No association between loss-of-function mutations in filaggrin and diabetes, cardiovascular disease, and all-cause mortality.
<h4>Background</h4>Common loss-of-function mutations in the filaggrin gene (FLG) are a major predisposing risk factor for atopic disease due to reduced epidermal filaggrin protein levels. We previously observed an association between these mutations and type 2 diabetes and hypothesized t...
Guardado en:
Autores principales: | Lise Lotte N Husemoen, Tea Skaaby, Torben Jørgensen, Jacob P Thyssen, Michael Meldgaard, Pal B Szecsi, Steen Stender, Jeanne Duus Johansen, Allan Linneberg |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2013
|
Materias: | |
Acceso en línea: | https://doaj.org/article/29c7f2d290364ef7940f2bd50528f75a |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Vitamin D status, filaggrin genotype, and cardiovascular risk factors: a Mendelian randomization approach.
por: Tea Skaaby, et al.
Publicado: (2013) -
Vitamin D status and chronic obstructive pulmonary disease: a prospective general population study.
por: Tea Skaaby, et al.
Publicado: (2014) -
The association of alcohol and alcohol metabolizing gene variants with diabetes and coronary heart disease risk factors in a white population.
por: Lise Lotte N Husemoen, et al.
Publicado: (2010) -
Clinical presentation of atopic dermatitis by filaggrin gene mutation status during the first 7 years of life in a prospective cohort study.
por: Charlotte Giwercman Carson, et al.
Publicado: (2012) -
TSLP is a direct trigger for T cell migration in filaggrin-deficient skin equivalents
por: Leonie Wallmeyer, et al.
Publicado: (2017)