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Items: 1 to 20 of 76

1.

Filamin-interacting proteins, Cfm1 and Cfm2, are essential for the formation of cartilaginous skeletal elements.

Mizuhashi K, Kanamoto T, Moriishi T, Muranishi Y, Miyazaki T, Terada K, Omori Y, Ito M, Komori T, Furukawa T.

Hum Mol Genet. 2014 Jun 1;23(11):2953-67. doi: 10.1093/hmg/ddu007. Epub 2014 Jan 16.

PMID:
24436304
2.

Filamin B mutations cause chondrocyte defects in skeletal development.

Lu J, Lian G, Lenkinski R, De Grand A, Vaid RR, Bryce T, Stasenko M, Boskey A, Walsh C, Sheen V.

Hum Mol Genet. 2007 Jul 15;16(14):1661-75. Epub 2007 May 17.

PMID:
17510210
3.

Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development.

Zhou X, Tian F, Sandzén J, Cao R, Flaberg E, Szekely L, Cao Y, Ohlsson C, Bergo MO, Borén J, Akyürek LM.

Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):3919-24. Epub 2007 Feb 26.

4.

Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome.

Farrington-Rock C, Kirilova V, Dillard-Telm L, Borowsky AD, Chalk S, Rock MJ, Cohn DH, Krakow D.

Hum Mol Genet. 2008 Mar 1;17(5):631-41. Epub 2007 Jul 17.

5.

TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions.

Zieba J, Forlenza KN, Khatra JS, Sarukhanov A, Duran I, Rigueur D, Lyons KM, Cohn DH, Merrill AE, Krakow D.

PLoS Genet. 2016 Mar 28;12(3):e1005936. doi: 10.1371/journal.pgen.1005936. eCollection 2016 Mar.

6.

Formin 1 and filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plate.

Hu J, Lu J, Lian G, Ferland RJ, Dettenhofer M, Sheen VL.

Hum Mol Genet. 2014 Sep 1;23(17):4663-73. doi: 10.1093/hmg/ddu186. Epub 2014 Apr 23.

7.

Filamin B represses chondrocyte hypertrophy in a Runx2/Smad3-dependent manner.

Zheng L, Baek HJ, Karsenty G, Justice MJ.

J Cell Biol. 2007 Jul 2;178(1):121-8.

8.

Filamin B regulates chondrocyte proliferation and differentiation through Cdk1 signaling.

Hu J, Lu J, Lian G, Zhang J, Hecht JL, Sheen VL.

PLoS One. 2014 Feb 14;9(2):e89352. doi: 10.1371/journal.pone.0089352. eCollection 2014.

9.

Opposing FlnA and FlnB interactions regulate RhoA activation in guiding dynamic actin stress fiber formation and cell spreading.

Hu J, Lu J, Goyal A, Wong T, Lian G, Zhang J, Hecht JL, Feng Y, Sheen VL.

Hum Mol Genet. 2017 Apr 1;26(7):1294-1304. doi: 10.1093/hmg/ddx047.

10.

Filamin B: The next hotspot in skeletal research?

Xu Q, Wu N, Cui L, Wu Z, Qiu G.

J Genet Genomics. 2017 Jul 20;44(7):335-342. doi: 10.1016/j.jgg.2017.04.007. Epub 2017 Jul 6. Review.

PMID:
28739045
11.

Cartilage abnormalities are associated with abnormal Phex expression and with altered matrix protein and MMP-9 localization in Hyp mice.

Miao D, Bai X, Panda DK, Karaplis AC, Goltzman D, McKee MD.

Bone. 2004 Apr;34(4):638-47.

PMID:
15050894
12.

Targeted disruption of Shp2 in chondrocytes leads to metachondromatosis with multiple cartilaginous protrusions.

Kim HK, Feng GS, Chen D, King PD, Kamiya N.

J Bone Miner Res. 2014 Mar;29(3):761-9. doi: 10.1002/jbmr.2062.

13.

Cartilage-specific overexpression of ERRγ results in Chondrodysplasia and reduced chondrocyte proliferation.

Cardelli M, Zirngibl RA, Boetto JF, McKenzie KP, Troy TC, Turksen K, Aubin JE.

PLoS One. 2013 Dec 9;8(12):e81511. doi: 10.1371/journal.pone.0081511. eCollection 2013.

14.
15.

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact.

Sheen VL, Feng Y, Graham D, Takafuta T, Shapiro SS, Walsh CA.

Hum Mol Genet. 2002 Nov 1;11(23):2845-54.

PMID:
12393796
16.

The role of hyaluronan produced by Has2 gene expression in development of the spine.

Roughley PJ, Lamplugh L, Lee ER, Matsumoto K, Yamaguchi Y.

Spine (Phila Pa 1976). 2011 Jun 15;36(14):E914-20. doi: 10.1097/BRS.0b013e3181f1e84f.

PMID:
21224752
17.

Evidence for regulation of cartilage differentiation by the homeobox gene Hoxc-8.

Yueh YG, Gardner DP, Kappen C.

Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9956-61.

18.

EXT 1 gene mutation induces chondrocyte cytoskeletal abnormalities and defective collagen expression in the exostoses.

Legeai-Mallet L, Rossi A, Benoist-Lasselin C, Piazza R, Mallet JF, Delezoide AL, Munnich A, Bonaventure J, Zylberberg L.

J Bone Miner Res. 2000 Aug;15(8):1489-500.

19.

The filamin-B-refilin axis - spatiotemporal regulators of the actin-cytoskeleton in development and disease.

Baudier J, Jenkins ZA, Robertson SP.

J Cell Sci. 2018 Apr 13;131(8). pii: jcs213959. doi: 10.1242/jcs.213959. Review.

20.

ALK2 functions as a BMP type I receptor and induces Indian hedgehog in chondrocytes during skeletal development.

Zhang D, Schwarz EM, Rosier RN, Zuscik MJ, Puzas JE, O'Keefe RJ.

J Bone Miner Res. 2003 Sep;18(9):1593-604.

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