Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Jesús Purroy"'
Autor:
Kunjan R. Dave, Ami P. Raval, Jesús Purroy, Ilias G. Kirkinezos, Carlos T. Moraes, Walter G. Bradley, Miguel A. Pérez-Pinzón
Publikováno v:
Neurobiology of Disease, Vol 18, Iss 1, Pp 126-133 (2005)
Protein kinase C (PKC) was suggested to play a role in the pathology of amyotrophic lateral sclerosis (ALS) patients. Activation of PKC delta (δPKC) modulates mitochondrially induced apoptosis. The goal of the present study was to define whether δP
Externí odkaz:
https://doaj.org/article/4fe0b2119d044d27be734cb168c62a6a
Autor:
Jesús Purroy
LA INGENIERÍA GENÉTICA AL SERVICIO DE LA MEDICINA Hace ciento cincuenta años, Mendel dio a conocer los mecanismos de la genética. Desde entonces, la investigación sobre los genes y los rasgos hereditarios ha avanzado a un ritmo vertiginoso, espe
Autor:
Maria Calvo, Pierre-Yves Fortin, Carles Justicia, Angélica Salas-Perdomo, Franck Couillaud, Xavier de la Rosa, Tomàs Santalucía, Anna M. Planas, Jesús Purroy
Publikováno v:
European Journal of Nuclear Medicine and Molecular Imaging
European Journal of Nuclear Medicine and Molecular Imaging; Vol 40
Digital.CSIC. Repositorio Institucional del CSIC
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European Journal of Nuclear Medicine and Molecular Imaging; Vol 40
Digital.CSIC. Repositorio Institucional del CSIC
instname
El pdf del artículo es la versión post-print.-- et al.
Purpose: Stroke induces strong expression of the 72-kDa heat-shock protein (HSP-70) in the ischaemic brain, and neuronal expression of HSP-70 is associated with the ischaemic penumbra. The
Purpose: Stroke induces strong expression of the 72-kDa heat-shock protein (HSP-70) in the ischaemic brain, and neuronal expression of HSP-70 is associated with the ischaemic penumbra. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eec3edc3df311c39cfc414b56f02338
Autor:
Valeria Marigo, Giuseppe Borsani, Maria Teresa Bassi, Marta Pineda, Manuel Palacín, Marta Manzoni, Esperanza Fernández, Jesús Purroy, Mariona Font, Virginia Nunes, Antonio Zorzano, Rafael Martín del Río
Publikováno v:
Kidney International. 66:1453-1464
The amino acid transporter asc-1 is not involved in cystinuria. Background The human amino acid transporter asc-1 ( SLC7A10 ) exhibits substrate selectivity for small neutral amino acids, including cysteine, is expressed in kidney, is located close t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb98a7defd4f08043b51eebc7fde11ad
https://doi.org/10.1111/j.1523-1755.2004.00908.x
https://doi.org/10.1111/j.1523-1755.2004.00908.x
Autor:
Ercole Beccia, Adamo Pio d'Adamo, Paolo Gasparini, Virginia Nunes, Maite Jiménez-Vidal, Gianfranco Rizzoni, Manuel Palacín, Rosa Penza, Michele Gallucci, Leopoldo Zelante, Luigi Bisceglia, Ferran Rousaud, Jesús Purroy
Publikováno v:
Kidney International. 59:1250-1256
Cystinuria type I: Identification of eight new mutations inSLC3A1.BackgroundCystinuria is a heritable disorder of amino acid transport characterized by the defective transport of cystine and the dibasic amino acids through the brush border epithelial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18bde09b6a564f61e434c2b76164f78d
https://doi.org/10.1046/j.1523-1755.2001.0590041250.x
https://doi.org/10.1046/j.1523-1755.2001.0590041250.x
Publikováno v:
Human Mutation. 15:373-379
Cystinuria is an autosomal recessive aminoaciduria in which two clinical types have been described (type I and non-type I). Cystinuria type I is caused by mutations in SLC3A1, a gene located in 2p16 coding for an amino acid transporter named rBAT. Us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dac9077065427a9d5798739384e76674
https://doi.org/10.1002/(sici)1098-1004(200004)15:4<373::aid-humu10>3.0.co
https://doi.org/10.1002/(sici)1098-1004(200004)15:4<373::aid-humu10>3.0.co
Autor:
Jesús Purroy
Vivimos rodeados por los resultados de los adelantos científicos y tecnológicos, pero conocemos muy poco sobre el funcionamiento de la ciencia. Precisamente, Todo lo que hay que saber para saberlo todo aborda con rigor y amenidad estas cuestiones:
Autor:
Santiago Rojas, Vanessa Gómez, Maria J. Arranz, Deborah Pareto, Abraham Martín, Esther Verdaguer, Joan D. Gispert, Jesús Purroy, Jordi Llop, Anna M. Planas, Olga Millán, Ángel Chamorro
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
[11C]PK11195 is used in positron emission tomography (PET) studies for imaging brain inflammation in vivo as it binds to the peripheral-type benzodiazepine receptor (PBR) expressed by reactive glia and macrophages. However, features of the cellular r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a71a4b9baeebba7c706ec6ec334d7a15
http://hdl.handle.net/10261/89381
http://hdl.handle.net/10261/89381
Autor:
Nigel K. Spurr, Jesús Purroy
Publikováno v:
Human molecular genetics. 11(20)
The molecular mechanisms regulating bone remodelling are only partially understood. One of the controversial issues discussed during the past few years is the role that calcium signalling plays in this process and, in particular, in the functioning o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ed65a0b5d2e934c5c533cba662914fe
https://pubmed.ncbi.nlm.nih.gov/12351573
https://pubmed.ncbi.nlm.nih.gov/12351573
Autor:
Xavier Testar, Xavier Estivill, Luigi Bisceglia, Virginia Nunes, Jesús Purroy, Maria Julia Calonge, Manuel Palacín, Paolo Gasparini, Antonio Zorzano, Leopoldo Zelante
Publikováno v:
Genomics. 37(2)
Cystinuria is an autosomal recessive disorder of amino acid transport, manifesting as three phenotypes (I, II, and III). An amino acid transport gene, rBAT, is responsible for cystinuria. Mutation and linkage analyses have demonstrated the disease to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc91e9122abc38428f95c0acdef194ef
https://pubmed.ncbi.nlm.nih.gov/8921402
https://pubmed.ncbi.nlm.nih.gov/8921402