Gema Ariceta Iraola

Institutions of which they are part

Head of group
Kidney Physiopathology

Vall Hebron Institut de Recerca

Gema Ariceta Iraola

Institutions of which they are part

Head of group
Kidney Physiopathology

Vall Hebron Institut de Recerca

Projects

Ultrasecuenciación de RNAm y microRNAs en exosomas de pacientes con Hipomagnesia Hipercalciuria y Nefrocalcinosis Familiar HFHNC con mutaciones

IP: Gema Ariceta Iraola
Collaborators: Ramón Vilalta Casas, Alvaro Domingo Madrid Aris, Luis Enrique Lara Moctezuma, Marina Muñoz López
Funding agency: Instituto de Salud Carlos III
Funding: 148830
Reference: PI14/01107
Duration: 01/01/2015 - 31/12/2018

Related news

Vall d’Hebron and Hipofam promote a project to study a rare kidney disease

The aim of the project is to establish kidney organoids derived from patients with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis, which will be essential tools for studying the disease and testing new treatments.

Equip del grup de Fisiopatologia Renal que ha participat en l'estudi

Vall d'Hebron identifies key genetic factors in the progression of an rare kidney disease

The work identifies variants in genes such as NFU1 that, combined with the disease-causing mutation, can accelerate kidney deterioration.

A study presented by Vall d’Hebron has been awarded Best Communication at the ESPN

The communication is part of a study aimed at identifying the mechanisms of progression of Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis, a rare disease that affects the kidneys.