Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch-Schönlein purpura (IgA vasculitis).

López-Mejías, Raquel; Genre, Fernanda; Remuzgo-Martínez, Sara; Pérez, Belén Sevilla; Castañeda, Santos; Llorca, Javier; Ortego-Centeno, Norberto; Ubilla, Begoña; Mijares, Verónica; Pina, Trinitario; Calvo-Río, Vanesa; Palmou, Natalia; Miranda-Filloy, José A; Parejo, Antonio Navas; Argila, Diego; Sánchez-Pérez, Javier; Rubio, Esteban; Luque, Manuel León; Blanco-Madrigal, Juan María; Galíndez-Aguirregoikoa, Eva; Ocejo-Vinyals, J Gonzalo; Martín, Javier; Blanco, Ricardo; González-Gay, Miguel Ángel

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Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12530/20455

Title:	Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch-Schönlein purpura (IgA vasculitis).
Authors:	López-Mejías, Raquel Genre, Fernanda Remuzgo-Martínez, Sara Pérez, Belén Sevilla Castañeda, Santos Llorca, Javier Ortego-Centeno, Norberto Ubilla, Begoña Mijares, Verónica Pina, Trinitario Calvo-Río, Vanesa Palmou, Natalia Miranda-Filloy, José A Parejo, Antonio Navas Argila, Diego Sánchez-Pérez, Javier Rubio, Esteban Luque, Manuel León Blanco-Madrigal, Juan María Galíndez-Aguirregoikoa, Eva Ocejo-Vinyals, J Gonzalo Martín, Javier Blanco, Ricardo González-Gay, Miguel Ángel View more
Mesh:	Adult Child Female Gene Frequency Genetic Predisposition to Disease Genotype Humans Male Protein Tyrosine Phosphatase, Non-Receptor Type 22 Purpura, Schoenlein-Henoch Real-Time Polymerase Chain Reaction Spain src-Family Kinases Polymorphism, Single Nucleotide View more
Issue Date:	13-Oct-2015
Citation:	Arthritis Res. Ther..2015 Oct;(17):286
Abstract:	To determine whether the PTPN22 (protein tyrosine phosphatase nonreceptor 22)/CSK (c-src tyrosine kinase) pathway is implicated in the susceptibility and clinical heterogeneity of Henoch-Schönlein purpura (HSP) in the largest series of Caucasian HSP patients ever assessed for genetic studies.
PMID:	26458874
URI:	https://hdl.handle.net/20.500.12530/20455
Rights:	openAccess
Appears in Collections:	Fundaciones e Institutos de Investigación > IIS H. U. La Princesa > Artículos

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