Detalhe da pesquisa
1.
Degradomic Identification of Membrane Type 1-Matrix Metalloproteinase as an ADAMTS9 and ADAMTS20 Substrate.
Mol Cell Proteomics
; 22(6): 100566, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37169079
2.
Emerging roles for the ADAMTS-like family of matricellular proteins in cardiovascular disease through regulation of the extracellular microenvironment.
Mol Biol Rep
; 51(1): 280, 2024 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38324186
3.
Regulation of extracellular matrix composition by fibroblasts during perinatal cardiac maturation.
J Mol Cell Cardiol
; 169: 84-95, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35569524
4.
Proteolysis: a key post-translational modification regulating proteoglycans.
Am J Physiol Cell Physiol
; 323(3): C651-C665, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35785985
5.
Post-translational regulation and proteolytic activity of the metalloproteinase ADAMTS8.
J Biol Chem
; 297(5): 101323, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34687701
6.
Mutations of ADAMTS9 Cause Nephronophthisis-Related Ciliopathy.
Am J Hum Genet
; 104(1): 45-54, 2019 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30609407
7.
Alternative splicing of the metalloprotease ADAMTS17 spacer regulates secretion and modulates autoproteolytic activity.
FASEB J
; 35(2): e21310, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33484187
8.
O-Fucosylation of ADAMTSL2 is required for secretion and is impacted by geleophysic dysplasia-causing mutations.
J Biol Chem
; 295(46): 15742-15753, 2020 11 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32913123
9.
ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in mouse model of Peters plus syndrome.
Hum Mol Genet
; 28(24): 4053-4066, 2019 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31600785
10.
ADAMTSL5 is an epigenetically activated gene underlying tumorigenesis and drug resistance in hepatocellular carcinoma.
J Hepatol
; 74(4): 893-906, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33197513
11.
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
12.
Disruption of the Extracellular Matrix Progressively Impairs Central Nervous System Vascular Maturation Downstream of ß-Catenin Signaling.
Arterioscler Thromb Vasc Biol
; 39(7): 1432-1447, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31242033
13.
A Selective Extracellular Matrix Proteomics Approach Identifies Fibronectin Proteolysis by A Disintegrin-like and Metalloprotease Domain with Thrombospondin Type 1 Motifs (ADAMTS16) and Its Impact on Spheroid Morphogenesis.
Mol Cell Proteomics
; 17(7): 1410-1425, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29669734
14.
Immunoregulatory roles of versican proteolysis in the myeloma microenvironment.
Blood
; 128(5): 680-5, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27259980
15.
Identification and functional analysis of an ADAMTSL1 variant associated with a complex phenotype including congenital glaucoma, craniofacial, and other systemic features in a three-generation human pedigree.
Hum Mutat
; 38(11): 1485-1490, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28722276
16.
Genetic and biochemical evidence that gastrulation defects in Pofut2 mutants result from defects in ADAMTS9 secretion.
Dev Biol
; 416(1): 111-122, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27297885
17.
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation.
Hum Mol Genet
; 24(24): 6958-74, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26405179
18.
Corrigendum to: ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in mouse model of Peters plus syndrome.
Hum Mol Genet
; 29(17): 2986-2987, 2020 10 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32533185
19.
Anti-ADAMTS5 monoclonal antibodies: implications for aggrecanase inhibition in osteoarthritis.
Biochem J
; 473(1): e1-4, 2016 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26657033
20.
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