307 related articles for article (PubMed ID: 10448709)
1. Overexpression of thyroid hormone receptor alpha 1 during zebrafish embryogenesis disrupts hindbrain patterning and implicates retinoic acid receptors in the control of hox gene expression.
Essner JJ; Johnson RG; Hackett PB
Differentiation; 1999 Jul; 65(1):1-11. PubMed ID: 10448709
[TBL] [Abstract][Full Text] [Related]
2. The zebrafish thyroid hormone receptor alpha 1 is expressed during early embryogenesis and can function in transcriptional repression.
Essner JJ; Breuer JJ; Essner RD; Fahrenkrug SC; Hackett PB
Differentiation; 1997 Dec; 62(3):107-17. PubMed ID: 9447705
[TBL] [Abstract][Full Text] [Related]
3. Retinoic acid-dependent establishment of positional information in the hindbrain was conserved during vertebrate evolution.
Ishioka A; Jindo T; Kawanabe T; Hatta K; Parvin MS; Nikaido M; Kuroyanagi Y; Takeda H; Yamasu K
Dev Biol; 2011 Feb; 350(1):154-68. PubMed ID: 20969843
[TBL] [Abstract][Full Text] [Related]
4. Ectopic expression of hoxb2 after retinoic acid treatment or mRNA injection: disruption of hindbrain and craniofacial morphogenesis in zebrafish embryos.
Yan YL; Jowett T; Postlethwait JH
Dev Dyn; 1998 Dec; 213(4):370-85. PubMed ID: 9853959
[TBL] [Abstract][Full Text] [Related]
5. Independent roles for retinoic acid in segmentation and neuronal differentiation in the zebrafish hindbrain.
Linville A; Gumusaneli E; Chandraratna RA; Schilling TF
Dev Biol; 2004 Jun; 270(1):186-99. PubMed ID: 15136149
[TBL] [Abstract][Full Text] [Related]
6. Dynamic and sequential patterning of the zebrafish posterior hindbrain by retinoic acid.
Maves L; Kimmel CB
Dev Biol; 2005 Sep; 285(2):593-605. PubMed ID: 16102743
[TBL] [Abstract][Full Text] [Related]
7. Modulation of normal erythroid differentiation by the endogenous thyroid hormone and retinoic acid receptors: a possible target for v-erbA oncogene action.
Schroeder C; Gibson L; Zenke M; Beug H
Oncogene; 1992 Feb; 7(2):217-27. PubMed ID: 1347914
[TBL] [Abstract][Full Text] [Related]
8. Domains of retinoid signalling and neurectodermal expression of zebrafish otx1 and goosecoid are mutually exclusive.
Joore J; Timmermans A; van de Water S; Folkers GE; van der Saag PT; Zivkovic D
Biochem Cell Biol; 1997; 75(5):601-12. PubMed ID: 9551182
[TBL] [Abstract][Full Text] [Related]
9. Retinoic acid and hindbrain patterning.
Glover JC; Renaud JS; Rijli FM
J Neurobiol; 2006 Jun; 66(7):705-25. PubMed ID: 16688767
[TBL] [Abstract][Full Text] [Related]
10. Involvement of wnt1 and pax2 in the formation of the midbrain-hindbrain boundary in the zebrafish gastrula.
Kelly GM; Moon RT
Dev Genet; 1995; 17(2):129-40. PubMed ID: 7586754
[TBL] [Abstract][Full Text] [Related]
11. Segmental development of reticulospinal and branchiomotor neurons in lamprey: insights into the evolution of the vertebrate hindbrain.
Murakami Y; Pasqualetti M; Takio Y; Hirano S; Rijli FM; Kuratani S
Development; 2004 Mar; 131(5):983-95. PubMed ID: 14973269
[TBL] [Abstract][Full Text] [Related]
12. Retinoic acid alters hindbrain Hox code and induces transformation of rhombomeres 2/3 into a 4/5 identity.
Marshall H; Nonchev S; Sham MH; Muchamore I; Lumsden A; Krumlauf R
Nature; 1992 Dec 24-31; 360(6406):737-41. PubMed ID: 1361214
[TBL] [Abstract][Full Text] [Related]
13. Retinoic acid and thyroid hormone induce gene expression through a common responsive element.
Umesono K; Giguere V; Glass CK; Rosenfeld MG; Evans RM
Nature; 1988 Nov; 336(6196):262-5. PubMed ID: 2848197
[TBL] [Abstract][Full Text] [Related]
14. The v-erbA oncogene requires cooperation with tyrosine kinases to arrest erythroid differentiation induced by ligand-activated endogenous c-erbA and retinoic acid receptor.
Schroeder C; Gibson L; Beug H
Oncogene; 1992 Feb; 7(2):203-16. PubMed ID: 1347913
[TBL] [Abstract][Full Text] [Related]
15. N-CoR is required for patterning the anterior-posterior axis of zebrafish hindbrain by actively repressing retinoid signaling.
Xu F; Li K; Tian M; Hu P; Song W; Chen J; Gao X; Zhao Q
Mech Dev; 2009 Oct; 126(10):771-80. PubMed ID: 19735730
[TBL] [Abstract][Full Text] [Related]
16. Retinoic acid is required for endodermal pouch morphogenesis and not for pharyngeal endoderm specification.
Kopinke D; Sasine J; Swift J; Stephens WZ; Piotrowski T
Dev Dyn; 2006 Oct; 235(10):2695-709. PubMed ID: 16871626
[TBL] [Abstract][Full Text] [Related]
17. Combinatorial roles for zebrafish retinoic acid receptors in the hindbrain, limbs and pharyngeal arches.
Linville A; Radtke K; Waxman JS; Yelon D; Schilling TF
Dev Biol; 2009 Jan; 325(1):60-70. PubMed ID: 18929555
[TBL] [Abstract][Full Text] [Related]
18. Molecular mechanisms of segmental patterning in the vertebrate hindbrain.
Wilkinson DG
Perspect Dev Neurobiol; 1993; 1(3):117-25. PubMed ID: 7916256
[TBL] [Abstract][Full Text] [Related]
19. Early requirement for fgf8 function during hindbrain pattern formation in zebrafish.
Wiellette EL; Sive H
Dev Dyn; 2004 Feb; 229(2):393-9. PubMed ID: 14745965
[TBL] [Abstract][Full Text] [Related]
20. c-ErbA, but not v-ErbA, competes with a putative erythroid repressor for binding to the carbonic anhydrase II promoter.
Rascle A; Ghysdael J; Samarut J
Oncogene; 1994 Oct; 9(10):2853-67. PubMed ID: 7916146
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
