Associated Papers
The molecular spectrum of Turkish osteopetrosis and related osteoclast disorders with natural history, including a candidate gene, CCDC120.
Tüysüz B et al.
Bone, 2023
Identification of Key Amino Acid Residues Involved in the Localization of Sorting Nexin 10 and Induction of Vacuole Formation.
Xiao B et al.
Biochemistry. Biokhimiia, 2021
The molecular structure and function of sorting nexin 10 in skeletal disorders, cancers, and other pathological conditions.
Xu J et al.
Journal of Cellular Physiology, 2021
Sorting Nexin 10 as a Key Regulator of Membrane Trafficking in Bone-Resorbing Osteoclasts: Lessons Learned From Osteopetrosis.
Elson A et al.
Frontiers in Cell and Developmental Biology, 2021
Structure of human SNX10 reveals insights into its role in human autosomal recessive osteopetrosis.
Xu T et al.
Proteins, 2014
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity.
Pangrazio A et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research, 2013
Snx10: a newly identified locus associated with human osteopetrosis.
Ye L et al.
Ibms Bonekey, 2013
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