Detalhe da pesquisa
1.
EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis.
Am J Hum Genet
; 109(12): 2230-2252, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36351433
2.
Interleukin-4 Receptor α Signaling in Myeloid Cells Controls Collagen Fibril Assembly in Skin Repair.
Immunity
; 43(4): 803-16, 2015 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-26474656
3.
Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2.
Am J Hum Genet
; 107(5): 989-999, 2020 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33053334
4.
The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal-Epidermal Junction of Mouse Skin.
Int J Mol Sci
; 24(7)2023 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37047755
5.
Collagen type VI is the antigen recognized by the ER-TR7 antibody.
Eur J Immunol
; 51(9): 2345-2347, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34180542
6.
Structure of a collagen VI α3 chain VWA domain array: adaptability and functional implications of myopathy causing mutations.
J Biol Chem
; 295(36): 12755-12771, 2020 09 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32719005
7.
C-terminal proteolysis of the collagen VI α3 chain by BMP-1 and proprotein convertase(s) releases endotrophin in fragments of different sizes.
J Biol Chem
; 294(37): 13769-13780, 2019 09 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31346034
8.
Collagen VI Contains Multiple Host Defense Peptides with Potent In Vivo Activity.
J Immunol
; 201(3): 1007-1020, 2018 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29925677
9.
Mice Lacking the Matrilin Family of Extracellular Matrix Proteins Develop Mild Skeletal Abnormalities and Are Susceptible to Age-Associated Osteoarthritis.
Int J Mol Sci
; 21(2)2020 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31963938
10.
The cartilage-specific lectin C-type lectin domain family 3 member A (CLEC3A) enhances tissue plasminogen activator-mediated plasminogen activation.
J Biol Chem
; 293(1): 203-214, 2018 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29146595
11.
The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta.
Hum Mol Genet
; 26(15): 2897-2911, 2017 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28475764
12.
Gene Expression Profiling of the Extracellular Matrix Signature in Macrophages of Different Activation Status: Relevance for Skin Wound Healing.
Int J Mol Sci
; 20(20)2019 Oct 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-31615030
13.
Identification of antibodies against extracellular matrix proteins in human osteoarthritis.
Biochem Biophys Res Commun
; 503(3): 1273-1277, 2018 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30001809
14.
Heterogeneity of Collagen VI Microfibrils: STRUCTURAL ANALYSIS OF NON-COLLAGENOUS REGIONS.
J Biol Chem
; 291(10): 5247-58, 2016 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26742845
15.
Matrilin-1 is essential for zebrafish development by facilitating collagen II secretion.
J Biol Chem
; 289(3): 1505-18, 2014 Jan 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-24293366
16.
A mouse model for dominant collagen VI disorders: heterozygous deletion of Col6a3 Exon 16.
J Biol Chem
; 289(15): 10293-10307, 2014 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-24563484
17.
Characterization of recombinantly expressed matrilin VWA domains.
Protein Expr Purif
; 107: 20-8, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25462806
18.
ANTXR1 deficiency promotes fibroblast senescence: implications for GAPO syndrome as a progeroid disorder.
Sci Rep
; 14(1): 9321, 2024 04 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38653789
19.
EMILIN-3, peculiar member of elastin microfibril interface-located protein (EMILIN) family, has distinct expression pattern, forms oligomeric assemblies, and serves as transforming growth factor ß (TGF-ß) antagonist.
J Biol Chem
; 287(14): 11498-515, 2012 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-22334695
20.
Genetic analysis of fin development in zebrafish identifies furin and hemicentin1 as potential novel fraser syndrome disease genes.
PLoS Genet
; 6(4): e1000907, 2010 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20419147