Navegar por término MeSH "Haplotypes"

Mostrando ítems 1-13 de 13

A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy

2013- Rojas, J.; Fernandez, I.; Pastor, J. C.; MacLaren, R. E.; Ramkissoon, Y.; [et al.]
AGT haplotype in ITGA4 gene is related to antibody-mediated rejection in heart transplant patients

2019- Nuñez Fernandez, Lucia; Marron Liñares, Grecia; Crespo Leiro, Marisa; Barge Caballero, Eduardo; Alvarez López, Eloy; [et al.]
Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population

2019- Esperón Moldes, Uxía Saraiva; Pardo Seco, Jacobo José; Montalván-Suárez, M.; Fachal Vilar, Laura; Ginarte Val, Manuel Javier; [et al.]
HLA-DRB1 Amino Acid Positions 11/13, 71, and 74 Are Associated With Inflammation Level, Disease Activity, and the Health Assessment Questionnaire Score in Patients With Inflammatory Polyarthritis.

2016-11- Ling, Stephanie F.; Viatte, Sebastien; Lunt, Mark; Van Sijl, Alper M; Silva Fernández, Lucía; [et al.]
Impaired Metabolic Flexibility in the Osteoarthritis Process: A Study on Transmitochondrial Cybrids

2020- Dalmao Fernández, Andrea; Lund, Jenny; Hermida Gómez, Tamara; Vázquez Mosquera, María Eugenia; Rego Pérez, Ignacio; [et al.]
Multiple Local and Recent Founder Effects of TGM1 in Spanish Families

2012- Fachal Vilar, Laura; Rodríguez Pazos, Laura; Ginarte Val, Manuel Javier; Toribio Pérez, Jaime; Salas Ellacuriaga, Antonio; [et al.]
N-acetyltransferase 2 polymorphisms and risk of anti-tuberculosis drug-induced hepatotoxicity in Caucasians

2011- Leiro Fernández, Virginia; Valverde, D.; Vázquez Gallardo, Eladio Rafael; Botana Rial, María Isabel; Constenla Caramés, Lucia; [et al.]
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation

2020- Esperón Moldes, Uxía Saraiva; Ginarte Val, Manuel Javier; Rodríguez Pazos, Laura; Fachal Vilar, Laura; Martín-Santiago, A.; [et al.]
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation

2020- Esperón Moldes, Uxía Saraiva; Ginarte Val, Manuel Javier; Rodriguez-Pazos, L; Fachal Vilar, Laura; Martin-Santiago, A; [et al.]
Phylogeography of SARS-CoV-2 pandemic in Spain: a story of multiple introductions, micro-geographic stratification, founder effects, and super-spreaders

2020- Gómez Carballa, Alberto; Bello Paderne, Xabier; Pardo Seco, Jacobo José; Pérez del Molino Bernal, María Luisa; Martinón Torres, Federico; [et al.]
Polymorphisms at phase I-metabolizing enzyme and hormone receptor loci influence the response to anti-TNF therapy in rheumatoid arthritis patients

2019- Canet, L. M.; Sanchez-Maldonado, J. M.; Caliz, R.; Rodriguez-Ramos, A.; Lupianez, C. B.; [et al.]
Steroid hormone-related polymorphisms associate with the development of bone erosions in rheumatoid arthritis and help to predict disease progression: Results from the REPAIR consortium

2019- Sánchez-Maldonado, J. M.; Cáliz, R.; Canet, L.; Horst, R.; Bakker, O.; [et al.]
The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive disease

2014- Fu, Y. P.; Kohaar, I.; Moore, L. E.; Lenz, P.; Figueroa, J. D.; [et al.]