Found: 4
Select item for more details and to access through your institution.
Loss of Type I Collagen Telopeptide Lysyl Hydroxylation Causes Musculoskeletal Abnormalities in a Zebrafish Model of Bruck Syndrome.
- Published in:
- Journal of Bone & Mineral Research, 2016, v. 31, n. 11, p. 1930, doi. 10.1002/jbmr.2977
- By:
- Publication type:
- Article
MicroCT-based phenomics in the zebrafish skeleton reveals virtues of deep phenotyping in a distributed organ system.
- Published in:
- eLife, 2017, p. 1, doi. 10.7554/eLife.26014
- By:
- Publication type:
- Article
Abnormal Bone Collagen Cross‐Linking in Osteogenesis Imperfecta/Bruck Syndrome Caused by Compound Heterozygous PLOD2 Mutations.
- Published in:
- JBMR Plus, 2021, v. 5, n. 3, p. 1, doi. 10.1002/jbm4.10454
- By:
- Publication type:
- Article
Purification of high-quality RNA from a small number of fluorescence activated cell sorted zebrafish cells for RNA sequencing purposes.
- Published in:
- BMC Genomics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12864-019-5608-2
- By:
- Publication type:
- Article