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UnknownThe contribution of rare variation to prostate cancer heritability.
Not available
S-EPMC7534691 | biostudies-literature
UnknownAbnormal Bone Collagen Cross-Linking in Osteogenesis Imperfecta/Bruck Syndrome Caused by Compound Heterozygous PLOD2 Mutations.
Not available
S-EPMC7990156 | biostudies-literature
UnknownA Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen.
Not available
S-EPMC5466459 | biostudies-literature
UnknownLoss of the long form of Plod2 phenocopies contractures of Bruck syndrome-osteogenesis imperfecta.
Not available
S-EPMC11371901 | biostudies-literature
UnknownHSP47 and FKBP65 cooperate in the synthesis of type I procollagen.
Not available
S-EPMC4355024 | biostudies-literature
UnknownLocalized chondro-ossification underlies joint dysfunction and motor deficits in the Fkbp10 mouse model of osteogenesis imperfecta.
Not available
S-EPMC8237619 | biostudies-literature
UnknownConnective tissue alterations in Fkbp10-/- mice.
Not available
S-EPMC4140464 | biostudies-literature
UnknownFkbp10 Deletion in Osteoblasts Leads to Qualitative Defects in Bone.
Not available
S-EPMC5466482 | biostudies-literature
UnknownIdentification of SOX3 as an XX male sex reversal gene in mice and humans.
Not available
S-EPMC3007141 | biostudies-literature
UnknownCRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.
Not available
S-EPMC2671575 | biostudies-literature
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