BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 10648246)

  • 1. OVO transcription factors function antagonistically in the Drosophila female germline.
    Andrews J; Garcia-Estefania D; Delon I; Lü J; Mével-Ninio M; Spierer A; Payre F; Pauli D; Oliver B
    Development; 2000 Feb; 127(4):881-92. PubMed ID: 10648246
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Core promoter sequences contribute to ovo-B regulation in the Drosophila melanogaster germline.
    Bielinska B; Lü J; Sturgill D; Oliver B
    Genetics; 2005 Jan; 169(1):161-72. PubMed ID: 15371353
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Regulatory and functional interactions between ovarian tumor and ovo during Drosophila oogenesis.
    Hinson S; Pettus J; Nagoshi RN
    Mech Dev; 1999 Oct; 88(1):3-14. PubMed ID: 10525184
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The three dominant female-sterile mutations of the Drosophila ovo gene are point mutations that create new translation-initiator AUG codons.
    Mével-Ninio M; Fouilloux E; Guénal I; Vincent A
    Development; 1996 Dec; 122(12):4131-8. PubMed ID: 9012532
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Drosophila OVO zinc-finger protein regulates ovo and ovarian tumor target promoters.
    Lü J; Andrews J; Pauli D; Oliver B
    Dev Genes Evol; 1998 Jun; 208(4):213-22. PubMed ID: 9634487
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Drosophila OVO regulates ovarian tumor transcription by binding unusually near the transcription start site.
    Lü J; Oliver B
    Development; 2001 May; 128(9):1671-86. PubMed ID: 11290304
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New AUG initiation codons in a long 5' UTR create four dominant negative alleles of the Drosophila C2H2 zinc-finger gene ovo.
    Andrews J; Levenson I; Oliver B
    Dev Genes Evol; 1998 Jan; 207(7):482-7. PubMed ID: 9510543
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Regulatory and functional interactions between the somatic sex regulatory gene transformer and the germline genes ovo and ovarian tumor.
    Hinson S; Nagoshi RN
    Development; 1999 Feb; 126(5):861-71. PubMed ID: 9927588
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A germline-specific splicing generates an extended ovo protein isoform required for Drosophila oogenesis.
    Salles C; Mével-Ninio M; Vincent A; Payre F
    Dev Biol; 2002 Jun; 246(2):366-76. PubMed ID: 12051822
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of the isoforms of MOVO zinc finger protein, a mouse homologue of Drosophila Ovo, as transcription factors.
    Unezaki S; Nishizawa M; Okuda-Ashitaka E; Masu Y; Mukai M; Kobayashi S; Sawamoto K; Okano H; Ito S
    Gene; 2004 Jul; 336(1):47-58. PubMed ID: 15225875
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sex determination signals control ovo-B transcription in Drosophila melanogaster germ cells.
    Andrews J; Oliver B
    Genetics; 2002 Feb; 160(2):537-45. PubMed ID: 11861560
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The dual function of ovo/shavenbaby in germline and epidermis differentiation is conserved between Drosophila melanogaster and the olive fruit fly Bactrocera oleae.
    Khila A; El Haidani A; Vincent A; Payre F; Souda SI
    Insect Biochem Mol Biol; 2003 Jul; 33(7):691-9. PubMed ID: 12826096
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Conserved role of Ovo in germline development in mouse and Drosophila.
    Hayashi M; Shinozuka Y; Shigenobu S; Sato M; Sugimoto M; Ito S; Abe K; Kobayashi S
    Sci Rep; 2017 Jan; 7():40056. PubMed ID: 28059165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The ovo gene required for cuticle formation and oogenesis in flies is involved in hair formation and spermatogenesis in mice.
    Dai X; Schonbaum C; Degenstein L; Bai W; Mahowald A; Fuchs E
    Genes Dev; 1998 Nov; 12(21):3452-63. PubMed ID: 9808631
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of Drosophila OVO protein DNA binding specificity using random DNA oligomer selection suggests zinc finger degeneration.
    Lee S; Garfinkel MD
    Nucleic Acids Res; 2000 Feb; 28(3):826-34. PubMed ID: 10637336
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trithorax and ASH1 interact directly and associate with the trithorax group-responsive bxd region of the Ultrabithorax promoter.
    Rozovskaia T; Tillib S; Smith S; Sedkov Y; Rozenblatt-Rosen O; Petruk S; Yano T; Nakamura T; Ben-Simchon L; Gildea J; Croce CM; Shearn A; Canaani E; Mazo A
    Mol Cell Biol; 1999 Sep; 19(9):6441-7. PubMed ID: 10454589
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Suppression of distinct ovo phenotypes in the Drosophila female germline by maleless- and Sex-lethal.
    Oliver B; Pauli D
    Dev Genet; 1998; 23(4):335-46. PubMed ID: 9883585
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PDP1, a novel Drosophila PAR domain bZIP transcription factor expressed in developing mesoderm, endoderm and ectoderm, is a transcriptional regulator of somatic muscle genes.
    Lin SC; Lin MH; Horváth P; Reddy KL; Storti RV
    Development; 1997 Nov; 124(22):4685-96. PubMed ID: 9409684
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ovo, a Drosophila gene required for ovarian development, is specifically expressed in the germline and shares most of its coding sequences with shavenbaby, a gene involved in embryo patterning.
    Mével-Ninio M; Terracol R; Salles C; Vincent A; Payre F
    Mech Dev; 1995 Jan; 49(1-2):83-95. PubMed ID: 7748792
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bicoid occurrence and Bicoid-dependent hunchback regulation in lower cyclorrhaphan flies.
    Lemke S; Stauber M; Shaw PJ; Rafiqi AM; Prell A; Schmidt-Ott U
    Evol Dev; 2008; 10(4):413-20. PubMed ID: 18638318
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.