Add to ORKGThe skeletal phenotype of chondroadherin deficient mice.PLOS One, 8(6), [e63080]
Cartilage oligomeric matrix protein (COMP) belongs to the thrombospondin family and is a homopentame...
Osteoporosis is a common polygenic disease and global healthcare priority but its genetic basis rema...
A new autosomal recessive lethal mutation in the mouse designated cartilage matrix deficiency (cmd) ...
The skeletal phenotype of chondroadherin deficient mice.PLOS One, 8(6), [e63080]
Chondroadherin, a leucine rich repeat extracellular matrix protein with functions in cell to matrix ...
Chondroadherin, a leucine rich repeat extracellular matrix protein with functions in cell to matrix ...
Chondroadherin, a leucine rich repeat extracellular matrix protein with functions in cell to matrix ...
BBSRC. Grant Numbers: BB/J004316/1, BB/I014608/1 Arthritis Research UK. Grant Numbers: 20413, 20581...
Studies of a number of mouse mutations with skeletal defects have contributed significantly to the u...
The complexity of skeletal pathologies makes use of in vivo models essential to elucidate the pathog...
The complexity of skeletal pathologies makes use of in vivo models essential to elucidate the pathog...
<p>(A) Quantification of the chondrocyte number per cartilage area in femur and tibia sections from ...
The critical importance of hypoxia-inducible factor (HIF)s in the regulation of endochondral bone fo...
Short-limbed dwarfism (SLW) is a new mutant mouse characterized by a dwarf phenotype with markedly s...
<p>(A) Alcian blue/alizarin red staining of P7 mice pups. Alcian blue and alizarin red stain cartila...
Cartilage oligomeric matrix protein (COMP) belongs to the thrombospondin family and is a homopentame...
Osteoporosis is a common polygenic disease and global healthcare priority but its genetic basis rema...
A new autosomal recessive lethal mutation in the mouse designated cartilage matrix deficiency (cmd) ...
The skeletal phenotype of chondroadherin deficient mice.PLOS One, 8(6), [e63080]
Chondroadherin, a leucine rich repeat extracellular matrix protein with functions in cell to matrix ...
Chondroadherin, a leucine rich repeat extracellular matrix protein with functions in cell to matrix ...
Chondroadherin, a leucine rich repeat extracellular matrix protein with functions in cell to matrix ...
BBSRC. Grant Numbers: BB/J004316/1, BB/I014608/1 Arthritis Research UK. Grant Numbers: 20413, 20581...
Studies of a number of mouse mutations with skeletal defects have contributed significantly to the u...
The complexity of skeletal pathologies makes use of in vivo models essential to elucidate the pathog...
The complexity of skeletal pathologies makes use of in vivo models essential to elucidate the pathog...
<p>(A) Quantification of the chondrocyte number per cartilage area in femur and tibia sections from ...
The critical importance of hypoxia-inducible factor (HIF)s in the regulation of endochondral bone fo...
Short-limbed dwarfism (SLW) is a new mutant mouse characterized by a dwarf phenotype with markedly s...
<p>(A) Alcian blue/alizarin red staining of P7 mice pups. Alcian blue and alizarin red stain cartila...
Cartilage oligomeric matrix protein (COMP) belongs to the thrombospondin family and is a homopentame...
Osteoporosis is a common polygenic disease and global healthcare priority but its genetic basis rema...
A new autosomal recessive lethal mutation in the mouse designated cartilage matrix deficiency (cmd) ...