Is the 32-kDa fragment the functional enamelin unit in all species?
- Published in:
- European Journal of Oral Sciences, 2011, v. 119, p. 345, doi. 10.1111/j.1600-0722.2011.00869.x
- By:
- Publication type:
- Article
Works by Martin J. Barron
Results: 9
1
2
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 10, p. 1863, doi. 10.1093/hmg/ddx090
- By:
- Publication type:
- Article
3
Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrate.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 9, p. 2468, doi. 10.1093/hmg/ddt642
- By:
- Publication type:
- Article
4
Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions.
- Published in:
- Brain: A Journal of Neurology, 2006, v. 129, n. 12, p. 3391, doi. 10.1093/brain/awl282
- By:
- Publication type:
- Article
5
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.
- Published in:
- 2008
- By:
- Publication type:
- journal article
6
Familial myopathy: New insights into the T14709C mitochondrial tRNA mutation.
- Published in:
- Annals of Neurology, 2004, v. 55, n. 4, p. 478
- By:
- Publication type:
- Article
7
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 7, p. 1230, doi. 10.1093/hmg/ddq001
- By:
- Publication type:
- Article
8
The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3509, doi. 10.1093/hmg/ddn243
- By:
- Publication type:
- Article
9
The Unfolded Protein Response in Amelogenesis and Enamel Pathologies.
- Published in:
- Frontiers in Physiology, 2017, p. 1, doi. 10.3389/fphys.2017.00653
- By:
- Publication type:
- Article