1050 related articles for article (PubMed ID: 10192400)
1. Embryonic retinoic acid synthesis is essential for early mouse post-implantation development.
Niederreither K; Subbarayan V; Dollé P; Chambon P
Nat Genet; 1999 Apr; 21(4):444-8. PubMed ID: 10192400
[TBL] [Abstract][Full Text] [Related]
2. Dorsal pancreas agenesis in retinoic acid-deficient Raldh2 mutant mice.
Martín M; Gallego-Llamas J; Ribes V; Kedinger M; Niederreither K; Chambon P; Dollé P; Gradwohl G
Dev Biol; 2005 Aug; 284(2):399-411. PubMed ID: 16026781
[TBL] [Abstract][Full Text] [Related]
3. Rescue of morphogenetic defects and of retinoic acid signaling in retinaldehyde dehydrogenase 2 (Raldh2) mouse mutants by chimerism with wild-type cells.
Vermot J; Messaddeq N; Niederreither K; Dierich A; Dollé P
Differentiation; 2006 Dec; 74(9-10):661-8. PubMed ID: 17177861
[TBL] [Abstract][Full Text] [Related]
4. Control of retinoic acid synthesis and FGF expression in the nasal pit is required to pattern the craniofacial skeleton.
Song Y; Hui JN; Fu KK; Richman JM
Dev Biol; 2004 Dec; 276(2):313-29. PubMed ID: 15581867
[TBL] [Abstract][Full Text] [Related]
5. Retinaldehyde dehydrogenase 2 (RALDH2)-mediated retinoic acid synthesis regulates early mouse embryonic forebrain development by controlling FGF and sonic hedgehog signaling.
Ribes V; Wang Z; Dollé P; Niederreither K
Development; 2006 Jan; 133(2):351-61. PubMed ID: 16368932
[TBL] [Abstract][Full Text] [Related]
6. Activation of fgf4 gene expression in the myotomes is regulated by myogenic bHLH factors and by sonic hedgehog.
Fraidenraich D; Iwahori A; Rudnicki M; Basilico C
Dev Biol; 2000 Sep; 225(2):392-406. PubMed ID: 10985858
[TBL] [Abstract][Full Text] [Related]
7. Retinoic acid controls the bilateral symmetry of somite formation in the mouse embryo.
Vermot J; Gallego Llamas J; Fraulob V; Niederreither K; Chambon P; Dollé P
Science; 2005 Apr; 308(5721):563-6. PubMed ID: 15731404
[TBL] [Abstract][Full Text] [Related]
8. Identification of endogenous retinoids, enzymes, binding proteins, and receptors during early postimplantation development in mouse: important role of retinal dehydrogenase type 2 in synthesis of all-trans-retinoic acid.
Ulven SM; Gundersen TE; Weedon MS; Landaas VO; Sakhi AK; Fromm SH; Geronimo BA; Moskaug JO; Blomhoff R
Dev Biol; 2000 Apr; 220(2):379-91. PubMed ID: 10753524
[TBL] [Abstract][Full Text] [Related]
9. Establishment of embryonic neuroepithelial cell lines exhibiting an epiplastic expression pattern of region specific markers.
Nardelli J; Catala M; Charnay P
J Neurosci Res; 2003 Sep; 73(6):737-52. PubMed ID: 12949900
[TBL] [Abstract][Full Text] [Related]
10. Embryonic retinoic acid synthesis is required for forelimb growth and anteroposterior patterning in the mouse.
Niederreither K; Vermot J; Schuhbaur B; Chambon P; Dollé P
Development; 2002 Aug; 129(15):3563-74. PubMed ID: 12117807
[TBL] [Abstract][Full Text] [Related]
11. Retinoic acid coordinates somitogenesis and left-right patterning in vertebrate embryos.
Vermot J; Pourquié O
Nature; 2005 May; 435(7039):215-20. PubMed ID: 15889094
[TBL] [Abstract][Full Text] [Related]
12. Inhibition of Tgf beta signaling by endogenous retinoic acid is essential for primary lung bud induction.
Chen F; Desai TJ; Qian J; Niederreither K; Lü J; Cardoso WV
Development; 2007 Aug; 134(16):2969-79. PubMed ID: 17634193
[TBL] [Abstract][Full Text] [Related]
13. Retinoic acid is essential for Shh/Hoxd signaling during rat limb outgrowth but not for limb initiation.
Power SC; Lancman J; Smith SM
Dev Dyn; 1999 Dec; 216(4-5):469-80. PubMed ID: 10633866
[TBL] [Abstract][Full Text] [Related]
14. Retinoic acid synthesis controlled by Raldh2 is required early for limb bud initiation and then later as a proximodistal signal during apical ectodermal ridge formation.
Mic FA; Sirbu IO; Duester G
J Biol Chem; 2004 Jun; 279(25):26698-706. PubMed ID: 15069081
[TBL] [Abstract][Full Text] [Related]
15. The Hand1 bHLH transcription factor is essential for placentation and cardiac morphogenesis.
Riley P; Anson-Cartwright L; Cross JC
Nat Genet; 1998 Mar; 18(3):271-5. PubMed ID: 9500551
[TBL] [Abstract][Full Text] [Related]
16. The mouse polydactylous mutation, luxate (lx), causes anterior shift of the anteroposterior border in the developing hindlimb bud.
Yada Y; Makino S; Chigusa-Ishiwa S; Shiroishi T
Int J Dev Biol; 2002; 46(7):975-82. PubMed ID: 12455637
[TBL] [Abstract][Full Text] [Related]
17. Effects of all-trans-retinoic acid on skeletal pattern, 5'HoxD gene expression, and RAR beta 2/beta 4 promoter activity in embryonic mouse limbs.
Wood HB; Ward SJ; Morriss-Kay GM
Dev Genet; 1996; 19(1):74-84. PubMed ID: 8792611
[TBL] [Abstract][Full Text] [Related]
18. Rescue of cytochrome P450 oxidoreductase (Por) mouse mutants reveals functions in vasculogenesis, brain and limb patterning linked to retinoic acid homeostasis.
Ribes V; Otto DM; Dickmann L; Schmidt K; Schuhbaur B; Henderson C; Blomhoff R; Wolf CR; Tickle C; Dollé P
Dev Biol; 2007 Mar; 303(1):66-81. PubMed ID: 17126317
[TBL] [Abstract][Full Text] [Related]
19. Retinoic acid generated by Raldh2 in mesoderm is required for mouse dorsal endodermal pancreas development.
Molotkov A; Molotkova N; Duester G
Dev Dyn; 2005 Apr; 232(4):950-7. PubMed ID: 15739227
[TBL] [Abstract][Full Text] [Related]
20. A conserved enhancer element that drives FGF4 gene expression in the embryonic myotomes is synergistically activated by GATA and bHLH proteins.
Iwahori A; Fraidenraich D; Basilico C
Dev Biol; 2004 Jun; 270(2):525-37. PubMed ID: 15183731
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
