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Disruption of basal JNK activity differentially affects key fibroblast functions important for wound healing.

Javelaud D, Laboureau J, Gabison E, Verrecchia F, Mauviel A.

J Biol Chem. 2003 Jul 4;278(27):24624-8. Epub 2003 May 1.


Beta-catenin regulates wound size and mediates the effect of TGF-beta in cutaneous healing.

Cheon SS, Wei Q, Gurung A, Youn A, Bright T, Poon R, Whetstone H, Guha A, Alman BA.

FASEB J. 2006 Apr;20(6):692-701.


Effects of TGF-beta s on the growth, collagen synthesis and collagen lattice contraction of human dental pulp fibroblasts in vitro.

Chan CP, Lan WH, Chang MC, Chen YJ, Lan WC, Chang HH, Jeng JH.

Arch Oral Biol. 2005 May;50(5):469-79. Epub 2004 Dec 10.


Beta-catenin is a mediator of the response of fibroblasts to irradiation.

Gurung A, Uddin F, Hill RP, Ferguson PC, Alman BA.

Am J Pathol. 2009 Jan;174(1):248-55. doi: 10.2353/ajpath.2009.080576. Epub 2008 Nov 26.


Beta-catenin signaling plays a disparate role in different phases of fracture repair: implications for therapy to improve bone healing.

Chen Y, Whetstone HC, Lin AC, Nadesan P, Wei Q, Poon R, Alman BA.

PLoS Med. 2007 Jul 31;4(7):e249.


The pro-fibrogenic effect of nerve growth factor on conjunctival fibroblasts is mediated by transforming growth factor-beta.

Micera A, Puxeddu I, Lambiase A, Antonelli A, Bonini S, Bonini S, Aloe L, Pe'er J, Levi-Schaffer F.

Clin Exp Allergy. 2005 May;35(5):650-6.


Type-1 Collagen differentially alters beta-catenin accumulation in primary Dupuytren's Disease cord and adjacent palmar fascia cells.

Vi L, Njarlangattil A, Wu Y, Gan BS, O'Gorman DB.

BMC Musculoskelet Disord. 2009 Jun 19;10:72. doi: 10.1186/1471-2474-10-72.


The role of the tetraspanin CD151 in primary keratinocyte and fibroblast functions: implications for wound healing.

Geary SM, Cowin AJ, Copeland B, Baleato RM, Miyazaki K, Ashman LK.

Exp Cell Res. 2008 Jul 1;314(11-12):2165-75. doi: 10.1016/j.yexcr.2008.04.011. Epub 2008 May 3.


The effect of growth factor signaling on keratocytes in vitro and its relationship to the phases of stromal wound repair.

Etheredge L, Kane BP, Hassell JR.

Invest Ophthalmol Vis Sci. 2009 Jul;50(7):3128-36. doi: 10.1167/iovs.08-3077. Epub 2009 Feb 21.


Regulation of proliferation, motility, and contractivity of cultured human endometrial stromal cells by transforming growth factor-beta isoforms.

Nasu K, Nishida M, Matsumoto H, Bing S, Inoue C, Kawano Y, Miyakawa I.

Fertil Steril. 2005 Oct;84 Suppl 2:1114-23.


Fetal fibroblast contraction of collagen matrices in vitro: the effects of epidermal growth factor and transforming growth factor-beta.

Piscatelli SJ, Michaels BM, Gregory P, Jennings RW, Longaker MT, Harrison MR, Siebert JW.

Ann Plast Surg. 1994 Jul;33(1):38-45.


Collagen and collagenase gene expression in three-dimensional collagen lattices are differentially regulated by alpha 1 beta 1 and alpha 2 beta 1 integrins.

Langholz O, Röckel D, Mauch C, Kozlowska E, Bank I, Krieg T, Eckes B.

J Cell Biol. 1995 Dec;131(6 Pt 2):1903-15.


Fibroblasts in mechanically stressed collagen lattices assume a "synthetic" phenotype.

Kessler D, Dethlefsen S, Haase I, Plomann M, Hirche F, Krieg T, Eckes B.

J Biol Chem. 2001 Sep 28;276(39):36575-85. Epub 2001 Jul 23.


Cell surface CD44-related chondroitin sulfate proteoglycan is required for transforming growth factor-beta-stimulated mouse melanoma cell motility and invasive behavior on type I collagen.

Faassen AE, Mooradian DL, Tranquillo RT, Dickinson RB, Letourneau PC, Oegema TR, McCarthy JB.

J Cell Sci. 1993 Jun;105 ( Pt 2):501-11.


Wnt3a induces myofibroblast differentiation by upregulating TGF-β signaling through SMAD2 in a β-catenin-dependent manner.

Carthy JM, Garmaroudi FS, Luo Z, McManus BM.

PLoS One. 2011;6(5):e19809. doi: 10.1371/journal.pone.0019809. Epub 2011 May 18.

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