Detalhe da pesquisa
1.
A disintegrin-like and metalloproteinase domain with thrombospondin type 1 motif 9 (ADAMTS9) regulates fibronectin fibrillogenesis and turnover.
J Biol Chem
; 294(25): 9924-9936, 2019 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-31085586
2.
ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulation.
Nat Genet
; 40(9): 1119-23, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18677313
3.
Time-resolved analysis of the matrix metalloproteinase 10 substrate degradome.
Mol Cell Proteomics
; 13(2): 580-93, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24281761
4.
Mutations in the TGFß binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias.
Am J Hum Genet
; 89(1): 7-14, 2011 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21683322
5.
ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts.
J Biol Chem
; 286(19): 17156-67, 2011 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-21402694
6.
Proteolysis of fibrillin-2 microfibrils is essential for normal skeletal development.
Elife
; 112022 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35503090
7.
ADAMTS9 is a cell-autonomously acting, anti-angiogenic metalloprotease expressed by microvascular endothelial cells.
Am J Pathol
; 176(3): 1494-504, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20093484
8.
Post-translational modification of thrombospondin type-1 repeats in ADAMTS-like 1/punctin-1 by C-mannosylation of tryptophan.
J Biol Chem
; 284(44): 30004-15, 2009 Oct 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-19671700
9.
Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis.
Nat Commun
; 10(1): 953, 2019 02 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-30814516
10.
Adamts10 inactivation in mice leads to persistence of ocular microfibrils subsequent to reduced fibrillin-2 cleavage.
Matrix Biol
; 77: 117-128, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30201140
11.
Functional analysis of an ADAMTS10 signal peptide mutation in Weill-Marchesani syndrome demonstrates a long-range effect on secretion of the full-length enzyme.
Hum Mutat
; 29(12): 1425-34, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18567016
12.
Impaired ADAMTS9 secretion: A potential mechanism for eye defects in Peters Plus Syndrome.
Sci Rep
; 6: 33974, 2016 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-27687499
13.
Adamtsl2 deletion results in bronchial fibrillin microfibril accumulation and bronchial epithelial dysplasia--a novel mouse model providing insights into geleophysic dysplasia.
Dis Model Mech
; 8(5): 487-99, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25762570
14.
Hedgehog pathway inhibition in chondrosarcoma using the smoothened inhibitor IPI-926 directly inhibits sarcoma cell growth.
Mol Cancer Ther
; 13(5): 1259-69, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24634412
15.
Nonselective assembly of fibrillin 1 and fibrillin 2 in the rodent ocular zonule and in cultured cells: implications for Marfan syndrome.
Invest Ophthalmol Vis Sci
; 54(13): 8337-44, 2013 Dec 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-24265020
16.
A disintegrin-like and metalloprotease domain containing thrombospondin type 1 motif-like 5 (ADAMTSL5) is a novel fibrillin-1-, fibrillin-2-, and heparin-binding member of the ADAMTS superfamily containing a netrin-like module.
Matrix Biol
; 31(7-8): 398-411, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23010571
17.
ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis.
Invest Ophthalmol Vis Sci
; 53(1): 461-9, 2012 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-21989719
18.
An ADAMTSL2 founder mutation causes Musladin-Lueke Syndrome, a heritable disorder of beagle dogs, featuring stiff skin and joint contractures.
PLoS One
; 5(9)2010 Sep 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-20862248
19.
O-fucosylation of thrombospondin type 1 repeats in ADAMTS-like-1/punctin-1 regulates secretion: implications for the ADAMTS superfamily.
J Biol Chem
; 282(23): 17024-31, 2007 Jun 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-17395588
20.
ADAMTS7B, the full-length product of the ADAMTS7 gene, is a chondroitin sulfate proteoglycan containing a mucin domain.
J Biol Chem
; 279(34): 35159-75, 2004 Aug 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-15192113