BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

715 related articles for article (PubMed ID: 17641088)

  • 1. Analysis of TATA-binding protein 2 (TBP2) and TBP expression suggests different roles for the two proteins in regulation of gene expression during oogenesis and early mouse development.
    Gazdag E; Rajkovic A; Torres-Padilla ME; Tora L
    Reproduction; 2007 Jul; 134(1):51-62. PubMed ID: 17641088
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Regulated expression of TATA-binding protein-related factor 3 (TRF3) during early embryogenesis.
    Yang Y; Cao J; Huang L; Fang HY; Sheng HZ
    Cell Res; 2006 Jul; 16(7):610-21. PubMed ID: 16721357
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spatiotemporal expression of transcriptional regulators in concert with the maternal-to-embryonic transition during bovine in vitro embryogenesis.
    Vigneault C; McGraw S; Sirard MA
    Reproduction; 2009 Jan; 137(1):13-21. PubMed ID: 18805820
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Regulation of gene expression in the preimplantation mouse embryo: temporal and spatial patterns of expression of the transcription factor Sp1.
    Worrad DM; Schultz RM
    Mol Reprod Dev; 1997 Mar; 46(3):268-77. PubMed ID: 9041129
    [TBL] [Abstract][Full Text] [Related]  

  • 5. TAF4b, a TBP associated factor, is required for oocyte development and function.
    Falender AE; Shimada M; Lo YK; Richards JS
    Dev Biol; 2005 Dec; 288(2):405-19. PubMed ID: 16289522
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Factors affecting oocyte quality: who is driving the follicle?
    Mermillod P; Dalbiès-Tran R; Uzbekova S; Thélie A; Traverso JM; Perreau C; Papillier P; Monget P
    Reprod Domest Anim; 2008 Jul; 43 Suppl 2():393-400. PubMed ID: 18638152
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linker histone transitions during mammalian oogenesis and embryogenesis.
    Clarke HJ; McLay DW; Mohamed OA
    Dev Genet; 1998; 22(1):17-30. PubMed ID: 9499577
    [TBL] [Abstract][Full Text] [Related]  

  • 8. TBP2 is essential for germ cell development by regulating transcription and chromatin condensation in the oocyte.
    Gazdag E; Santenard A; Ziegler-Birling C; Altobelli G; Poch O; Tora L; Torres-Padilla ME
    Genes Dev; 2009 Sep; 23(18):2210-23. PubMed ID: 19759265
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Analysis of transcription factor expression during oogenesis and preimplantation development in mice.
    Kageyama S; Gunji W; Nakasato M; Murakami Y; Nagata M; Aoki F
    Zygote; 2007 May; 15(2):117-28. PubMed ID: 17462104
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The TATA binding protein in the sea urchin embryo is maternally derived.
    Edelmann L; Zheng L; Wang ZF; Marzluff W; Wessel GM; Childs G
    Dev Biol; 1998 Dec; 204(1):293-304. PubMed ID: 9851860
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Oocyte-specific knockout: a novel in vivo approach for studying gene functions during folliculogenesis, oocyte maturation, fertilization, and embryogenesis.
    Sun QY; Liu K; Kikuchi K
    Biol Reprod; 2008 Dec; 79(6):1014-20. PubMed ID: 18753607
    [TBL] [Abstract][Full Text] [Related]  

  • 12. GATA-like protein-1 (GLP-1) is required for normal germ cell development during embryonic oogenesis.
    Strauss TJ; Castrillon DH; Hammes SR
    Reproduction; 2011 Feb; 141(2):173-81. PubMed ID: 21123517
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Transcriptional regulation of early oogenesis: in search of masters.
    Pangas SA; Rajkovic A
    Hum Reprod Update; 2006; 12(1):65-76. PubMed ID: 16143663
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel maternally transcribed homeobox gene, Eso-1, is preferentially expressed in oocytes and regulated by cytoplasmic polyadenylation.
    Li H; Tsai MS; Chen CY; Lian WC; Chiu YT; Chen GD; Wang SH
    Mol Reprod Dev; 2006 Jul; 73(7):825-33. PubMed ID: 16596637
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Major chromatin remodeling in the germinal vesicle (GV) of mammalian oocytes is dispensable for global transcriptional silencing but required for centromeric heterochromatin function.
    De La Fuente R; Viveiros MM; Burns KH; Adashi EY; Matzuk MM; Eppig JJ
    Dev Biol; 2004 Nov; 275(2):447-58. PubMed ID: 15501230
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expression pattern and developmental behaviour of cellular nucleic acid-binding protein (CNBP) during folliculogenesis and oogenesis in fish.
    Liu JX; Gui JF
    Gene; 2005 Aug; 356():181-92. PubMed ID: 16002243
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The RNA-binding proteins PUF-5, PUF-6, and PUF-7 reveal multiple systems for maternal mRNA regulation during C. elegans oogenesis.
    Lublin AL; Evans TC
    Dev Biol; 2007 Mar; 303(2):635-49. PubMed ID: 17234175
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Intercellular communication via connexin43 gap junctions is required for ovarian folliculogenesis in the mouse.
    Ackert CL; Gittens JE; O'Brien MJ; Eppig JJ; Kidder GM
    Dev Biol; 2001 May; 233(2):258-70. PubMed ID: 11336494
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression.
    Rajkovic A; Pangas SA; Ballow D; Suzumori N; Matzuk MM
    Science; 2004 Aug; 305(5687):1157-9. PubMed ID: 15326356
    [TBL] [Abstract][Full Text] [Related]  

  • 20. KIT/KIT ligand in mammalian oogenesis and folliculogenesis: roles in rabbit and murine ovarian follicle activation and oocyte growth.
    Hutt KJ; McLaughlin EA; Holland MK
    Biol Reprod; 2006 Sep; 75(3):421-33. PubMed ID: 16790689
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 36.