148 related articles for article (PubMed ID: 32141660)
1. ADAMTSL6β promotes fibrillin-1 microfibril assembly, which is possibly mediated via binding through the third thrombospondin type I domain to fibrillin-1.
Orimoto A; Fukuda T
Cell Biol Int; 2020 Jul; 44(7):1436-1446. PubMed ID: 32141660
[TBL] [Abstract][Full Text] [Related]
2. ADAMTSL6β protein rescues fibrillin-1 microfibril disorder in a Marfan syndrome mouse model through the promotion of fibrillin-1 assembly.
Saito M; Kurokawa M; Oda M; Oshima M; Tsutsui K; Kosaka K; Nakao K; Ogawa M; Manabe RI; Suda N; Ganjargal G; Hada Y; Noguchi T; Teranaka T; Sekiguchi K; Yoneda T; Tsuji T
J Biol Chem; 2011 Nov; 286(44):38602-38613. PubMed ID: 21880733
[TBL] [Abstract][Full Text] [Related]
3. [Molecular mechanisms for the improvement of wound healing ability of periodontal ligament in Marfan's syndrome].
Saito M; Tsuji T
Clin Calcium; 2012 Jan; 22(1):35-42. PubMed ID: 22201097
[TBL] [Abstract][Full Text] [Related]
4. ADAMTSL-6 is a novel extracellular matrix protein that binds to fibrillin-1 and promotes fibrillin-1 fibril formation.
Tsutsui K; Manabe R; Yamada T; Nakano I; Oguri Y; Keene DR; Sengle G; Sakai LY; Sekiguchi K
J Biol Chem; 2010 Feb; 285(7):4870-82. PubMed ID: 19940141
[TBL] [Abstract][Full Text] [Related]
5. New insights into the structure, assembly and biological roles of 10-12 nm connective tissue microfibrils from fibrillin-1 studies.
Jensen SA; Handford PA
Biochem J; 2016 Apr; 473(7):827-38. PubMed ID: 27026396
[TBL] [Abstract][Full Text] [Related]
6. Genetic and functional linkage between ADAMTS superfamily proteins and fibrillin-1: a novel mechanism influencing microfibril assembly and function.
Hubmacher D; Apte SS
Cell Mol Life Sci; 2011 Oct; 68(19):3137-48. PubMed ID: 21858451
[TBL] [Abstract][Full Text] [Related]
7. Microfibrils: a cornerstone of extracellular matrix and a key to understand Marfan syndrome.
Bonetti MI
Ital J Anat Embryol; 2009; 114(4):201-24. PubMed ID: 20578676
[TBL] [Abstract][Full Text] [Related]
8. ADAMTS proteins as modulators of microfibril formation and function.
Hubmacher D; Apte SS
Matrix Biol; 2015 Sep; 47():34-43. PubMed ID: 25957949
[TBL] [Abstract][Full Text] [Related]
9. In vivo studies of mutant fibrillin-1 microfibrils.
Charbonneau NL; Carlson EJ; Tufa S; Sengle G; Manalo EC; Carlberg VM; Ramirez F; Keene DR; Sakai LY
J Biol Chem; 2010 Aug; 285(32):24943-55. PubMed ID: 20529844
[TBL] [Abstract][Full Text] [Related]
10. Fibrillin-rich microfibrils: Structural determinants of morphogenetic and homeostatic events.
Ramirez F; Dietz HC
J Cell Physiol; 2007 Nov; 213(2):326-30. PubMed ID: 17708531
[TBL] [Abstract][Full Text] [Related]
11. Adamtsl2 deletion results in bronchial fibrillin microfibril accumulation and bronchial epithelial dysplasia--a novel mouse model providing insights into geleophysic dysplasia.
Hubmacher D; Wang LW; Mecham RP; Reinhardt DP; Apte SS
Dis Model Mech; 2015 May; 8(5):487-99. PubMed ID: 25762570
[TBL] [Abstract][Full Text] [Related]
12. Biogenesis of extracellular microfibrils: Multimerization of the fibrillin-1 C terminus into bead-like structures enables self-assembly.
Hubmacher D; El-Hallous EI; Nelea V; Kaartinen MT; Lee ER; Reinhardt DP
Proc Natl Acad Sci U S A; 2008 May; 105(18):6548-53. PubMed ID: 18448684
[TBL] [Abstract][Full Text] [Related]
13. ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis.
Gabriel LA; Wang LW; Bader H; Ho JC; Majors AK; Hollyfield JG; Traboulsi EI; Apte SS
Invest Ophthalmol Vis Sci; 2012 Jan; 53(1):461-9. PubMed ID: 21989719
[TBL] [Abstract][Full Text] [Related]
14. Heparin/heparan sulfate controls fibrillin-1, -2 and -3 self-interactions in microfibril assembly.
Sabatier L; Djokic J; Hubmacher D; Dzafik D; Nelea V; Reinhardt DP
FEBS Lett; 2014 Aug; 588(17):2890-7. PubMed ID: 25034023
[TBL] [Abstract][Full Text] [Related]
15. A microfibril assembly assay identifies different mechanisms of dominance underlying Marfan syndrome, stiff skin syndrome and acromelic dysplasias.
Jensen SA; Iqbal S; Bulsiewicz A; Handford PA
Hum Mol Genet; 2015 Aug; 24(15):4454-63. PubMed ID: 25979247
[TBL] [Abstract][Full Text] [Related]
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.
Bader HL; Wang LW; Ho JC; Tran T; Holden P; Fitzgerald J; Atit RP; Reinhardt DP; Apte SS
Matrix Biol; 2012; 31(7-8):398-411. PubMed ID: 23010571
[TBL] [Abstract][Full Text] [Related]
17. Assembly assay identifies a critical region of human fibrillin-1 required for 10-12 nm diameter microfibril biogenesis.
Jensen SA; Atwa O; Handford PA
PLoS One; 2021; 16(3):e0248532. PubMed ID: 33735269
[TBL] [Abstract][Full Text] [Related]
18. Basic components of connective tissues and extracellular matrix: elastin, fibrillin, fibulins, fibrinogen, fibronectin, laminin, tenascins and thrombospondins.
Halper J; Kjaer M
Adv Exp Med Biol; 2014; 802():31-47. PubMed ID: 24443019
[TBL] [Abstract][Full Text] [Related]
19. Metal ion dependency of microfibrils supports a rod-like conformation for fibrillin-1 calcium-binding epidermal growth factor-like domains.
Cardy CM; Handford PA
J Mol Biol; 1998 Mar; 276(5):855-60. PubMed ID: 9566191
[TBL] [Abstract][Full Text] [Related]
20. Fibrillin: from microfibril assembly to biomechanical function.
Kielty CM; Baldock C; Lee D; Rock MJ; Ashworth JL; Shuttleworth CA
Philos Trans R Soc Lond B Biol Sci; 2002 Feb; 357(1418):207-17. PubMed ID: 11911778
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]