Found: 9
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Mutations in SERPINF1 cause osteogenesis imperfecta type VI.
- Published in:
- Journal of Bone & Mineral Research, 2011, v. 26, n. 12, p. 2798, doi. 10.1002/jbmr.487
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- Publication type:
- Article
Excessive transforming growth factor-β signaling is a common mechanism in osteogenesis imperfecta.
- Published in:
- Nature Medicine, 2014, v. 20, n. 6, p. 670, doi. 10.1038/nm.3544
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- Publication type:
- Article
Generalized Connective Tissue Disease in Crtap-/- Mouse.
- Published in:
- PLoS ONE, 2010, v. 5, n. 5, p. 1, doi. 10.1371/journal.pone.0010560
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- Publication type:
- Article
FoxK1 and FoxK2 in insulin regulation of cellular and mitochondrial metabolism.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09418-0
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- Publication type:
- Article
Connective tissue alterations in Fkbp10−/− mice.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 18, p. 4822, doi. 10.1093/hmg/ddu197
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- Publication type:
- Article
Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B.
- Published in:
- American Journal of Hematology, 2007, v. 82, n. 3, p. 179, doi. 10.1002/ajh.20800
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- Publication type:
- Article
Differential Effects of Collagen Prolyl 3-Hydroxylation on Skeletal Tissues.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 1, p. 1, doi. 10.1371/journal.pgen.1004121
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- Publication type:
- Article
Sclerostin Antibody Treatment Improves the Bone Phenotype of Crtap<sup>-/-</sup> Mice, a Model of Recessive Osteogenesis Imperfecta.
- Published in:
- Journal of Bone & Mineral Research, 2016, v. 31, n. 5, p. 1030, doi. 10.1002/jbmr.2776
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- Publication type:
- Article
Lipodystrophy Due to Adipose Tissue-Specific Insulin Receptor Knockout Results in Progressive NAFLD.
- Published in:
- 2016
- By:
- Publication type:
- journal article