188 related articles for article (PubMed ID: 9256350)
1. Insertional mutation of the mouse Msx1 homeobox gene by an nlacZ reporter gene.
Houzelstein D; Cohen A; Buckingham ME; Robert B
Mech Dev; 1997 Jul; 65(1-2):123-33. PubMed ID: 9256350
[TBL] [Abstract][Full Text] [Related]
2. The homeobox gene Msx1 is expressed in a subset of somites, and in muscle progenitor cells migrating into the forelimb.
Houzelstein D; Auda-Boucher G; Chéraud Y; Rouaud T; Blanc I; Tajbakhsh S; Buckingham ME; Fontaine-Pérus J; Robert B
Development; 1999 Jun; 126(12):2689-701. PubMed ID: 10331980
[TBL] [Abstract][Full Text] [Related]
3. A signaling cascade involving endothelin-1, dHAND and msx1 regulates development of neural-crest-derived branchial arch mesenchyme.
Thomas T; Kurihara H; Yamagishi H; Kurihara Y; Yazaki Y; Olson EN; Srivastava D
Development; 1998 Aug; 125(16):3005-14. PubMed ID: 9671575
[TBL] [Abstract][Full Text] [Related]
4. Msx1 and Msx2 regulate survival of secondary heart field precursors and post-migratory proliferation of cardiac neural crest in the outflow tract.
Chen YH; Ishii M; Sun J; Sucov HM; Maxson RE
Dev Biol; 2007 Aug; 308(2):421-37. PubMed ID: 17601530
[TBL] [Abstract][Full Text] [Related]
5. Cranial neural crest-derived mesenchymal proliferation is regulated by Msx1-mediated p19(INK4d) expression during odontogenesis.
Han J; Ito Y; Yeo JY; Sucov HM; Maas R; Chai Y
Dev Biol; 2003 Sep; 261(1):183-96. PubMed ID: 12941628
[TBL] [Abstract][Full Text] [Related]
6. LIM homeobox transcription factor Lhx2 inhibits skeletal muscle differentiation in part via transcriptional activation of Msx1 and Msx2.
Kodaka Y; Tanaka K; Kitajima K; Tanegashima K; Matsuda R; Hara T
Exp Cell Res; 2015 Feb; 331(2):309-19. PubMed ID: 25460335
[TBL] [Abstract][Full Text] [Related]
7. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development.
Satokata I; Maas R
Nat Genet; 1994 Apr; 6(4):348-56. PubMed ID: 7914451
[TBL] [Abstract][Full Text] [Related]
8. [Genetic and experimental approach to bony craniofacial growth: the role of the divergent homeobox gene Msx1].
Vi-Fane B; Nefussi JR; Orestes-Cardoso S; Hotton D; Robert B; Chabre C; Berdal A; Davideau JL
Orthod Fr; 2003 Mar; 74(1):103-13. PubMed ID: 15301380
[TBL] [Abstract][Full Text] [Related]
9. Concerted action of Msx1 and Msx2 in regulating cranial neural crest cell differentiation during frontal bone development.
Han J; Ishii M; Bringas P; Maas RL; Maxson RE; Chai Y
Mech Dev; 2007; 124(9-10):729-45. PubMed ID: 17693062
[TBL] [Abstract][Full Text] [Related]
10. Differential impact of MSX1 and MSX2 homeogenes on mouse maxillofacial skeleton.
Berdal A; Molla M; Hotton D; Aïoub M; Lézot F; Néfussi JR; Goubin G
Cells Tissues Organs; 2009; 189(1-4):126-32. PubMed ID: 18769023
[TBL] [Abstract][Full Text] [Related]
11. Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice.
Winograd J; Reilly MP; Roe R; Lutz J; Laughner E; Xu X; Hu L; Asakura T; vander Kolk C; Strandberg JD; Semenza GL
Hum Mol Genet; 1997 Mar; 6(3):369-79. PubMed ID: 9147639
[TBL] [Abstract][Full Text] [Related]
12. BMP-mediated functional cooperation between Dlx5;Dlx6 and Msx1;Msx2 during mammalian limb development.
Vieux-Rochas M; Bouhali K; Mantero S; Garaffo G; Provero P; Astigiano S; Barbieri O; Caratozzolo MF; Tullo A; Guerrini L; Lallemand Y; Robert B; Levi G; Merlo GR
PLoS One; 2013; 8(1):e51700. PubMed ID: 23382810
[TBL] [Abstract][Full Text] [Related]
13. Msx homeobox gene family and craniofacial development.
Alappat S; Zhang ZY; Chen YP
Cell Res; 2003 Dec; 13(6):429-42. PubMed ID: 14728799
[TBL] [Abstract][Full Text] [Related]
14. Expression of muscle segment homeobox genes in the developing myocardium.
Boogerd CJ; Moorman AF; Barnett P
Anat Rec (Hoboken); 2010 Jun; 293(6):998-1001. PubMed ID: 20225205
[TBL] [Abstract][Full Text] [Related]
15. Alterations in gene expression during mesoderm formation and axial patterning in Brachyury (T) embryos.
Rashbass P; Wilson V; Rosen B; Beddington RS
Int J Dev Biol; 1994 Mar; 38(1):35-44. PubMed ID: 7915533
[TBL] [Abstract][Full Text] [Related]
16. The expression of the homeobox gene Msx1 reveals two populations of dermal progenitor cells originating from the somites.
Houzelstein D; Chéraud Y; Auda-Boucher G; Fontaine-Pérus J; Robert B
Development; 2000 May; 127(10):2155-64. PubMed ID: 10769239
[TBL] [Abstract][Full Text] [Related]
17. Combined deficiencies of Msx1 and Msx2 cause impaired patterning and survival of the cranial neural crest.
Ishii M; Han J; Yen HY; Sucov HM; Chai Y; Maxson RE
Development; 2005 Nov; 132(22):4937-50. PubMed ID: 16221730
[TBL] [Abstract][Full Text] [Related]
18. Malleal processus brevis is dispensable for normal hearing in mice.
Zhang Z; Zhang X; Avniel WA; Song Y; Jones SM; Jones TA; Fermin C; Chen Y
Dev Dyn; 2003 May; 227(1):69-77. PubMed ID: 12701100
[TBL] [Abstract][Full Text] [Related]
19. Msx1 and Msx2 in limb mesenchyme modulate digit number and identity.
Bensoussan-Trigano V; Lallemand Y; Saint Cloment C; Robert B
Dev Dyn; 2011 May; 240(5):1190-202. PubMed ID: 21465616
[TBL] [Abstract][Full Text] [Related]
20. Analysis of Msx1; Msx2 double mutants reveals multiple roles for Msx genes in limb development.
Lallemand Y; Nicola MA; Ramos C; Bach A; Cloment CS; Robert B
Development; 2005 Jul; 132(13):3003-14. PubMed ID: 15930102
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
