List of works - Manuel D Díaz-Muñoz

Alternative Translation Initiation Generates a Functionally Distinct Isoform of the Stress-Activated Protein Kinase MK2

scientific article published on 01 June 2019

Characterization of the B Cell Transcriptome Bound by RNA-Binding Proteins with iCLIP.

scientific article published on January 2017

Cyclooxygenase-2 deficiency in macrophages leads to defective p110γ PI3K signaling and impairs cell adhesion and migration.

scientific article published on 3 June 2013

Deletion of AU-rich elements within the Bcl2 3'UTR reduces protein expression and B cell survival in vivo

scientific article

Dose-dependent effects of prostaglandin E2 in macrophage adhesion and migration.

scientific article

Generation of functionally distinct isoforms of PTBP3 by alternative splicing and translation initiation.

scientific article published on 4 May 2015

Involvement of PGE2 and the cAMP signalling pathway in the up-regulation of COX-2 and mPGES-1 expression in LPS-activated macrophages.

scientific article published on April 2012

Prostanoid function and cardiovascular disease

scientific article published on 01 July 2008

R-Ras2 is required for germinal center formation to aid B cells during energetically demanding processes

scientific article published on 29 May 2018

RNA-binding proteins ZFP36L1 and ZFP36L2 promote cell quiescence

scientific journal article

RNA-binding proteins control gene expression and cell fate in the immune system.

scientific article published on 18 January 2018

Role of peroxisome proliferator-activated receptor alpha in the control of cyclooxygenase 2 and vascular endothelial growth factor: involvement in tumor growth.

scientific article published on January 2008

The RNA-binding protein HuR is essential for the B cell antibody response.

scientific article published on 23 February 2015

The RNA-binding protein HuR is required for maintenance of the germinal centre response

scientific article published on 12 November 2021

The RNA-binding protein PTBP1 is necessary for B cell selection in germinal centers

scientific article

Tia1 dependent regulation of mRNA subcellular location and translation controls p53 expression in B cells.

scientific article published on 13 September 2017

Uncovering the Role of RNA-Binding Proteins in Gene Expression in the Immune System.

scientific article published on 23 May 2018

List of works by Manuel D Díaz-Muñoz

Alternative Translation Initiation Generates a Functionally Distinct Isoform of the Stress-Activated Protein Kinase MK2

Characterization of the B Cell Transcriptome Bound by RNA-Binding Proteins with iCLIP.

Cyclooxygenase-2 deficiency in macrophages leads to defective p110γ PI3K signaling and impairs cell adhesion and migration.

Deletion of AU-rich elements within the Bcl2 3'UTR reduces protein expression and B cell survival in vivo

Dose-dependent effects of prostaglandin E2 in macrophage adhesion and migration.

Generation of functionally distinct isoforms of PTBP3 by alternative splicing and translation initiation.

Involvement of PGE2 and the cAMP signalling pathway in the up-regulation of COX-2 and mPGES-1 expression in LPS-activated macrophages.

Prostanoid function and cardiovascular disease

R-Ras2 is required for germinal center formation to aid B cells during energetically demanding processes

RNA-binding proteins ZFP36L1 and ZFP36L2 promote cell quiescence

RNA-binding proteins control gene expression and cell fate in the immune system.

Role of peroxisome proliferator-activated receptor alpha in the control of cyclooxygenase 2 and vascular endothelial growth factor: involvement in tumor growth.

The RNA-binding protein HuR is essential for the B cell antibody response.

The RNA-binding protein HuR is required for maintenance of the germinal centre response

The RNA-binding protein PTBP1 is necessary for B cell selection in germinal centers

Tia1 dependent regulation of mRNA subcellular location and translation controls p53 expression in B cells.

Uncovering the Role of RNA-Binding Proteins in Gene Expression in the Immune System.