Detalhe da pesquisa
1.
Microscale mapping of extracellular matrix elasticity of mouse joint cartilage: an approach to extracting bulk elasticity of soft matter with surface roughness.
Soft Matter
; 14(15): 2879-2892, 2018 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-29582024
2.
Haploinsufficiency for either one of the type-II regulatory subunits of protein kinase A improves the bone phenotype of Prkar1a+/- mice.
Hum Mol Genet
; 24(21): 6080-92, 2015 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26246497
3.
Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfecta.
PLoS Genet
; 10(6): e1004465, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24968150
4.
Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutations.
Hum Mutat
; 34(9): 1279-88, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23712425
5.
Matrix disruptions, growth, and degradation of cartilage with impaired sulfation.
J Biol Chem
; 287(26): 22030-42, 2012 Jun 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-22556422
6.
Alternate protein kinase A activity identifies a unique population of stromal cells in adult bone.
Proc Natl Acad Sci U S A
; 107(19): 8683-8, 2010 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-20421483
7.
A facile, one-step nanocarbon functionalization for biomedical applications.
Nano Lett
; 12(7): 3613-20, 2012 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-22694219
8.
Bone Formation in 2D Culture of Primary Cells.
JBMR Plus
; 7(1): e10701, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36699640
9.
Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix.
Hum Mutat
; 33(11): 1589-98, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22718341
10.
In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knockin murine model for classical, dominant osteogenesis imperfecta.
Blood
; 114(2): 459-68, 2009 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-19414862
11.
Substitutions for arginine at position 780 in triple helical domain of the α1(I) chain alter folding of the type I procollagen molecule and cause osteogenesis imperfecta.
PLoS One
; 13(7): e0200264, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29990383
12.
Conditions for insensitivity of the microscopic-scale dielectric response to structural details of dipolar liquids.
Phys Rev E Stat Nonlin Soft Matter Phys
; 76(6 Pt 1): 062503, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18233884
13.
Celecoxib treatment of fibrous dysplasia (FD) in a human FD cell line and FD-like lesions in mice with protein kinase A (PKA) defects.
Mol Cell Endocrinol
; 439: 165-174, 2017 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27498419
14.
Osteoblast Malfunction Caused by Cell Stress Response to Procollagen Misfolding in α2(I)-G610C Mouse Model of Osteogenesis Imperfecta.
J Bone Miner Res
; 31(8): 1608-1616, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26925839
15.
Structural heterogeneity of type I collagen triple helix and its role in osteogenesis imperfecta.
J Biol Chem
; 283(8): 4787-98, 2008 Feb 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-18073209
16.
Anomalous microscopic dielectric response of dipolar solvents and water.
J Phys Chem A
; 109(1): 44-56, 2005 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-16839088
17.
Interactions of inorganic phosphate and sulfate anions with collagen.
Biochemistry
; 43(47): 14901-12, 2004 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-15554697