229 related articles for article (PubMed ID: 33516761)
1. The mgΔ
Souza RB; Gyuricza IG; Cassiano LL; Farinha-Arcieri LE; Alvim Liberatore AM; Schuindt do Carmo S; Caldeira W; Cruz MV; Ribeiro AF; Tedesco RC; Reinhardt DP; Smith R; Jun Koh IH; Pereira LV
Exp Eye Res; 2021 Mar; 204():108461. PubMed ID: 33516761
[TBL] [Abstract][Full Text] [Related]
2. Nonselective assembly of fibrillin 1 and fibrillin 2 in the rodent ocular zonule and in cultured cells: implications for Marfan syndrome.
Beene LC; Wang LW; Hubmacher D; Keene DR; Reinhardt DP; Annis DS; Mosher DF; Mecham RP; Traboulsi EI; Apte SS
Invest Ophthalmol Vis Sci; 2013 Dec; 54(13):8337-44. PubMed ID: 24265020
[TBL] [Abstract][Full Text] [Related]
3. Targeted deletion of fibrillin-1 in the mouse eye results in ectopia lentis and other ocular phenotypes associated with Marfan syndrome.
Jones W; Rodriguez J; Bassnett S
Dis Model Mech; 2019 Jan; 12(1):. PubMed ID: 30642872
[TBL] [Abstract][Full Text] [Related]
4. Development, composition, and structural arrangements of the ciliary zonule of the mouse.
Shi Y; Tu Y; De Maria A; Mecham RP; Bassnett S
Invest Ophthalmol Vis Sci; 2013 Apr; 54(4):2504-15. PubMed ID: 23493297
[TBL] [Abstract][Full Text] [Related]
5. Ocular pathology in bovine Marfan's syndrome with demonstration of altered fibrillin immunoreactivity in explanted ciliary body cells.
Pessier AP; Potter KA
Lab Invest; 1996 Jul; 75(1):87-95. PubMed ID: 8683943
[TBL] [Abstract][Full Text] [Related]
6. Human eye development is characterized by coordinated expression of fibrillin isoforms.
Hubmacher D; Reinhardt DP; Plesec T; Schenke-Layland K; Apte SS
Invest Ophthalmol Vis Sci; 2014 Nov; 55(12):7934-44. PubMed ID: 25406291
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Fibrillin-1 mgΔ(lpn) Marfan syndrome mutation associates with preserved proteostasis and bypass of a protein disulfide isomerase-dependent quality checkpoint.
Meirelles T; Araujo TLS; Nolasco P; Moretti AIS; Guido MC; Debbas V; Pereira LV; Laurindo FR
Int J Biochem Cell Biol; 2016 Feb; 71():81-91. PubMed ID: 26718974
[TBL] [Abstract][Full Text] [Related]
9. Fibrillin-1 genetic deficiency leads to pathological ageing of arteries in mice.
Mariko B; Pezet M; Escoubet B; Bouillot S; Andrieu JP; Starcher B; Quaglino D; Jacob MP; Huber P; Ramirez F; Faury G
J Pathol; 2011 May; 224(1):33-44. PubMed ID: 21432852
[TBL] [Abstract][Full Text] [Related]
10. Adamts10 inactivation in mice leads to persistence of ocular microfibrils subsequent to reduced fibrillin-2 cleavage.
Wang LW; Kutz WE; Mead TJ; Beene LC; Singh S; Jenkins MW; Reinhardt DP; Apte SS
Matrix Biol; 2019 Apr; 77():117-128. PubMed ID: 30201140
[TBL] [Abstract][Full Text] [Related]
11. Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome.
Kainulainen K; Karttunen L; Puhakka L; Sakai L; Peltonen L
Nat Genet; 1994 Jan; 6(1):64-9. PubMed ID: 8136837
[TBL] [Abstract][Full Text] [Related]
12. [Computer construction and analysis of protein models of mutant fibrillin-1 gene in Marfan's syndrome].
Shentu XC; Tang XJ; Ye PP; Jin CF; Wang W; Yao K
Zhonghua Yan Ke Za Zhi; 2009 Aug; 45(8):699-702. PubMed ID: 20021881
[TBL] [Abstract][Full Text] [Related]
13. Hyperkyphosis is not dependent on bone mass and quality in the mouse model of Marfan syndrome.
Souza RB; Kawahara EI; Farinha-Arcieri LE; Gyuricza IG; Neofiti-Papi B; Miranda-Rodrigues M; Teixeira MBCG; Fernandes GR; Lemes RB; Reinhardt DP; Gouveia CH; Pereira LV
Bone; 2021 Nov; 152():116073. PubMed ID: 34171513
[TBL] [Abstract][Full Text] [Related]
14. Fibrillin-rich microfibrils of the extracellular matrix: ultrastructure and assembly.
Sherratt MJ; Wess TJ; Baldock C; Ashworth J; Purslow PP; Shuttleworth CA; Kielty CM
Micron; 2001 Feb; 32(2):185-200. PubMed ID: 10936461
[TBL] [Abstract][Full Text] [Related]
15. The roles of two novel FBN1 gene mutations in the genotype-phenotype correlations of Marfan syndrome and ectopia lentis patients with marfanoid habitus.
Li D; Yu J; Gu F; Pang X; Ma X; Li R; Liu N; Ma X
Genet Test; 2008 Jun; 12(2):325-30. PubMed ID: 18471089
[TBL] [Abstract][Full Text] [Related]
16. Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome.
Loeys B; Nuytinck L; Delvaux I; De Bie S; De Paepe A
Arch Intern Med; 2001 Nov; 161(20):2447-54. PubMed ID: 11700157
[TBL] [Abstract][Full Text] [Related]
17. Marfan syndrome: fibrillin expression and microfibrillar abnormalities in a family with predominant ocular defects.
Kielty CM; Davies SJ; Phillips JE; Jones CJ; Shuttleworth CA; Charles SJ
J Med Genet; 1995 Jan; 32(1):1-6. PubMed ID: 7897619
[TBL] [Abstract][Full Text] [Related]
18. A new mouse model for marfan syndrome presents phenotypic variability associated with the genetic background and overall levels of Fbn1 expression.
Lima BL; Santos EJ; Fernandes GR; Merkel C; Mello MR; Gomes JP; Soukoyan M; Kerkis A; Massironi SM; Visintin JA; Pereira LV
PLoS One; 2010 Nov; 5(11):e14136. PubMed ID: 21152435
[TBL] [Abstract][Full Text] [Related]
19. Immunohistochemical evaluation of conjunctival fibrillin-1 in Marfan syndrome.
Ganesh A; Smith C; Chan W; Unger S; Quercia N; Godfrey M; Kraft S; Buncic R; Levin A
Arch Ophthalmol; 2006 Feb; 124(2):205-9. PubMed ID: 16476890
[TBL] [Abstract][Full Text] [Related]
20. Marfan syndrome caused by a novel FBN1 mutation with associated pigmentary glaucoma.
Kuchtey J; Chang TC; Panagis L; Kuchtey RW
Am J Med Genet A; 2013 Apr; 161A(4):880-3. PubMed ID: 23444230
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
