Altered hypoxia inducible factor regulation in hereditary haemorrhagic telangiectasia

Patients with hereditary haemorrhagic telangiectasia (HHT), also known as Rendu–Osler–Weber syndrome, suffer from the consequences of abnormal vessel structures. These structures can lead to haemorrhages or shunt effects in liver, lungs and brain. This inherited and rare disease is characterized by...

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Detalles Bibliográficos
Autores principales: Wrobeln, Anna, Leu, Tristan, Jablonska, Jadwiga, Geisthoff, Urban, Lang, Stephan, Fandrey, Joachim, Droege, Freya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988913/
https://www.ncbi.nlm.nih.gov/pubmed/35393474
http://dx.doi.org/10.1038/s41598-022-09759-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988913/
https://www.ncbi.nlm.nih.gov/pubmed/35393474
http://dx.doi.org/10.1038/s41598-022-09759-9

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