In this article, Millard and colleagues show that intrauterine bone marrow transplantation in the oim/oim mouse model of osteogenesis imperfecta yields hematopoietic microchimerism in the absence of donor osteopoiesis or phenotypic improvement. Bone-associated donor cells were not bone-forming osteoblasts, but osteoclasts (bone resorbing cells of the hematopoietic lineage) and osteal macrophages (bone regulatory cells of the hematopoietic lineage)
Transplantation of whole bone marrow (BMT) as well as ex vivo-expanded mesenchymal stromal cells (MS...
Bone and bone marrow are closely aligned physiologic compartments, suggesting that these tissues may...
Osteoblasts play a crucial role in the hematopoietic stem cell (HSC) niche; however, an overall incr...
The inherited skeletal dysplasia osteogenesis imperfecta (01) results in multiple fractures and is c...
The inherited skeletal dysplasia osteogenesis imperfecta (OI) results in multiple fractures and is c...
n principle,bone marrow transplantation should offer effective treatment for disorders originating f...
Infantile malignant osteopetrosis (IMO) is caused by lack of functional osteoclasts leading to skele...
Osteogenesis imperfecta (OI or brittle bone disease) is a disorder of connective tissues caused by m...
OBJECTIVE: Based on the recognition that marrow contains progenitors for bone as well as blood, we u...
OBJECTIVE: Transplantable osteoprogenitors, as well as hematopoietic progenitors, reside in bone mar...
The osteoclast is vital for establishment of normal hematopoiesis in the developing animal. However,...
Infantile malignant osteopetrosis (IMO) is caused by lack of functional osteoclasts leading to skele...
Objective. Based on the recognition that marrow contains progenitors for bone as well as blood, we u...
Copyright © 2009 by American Society of HematologyAutosomal dominant osteogenesis imperfecta (OI) ca...
Autosomal dominant osteogenesis imperfecta (OI) caused by glycine substitutions in type I collagen i...
Transplantation of whole bone marrow (BMT) as well as ex vivo-expanded mesenchymal stromal cells (MS...
Bone and bone marrow are closely aligned physiologic compartments, suggesting that these tissues may...
Osteoblasts play a crucial role in the hematopoietic stem cell (HSC) niche; however, an overall incr...
The inherited skeletal dysplasia osteogenesis imperfecta (01) results in multiple fractures and is c...
The inherited skeletal dysplasia osteogenesis imperfecta (OI) results in multiple fractures and is c...
n principle,bone marrow transplantation should offer effective treatment for disorders originating f...
Infantile malignant osteopetrosis (IMO) is caused by lack of functional osteoclasts leading to skele...
Osteogenesis imperfecta (OI or brittle bone disease) is a disorder of connective tissues caused by m...
OBJECTIVE: Based on the recognition that marrow contains progenitors for bone as well as blood, we u...
OBJECTIVE: Transplantable osteoprogenitors, as well as hematopoietic progenitors, reside in bone mar...
The osteoclast is vital for establishment of normal hematopoiesis in the developing animal. However,...
Infantile malignant osteopetrosis (IMO) is caused by lack of functional osteoclasts leading to skele...
Objective. Based on the recognition that marrow contains progenitors for bone as well as blood, we u...
Copyright © 2009 by American Society of HematologyAutosomal dominant osteogenesis imperfecta (OI) ca...
Autosomal dominant osteogenesis imperfecta (OI) caused by glycine substitutions in type I collagen i...
Transplantation of whole bone marrow (BMT) as well as ex vivo-expanded mesenchymal stromal cells (MS...
Bone and bone marrow are closely aligned physiologic compartments, suggesting that these tissues may...
Osteoblasts play a crucial role in the hematopoietic stem cell (HSC) niche; however, an overall incr...