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Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 04/2011, Volume 7, Issue 4, p. e1002050
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 7/2003, Volume 162, Issue 1, pp. 139 - 148
Chondrocyte proliferation and differentiation requires their attachment to the collagen type II-rich matrix of developing bone. This interaction is mediated by... 
Cell growth | Chondrocytes | Collagens | Alleles | Epiphyses | Mice | Gene expression regulation | Cyclins | Cells | Integrins | Cre-lox | Integrin-linked kinase | Gene targeting | Cyclin D1 | chondrocytes | CANCER CELLS | PROTEIN-KINASE | gene targeting | CRE RECOMBINASE | CELL-ADHESION | BETA-CATENIN | CELL BIOLOGY | ENDOCHONDRAL BONE-DEVELOPMENT | cyclin D1 | CYCLIN D1 GENE | EXTRACELLULAR-MATRIX | integrin-linked kinase | EXPRESSION | TRANSGENIC MICE | Growth Plate - pathology | Cyclin D1 - metabolism | Protein-Serine-Threonine Kinases - deficiency | Growth Plate - enzymology | Chondrogenesis - genetics | Gene Expression Regulation, Developmental - genetics | Apoptosis - genetics | Male | Integrins - metabolism | Collagen Type II - metabolism | Growth Plate - abnormalities | Cell Differentiation - genetics | Exostoses, Multiple Hereditary - genetics | Female | Dwarfism - physiopathology | Osteogenesis - genetics | Disease Models, Animal | Cell Division - genetics | Chondrocytes - pathology | Cell Adhesion - genetics | Transgenes - genetics | Protein-Serine-Threonine Kinases - genetics | Viral Proteins - genetics | Cartilage - physiopathology | Down-Regulation - genetics | Mice, Knockout | Exostoses, Multiple Hereditary - enzymology | Cartilage - abnormalities | Chondrocytes - enzymology | Dwarfism - genetics | Animals | Dwarfism - enzymology | Cartilage - enzymology | Integrases - genetics | Physiological aspects | Cartilage cells | Research | integrin-linked kinase; chondrocytes; Cre-lox; cyclin D1; gene targeting
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2012, Volume 91, Issue 1, pp. 56 - 72
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 12699 - 14
Transdifferentiation of hypertrophic chondrocytes into bone-forming osteoblasts has been reported, yet the underlying molecular mechanism remains incompletely... 
CONDITIONAL INACTIVATION | TRANSCRIPTION FACTOR SOX9 | OSTEOBLAST DIFFERENTIATION | MESENCHYMAL PROGENITORS | ENDOCHONDRAL BONE-FORMATION | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | CRE RECOMBINASE | BETA-CATENIN | PROTEIN-TYROSINE-PHOSPHATASE | NOONAN-SYNDROME | Growth Plate - pathology | Cartilage - pathology | Chondrogenesis - genetics | Humans | Exostoses, Multiple Hereditary - physiopathology | Cell Transdifferentiation - genetics | Hypertrophy - pathology | Growth Plate - growth & development | Cell Differentiation - genetics | Bone Neoplasms - physiopathology | Hypertrophy - genetics | Exostoses, Multiple Hereditary - genetics | Bone Neoplasms - genetics | Chondrocytes - metabolism | Osteogenesis - genetics | Cartilage - growth & development | Chondrocytes - pathology | Cell Proliferation - genetics | Chondromatosis - physiopathology | Cartilage - metabolism | Growth Plate - metabolism | Animals | Chondromatosis - genetics | Mice | Bone Development - genetics | Protein Tyrosine Phosphatase, Non-Receptor Type 11 - genetics | Osteoblasts - metabolism | SOX9 Transcription Factor - genetics | Tyrosine | Therapeutic applications | Sox9 protein | Homeostasis | Bone diseases | Gestation | Osteoblasts | Chondrodystrophy | Ossification | Dwarfism | Cartilage | Growth plate | Osteoporosis | Osteoblastogenesis | Collagen | Rodents | Chondrocytes | Skeleton | Chondrogenesis | Bone (endochondral) | Osteopenia | Protein-tyrosine-phosphatase
Journal Article
PLoS Genetics, ISSN 1553-7390, 04/2017, Volume 13, Issue 4, p. e1006742
Hereditary Multiple Exostoses (HME) is a rare pediatric disorder caused by loss-of-function mutations in the genes encoding the heparan sulfate... 
ENDOCHONDRAL OSSIFICATION | CRE ACTIVITY | MOUSE MODEL | GENETICS & HEREDITY | GROWTH-PLATE | HEPARAN-SULFATE PROTEOGLYCANS | SKELETAL DEVELOPMENT | CHONDROGENESIS | EXT2 GENES | LONG BONES | CARTILAGE | Growth Plate - pathology | Heparitin Sulfate - biosynthesis | Exostoses, Multiple Hereditary - diagnostic imaging | Chondrogenesis - genetics | Humans | N-Acetylglucosaminyltransferases - genetics | Bone Morphogenetic Proteins - metabolism | Osteochondroma - pathology | Smad1 Protein - genetics | Exostoses, Multiple Hereditary - genetics | Osteochondroma - diagnostic imaging | Bone Morphogenetic Proteins - genetics | Disease Models, Animal | Pyrimidines - administration & dosage | Cervical Cord - pathology | Embryonic Development - genetics | Osteochondroma - genetics | Growth Plate - metabolism | Exostoses, Multiple Hereditary - pathology | Mice, Knockout | Exostoses, Multiple Hereditary - drug therapy | Magnetic Resonance Imaging | Pyrazoles - administration & dosage | Animals | Cervical Cord - metabolism | Mice | Tomography, Emission-Computed | Mutation | Antagonists (Biochemistry) | CT imaging | Usage | Care and treatment | Hereditary multiple exostoses | Analysis | Osteochondroma | Genetic aspects | Research | Pediatrics | Electronic mail systems | Spine | Colleges & universities | Embryo cells | AKT protein | Biochemistry | Cartilage | Computed tomography | Surgery | Biocompatibility | Skin diseases | Inhibition | Evaluation | Enzymes | Data acquisition | Abnormalities | Benign | Gene expression | Patients | Hereditary diseases | Osteoblastogenesis | Stem cells | Plates (structural members) | Animal models | Apert's syndrome | Medical services | Arthritis | Chin | Bone tumors | Bone diseases | Kinases | Defects | Biomedical materials | Pain | Rodents | Bone morphogenetic proteins | Bones | Division | Skeleton | Children | Lesions | Heart diseases | Heparan sulfate | Medicine | Effectors | Skull | Aggrecan | Differentiation | Cancer
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 01/2013, Volume 161, Issue 1, pp. 198 - 202
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 11/2018, Volume 26, Issue 11, pp. 1611 - 1622
Journal Article