Cargando…
Rare variants in complement system genes associate with endothelial damage after pediatric allogeneic hematopoietic stem cell transplantation
INTRODUCTION: Complement system has a postulated role in endothelial problems after hematopoietic stem cell transplantation (HSCT). In this retrospective, singlecenter study we studied genetic complement system variants in patients with documented endotheliopathy. In our previous study among pediatr...
Autores principales: | Leimi, Lilli, Koski, Jessica R., Kilpivaara, Outi, Vettenranta, Kim, Lokki, A. Inkeri, Meri, Seppo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525714/ https://www.ncbi.nlm.nih.gov/pubmed/37771589 http://dx.doi.org/10.3389/fimmu.2023.1249958 |
Ejemplares similares
-
P1263: SINGLE NUCLEOTIDE POLYMORPHISMS IN PATIENTS WITH ENDOTHELIAL DAMAGE AFTER PEDIATRIC ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION
por: Leimi, Lilli, et al.
Publicado: (2023) -
Early vascular toxicity after pediatric allogeneic hematopoietic stem cell transplantation
por: Leimi, Lilli, et al.
Publicado: (2022) -
Clinically relevant germline variants in allogeneic hematopoietic stem cell transplant recipients
por: Lahtinen, Atte K., et al.
Publicado: (2022) -
Complement Activation and Regulation in Preeclamptic Placenta
por: Lokki, Anna Inkeri, et al.
Publicado: (2014) -
Genetic Analysis of Membrane Cofactor Protein (CD46) of the Complement System in Women with and without Preeclamptic Pregnancies
por: Lokki, A. Inkeri, et al.
Publicado: (2015)