BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 12481294)

  • 1. What cardiovascular defect does my prenatal mouse mutant have, and why?
    Conway SJ; Kruzynska-Frejtag A; Kneer PL; Machnicki M; Koushik SV
    Genesis; 2003 Jan; 35(1):1-21. PubMed ID: 12481294
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Death before birth: clues from gene knockouts and mutations.
    Copp AJ
    Trends Genet; 1995 Mar; 11(3):87-93. PubMed ID: 7732578
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.
    Stalmans I
    Verh K Acad Geneeskd Belg; 2005; 67(4):229-76. PubMed ID: 16334858
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cardiac abnormalities cause early lethality of jumonji mutant mice.
    Takahashi M; Kojima M; Nakajima K; Suzuki-Migishima R; Motegi Y; Yokoyama M; Takeuchi T
    Biochem Biophys Res Commun; 2004 Nov; 324(4):1319-23. PubMed ID: 15504358
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cardiovascular abnormalities in Folr1 knockout mice and folate rescue.
    Zhu H; Wlodarczyk BJ; Scott M; Yu W; Merriweather M; Gelineau-van Waes J; Schwartz RJ; Finnell RH
    Birth Defects Res A Clin Mol Teratol; 2007 Apr; 79(4):257-68. PubMed ID: 17286298
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mouse model of heterotaxy with single ventricle spectrum of cardiac anomalies.
    Aune CN; Chatterjee B; Zhao XQ; Francis R; Bracero L; Yu Q; Rosenthal J; Leatherbury L; Lo CW
    Pediatr Res; 2008 Jan; 63(1):9-14. PubMed ID: 18043505
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Separating genetic and hemodynamic defects in neuropilin 1 knockout embryos.
    Jones EA; Yuan L; Breant C; Watts RJ; Eichmann A
    Development; 2008 Aug; 135(14):2479-88. PubMed ID: 18550715
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rotation of the myocardial wall of the outflow tract is implicated in the normal positioning of the great arteries.
    Bajolle F; Zaffran S; Kelly RG; Hadchouel J; Bonnet D; Brown NA; Buckingham ME
    Circ Res; 2006 Feb; 98(3):421-8. PubMed ID: 16397144
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lack of Gata3 results in conotruncal heart anomalies in mouse.
    Raid R; Krinka D; Bakhoff L; Abdelwahid E; Jokinen E; Kärner M; Malva M; Meier R; Pelliniemi LJ; Ploom M; Sizarov A; Pooga M; Karis A
    Mech Dev; 2009; 126(1-2):80-9. PubMed ID: 18955134
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Development of a lethal congenital heart defect in the splotch (Pax3) mutant mouse.
    Conway SJ; Henderson DJ; Kirby ML; Anderson RH; Copp AJ
    Cardiovasc Res; 1997 Nov; 36(2):163-73. PubMed ID: 9463628
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Temporal-spatial ablation of neural crest in the mouse results in cardiovascular defects.
    Porras D; Brown CB
    Dev Dyn; 2008 Jan; 237(1):153-62. PubMed ID: 18058916
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Early postnatal lethality and cardiovascular defects in CXCR7-deficient mice.
    Gerrits H; van Ingen Schenau DS; Bakker NE; van Disseldorp AJ; Strik A; Hermens LS; Koenen TB; Krajnc-Franken MA; Gossen JA
    Genesis; 2008 May; 46(5):235-45. PubMed ID: 18442043
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cardiac neural crest expression of Hand2 regulates outflow and second heart field development.
    Morikawa Y; Cserjesi P
    Circ Res; 2008 Dec; 103(12):1422-9. PubMed ID: 19008477
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Atrophin 2 recruits histone deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis.
    Zoltewicz JS; Stewart NJ; Leung R; Peterson AS
    Development; 2004 Jan; 131(1):3-14. PubMed ID: 14645126
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cardiovascular malformations among preterm infants.
    Tanner K; Sabrine N; Wren C
    Pediatrics; 2005 Dec; 116(6):e833-8. PubMed ID: 16322141
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Msx1 and Msx2 regulate survival of secondary heart field precursors and post-migratory proliferation of cardiac neural crest in the outflow tract.
    Chen YH; Ishii M; Sun J; Sucov HM; Maxson RE
    Dev Biol; 2007 Aug; 308(2):421-37. PubMed ID: 17601530
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital heart disease reminiscent of partial trisomy 2p syndrome in mice transgenic for the transcription factor Lbh.
    Briegel KJ; Baldwin HS; Epstein JA; Joyner AL
    Development; 2005 Jul; 132(14):3305-16. PubMed ID: 15958514
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Histopathological analysis of neonatal mouse hearts with connexin43 gene defects].
    Xie LJ; Huang GY; Zhao XQ; Shen Y; Zhou GM
    Zhonghua Yi Xue Za Zhi; 2005 May; 85(18):1249-51. PubMed ID: 16029609
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation.
    Araki T; Mohi MG; Ismat FA; Bronson RT; Williams IR; Kutok JL; Yang W; Pao LI; Gilliland DG; Epstein JA; Neel BG
    Nat Med; 2004 Aug; 10(8):849-57. PubMed ID: 15273746
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interpreting neonatal lethal phenotypes in mouse mutants: insights into gene function and human diseases.
    Turgeon B; Meloche S
    Physiol Rev; 2009 Jan; 89(1):1-26. PubMed ID: 19126753
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.