Found: 12
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Identification of osteopontin phosphorylation sites involved in bone remodeling and inhibition of pathological calcification.
- Published in:
- Journal of Cellular Biochemistry, 2008, v. 103, n. 3, p. 852, doi. 10.1002/jcb.21453
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- Article
Editorial: Organs integrative endocrinology - the interplay between the pathways regulating endocrine organs.
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- Frontiers in Endocrinology, 2023, p. 1, doi. 10.3389/fendo.2023.1323185
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- Article
Novel insights into the complex architecture of osteoporosis molecular genetics.
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- Annals of the New York Academy of Sciences, 2020, v. 1462, n. 1, p. 37, doi. 10.1111/nyas.14231
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- Article
Advances in Dystrophinopathy Diagnosis and Therapy.
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- Biomolecules (2218-273X), 2023, v. 13, n. 9, p. 1319, doi. 10.3390/biom13091319
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- Article
Age dependence of expression of growth factor receptors in porcine ACL fibroblasts.
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- Journal of Orthopaedic Research, 2010, v. 28, n. 8, p. 1107, doi. 10.1002/jor.21111
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- Article
VEGF receptor mRNA expression by ACL fibroblasts is associated with functional healing of the ACL.
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- Knee Surgery, Sports Traumatology, Arthroscopy, 2011, v. 19, n. 10, p. 1675, doi. 10.1007/s00167-011-1443-y
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- Article
Novel mutations and polymorphisms in the human dystrophin gene detected by double-strand conformation analysis.
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- Human Mutation, 1997, v. 9, n. 2, p. 188, doi. 10.1002/(SICI)1098-1004(1997)9:2<188::AID-HUMU15>3.0.CO;2-Z
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- Article
Scheimpflug Imaging in Operated Primary Congenital Glaucoma.
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- Journal of Pediatric Ophthalmology & Strabismus, 2021, v. 58, n. 4, p. 218, doi. 10.3928/01913913-20210211-02
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- Article
Up-regulation of soluble vascular endothelial growth factor receptor-1 prevents angiogenesis in hypertrophied myocardium.
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- Cardiovascular Research, 2011, v. 89, n. 2, p. 410, doi. 10.1093/cvr/cvq321
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- Article
Proteomic analysis of mineralising osteoblasts identifies novel genes related to bone matrix mineralisation.
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- International Orthopaedics, 2011, v. 35, n. 3, p. 447, doi. 10.1007/s00264-010-1076-7
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- Article
DXS997 localized to intron 48 of dystrophin.
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- Human Molecular Genetics, 1993, v. 2, n. 12, p. 2199
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- Article
A 3′ consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions.
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- Human Molecular Genetics, 1992, v. 1, n. 5, p. 345
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- Article