Detalhe da pesquisa
1.
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay.
Am J Hum Genet
; 108(9): 1710-1724, 2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34450031
2.
Loading-induced bone formation is mediated by Wnt1 induction in osteoblast-lineage cells.
FASEB J
; 36(9): e22502, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35969160
3.
Rac1 activation controls nuclear localization of beta-catenin during canonical Wnt signaling.
Cell
; 133(2): 340-53, 2008 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-18423204
4.
P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA.
J Biol Chem
; 292(9): 3877-3887, 2017 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28115524
5.
Heterozygous WNT1 variant causing a variable bone phenotype.
Am J Med Genet A
; 176(11): 2419-2424, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30246918
6.
Up-regulation of glycolytic metabolism is required for HIF1α-driven bone formation.
Proc Natl Acad Sci U S A
; 111(23): 8673-8, 2014 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-24912186
7.
WNT7B promotes bone formation in part through mTORC1.
PLoS Genet
; 10(1): e1004145, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24497849
8.
Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutations.
J Biol Chem
; 290(13): 8613-22, 2015 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-25645914
9.
The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations.
Hum Mol Genet
; 23(15): 4035-42, 2014 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24634143
10.
WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta.
N Engl J Med
; 368(19): 1809-16, 2013 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-23656646
11.
Restoration of the serum level of SERPINF1 does not correct the bone phenotype in Serpinf1 null mice.
Mol Genet Metab
; 117(3): 378-82, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26693895
12.
Characterization of TGFß1-induced tendon-like structure in the scaffold-free three-dimensional tendon cell culture system.
Sci Rep
; 14(1): 9495, 2024 04 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38664570
13.
Indian hedgehog requires additional effectors besides Runx2 to induce osteoblast differentiation.
Dev Biol
; 362(1): 76-82, 2012 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22155527
14.
Indian Hedgehog signalling triggers Nkx3.2 protein degradation during chondrocyte maturation.
Biochem J
; 443(3): 789-98, 2012 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22507129
15.
Long lifespan in worms with long telomeric DNA.
Nat Genet
; 36(6): 607-11, 2004 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15122256
16.
Lrp5 and Lrp6 redundantly control skeletal development in the mouse embryo.
Dev Biol
; 359(2): 222-9, 2011 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21924256
17.
Noncanonical Wnt signaling through G protein-linked PKCdelta activation promotes bone formation.
Dev Cell
; 12(1): 113-27, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17199045
18.
The Gli2 transcriptional activator is a crucial effector for Ihh signaling in osteoblast development and cartilage vascularization.
Development
; 136(24): 4177-85, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19906844
19.
Transient expansion and myofibroblast conversion of adipogenic lineage precursors mediate bone marrow repair after radiation.
JCI Insight
; 7(7)2022 04 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35393948
20.
Heterozygous variant in WNT1 gene in two brothers with early onset osteoporosis.
Bone Rep
; 15: 101118, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34458510