Found: 12
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Osteogenesis imperfecta without features of type V caused by a mutation in the IFITM 5 gene.
- Published in:
- Journal of Bone & Mineral Research, 2013, v. 28, n. 11, p. 2333, doi. 10.1002/jbmr.1983
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- Article
Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM 5 Mutation.
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- Journal of Bone & Mineral Research, 2013, v. 28, n. 7, p. 1523, doi. 10.1002/jbmr.1891
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- Article
Mutations in SERPINF1 cause osteogenesis imperfecta type VI.
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- Journal of Bone & Mineral Research, 2011, v. 26, n. 12, p. 2798, doi. 10.1002/jbmr.487
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- Article
Excessive transforming growth factor-β signaling is a common mechanism in osteogenesis imperfecta.
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- Nature Medicine, 2014, v. 20, n. 6, p. 670, doi. 10.1038/nm.3544
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- Article
Small proline‐rich repeat 3 is a novel coordinator of PDGFRβ and integrin β1 crosstalk to augment proliferation and matrix synthesis by cardiac fibroblasts.
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- FASEB Journal, 2020, v. 34, n. 6, p. 7885, doi. 10.1096/fj.201902815R
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- Article
Connective tissue alterations in Fkbp10−/− mice.
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- Human Molecular Genetics, 2014, v. 23, n. 18, p. 4822, doi. 10.1093/hmg/ddu197
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- Article
Differential Effects of Collagen Prolyl 3-Hydroxylation on Skeletal Tissues.
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- PLoS Genetics, 2014, v. 10, n. 1, p. 1, doi. 10.1371/journal.pgen.1004121
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- Article
A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen.
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- Journal of Bone & Mineral Research, 2017, v. 32, n. 6, p. 1309, doi. 10.1002/jbmr.3095
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- Article
Fkbp10 Deletion in Osteoblasts Leads to Qualitative Defects in Bone.
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- Journal of Bone & Mineral Research, 2017, v. 32, n. 6, p. 1354, doi. 10.1002/jbmr.3108
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- Article
Sclerostin Antibody Treatment Improves the Bone Phenotype of Crtap<sup>-/-</sup> Mice, a Model of Recessive Osteogenesis Imperfecta.
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- Journal of Bone & Mineral Research, 2016, v. 31, n. 5, p. 1030, doi. 10.1002/jbmr.2776
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- Article
A Transgenic Mouse Model of OI Type V Supports a Neomorphic Mechanism of the IFITM5 Mutation.
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- Journal of Bone & Mineral Research, 2015, v. 30, n. 3, p. 498, doi. 10.1002/jbmr.2363
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- Article
Loss of SPRR3 in ApoE<sup>-/-</sup> mice leads to atheroma vulnerability through Akt dependent and independent effects in VSMCs.
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- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0184620
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- Article