VCAM1 modulation on endothelial cells – implications for vasculopathy in sickle cell anemia

Sickle cell anemia (SCA) is a highly heterogeneous and multifactorial-like monogenic disease that arises from homozygosity for the c.20A>T mutation in the HBB gene. Vascular disease is systemic in SCA, with profound effects in organs like the brain, where stroke is the most severe end of the cere...

Full description

Bibliographic Details
Main Author: Silva, Marisa (author)
Other Authors: Vargas, Sofia (author), Coelho, Andreia (author), Lavinha, João (author), Faustino, Paula (author)
Format: conferenceObject
Language:eng
Published: 2020
Subjects:
Sickle Cell Anemia
Drepanocitose
Anemia das Células Falciformes
AVC
Medicina personalizada
VCAM1
Vasculopatia cerebral
Hemoglobinopatias
Doenças Genéticas
Doenças Raras
Online Access:http://hdl.handle.net/10400.18/6724
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/6724

Internet

http://hdl.handle.net/10400.18/6724

Similar Items