Zobrazeno 1 - 10
of 54
pro vyhledávání: '"de la Calle, Hermenegildo"'
Autor:
Santiago, Jose Luis, Martínez, Alfonso, Núñez, Concepción, de la Calle, Hermenegildo, Fernández-Arquero, Miguel, de la Concha, Emilio G., Urcelay, E.
Publikováno v:
In Human Immunology 2008 69(2):112-115
Autor:
Santiago, José L., Martínez, Alfonso, de La Calle, Hermenegildo, Fernández-Arquero, Miguel, de La Concha, Emilio G., Urcelay, Elena
Publikováno v:
In Human Immunology 2005 66(8):897-902
Autor:
Arroyo, Jaime, Badía, Xavier, de la Calle, Hermenegildo, Díez, Javier, Estmatjes, Enric, Fernández, Isabel, Filozof, Claudia, Franch, Josep, Gambús, Gemma, Gomis, Ramón, Navarro, Javier, de Pablos, Pedro
Publikováno v:
In Medicina Clinica 2005 125(5):166-172
Autor:
de la Calle, Hermenegildo, Costa, Àngels *, Díez-Espino, Javier, Franch, Josep, Goday, Albert
Publikováno v:
In Medicina Clinica 2003 120(12):446-450
Polymorphisms in the selenoprotein S gene: lack of association with autoimmune inflammatory diseases
Autor:
Díaz-Rubio Manuel, de la Calle Hermenegildo, Mendoza Juan, Lamas José, Márquez Ana, Varadé Jezabel, Santiago Jose, Martínez Alfonso, de la Concha Emilio G, Fernández-Gutiérrez Benjamín, Urcelay Elena
Publikováno v:
BMC Genomics, Vol 9, Iss 1, p 329 (2008)
Abstract Background Selenoprotein S (SelS) protects the functional integrity of the endoplasmic reticulum against the deleterious effects of metabolic stress. SEPS1/SelS polymorphisms have been involved in the increased release of pro-inflammatory cy
Externí odkaz:
https://doaj.org/article/17e281d741804d32bdfbd2da4b4fa250
Autor:
Figueredo M Ángeles, Fernández-Arquero Miguel, de la Calle Hermenegildo, Martínez Alfonso, Santiago Jose, de la Concha Emilio G, Urcelay Elena
Publikováno v:
BMC Medical Genetics, Vol 8, Iss 1, p 54 (2007)
Abstract Background The protein tyrosine phosphatase N22 gene (PTPN22) encodes a lymphoid-specific phosphatase (LYP) which is an important downregulator of T cell activation. A PTPN22 polymorphism, C1858T, was found associated with type 1 diabetes (T
Externí odkaz:
https://doaj.org/article/a355dd65e5fe4a3c9523604dcd4862c9
Autor:
Figueredo M Ángeles, Fernández-Arquero Miguel, de la Calle Hermenegildo, Martínez Alfonso, Santiago Jose, de la Concha Emilio G, Urcelay Elena
Publikováno v:
BMC Medical Genetics, Vol 7, Iss 1, p 54 (2006)
Abstract Background Type 1 diabetes (T1D) is a chronic, autoimmune and multifactorial disease characterized by abnormal metabolism of carbohydrate and fat. Diminished carnitine plasma levels have been previously reported in T1D patients and carnitine
Externí odkaz:
https://doaj.org/article/72fd05a6d1b046e68da8adedadafa129
Autor:
Ibarra José M, Méndez Julián, Martínez Alfonso, de la Calle Hermenegildo, Santiago José L, Urcelay Elena, Maluenda Carlos, Fernández-Arquero Miguel, de la Concha Emilio G
Publikováno v:
BMC Genomics, Vol 6, Iss 1, p 56 (2005)
Abstract Background The Major Histocompatibility Complex is the main genetic contributor to susceptibility to type 1 diabetes (T1D); genome-wide scans have consistently mapped increased predisposition to this region. The highest disease risk has been
Externí odkaz:
https://doaj.org/article/ed3ead23d1b04c4580e05f2268f8e7f0
Autor:
Espino-Paisán, Laura1 (AUTHOR), De La Calle, Hermenegildo2 (AUTHOR), Fernández-Arquero, Miguel1 (AUTHOR), Figueredo, M. Angeles1 (AUTHOR), De La Concha, Emilio G.1 (AUTHOR), Urcelay, Elena1 (AUTHOR), Santiago, Jose Luis1 (AUTHOR) jlsantial@gmail.com
Publikováno v:
Autoimmunity. Dec2011, Vol. 44 Issue 8, p624-630. 7p. 1 Diagram, 3 Charts.
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