Neutral Sphingomyelinase (SMPD3) Deficiency Causes a Novel Form of Chondrodysplasia and Dwarfism That Is Rescued by Col2A1-Driven smpd3 Transgene Expression

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

Francis Rousseau, Jacky Bonaventure, Laurence Legeai‐Mallet et al. · Nature · 1994 · 928 citations

Fibrosis, Genetic Disorder, Genetics +5

Osteopontin--a possible anchor of osteoclasts to bone.

Finn P. Reinholt, Kjell Hultenby, Å Oldberg et al. · Proceedings of the National Academy of Sciences · 1990 · 824 citations

Mechanobiology, Bone Surface, Biochemistry +13

COMP (cartilage oligomeric matrix protein) is structurally related to the thrombospondins.

Å Oldberg, Per Antonsson, Karin Lindblom et al. · Journal of Biological Chemistry · 1992 · 326 citations · Full text

Protein Function, Signal Transduction, Musculoskeletal Research +15

Cloning and characterization of the mammalian brain-specific, Mg ²⁺ -dependent neutral sphingomyelinase

Kay Hofmann, Stefan Tomiuk, Gabriela Wolff et al. · Proceedings of the National Academy of Sciences · 2000 · 298 citations

Cloned mammalian neutral sphingomyelinase: Functions in sphingolipid signaling?

Stefan Tomiuk, Kay Hofmann, Michael Nix et al. · Proceedings of the National Academy of Sciences · 1998 · 266 citations · Full text