Collagen type XI is a quantitatively minor yet essential component of the collagen fibrils within cartilage. It functions in the assembly of embryonic cartilage collagen fibrils as the diameter of cartilage collagen fibrils is dependent on the relative ratioand microfibril structure of collagen types II and XI. However, very little is known about the role of collagen type XI in the formation of mineralized tissue. In this study, skeletal mineralization was evaluated in the absence and presence of collagen α1(XI) using the chondrodysplasia (cho) mouse. Skeletal deformities in the cho mouse indicate that collagen type XI acts in skeletal development distinct from its function in nucleating the formation and limiting the diameter of cartilage ...
Skeletal biology has entered an exciting period with the technological advances in murine transgenes...
The bone matrix is constantly remodeled by the coordinated activities of bone-forming osteoblasts an...
AbstractMice that are homozygous for the autosomal recessive chondrodysplasia (cho) mutation die at ...
Collagen type XI is a quantitatively minor yet essential component of the collagen fibrils within ca...
Collagen XI alpha 1 (Col11a1) is an extracellular matrix molecule required for embryonic development...
Skeletogenesis occurs through both intramembranous ossification, and endochondral ossification, the ...
Mutation or loss of collagen VI has been linked to a variety of musculoskeletal abnormalities, parti...
Mutation or loss of collagen VI has been linked to a variety of musculoskeletal abnormalities, parti...
Collagen, the most abundant protein in the body, can be found throughout in a variety of places incl...
Mice that are homozygous for the autosomal recessive chondrodysplasia (cho) mutation die at birth wi...
Collagen II is a fibril-forming collagen that is mainly expressed in cartilage. Collagen II-deficien...
licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that th...
Abstract Type XIII collagen is a type II transmembrane protein which is expressed in many tissues th...
The bone matrix is constantly remodeled by the coordinated activities of bone-forming osteoblasts an...
The establishment of a complex collagen network is critical for the architecture and mechanical prop...
Skeletal biology has entered an exciting period with the technological advances in murine transgenes...
The bone matrix is constantly remodeled by the coordinated activities of bone-forming osteoblasts an...
AbstractMice that are homozygous for the autosomal recessive chondrodysplasia (cho) mutation die at ...
Collagen type XI is a quantitatively minor yet essential component of the collagen fibrils within ca...
Collagen XI alpha 1 (Col11a1) is an extracellular matrix molecule required for embryonic development...
Skeletogenesis occurs through both intramembranous ossification, and endochondral ossification, the ...
Mutation or loss of collagen VI has been linked to a variety of musculoskeletal abnormalities, parti...
Mutation or loss of collagen VI has been linked to a variety of musculoskeletal abnormalities, parti...
Collagen, the most abundant protein in the body, can be found throughout in a variety of places incl...
Mice that are homozygous for the autosomal recessive chondrodysplasia (cho) mutation die at birth wi...
Collagen II is a fibril-forming collagen that is mainly expressed in cartilage. Collagen II-deficien...
licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that th...
Abstract Type XIII collagen is a type II transmembrane protein which is expressed in many tissues th...
The bone matrix is constantly remodeled by the coordinated activities of bone-forming osteoblasts an...
The establishment of a complex collagen network is critical for the architecture and mechanical prop...
Skeletal biology has entered an exciting period with the technological advances in murine transgenes...
The bone matrix is constantly remodeled by the coordinated activities of bone-forming osteoblasts an...
AbstractMice that are homozygous for the autosomal recessive chondrodysplasia (cho) mutation die at ...