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 *

216 related articles for article (PubMed ID: 24361260)

  • 1. Coordinated activity of Spry1 and Spry2 is required for normal development of the external genitalia.
    Ching ST; Cunha GR; Baskin LS; Basson MA; Klein OD
    Dev Biol; 2014 Feb; 386(1):1-11. PubMed ID: 24361260
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spry1 and Spry2 are necessary for eyelid closure.
    Kuracha MR; Siefker E; Licht JD; Govindarajan V
    Dev Biol; 2013 Nov; 383(2):227-38. PubMed ID: 24055172
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular analysis of external genitalia formation: the role of fibroblast growth factor (Fgf) genes during genital tubercle formation.
    Haraguchi R; Suzuki K; Murakami R; Sakai M; Kamikawa M; Kengaku M; Sekine K; Kawano H; Kato S; Ueno N; Yamada G
    Development; 2000 Jun; 127(11):2471-9. PubMed ID: 10804187
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cooperative and independent functions of FGF and Wnt signaling during early inner ear development.
    Wright KD; Mahoney Rogers AA; Zhang J; Shim K
    BMC Dev Biol; 2015 Oct; 15():33. PubMed ID: 26443994
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sprouty genes prevent excessive FGF signalling in multiple cell types throughout development of the cerebellum.
    Yu T; Yaguchi Y; Echevarria D; Martinez S; Basson MA
    Development; 2011 Jul; 138(14):2957-68. PubMed ID: 21693512
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tissue-specific roles of FGF signaling in external genitalia development.
    Harada M; Omori A; Nakahara C; Nakagata N; Akita K; Yamada G
    Dev Dyn; 2015 Jun; 244(6):759-73. PubMed ID: 25820239
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sprouty genes function in suppression of prostate tumorigenesis.
    Schutzman JL; Martin GR
    Proc Natl Acad Sci U S A; 2012 Dec; 109(49):20023-8. PubMed ID: 23150596
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A dosage-dependent role for Spry2 in growth and patterning during palate development.
    Welsh IC; Hagge-Greenberg A; O'Brien TP
    Mech Dev; 2007; 124(9-10):746-61. PubMed ID: 17693063
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sprouty genes are essential for the normal development of epibranchial ganglia in the mouse embryo.
    Simrick S; Lickert H; Basson MA
    Dev Biol; 2011 Oct; 358(1):147-55. PubMed ID: 21806979
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spry1 and Spry2 are necessary for lens vesicle separation and corneal differentiation.
    Kuracha MR; Burgess D; Siefker E; Cooper JT; Licht JD; Robinson ML; Govindarajan V
    Invest Ophthalmol Vis Sci; 2011 Aug; 52(9):6887-97. PubMed ID: 21743007
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unique functions of Sonic hedgehog signaling during external genitalia development.
    Haraguchi R; Mo R; Hui C; Motoyama J; Makino S; Shiroishi T; Gaffield W; Yamada G
    Development; 2001 Nov; 128(21):4241-50. PubMed ID: 11684660
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sonic hedgehog signaling from the urethral epithelium controls external genital development.
    Perriton CL; Powles N; Chiang C; Maconochie MK; Cohn MJ
    Dev Biol; 2002 Jul; 247(1):26-46. PubMed ID: 12074550
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tissue-specific roles of Fgfr2 in development of the external genitalia.
    Gredler ML; Seifert AW; Cohn MJ
    Development; 2015 Jun; 142(12):2203-12. PubMed ID: 26081573
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spry1 and spry2 are essential for development of the temporomandibular joint.
    Purcell P; Jheon A; Vivero MP; Rahimi H; Joo A; Klein OD
    J Dent Res; 2012 Apr; 91(4):387-93. PubMed ID: 22328578
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multiphasic and tissue-specific roles of sonic hedgehog in cloacal septation and external genitalia development.
    Seifert AW; Bouldin CM; Choi KS; Harfe BD; Cohn MJ
    Development; 2009 Dec; 136(23):3949-57. PubMed ID: 19906862
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sprouty proteins regulate ureteric branching by coordinating reciprocal epithelial Wnt11, mesenchymal Gdnf and stromal Fgf7 signalling during kidney development.
    Chi L; Zhang S; Lin Y; Prunskaite-Hyyryläinen R; Vuolteenaho R; Itäranta P; Vainio S
    Development; 2004 Jul; 131(14):3345-56. PubMed ID: 15201220
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Repression of Fgf signaling by sprouty1-2 regulates cortical patterning in two distinct regions and times.
    Faedo A; Borello U; Rubenstein JL
    J Neurosci; 2010 Mar; 30(11):4015-23. PubMed ID: 20237272
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sprouty1 and Sprouty2 limit both the size of the otic placode and hindbrain Wnt8a by antagonizing FGF signaling.
    Mahoney Rogers AA; Zhang J; Shim K
    Dev Biol; 2011 May; 353(1):94-104. PubMed ID: 21362415
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular Characterization of the Genital Organizer: Gene Expression Profile of the Mouse Urethral Plate Epithelium.
    Armfield BA; Seifert AW; Zheng Z; Merton EM; Rock JR; Lopez MC; Baker HV; Cohn MJ
    J Urol; 2016 Oct; 196(4):1295-302. PubMed ID: 27173853
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dosage-dependent hedgehog signals integrated with Wnt/beta-catenin signaling regulate external genitalia formation as an appendicular program.
    Miyagawa S; Moon A; Haraguchi R; Inoue C; Harada M; Nakahara C; Suzuki K; Matsumaru D; Kaneko T; Matsuo I; Yang L; Taketo MM; Iguchi T; Evans SM; Yamada G
    Development; 2009 Dec; 136(23):3969-78. PubMed ID: 19906864
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.