Characterization and management of hypercalcemia …

Characterization and management of hypercalcemia following transplantation for osteopetrosis Bone Marrow Transplantation advance online publication, October 5, 2009. doi:10.1038/bmt.2009.277 Authors: C Martinez, L E

Osteopetrosis with micro-lacunar resorption because …

Osteopetrosis with micro-lacunar resorption because of defective integrin organization Laboratory Investigation advance online publication, June 22, 2009. doi:10.1038/labinvest.2009.58 Authors: Harry C Blair

Genetic analysis of autosomal recessive osteopetrosis …

Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect European Journal of Human Genetics advance online publication, January

Osteoclast-poor human osteopetrosis due to mutations …

Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL Nature Genetics 39, 960 (2007). doi:10.1038/ng2076 Authors: Cristina Sobacchi, Annalisa Frattini, Matteo M Guerrini, Mario Abinun

Patients with autosomal-recessive osteopetrosis …

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UW researchers help identify fatal disease in Red Angus

… osteopetrosis (OS), which is commonly referred to as marble bone disease because the bones of affected calves shatter easily, like ...

Leukocyte adhesion deficiency-III is caused by …

… osteopetrosis, which Malinin et al. showed could be corrected by bone marrow transplantation (pages 249–250, 300–305 and 313–318).

A point mutation in KINDLIN3 ablates activation of …

… osteopetrosis, which Malinin et al. showed could be corrected by bone marrow transplantation (pages 249–250, 300–305 and 306–312).

The Cl-/H+ antiporter ClC-7 is the primary chloride …

… osteopetrosis. Several mammalian members of the CLC family have been characterized in detail; some (including ClC-0, ClC-1 and ClC-2) function as Cl--conducting ion channels, whereas others act as Cl-/H+antiporters

The Cl-/H+ antiporter ClC-7 is the primary chloride …

… osteopetrosis. Several mammalian members of the CLC family have been characterized in detail; some (including ClC-0, ClC-1 and ClC-2) function as Cl--conducting ion channels, whereas others act as Cl-/H+antiporters