These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 16938278)

  • 1. Six1 and Six4 promote survival of sensory neurons during early trigeminal gangliogenesis.
    Konishi Y; Ikeda K; Iwakura Y; Kawakami K
    Brain Res; 2006 Oct; 1116(1):93-102. PubMed ID: 16938278
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Six1 and Six4 are essential for Gdnf expression in the metanephric mesenchyme and ureteric bud formation, while Six1 deficiency alone causes mesonephric-tubule defects.
    Kobayashi H; Kawakami K; Asashima M; Nishinakamura R
    Mech Dev; 2007 Apr; 124(4):290-303. PubMed ID: 17300925
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Slc12a2 is a direct target of two closely related homeobox proteins, Six1 and Six4.
    Ando Z; Sato S; Ikeda K; Kawakami K
    FEBS J; 2005 Jun; 272(12):3026-41. PubMed ID: 15955062
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Activation of Six1 Expression in Vertebrate Sensory Neurons.
    Sato S; Yajima H; Furuta Y; Ikeda K; Kawakami K
    PLoS One; 2015; 10(8):e0136666. PubMed ID: 26313368
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Support of trigeminal sensory neurons by nonneuronal p75 neurotrophin receptors.
    Fan L; Girnius S; Oakley B
    Brain Res Dev Brain Res; 2004 May; 150(1):23-39. PubMed ID: 15126035
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genesis of muscle fiber-type diversity during mouse embryogenesis relies on Six1 and Six4 gene expression.
    Richard AF; Demignon J; Sakakibara I; Pujol J; Favier M; Strochlic L; Le Grand F; Sgarioto N; Guernec A; Schmitt A; Cagnard N; Huang R; Legay C; Guillet-Deniau I; Maire P
    Dev Biol; 2011 Nov; 359(2):303-20. PubMed ID: 21884692
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death.
    Andrieu D; Meziane H; Marly F; Angelats C; Fernandez PA; Muscatelli F
    BMC Dev Biol; 2006 Nov; 6():56. PubMed ID: 17116257
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Regulation of FGF10 by POU transcription factor Brn3a in the developing trigeminal ganglion.
    Cox E; Lanier J; Quina L; Eng SR; Turner EE
    J Neurobiol; 2006 Sep; 66(10):1075-83. PubMed ID: 16838370
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Involvement of DRG11 in the development of the primary afferent nociceptive system.
    Rebelo S; Chen ZF; Anderson DJ; Lima D
    Mol Cell Neurosci; 2006 Nov; 33(3):236-46. PubMed ID: 16978876
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Six1 and Six4 gene expression is necessary to activate the fast-type muscle gene program in the mouse primary myotome.
    Niro C; Demignon J; Vincent S; Liu Y; Giordani J; Sgarioto N; Favier M; Guillet-Deniau I; Blais A; Maire P
    Dev Biol; 2010 Feb; 338(2):168-82. PubMed ID: 19962975
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brn3a and Klf7 cooperate to control TrkA expression in sensory neurons.
    Lei L; Zhou J; Lin L; Parada LF
    Dev Biol; 2006 Dec; 300(2):758-69. PubMed ID: 17011544
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Retrograde BMP signaling regulates trigeminal sensory neuron identities and the formation of precise face maps.
    Hodge LK; Klassen MP; Han BX; Yiu G; Hurrell J; Howell A; Rousseau G; Lemaigre F; Tessier-Lavigne M; Wang F
    Neuron; 2007 Aug; 55(4):572-86. PubMed ID: 17698011
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rescue of NGF-deficient mice I: transgenic expression of NGF in skin rescues mice lacking endogenous NGF.
    Harrison SM; Davis BM; Nishimura M; Albers KM; Jones ME; Phillips HS
    Brain Res Mol Brain Res; 2004 Mar; 122(2):116-25. PubMed ID: 15010204
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Coordinated regulation of gene expression by Brn3a in developing sensory ganglia.
    Eng SR; Lanier J; Fedtsova N; Turner EE
    Development; 2004 Aug; 131(16):3859-70. PubMed ID: 15253936
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sensory neurons from N-syndecan-deficient mice are defective in survival.
    Paveliev M; Hienola A; Jokitalo E; Planken A; Bespalov MM; Rauvala H; Saarma M
    Neuroreport; 2008 Sep; 19(14):1397-400. PubMed ID: 18766019
    [TBL] [Abstract][Full Text] [Related]  

  • 16. TNFalpha contributes to the death of NGF-dependent neurons during development.
    Barker V; Middleton G; Davey F; Davies AM
    Nat Neurosci; 2001 Dec; 4(12):1194-8. PubMed ID: 11685224
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neuronal differentiation and maturation in the mouse trigeminal sensory system, in vivo and in vitro.
    Stainier DY; Gilbert W
    J Comp Neurol; 1991 Sep; 311(2):300-12. PubMed ID: 1753021
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Brn-3a is required for the generation of proprioceptors in the mesencephalic trigeminal tract nucleus.
    Ichikawa H; Qiu F; Xiang M; Sugimoto T
    Brain Res; 2005 Aug; 1053(1-2):203-6. PubMed ID: 16040009
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Six family genes control the proliferation and differentiation of muscle satellite cells.
    Yajima H; Motohashi N; Ono Y; Sato S; Ikeda K; Masuda S; Yada E; Kanesaki H; Miyagoe-Suzuki Y; Takeda S; Kawakami K
    Exp Cell Res; 2010 Oct; 316(17):2932-44. PubMed ID: 20696153
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neurofibromin negatively regulates neurotrophin signaling through p21ras in embryonic sensory neurons.
    Vogel KS; El-Afandi M; Parada LF
    Mol Cell Neurosci; 2000 Apr; 15(4):398-407. PubMed ID: 10845775
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.