229 related articles for article (PubMed ID: 15673568)
1. Distinct developmental programs require different levels of Bmp signaling during mouse retinal development.
Murali D; Yoshikawa S; Corrigan RR; Plas DJ; Crair MC; Oliver G; Lyons KM; Mishina Y; Furuta Y
Development; 2005 Mar; 132(5):913-23. PubMed ID: 15673568
[TBL] [Abstract][Full Text] [Related]
2. Developmental expression patterns of bone morphogenetic proteins, receptors, and binding proteins in the chick retina.
Belecky-Adams T; Adler R
J Comp Neurol; 2001 Feb; 430(4):562-72. PubMed ID: 11169487
[TBL] [Abstract][Full Text] [Related]
3. BMP receptor 1b is required for axon guidance and cell survival in the developing retina.
Liu J; Wilson S; Reh T
Dev Biol; 2003 Apr; 256(1):34-48. PubMed ID: 12654290
[TBL] [Abstract][Full Text] [Related]
4. Distinct functions for Bmp signaling in lip and palate fusion in mice.
Liu W; Sun X; Braut A; Mishina Y; Behringer RR; Mina M; Martin JF
Development; 2005 Mar; 132(6):1453-61. PubMed ID: 15716346
[TBL] [Abstract][Full Text] [Related]
5. BMP receptor IA is required in the mammalian embryo for endodermal morphogenesis and ectodermal patterning.
Davis S; Miura S; Hill C; Mishina Y; Klingensmith J
Dev Biol; 2004 Jun; 270(1):47-63. PubMed ID: 15136140
[TBL] [Abstract][Full Text] [Related]
6. BMP signaling through ACVRI is required for left-right patterning in the early mouse embryo.
Kishigami S; Yoshikawa S; Castranio T; Okazaki K; Furuta Y; Mishina Y
Dev Biol; 2004 Dec; 276(1):185-93. PubMed ID: 15531373
[TBL] [Abstract][Full Text] [Related]
7. Smad4 is required predominantly in the developmental processes dependent on the BMP branch of the TGF-β signaling system in the embryonic mouse retina.
Murali D; Kawaguchi-Niida M; Deng CX; Furuta Y
Invest Ophthalmol Vis Sci; 2011 May; 52(6):2930-7. PubMed ID: 21273545
[TBL] [Abstract][Full Text] [Related]
8. Contributions by members of the TGFbeta superfamily to lens development.
Beebe D; Garcia C; Wang X; Rajagopal R; Feldmeier M; Kim JY; Chytil A; Moses H; Ashery-Padan R; Rauchman M
Int J Dev Biol; 2004; 48(8-9):845-56. PubMed ID: 15558476
[TBL] [Abstract][Full Text] [Related]
9. BMPs regulate multiple aspects of growth-plate chondrogenesis through opposing actions on FGF pathways.
Yoon BS; Pogue R; Ovchinnikov DA; Yoshii I; Mishina Y; Behringer RR; Lyons KM
Development; 2006 Dec; 133(23):4667-78. PubMed ID: 17065231
[TBL] [Abstract][Full Text] [Related]
10. Altered BMP signaling disrupts chick diencephalic development.
Lim Y; Cho G; Minarcik J; Golden J
Mech Dev; 2005 Apr; 122(4):603-20. PubMed ID: 15804571
[TBL] [Abstract][Full Text] [Related]
11. Transgenic zebrafish reveal stage-specific roles for Bmp signaling in ventral and posterior mesoderm development.
Pyati UJ; Webb AE; Kimelman D
Development; 2005 May; 132(10):2333-43. PubMed ID: 15829520
[TBL] [Abstract][Full Text] [Related]
12. ALK2 functions as a BMP type I receptor and induces Indian hedgehog in chondrocytes during skeletal development.
Zhang D; Schwarz EM; Rosier RN; Zuscik MJ; Puzas JE; O'Keefe RJ
J Bone Miner Res; 2003 Sep; 18(9):1593-604. PubMed ID: 12968668
[TBL] [Abstract][Full Text] [Related]
13. The level of BMP4 signaling is critical for the regulation of distinct T-box gene expression domains and growth along the dorso-ventral axis of the optic cup.
Behesti H; Holt JK; Sowden JC
BMC Dev Biol; 2006 Dec; 6():62. PubMed ID: 17173667
[TBL] [Abstract][Full Text] [Related]
14. Cloning of rat type I receptor cDNA for bone morphogenetic protein-2 and bone morphogenetic protein-4, and the localization compared with that of the ligands.
Ikeda T; Takahashi H; Suzuki A; Ueno N; Yokose S; Yamaguchi A; Yoshiki S
Dev Dyn; 1996 Jul; 206(3):318-29. PubMed ID: 8896987
[TBL] [Abstract][Full Text] [Related]
15. BMPR1A signaling is necessary for hair follicle cycling and hair shaft differentiation in mice.
Yuhki M; Yamada M; Kawano M; Iwasato T; Itohara S; Yoshida H; Ogawa M; Mishina Y
Development; 2004 Apr; 131(8):1825-33. PubMed ID: 15084466
[TBL] [Abstract][Full Text] [Related]
16. Signaling through BMP type 1 receptors is required for development of interneuron cell types in the dorsal spinal cord.
Wine-Lee L; Ahn KJ; Richardson RD; Mishina Y; Lyons KM; Crenshaw EB
Development; 2004 Nov; 131(21):5393-403. PubMed ID: 15469980
[TBL] [Abstract][Full Text] [Related]
17. Temporal and spatial expression profiles of BMP receptors and noggin during BMP-2-induced ectopic bone formation.
Nakamura Y; Wakitani S; Nakayama J; Wakabayashi S; Horiuchi H; Takaoka K
J Bone Miner Res; 2003 Oct; 18(10):1854-62. PubMed ID: 14584896
[TBL] [Abstract][Full Text] [Related]
18. AcvR1-mediated BMP signaling in second heart field is required for arterial pole development: implications for myocardial differentiation and regional identity.
Thomas PS; Rajderkar S; Lane J; Mishina Y; Kaartinen V
Dev Biol; 2014 Jun; 390(2):191-207. PubMed ID: 24680892
[TBL] [Abstract][Full Text] [Related]
19. Bone morphogenetic proteins-2 and -4: negative growth regulators in adult retinal pigmented epithelium.
Mathura JR; Jafari N; Chang JT; Hackett SF; Wahlin KJ; Della NG; Okamoto N; Zack DJ; Campochiaro PA
Invest Ophthalmol Vis Sci; 2000 Feb; 41(2):592-600. PubMed ID: 10670493
[TBL] [Abstract][Full Text] [Related]
20. Alk2/ACVR1 and Alk3/BMPR1A Provide Essential Function for Bone Morphogenetic Protein-Induced Retinal Angiogenesis.
Lee HW; Chong DC; Ola R; Dunworth WP; Meadows S; Ka J; Kaartinen VM; Qyang Y; Cleaver O; Bautch VL; Eichmann A; Jin SW
Arterioscler Thromb Vasc Biol; 2017 Apr; 37(4):657-663. PubMed ID: 28232325
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
