Skip to main content

Cristina Martínez Martínez

Institutions of which they are part

Main researcher
Kidney Physiopathology
Vall Hebron Institut de Recerca

Cristina Martínez Martínez

Institutions of which they are part

Main researcher
Kidney Physiopathology
Vall Hebron Institut de Recerca

Projects

Candidatura Juan de la Cierva-incorporación

IP: Fco Javier Santos Vicente
Collaborators: Cristina Martínez Martínez
Funding agency: Ministerio Economía, Industria y Competitividad
Funding: 64000
Reference: IJCI-2015-26099
Duration: 09/01/2017 - 08/01/2019

Identificación de antígenos inductores de la respuesta humoral y de mecanismos de regulación de la inflamación intestinal en el síndrome del intestino irritable. Desarrollo de un panel diagnóstico diferencial.

IP: -
Collaborators: Inés de Torres Ramirez, Identificación de antígenos inductores de la respuesta humoral y de mecanismos de regulación de la inflamación intestinal en el , Marc Pigrau Pastor, Cristina Martínez Martínez, Danila Guagnozzi
Funding agency: Instituto de Salud Carlos III
Funding: 183012.5
Reference: PI16/00583
Duration: 01/01/2017 - 30/06/2020

Desarrollo de un panel diagnóstico innovador para el Síndrome del Intestino Irritable basado en la expresión sistémica diferencial de miRNAs, asociado a manifestaciones clínicas y a patología intestinal

IP: Fco Javier Santos Vicente
Collaborators: Ana Maria Gonzalez Castro, Cristina Martínez Martínez
Funding agency: Instituto de Salud Carlos III
Funding: 171215
Reference: PI14/00994
Duration: 01/01/2015 - 30/04/2018

HNF4A EXPRESSION AND REGULATION IN THE JEJUNUM OF IBS-D PATIENTS

IP: Fernando Azpiroz Vidaur
Collaborators: Cristina Martínez Martínez
Funding agency: Agència Gestió Ajuts Universitaris i de Recerca
Funding: 40604.62
Reference: 2011 BP_A2 00002
Duration: 01/02/2015 - 31/01/2016

Related news

Funding has been obtained for 43 projects under the calls for Health R&D&I Projects, Health Technology Development, and Independent Clinical Research

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.

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

Related professionals

Ana García de Frutos

Ana García de Frutos

Spine Research Unit
Read more
Ariadna Subirà González

Ariadna Subirà González

Research assistant
Maternal and Fetal Medicine
Read more
Deborah Pareto Onghena

Deborah Pareto Onghena

Main researcher
Neuroradiology
Read more
Adrian Avellaneda Rodriguez

Adrian Avellaneda Rodriguez

Research technician
Childhood Cancer and Blood Disorders
Read more

Subscribe to our newsletters and be part of the Campus life

We are a world-leading healthcare complex where healthcare, research, teaching and innovation go hand in hand.

This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.