort, J.; Robles, C.; Castejón, E.; Ruiz-Sala, P.; Bodoy, S.; Merinero, B.; López-Sala, A.; Dopazo, J.; Nunes, V.; Ugarte, M.; Artuch, R.; Palacín, M.; Rodríguez Pombo, P. (2014). Two novel mutations in the BCKDK gene (branched-chain keto-acid dehydrogenase kinase) are responsible of a neurobehavioral deficit in two paediatric unrelated patients. Human Mutation, 35(4), pp. 470 - 477 . https://doi.org/10.1002/humu.22513 . ISSN: 1059-7794

Bodoy S;Fotiadis D; Stoeger C; Kanai Y; Palacín M*. (2013). The small SLC43 family: facilitator system l amino acid transporters and the orphan EEG1. Molecular Aspects of Medicine, 34(2-3), pp. 638 - 645 . ISSN: 0098-2997