BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 16900517)

  • 1. Dlx5 and Dlx6 homeobox genes are required for specification of the mammalian vestibular apparatus.
    Robledo RF; Lufkin T
    Genesis; 2006 Sep; 44(9):425-37. PubMed ID: 16900517
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dlx gene expression during chick inner ear development.
    Brown ST; Wang J; Groves AK
    J Comp Neurol; 2005 Feb; 483(1):48-65. PubMed ID: 15672396
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The role of Pax2 in mouse inner ear development.
    Burton Q; Cole LK; Mulheisen M; Chang W; Wu DK
    Dev Biol; 2004 Aug; 272(1):161-75. PubMed ID: 15242798
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gbx2 is required for the morphogenesis of the mouse inner ear: a downstream candidate of hindbrain signaling.
    Lin Z; Cantos R; Patente M; Wu DK
    Development; 2005 May; 132(10):2309-18. PubMed ID: 15829521
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathway.
    Merlo GR; Paleari L; Mantero S; Zerega B; Adamska M; Rinkwitz S; Bober E; Levi G
    Dev Biol; 2002 Aug; 248(1):157-69. PubMed ID: 12142028
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hmx2 homeobox gene control of murine vestibular morphogenesis.
    Wang W; Chan EK; Baron S; Van de Water T; Lufkin T
    Development; 2001 Dec; 128(24):5017-29. PubMed ID: 11748138
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Retinoic acid-induced inner ear teratogenesis caused by defective Fgf3/Fgf10-dependent Dlx5 signaling.
    Liu W; Levi G; Shanske A; Frenz DA
    Birth Defects Res B Dev Reprod Toxicol; 2008 Apr; 83(2):134-44. PubMed ID: 18412219
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular mechanisms underlying inner ear patterning defects in kreisler mutants.
    Choo D; Ward J; Reece A; Dou H; Lin Z; Greinwald J
    Dev Biol; 2006 Jan; 289(2):308-17. PubMed ID: 16325169
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Otx2, Gbx2, and Fgf8 expression patterns in the chick developing inner ear and their possible roles in otic specification and early innervation.
    Sánchez-Calderón H; Martín-Partido G; Hidalgo-Sánchez M
    Gene Expr Patterns; 2004 Oct; 4(6):659-69. PubMed ID: 15465488
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The role of Six1 in mammalian auditory system development.
    Zheng W; Huang L; Wei ZB; Silvius D; Tang B; Xu PX
    Development; 2003 Sep; 130(17):3989-4000. PubMed ID: 12874121
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ectopic noggin blocks sensory and nonsensory organ morphogenesis in the chicken inner ear.
    Chang W; Nunes FD; De Jesus-Escobar JM; Harland R; Wu DK
    Dev Biol; 1999 Dec; 216(1):369-81. PubMed ID: 10588886
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A symphony of inner ear developmental control genes.
    Chatterjee S; Kraus P; Lufkin T
    BMC Genet; 2010 Jul; 11():68. PubMed ID: 20637105
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dlx5- and Dlx6-mediated chondrogenesis: Differential domain requirements for a conserved function.
    Hsu SH; Noamani B; Abernethy DE; Zhu H; Levi G; Bendall AJ
    Mech Dev; 2006 Nov; 123(11):819-30. PubMed ID: 17027239
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Six1 controls patterning of the mouse otic vesicle.
    Ozaki H; Nakamura K; Funahashi J; Ikeda K; Yamada G; Tokano H; Okamura HO; Kitamura K; Muto S; Kotaki H; Sudo K; Horai R; Iwakura Y; Kawakami K
    Development; 2004 Feb; 131(3):551-62. PubMed ID: 14695375
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Unraveling inner ear induction by gene manipulation using Pax2-Cre BAC transgenic mice.
    Ohyama T
    Brain Res; 2009 Jun; 1277():84-9. PubMed ID: 19265685
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Regulation of Dlx5 and Dlx6 gene expression by p63 is involved in EEC and SHFM congenital limb defects.
    Lo Iacono N; Mantero S; Chiarelli A; Garcia E; Mills AA; Morasso MI; Costanzo A; Levi G; Guerrini L; Merlo GR
    Development; 2008 Apr; 135(7):1377-88. PubMed ID: 18326838
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation.
    Shamseldin HE; Faden MA; Alashram W; Alkuraya FS
    J Med Genet; 2012 Jan; 49(1):16-20. PubMed ID: 22121204
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Absent expression of the osteoblast-specific maternally imprinted genes, DLX5 and DLX6, causes split hand/split foot malformation type I.
    Rattanasopha S; Tongkobpetch S; Srichomthong C; Kitidumrongsook P; Suphapeetiporn K; Shotelersuk V
    J Med Genet; 2014 Dec; 51(12):817-23. PubMed ID: 25332435
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hmx homeobox gene function in inner ear and nervous system cell-type specification and development.
    Wang W; Lufkin T
    Exp Cell Res; 2005 Jun; 306(2):373-9. PubMed ID: 15925593
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of direct downstream targets of Dlx5 during early inner ear development.
    Sajan SA; Rubenstein JL; Warchol ME; Lovett M
    Hum Mol Genet; 2011 Apr; 20(7):1262-73. PubMed ID: 21227998
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.