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Items: 1 to 20 of 88

1.

Bone lessons from Marfan syndrome and related disorders: fibrillin, TGF-B and BMP at the balance of too long and too short.

Loeys BL, Mortier G, Dietz HC.

Pediatr Endocrinol Rev. 2013 Jun;10 Suppl 2:417-23. Review.

PMID:
23858625
2.

Microfibrils: a cornerstone of extracellular matrix and a key to understand Marfan syndrome.

Bonetti MI.

Ital J Anat Embryol. 2009 Oct-Dec;114(4):201-24. Review.

PMID:
20578676
3.

Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes.

Cook JR, Carta L, Galatioto J, Ramirez F.

Clin Genet. 2015;87(1):11-20. doi: 10.1111/cge.12436. Epub 2014 Jul 10. Review.

PMID:
24867163
4.

[Molecular biological aspects of Marfan syndromes].

Belsing TZ, Lund AM, Abildstrøm SZ, Søndergaard L, Friis-Hansen L.

Ugeskr Laeger. 2011 Jan 31;173(5):333-7. Review. Danish.

PMID:
21276395
5.

Bone matrix to growth factors: location, location, location.

Rifkin DB, Todorovic V.

J Cell Biol. 2010 Sep 20;190(6):949-51. doi: 10.1083/jcb.201008116.

6.
7.

Cross talk among TGF-β signaling pathways, integrins, and the extracellular matrix.

Munger JS, Sheppard D.

Cold Spring Harb Perspect Biol. 2011 Nov 1;3(11):a005017. doi: 10.1101/cshperspect.a005017. Review.

8.

Fibrillin-1 and -2 differentially modulate endogenous TGF-β and BMP bioavailability during bone formation.

Nistala H, Lee-Arteaga S, Smaldone S, Siciliano G, Carta L, Ono RN, Sengle G, Arteaga-Solis E, Levasseur R, Ducy P, Sakai LY, Karsenty G, Ramirez F.

J Cell Biol. 2010 Sep 20;190(6):1107-21. doi: 10.1083/jcb.201003089.

9.

Marfan syndrome: from gene to therapy.

Bolar N, Van Laer L, Loeys BL.

Curr Opin Pediatr. 2012 Aug;24(4):498-504. doi: 10.1097/MOP.0b013e3283557d4c. Review.

PMID:
22705998
10.

Fibrillin-rich microfibrils: Structural determinants of morphogenetic and homeostatic events.

Ramirez F, Dietz HC.

J Cell Physiol. 2007 Nov;213(2):326-30. Review.

PMID:
17708531
11.

Targeting of bone morphogenetic protein growth factor complexes to fibrillin.

Sengle G, Charbonneau NL, Ono RN, Sasaki T, Alvarez J, Keene DR, Bächinger HP, Sakai LY.

J Biol Chem. 2008 May 16;283(20):13874-88. doi: 10.1074/jbc.M707820200. Epub 2008 Mar 13.

12.

TGF-β signalopathies as a paradigm for translational medicine.

Cannaerts E, van de Beek G, Verstraeten A, Van Laer L, Loeys B.

Eur J Med Genet. 2015 Dec;58(12):695-703. doi: 10.1016/j.ejmg.2015.10.010. Epub 2015 Oct 24. Review.

PMID:
26598797
13.

The prodomain of BMP-7 targets the BMP-7 complex to the extracellular matrix.

Gregory KE, Ono RN, Charbonneau NL, Kuo CL, Keene DR, Bächinger HP, Sakai LY.

J Biol Chem. 2005 Jul 29;280(30):27970-80. Epub 2005 Jun 1.

14.

TGF-beta-dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome.

Ng CM, Cheng A, Myers LA, Martinez-Murillo F, Jie C, Bedja D, Gabrielson KL, Hausladen JM, Mecham RP, Judge DP, Dietz HC.

J Clin Invest. 2004 Dec;114(11):1586-92.

15.

Recent progress in genetics of Marfan syndrome and Marfan-associated disorders.

Mizuguchi T, Matsumoto N.

J Hum Genet. 2007;52(1):1-12. Epub 2006 Oct 24. Review.

PMID:
17061023
16.

miR-29b participates in early aneurysm development in Marfan syndrome.

Merk DR, Chin JT, Dake BA, Maegdefessel L, Miller MO, Kimura N, Tsao PS, Iosef C, Berry GJ, Mohr FW, Spin JM, Alvira CM, Robbins RC, Fischbein MP.

Circ Res. 2012 Jan 20;110(2):312-24. doi: 10.1161/CIRCRESAHA.111.253740. Epub 2011 Nov 23.

17.

Mitral valve disease in Marfan syndrome and related disorders.

Judge DP, Rouf R, Habashi J, Dietz HC.

J Cardiovasc Transl Res. 2011 Dec;4(6):741-7. doi: 10.1007/s12265-011-9314-y. Epub 2011 Aug 25. Review.

PMID:
21866385
18.

Molecular genetics of Marfan syndrome.

Boileau C, Jondeau G, Mizuguchi T, Matsumoto N.

Curr Opin Cardiol. 2005 May;20(3):194-200. Review.

PMID:
15861007
19.

[Interactions between fibrillin-1 and tgf-beta: consequences and human pathology].

Wipff J, Allanore Y, Boileau C.

Med Sci (Paris). 2009 Feb;25(2):161-7. doi: 10.1051/medsci/2009252161. Review. French.

20.

Detection of 15 novel mutations in 52 children from 40 families with the Marfan or Loeys-Dietz syndrome and phenotype-genotype correlations.

Pees C, Michel-Behnke I, Hagl M, Laccone F.

Clin Genet. 2014 Dec;86(6):552-7. doi: 10.1111/cge.12314. Epub 2013 Dec 4.

PMID:
24199744

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