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

Unitat de Recerca del Sistema Digestiu (GRC)

IP: Fernando Azpiroz Vidaur
Collaborators: Fco Javier Santos Vicente, Beatriz Lobo Alvarez, Claudia Maria Herrera de Guise, Natalia Borruel Sainz, María Antolín Mate, Mar Guilarte Clavero, Francesc Casellas Jordá, Carmen Alonso Cotoner, Carolina Malagelada Prats, Ana Maria Gonzalez Castro, Marc Pigrau Pastor, Virginia Robles Alonso, Cristina Martínez Martínez, Chaysavanh Manichanh, Elizabeth Barba Orozco
Funding agency: Agència Gestió Ajuts Universitaris i de Recerca
Funding: 30000
Reference: 2014 SGR 1285
Duration: 01/01/2014 - 31/12/2016

Psychosocial and gender-related non-coding NRAs biomarkers in irritable bowel syndrome

IP: Fco Javier Santos Vicente
Collaborators: Marc Pigrau Pastor, Cristina Martínez Martínez
Funding agency: Instituto de Salud Carlos III
Funding: 200540.56
Reference: PI11/00716
Duration: 01/01/2012 - 31/12/2014

Role of mucosal eosinophols in the physiopathology of irritable bowel syndrome

IP: Fco Javier Santos Vicente
Collaborators: Beatriz Lobo Alvarez, Inés de Torres Ramirez, Carmen Alonso Cotoner, Cristina Martínez Martínez
Funding agency: Rome Foundation
Funding: 38959.02
Reference: ROMEF-2010
Duration: 01/07/2010 - 30/06/2011

Mecanismos moleculares subyacentes a la respuesta diferencial (género dependiente) de la barrera epitelial al estrés en el yeyuno humano. Papel del mastocito e implicaciones en el intestino irritable

IP: Fco Javier Santos Vicente
Collaborators: Victòria Cardona Dahl, Carmen Alonso Cotoner, Cristina Martínez Martínez
Funding agency: Instituto de Salud Carlos III
Funding: 246840
Reference: PI080940
Duration: 01/01/2009 - 31/12/2012

Related news

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.

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.

Related professionals

Maria Royo Lopez

Maria Royo Lopez

Research technician
Rheumatology
Read more
Gerard Roch Alba

Gerard Roch Alba

Research technician
Neurodegenerative Diseases
Read more
Marta Martinez Oliva

Marta Martinez Oliva

Shock, Organ Dysfunction and Resuscitation
Read more
Debora Sierra Nuñez

Debora Sierra Nuñez

Main researcher
Multidisciplinary Nursing Research Group
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.