Hematopoietic lineages cooperate with osteoblasts in the initiation and progression of neurofibromatosis type 1 associated skeletal deficits

Medicine and Dentistry

• Neurofibromatosis Type I 100%
• Pathogenesis 18%
• Clinical Study 18%
• Osteoblast 18%
• Osteoclast 18%
• Neurofibromatosis 18%
• Bone 18%
• Protein 9%
• Fracture 9%
• Plexiform Neurofibroma 9%
• Genetic Disorder 9%
• Tumor Suppressor Gene 9%
• Biosynthesis 9%
• Nonunion 9%
• Short Stature 9%
• Haploinsufficiency 9%
• Ras 9%
• Osteopenia 9%
• Pseudarthrosis 9%
• Autosomal Dominant Inheritance 9%
• Kyphoscoliosis 9%
• Spontaneous Mutation 9%
• Neurofibromin 1 9%
• Patient 9%
• Osteoporosis 9%

Biochemistry, Genetics and Molecular Biology

• Osteoclast 18%
• Osteoblast 18%
• Anabolism 9%
• Autosomal Dominant Inheritance 9%
• Myeloid 9%
• Haploinsufficiency 9%
• Body Height 9%
• Spontaneous Mutation 9%
• Protein 9%
• Genetic Disorder 9%