Progressive ankylosis, ank, a new recessive skeletal mutation causing a noninflammatory joint disease in mice is described. Preliminary observations suggest that three abnormal processes are involved: increased calcification of calcified cartilage and of joint tissues, hyperplasia of the cells and tissues of the joints, and degeneration within and around the tissues, tendons, and ligaments of the joints. The new mutation is closely linked, with about 4 percent recombination, to underwhite on chr 15
Objective The ank/ank mouse develops a phenotype similar to ankylosing spondylitis (AS) in humans. A...
Craniometaphyseal dysplasia (CMD) is a genetic disorder characterized by hyperostosis of craniofacia...
Osteochondrodystrophy (ocd) is a new autosomal recessive mouse mutation characterized by a short, sl...
Mutations in the progressive ankylosis gene (Ank/ANKH) cause surprisingly different skeletal phenoty...
The first objective of my work was to use the ank/ank (progressive ankylosis) mutant mice, which hav...
Chondrocalcinosis (CC) is a common cause of joint pain and arthritis that is caused by the depositio...
Craniometaphyseal dysplasia (CMD) is a bone dysplasia characterized by overgrowth and sclerosis of t...
CONTEXT: Mutations in ANKH cause the highly divergent conditions familial chondrocalcinosis and cran...
Abstract Introduction The diagnosis of ankylosing s...
Osteopetrosis (op/op) is a new mutation in the mouse that is transmitted as an autosomal recessive l...
Objective\ud \ud The ank/ank mouse develops a phenotype similar to ankylosing spondylitis (AS) in hu...
Abstract: We recently have reported on a novel ankylosis gene that is closely linked to the Enpp1 (e...
Inflammation is a complex cellular and humoral response against trauma and infection, and its presen...
Tarsal joint abnormalities have been observed in aged male mice on a C57BL background. This joint di...
Mutations in the pyrophosphate (PPi) transporter ANKH cause the autosomal dominant form of craniomet...
Objective The ank/ank mouse develops a phenotype similar to ankylosing spondylitis (AS) in humans. A...
Craniometaphyseal dysplasia (CMD) is a genetic disorder characterized by hyperostosis of craniofacia...
Osteochondrodystrophy (ocd) is a new autosomal recessive mouse mutation characterized by a short, sl...
Mutations in the progressive ankylosis gene (Ank/ANKH) cause surprisingly different skeletal phenoty...
The first objective of my work was to use the ank/ank (progressive ankylosis) mutant mice, which hav...
Chondrocalcinosis (CC) is a common cause of joint pain and arthritis that is caused by the depositio...
Craniometaphyseal dysplasia (CMD) is a bone dysplasia characterized by overgrowth and sclerosis of t...
CONTEXT: Mutations in ANKH cause the highly divergent conditions familial chondrocalcinosis and cran...
Abstract Introduction The diagnosis of ankylosing s...
Osteopetrosis (op/op) is a new mutation in the mouse that is transmitted as an autosomal recessive l...
Objective\ud \ud The ank/ank mouse develops a phenotype similar to ankylosing spondylitis (AS) in hu...
Abstract: We recently have reported on a novel ankylosis gene that is closely linked to the Enpp1 (e...
Inflammation is a complex cellular and humoral response against trauma and infection, and its presen...
Tarsal joint abnormalities have been observed in aged male mice on a C57BL background. This joint di...
Mutations in the pyrophosphate (PPi) transporter ANKH cause the autosomal dominant form of craniomet...
Objective The ank/ank mouse develops a phenotype similar to ankylosing spondylitis (AS) in humans. A...
Craniometaphyseal dysplasia (CMD) is a genetic disorder characterized by hyperostosis of craniofacia...
Osteochondrodystrophy (ocd) is a new autosomal recessive mouse mutation characterized by a short, sl...