389 related articles for article (PubMed ID: 24835466)
1. GATA6 levels modulate primitive endoderm cell fate choice and timing in the mouse blastocyst.
Schrode N; Saiz N; Di Talia S; Hadjantonakis AK
Dev Cell; 2014 May; 29(4):454-67. PubMed ID: 24835466
[TBL] [Abstract][Full Text] [Related]
2. Gata6, Nanog and Erk signaling control cell fate in the inner cell mass through a tristable regulatory network.
Bessonnard S; De Mot L; Gonze D; Barriol M; Dennis C; Goldbeter A; Dupont G; Chazaud C
Development; 2014 Oct; 141(19):3637-48. PubMed ID: 25209243
[TBL] [Abstract][Full Text] [Related]
3. Allocation of inner cells to epiblast vs primitive endoderm in the mouse embryo is biased but not determined by the round of asymmetric divisions (8→16- and 16→32-cells).
Krupa M; Mazur E; Szczepańska K; Filimonow K; Maleszewski M; Suwińska A
Dev Biol; 2014 Jan; 385(1):136-48. PubMed ID: 24041854
[TBL] [Abstract][Full Text] [Related]
4. FGF4 is required for lineage restriction and salt-and-pepper distribution of primitive endoderm factors but not their initial expression in the mouse.
Kang M; Piliszek A; Artus J; Hadjantonakis AK
Development; 2013 Jan; 140(2):267-79. PubMed ID: 23193166
[TBL] [Abstract][Full Text] [Related]
5. The transition from local to global patterns governs the differentiation of mouse blastocysts.
Fischer SC; Corujo-Simon E; Lilao-Garzon J; Stelzer EHK; Muñoz-Descalzo S
PLoS One; 2020; 15(5):e0233030. PubMed ID: 32413083
[TBL] [Abstract][Full Text] [Related]
6. Primitive endoderm differentiates via a three-step mechanism involving Nanog and RTK signaling.
Frankenberg S; Gerbe F; Bessonnard S; Belville C; Pouchin P; Bardot O; Chazaud C
Dev Cell; 2011 Dec; 21(6):1005-13. PubMed ID: 22172669
[TBL] [Abstract][Full Text] [Related]
7. Suppression of ERK signalling abolishes primitive endoderm formation but does not promote pluripotency in rabbit embryo.
Piliszek A; Madeja ZE; Plusa B
Development; 2017 Oct; 144(20):3719-3730. PubMed ID: 28935706
[TBL] [Abstract][Full Text] [Related]
8. Lineage Establishment and Progression within the Inner Cell Mass of the Mouse Blastocyst Requires FGFR1 and FGFR2.
Kang M; Garg V; Hadjantonakis AK
Dev Cell; 2017 Jun; 41(5):496-510.e5. PubMed ID: 28552559
[TBL] [Abstract][Full Text] [Related]
9. The combination of inhibitors of FGF/MEK/Erk and GSK3β signaling increases the number of OCT3/4- and NANOG-positive cells in the human inner cell mass, but does not improve stem cell derivation.
Van der Jeught M; O'Leary T; Ghimire S; Lierman S; Duggal G; Versieren K; Deforce D; Chuva de Sousa Lopes S; Heindryckx B; De Sutter P
Stem Cells Dev; 2013 Jan; 22(2):296-306. PubMed ID: 22784186
[TBL] [Abstract][Full Text] [Related]
10. Analysis of human embryos from zygote to blastocyst reveals distinct gene expression patterns relative to the mouse.
Niakan KK; Eggan K
Dev Biol; 2013 Mar; 375(1):54-64. PubMed ID: 23261930
[TBL] [Abstract][Full Text] [Related]
11. Depletion of Suds3 reveals an essential role in early lineage specification.
Zhang K; Dai X; Wallingford MC; Mager J
Dev Biol; 2013 Jan; 373(2):359-72. PubMed ID: 23123966
[TBL] [Abstract][Full Text] [Related]
12. Conversion from mouse embryonic to extra-embryonic endoderm stem cells reveals distinct differentiation capacities of pluripotent stem cell states.
Cho LT; Wamaitha SE; Tsai IJ; Artus J; Sherwood RI; Pedersen RA; Hadjantonakis AK; Niakan KK
Development; 2012 Aug; 139(16):2866-77. PubMed ID: 22791892
[TBL] [Abstract][Full Text] [Related]
13. Early lineage segregation between epiblast and primitive endoderm in mouse blastocysts through the Grb2-MAPK pathway.
Chazaud C; Yamanaka Y; Pawson T; Rossant J
Dev Cell; 2006 May; 10(5):615-24. PubMed ID: 16678776
[TBL] [Abstract][Full Text] [Related]
14.
Azami T; Waku T; Matsumoto K; Jeon H; Muratani M; Kawashima A; Yanagisawa J; Manabe I; Nagai R; Kunath T; Nakamura T; Kurimoto K; Saitou M; Takahashi S; Ema M
Development; 2017 Oct; 144(20):3706-3718. PubMed ID: 28870993
[TBL] [Abstract][Full Text] [Related]
15. The roles of FGF and MAP kinase signaling in the segregation of the epiblast and hypoblast cell lineages in bovine and human embryos.
Kuijk EW; van Tol LT; Van de Velde H; Wubbolts R; Welling M; Geijsen N; Roelen BA
Development; 2012 Mar; 139(5):871-82. PubMed ID: 22278923
[TBL] [Abstract][Full Text] [Related]
16. GATA6 phosphorylation by Erk1/2 propels exit from pluripotency and commitment to primitive endoderm.
Meng Y; Moore R; Tao W; Smith ER; Tse JD; Caslini C; Xu XX
Dev Biol; 2018 Apr; 436(1):55-65. PubMed ID: 29454706
[TBL] [Abstract][Full Text] [Related]
17. Formation of a polarised primitive endoderm layer in embryoid bodies requires fgfr/erk signalling.
Doughton G; Wei J; Tapon N; Welham MJ; Chalmers AD
PLoS One; 2014; 9(4):e95434. PubMed ID: 24752320
[TBL] [Abstract][Full Text] [Related]
18. Extensive co-binding and rapid redistribution of NANOG and GATA6 during emergence of divergent lineages.
Thompson JJ; Lee DJ; Mitra A; Frail S; Dale RK; Rocha PP
Nat Commun; 2022 Jul; 13(1):4257. PubMed ID: 35871075
[TBL] [Abstract][Full Text] [Related]
19. Bmi1 facilitates primitive endoderm formation by stabilizing Gata6 during early mouse development.
Lavial F; Bessonnard S; Ohnishi Y; Tsumura A; Chandrashekran A; Fenwick MA; Tomaz RA; Hosokawa H; Nakayama T; Chambers I; Hiiragi T; Chazaud C; Azuara V
Genes Dev; 2012 Jul; 26(13):1445-58. PubMed ID: 22713603
[TBL] [Abstract][Full Text] [Related]
20. Oct4 is required for lineage priming in the developing inner cell mass of the mouse blastocyst.
Le Bin GC; Muñoz-Descalzo S; Kurowski A; Leitch H; Lou X; Mansfield W; Etienne-Dumeau C; Grabole N; Mulas C; Niwa H; Hadjantonakis AK; Nichols J
Development; 2014 Mar; 141(5):1001-10. PubMed ID: 24504341
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]