Search filters

List of works by Michael D Briggs

A mouse model offers novel insights into the myopathy and tendinopathy often associated with pseudoachondroplasia and multiple epiphyseal dysplasia

scientific article

Abnormal chondrocyte apoptosis in the cartilage growth plate is influenced by genetic background and deletion of CHOP in a targeted mouse model of pseudoachondroplasia

scientific article

CRELD2 Is a Novel LRP1 Chaperone That Regulates Noncanonical WNT Signaling in Skeletal Development

scientific article published on 17 March 2020

Increased hippocampal excitability in miR-324-null mice

scientific article published on 17 May 2021

Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation

scientific article

Mild myopathy is associated with COMP but not MATN3 mutations in mouse models of genetic skeletal diseases

scientific article

Multiple epiphyseal dysplasia and related disorders; molecular genetics, disease mechanisms and therapeutic avenues

scientific article published on 07 July 2020

New developments in chondrocyte ER stress and related diseases

scientific article published on 24 April 2020

New therapeutic targets in rare genetic skeletal diseases

scientific article

Reduced cell proliferation and increased apoptosis are significant pathological mechanisms in a murine model of mild pseudoachondroplasia resulting from a mutation in the C-terminal domain of COMP

scientific article published in September 2007

Skeletal dysplasias associated with mild myopathy-a clinical and molecular review

scientific article published on 24 May 2010

The utility of mouse models to provide information regarding the pathomolecular mechanisms in human genetic skeletal diseases: The emerging role of endoplasmic reticulum stress (Review).

scientific article published on 30 March 2015

XBP1 signalling is essential for alleviating mutant protein aggregation in ER-stress related skeletal disease

scientific article published on 01 July 2019

Paulina is supported by:

About Paulina

Help