197 related articles for article (PubMed ID: 7758948)
1. The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages.
Martin JF; Bradley A; Olson EN
Genes Dev; 1995 May; 9(10):1237-49. PubMed ID: 7758948
[TBL] [Abstract][Full Text] [Related]
2. MHox and vertebrate skeletogenesis: the long and the short of it.
Brickell PM
Bioessays; 1995 Sep; 17(9):750-3. PubMed ID: 8763826
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. DeltaEF1, a zinc finger and homeodomain transcription factor, is required for skeleton patterning in multiple lineages.
Takagi T; Moribe H; Kondoh H; Higashi Y
Development; 1998 Jan; 125(1):21-31. PubMed ID: 9389660
[TBL] [Abstract][Full Text] [Related]
5. Prx1 and Prx2 in skeletogenesis: roles in the craniofacial region, inner ear and limbs.
ten Berge D; Brouwer A; Korving J; Martin JF; Meijlink F
Development; 1998 Oct; 125(19):3831-42. PubMed ID: 9729491
[TBL] [Abstract][Full Text] [Related]
6. Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2.
Zhang J; Hagopian-Donaldson S; Serbedzija G; Elsemore J; Plehn-Dujowich D; McMahon AP; Flavell RA; Williams T
Nature; 1996 May; 381(6579):238-41. PubMed ID: 8622766
[TBL] [Abstract][Full Text] [Related]
7. The expression pattern of the chick homeobox gene gMHox suggests a role in patterning of the limbs and face and in compartmentalization of somites.
Kuratani S; Martin JF; Wawersik S; Lilly B; Eichele G; Olson EN
Dev Biol; 1994 Feb; 161(2):357-69. PubMed ID: 7906232
[TBL] [Abstract][Full Text] [Related]
8. Bone morphogenetic protein regulation of forkhead/winged helix transcription factor Foxc2 (Mfh1) in a murine mesodermal cell line C1 and in skeletal precursor cells.
Nifuji A; Miura N; Kato N; Kellermann O; Noda M
J Bone Miner Res; 2001 Oct; 16(10):1765-71. PubMed ID: 11585339
[TBL] [Abstract][Full Text] [Related]
9. MHox: a mesodermally restricted homeodomain protein that binds an essential site in the muscle creatine kinase enhancer.
Cserjesi P; Lilly B; Bryson L; Wang Y; Sassoon DA; Olson EN
Development; 1992 Aug; 115(4):1087-101. PubMed ID: 1360403
[TBL] [Abstract][Full Text] [Related]
10. Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest.
Gendron-Maguire M; Mallo M; Zhang M; Gridley T
Cell; 1993 Dec; 75(7):1317-31. PubMed ID: 7903600
[TBL] [Abstract][Full Text] [Related]
11. Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.
Peters H; Neubüser A; Kratochwil K; Balling R
Genes Dev; 1998 Sep; 12(17):2735-47. PubMed ID: 9732271
[TBL] [Abstract][Full Text] [Related]
12. Identification of a prx1 limb enhancer.
Martin JF; Olson EN
Genesis; 2000 Apr; 26(4):225-9. PubMed ID: 10748458
[TBL] [Abstract][Full Text] [Related]
13. Hox group 3 paralogous genes act synergistically in the formation of somitic and neural crest-derived structures.
Manley NR; Capecchi MR
Dev Biol; 1997 Dec; 192(2):274-88. PubMed ID: 9441667
[TBL] [Abstract][Full Text] [Related]
14. Gdf11 is a negative regulator of chondrogenesis and myogenesis in the developing chick limb.
Gamer LW; Cox KA; Small C; Rosen V
Dev Biol; 2001 Jan; 229(2):407-20. PubMed ID: 11203700
[TBL] [Abstract][Full Text] [Related]
15. Targeted disruption of the homeobox transcription factor Bapx1 results in lethal skeletal dysplasia with asplenia and gastroduodenal malformation.
Akazawa H; Komuro I; Sugitani Y; Yazaki Y; Nagai R; Noda T
Genes Cells; 2000 Jun; 5(6):499-513. PubMed ID: 10886375
[TBL] [Abstract][Full Text] [Related]
16. Essential roles of the winged helix transcription factor MFH-1 in aortic arch patterning and skeletogenesis.
Iida K; Koseki H; Kakinuma H; Kato N; Mizutani-Koseki Y; Ohuchi H; Yoshioka H; Noji S; Kawamura K; Kataoka Y; Ueno F; Taniguchi M; Yoshida N; Sugiyama T; Miura N
Development; 1997 Nov; 124(22):4627-38. PubMed ID: 9409679
[TBL] [Abstract][Full Text] [Related]
17. Alx-4, a transcriptional activator whose expression is restricted to sites of epithelial-mesenchymal interactions.
Hudson R; Taniguchi-Sidle A; Boras K; Wiggan O; Hamel PA
Dev Dyn; 1998 Oct; 213(2):159-69. PubMed ID: 9786416
[TBL] [Abstract][Full Text] [Related]
18. In vivo impact of Dlx3 conditional inactivation in neural crest-derived craniofacial bones.
Duverger O; Isaac J; Zah A; Hwang J; Berdal A; Lian JB; Morasso MI
J Cell Physiol; 2013 Mar; 228(3):654-64. PubMed ID: 22886599
[TBL] [Abstract][Full Text] [Related]
19. Conserved molecular program regulating cranial and appendicular skeletogenesis.
Eames BF; Helms JA
Dev Dyn; 2004 Sep; 231(1):4-13. PubMed ID: 15305282
[TBL] [Abstract][Full Text] [Related]
20. Cellular expression of a mutant gene (cmd/cmd) causing limb and other defects in mouse embryos.
Kochhar DM
Prog Clin Biol Res; 1985; 163C():131-44. PubMed ID: 3991615
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
