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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

Validación e implementación de un panel molecular para el diagnóstico positivo del síndrome del intestino irritable con diarrea y para el diagnóstico diferencial de la diarrea crónica

IP: Fco Javier Santos Vicente
Collaborators: Ana Maria Gonzalez Castro, Lara Aguilera Castro, Marc Pigrau Pastor, Cristina Martínez Martínez, Adoración Nieto Ruiz
Funding agency: Instituto de Salud Carlos III
Funding: 220220
Reference: PI17/01902
Duration: 01/01/2018 - 30/06/2022

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, Elba Exposito Fernandez, 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

Related news

"Patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis present miRNA profiles in urinary extracellular vesicles associated with disease progression" was the awarded work.

Researchers at the VHIR have carried out a study showing that the ClC-5 protein regulates collagen levels through the β-catenin pathway and lysosomal degradation.

The research will perform a functional analysis of phenotype-modifying genetic variants in patients affected by familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (HFHNC).

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