About: Josep M. Argilés

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Cancer Research Group, Department of Biochemistry and Molecular Biology, Faculty of Biology, University of Barcelona

Attributes	Values
rdf:type	Item
description	wetenschapper (nl) дослідник (uk) spanischer Biochemiker und Molekularbiologe (de) Cancer Research Group, Department of Biochemistry and Molecular Biology, Faculty of Biology, University of Barcelona (en)
rdfs:label	Josep M Argilés (nl) Josep M. Argilés (de) Josep M. Argilés (en) Josep M. Argilés (es) Josep M. Argilés (fr) Josep M. Argilés (it) Josep M. Argilés (pl)
skos:prefLabel	Josep M Argilés (nl) Josep M. Argilés (de) Josep M. Argilés (en) Josep M. Argilés (es) Josep M. Argilés (fr) Josep M. Argilés (it) Josep M. Argilés (pl)
name	Josep M Argilés (nl) Josep M. Argilés (de) Josep M. Argilés (en) Josep M. Argilés (es) Josep M. Argilés (fr) Josep M. Argilés (it) Josep M. Argilés (pl)
Scopus author ID	wds:Q72997866-D6B8B5BD-2610-4155-A290-0E717DB5E171
Scopus author ID	23468738600
given name	wds:Q72997866-7B439ED5-BC2D-4A04-BBA1-CCAB54F3B908
given name	Josep
instance of	wds:Q72997866-112A9189-DD11-4954-B383-56452AF694BE
instance of	Homo sapiens
skos:altLabel	Josep Ma. Argilés Huguet (de) Josep Maria Argilés Huguet (de)
IxTheo authority ID	wds:Q72997866-B6616252-FE52-4ED4-B19F-8BE59C190463
occupation	wds:Q72997866-6FA8072F-DFF8-4110-A49F-DF0D592CBCFB wds:Q72997866-c6a57c6d-4056-04d7-2a2f-b686b18184ce
University of Barcelona authority ID	wds:Q72997866-51516A2A-BE17-4BA2-A0E9-921E7EA09D74
University of Barc...D (former scheme)	wds:Q72997866-06343DDF-CDE5-4366-92E1-9A1B4970AF36
different from	wds:Q72997866-7206e406-4c62-7dcc-2a06-42d023094bfd
sex or gender	wds:Q72997866-A157DAE1-EAD4-4A79-92E1-BBECA4138A7C
VIAF ID	wds:Q72997866-29F44148-76CA-4DE4-9FD0-143D4B47F133
GND ID	wds:Q72997866-c1a34181-4a73-d53e-7267-11b2bbbdbfec
IdRef ID	wds:Q72997866-65E7D1C2-D848-465E-9FB8-40ACD72E4CDC
National Library of Spain ID	wds:Q72997866-A5CDC19F-3B9A-4910-B79D-09DCBB5030E4
CANTIC ID	wds:Q72997866-575F4BEF-4B44-454C-9678-107B7C9AE7CC
GND ID	https://d-nb.info/gnd/1302743821
IdRef ID	http://www.idref.fr/066851025/id
National Library of Spain ID	http://datos.bne.es/resource/XX1022613
IxTheo authority ID	061966746
occupation	molecular biologist biochemist
University of Barcelona authority ID	981058523470206706
University of Barc...D (former scheme)	a1031846
different from	Josep Maria Argilés Bosch
sex or gender	male
GND ID	1302743821
IdRef ID	066851025
National Library of Spain ID	XX1022613
CANTIC ID	981058523470206706
ORCID iD	wds:Q72997866-5B787FAB-240E-4A50-A026-1E1BE9C4465D
ORCID iD	https://orcid.org/0000-0003-4683-5428
ORCID iD	0000-0003-4683-5428
ResearcherID	wds:Q72997866-6EF536A9-006A-465D-B06A-D8AAB9D3963E
ResearcherID	L-5741-2014
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q72997866
is author of	Roles of skeletal muscle and peroxisome proliferator-activated receptors in the development and treatment of obesity. Consensus definition of sarcopenia, cachexia and pre-cachexia: joint document elaborated by Special Interest Groups (SIG) "cachexia-anorexia in chronic wasting diseases" and "nutrition in geriatrics" Direct effects of doxorubicin on skeletal muscle contribute to fatigue. Formoterol treatment downregulates the myostatin system in skeletal muscle of cachectic tumour-bearing rats Inhibition of xanthine oxidase reduces wasting and improves outcome in a rat model of cancer cachexia. Sarcopenia with limited mobility: an international consensus Overexpression of interleukin-15 induces skeletal muscle hypertrophy in vitro: implications for treatment of muscle wasting disorders. Cachexia: a problem of energetic inefficiency. Cross-talk between skeletal muscle and adipose tissue: a link with obesity? Nuclear magnetic resonance in conjunction with functional genomics suggests mitochondrial dysfunction in a murine model of cancer cachexia Muscle wasting in cancer: the role of mitochondria. Skeletal muscle mitochondrial uncoupling in a murine cancer cachexia model Resveratrol does not ameliorate muscle wasting in different types of cancer cachexia models Interleukin-15 increases glucose uptake in skeletal muscle. An antidiabetogenic effect of the cytokine. Combined approach to counteract experimental cancer cachexia: eicosapentaenoic acid and training exercise Cancer-associated malnutrition. The role of cytokines in cancer cachexia Beneficial immune modulatory effects of a specific nutritional combination in a murine model for cancer cachexia. Effects of Eicosapentaenoic Acid (EPA) Treatment on Insulin Sensitivity in an Animal Model of Diabetes: Improvement of the Inflammatory Status Anticachectic effects of formoterol: a drug for potential treatment of muscle wasting. The potential of ghrelin in the treatment of cancer cachexia. Novel approaches to the treatment of cachexia. Mediators involved in the cancer anorexia-cachexia syndrome: past, present, and future. Cancer cachexia: understanding the molecular basis. Training depletes muscle glutathione in patients with chronic obstructive pulmonary disease and low body mass index Effects of IL-15 on rat brown adipose tissue: uncoupling proteins and PPARs Redox balance and carbonylated proteins in limb and heart muscles of cachectic rats. Nonmuscle Tissues Contribution to Cancer Cachexia Myostatin blockage using actRIIB antagonism in mice bearing the Lewis lung carcinoma results in the improvement of muscle wasting and physical performance. Mechanisms and treatment of cancer cachexia. Dose-dependent effects of leucine supplementation on preservation of muscle mass in cancer cachectic mice. Request for regulatory guidance for cancer cachexia intervention trials. Activation of UCPs gene expression in skeletal muscle can be independent on both circulating fatty acids and food intake. Involvement of ROS in a model of mouse cancer cachexia. l-Carnitine: An adequate supplement for a multi-targeted anti-wasting therapy in cancer

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