Ptpn11 deletion in a novel progenitor causes metachondromatosis by inducing hedgehog signalling

Noonan syndrome and clinically related disorders

(2011) Marco Tartaglia et al.   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

Ptpn11/Shp2 Acts as a Tumor Suppressor in Hepatocellular Carcinogenesis

(2011) Emilie A. Bard-Chapeau et al.   CANCER CELL

Relative percentage and zonal distribution of mesenchymal progenitor cells in human osteoarthritic and normal cartilage

(2011) David Pretzel et al.   ARTHRITIS RESEARCH & THERAPY

Loss-of-Function Mutations in PTPN11 Cause Metachondromatosis, but Not Ollier Disease or Maffucci Syndrome

(2011) Margot E. Bowen et al.   PLoS Genetics

Whole-Genome Sequencing of a Single Proband Together with Linkage Analysis Identifies a Mendelian Disease Gene

(2010) Nara L. M. Sobreira et al.   PLoS Genetics

Identification of a stem cell niche in the zone of Ranvier within the knee joint

(2009) Camilla Karlsson et al.   JOURNAL OF ANATOMY

Hereditary multiple exostoses and enchondromatosis

(2008) Stéphanie Pannier et al.   BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY