Skeletal Dysplasias Associated with Mild Myopathy—A Clinical and Molecular Review

Por Piróg, Katarzyna A., Briggs, Michael D.
Publicado em 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 (Re...

Por BRIGGS, MICHAEL D., BELL, PETER A., PIROG, KATARZYNA A.
Publicado no Int J Mol Med (2015)

Mild Myopathy Is Associated with COMP but Not MATN3 Mutations in Mouse Models of Genetic Skeletal Diseases

Por Piróg, Katarzyna A., Katakura, Yoshihisa, Mironov, Aleksandr, Briggs, Michael D.
Publicado em 2013

New therapeutic targets in rare genetic skeletal diseases

Por Briggs, Michael D, Bell, Peter A, Wright, Michael J, Pirog, Katarzyna A
Publicado no Expert Opin Orphan Drugs (2015)

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

Por Bell, Peter A, Piróg, Katarzyna A, Fresquet, Maryline, Thornton, David J, Boot-Handford, Raymond P, Briggs, Michael D
Publicado em 2012

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

Por Piróg, Katarzyna A., Jaka, Oihane, Katakura, Yoshihisa, Meadows, Roger S., Kadler, Karl E., Boot-Handford, Raymond P., Briggs, Michael D.
Publicado em 2010

Abnormal Chondrocyte Apoptosis in the Cartilage Growth Plate is Influenced by Genetic Background and Deletion of CHOP in a Targeted Mouse Model of Pseudoachondroplasia

Por Piróg, Katarzyna A., Irman, Andreja, Young, Siobhan, Halai, Poonam, Bell, Peter A., Boot-Handford, Raymond P., Briggs, Michael D.
Publicado em 2014

A Novel Form of Chondrocyte Stress is Triggered by a COMP Mutation Causing Pseudoachondroplasia

Por Suleman, Farhana, Gualeni, Benedetta, Gregson, Hannah J, Leighton, Matthew P, Piróg, Katarzyna A, Edwards, Sarah, Holden, Paul, Boot-Handford, Raymond P, Briggs, Michael D
Publicado em 2012