Detalhe da pesquisa
1.
The Osteogenesis Imperfecta Type V Mutant BRIL/IFITM5 Promotes Transcriptional Activation of MEF2, NFATc, and NR4A in Osteoblasts.
Int J Mol Sci
; 23(4)2022 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35216266
2.
Calvaria Bone Transcriptome in Mouse Models of Osteogenesis Imperfecta.
Int J Mol Sci
; 22(10)2021 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34069814
3.
Selective bacterial degradation of the extracellular matrix attaching the gingiva to the tooth.
Eur J Oral Sci
; 127(4): 313-322, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31230388
4.
Cole-Carpenter syndrome is caused by a heterozygous missense mutation in P4HB.
Am J Hum Genet
; 96(3): 425-31, 2015 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25683117
5.
Recessive osteogenesis imperfecta caused by missense mutations in SPARC.
Am J Hum Genet
; 96(6): 979-85, 2015 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26027498
6.
A polyadenylation site variant causes transcript-specific BMP1 deficiency and frequent fractures in children.
Hum Mol Genet
; 24(2): 516-24, 2015 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25214535
7.
Absence of the dermatan sulfate chain of decorin does not affect mouse development.
J Negat Results Biomed
; 16(1): 7, 2017 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28412940
8.
Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly is caused by a duplication in RUNX2.
Am J Hum Genet
; 92(2): 252-8, 2013 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23290074
9.
Osteogenesis Imperfecta Type I Caused by COL1A1 Deletions.
Calcif Tissue Int
; 98(1): 76-84, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26478226
10.
Osteogenesis Imperfecta Type VI in Individuals from Northern Canada.
Calcif Tissue Int
; 98(6): 566-72, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26815784
11.
Regulation of the bone-restricted IFITM-like (Bril) gene transcription by Sp and Gli family members and CpG methylation.
J Biol Chem
; 288(19): 13278-94, 2013 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23530031
12.
Osteogenic cell cultures cannot utilize exogenous sources of synthetic polyphosphate for mineralization.
J Cell Biochem
; 115(12): 2089-102, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25043819
13.
Characterisation of secretory calcium-binding phosphoprotein-proline-glutamine-rich 1: a novel basal lamina component expressed at cell-tooth interfaces.
Cell Tissue Res
; 358(3): 843-55, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25193156
14.
Targeted sequencing of a pediatric metabolic bone gene panel using a desktop semiconductor next-generation sequencer.
Calcif Tissue Int
; 95(4): 323-31, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25086671
15.
Mutations in WNT1 are a cause of osteogenesis imperfecta.
J Med Genet
; 50(5): 345-8, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23434763
16.
Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.-14C>T mutation in all patients.
J Med Genet
; 50(1): 21-4, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23240094
17.
Expression of odontogenic ameloblast-associated and amelotin proteins in the junctional epithelium.
Periodontol 2000
; 63(1): 59-66, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23931054
18.
Mechanical stress induces bone formation in the maxillary sinus in a short-term mouse model.
Clin Oral Investig
; 17(1): 131-7, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22373776
19.
RNA Sequencing of Urine-Derived Cells for the Characterization and Diagnosis of Osteogenesis Imperfecta.
J Bone Miner Res
; 38(8): 1125-1134, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37293821
20.
Requirements for ion and solute transport, and pH regulation during enamel maturation.
J Cell Physiol
; 227(4): 1776-85, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21732355