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Journal Article
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 01/2018, Volume 115, Issue 3, pp. E418 - E427
Fibrous dysplasia (FD; Online Mendelian Inheritance in Man no. 174800) is a crippling skeletal disease caused by activating mutations of the GNAS gene, which... 
Gnas | McCune-Albright syndrome | Fibrous dysplasia | Wnt/β-catenin | LGK-974 | Biological Sciences | β-catenin | PNAS Plus | McCune–Albright syndrome | fibrous dysplasia | Wnt
Journal Article
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN 0027-8424, 01/2018, Volume 115, Issue 3, pp. E418 - E427
Fibrous dysplasia (FD; Online Mendelian Inheritance in Man no. 174800) is a crippling skeletal disease caused by activating mutations of the GNAS gene, which... 
McCune-Albright syndrome | HORMONE-RELATED PEPTIDE | MULTIDISCIPLINARY SCIENCES | GS-ALPHA | STIMULATORY G-PROTEIN | METAPHYSEAL CHONDRODYSPLASIA | LGK-974 | MESSENGER-RNAS | ENDOCHONDRAL BONE-DEVELOPMENT | Wnt/beta-catenin | Gnas | INDIAN-HEDGEHOG | PARATHYROID-HORMONE | fibrous dysplasia | ACTIVATING G(S)ALPHA MUTATION
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 01/2018, Volume 115, Issue 3, p. E418
Fibrous dysplasia (FD; Online Mendelian Inheritance in Man no. 174800) is a crippling skeletal disease caused by activating mutations of the GNAS gene, which... 
Osteoprogenitor cells | Animal models | Wnt protein | Genes | Bone diseases | Genotype & phenotype | β-catenin | Biomedical materials | Pain | Wheelchairs | Rodents | Fibrous dysplasia | Bone marrow | Biocompatibility | Musculoskeletal diseases | Dysplasia | Deformation mechanisms | Therapeutic applications | Heredity | Embryos | Loci | Signaling | Molecular modelling | Stromal cells | Fibrosis | Mutation | Bone | GNAS protein
Journal Article