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Items: 1 to 20 of 410

1.

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. Epub 2005 Jun 15. Erratum in: Development. 2005 Sep;132(17):4015.

3.

The enigmatic role of the ankyrin repeat domain 1 gene in heart development and disease.

Mikhailov AT, Torrado M.

Int J Dev Biol. 2008;52(7):811-21. doi: 10.1387/ijdb.082655am. Review.

4.

Tbx5 specifies the left/right ventricles and ventricular septum position during cardiogenesis.

Takeuchi JK, Ohgi M, Koshiba-Takeuchi K, Shiratori H, Sakaki I, Ogura K, Saijoh Y, Ogura T.

Development. 2003 Dec;130(24):5953-64. Epub 2003 Oct 22.

5.

CARP, a cardiac ankyrin repeat protein, is downstream in the Nkx2-5 homeobox gene pathway.

Zou Y, Evans S, Chen J, Kuo HC, Harvey RP, Chien KR.

Development. 1997 Feb;124(4):793-804.

6.

A novel cardiac-restricted target for doxorubicin. CARP, a nuclear modulator of gene expression in cardiac progenitor cells and cardiomyocytes.

Jeyaseelan R, Poizat C, Baker RK, Abdishoo S, Isterabadi LB, Lyons GE, Kedes L.

J Biol Chem. 1997 Sep 5;272(36):22800-8.

7.

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. Review.

PMID:
16334858
8.

A human homolog of mouse Lbh gene, hLBH, expresses in heart and activates SRE and AP-1 mediated MAPK signaling pathway.

Ai J, Wang Y, Tan K, Deng Y, Luo N, Yuan W, Wang Z, Li Y, Wang Y, Mo X, Zhu C, Yin Z, Liu M, Wu X.

Mol Biol Rep. 2008 Jun;35(2):179-87. Epub 2007 Mar 28.

PMID:
17390236
10.

Transcriptional deregulation and a missense mutation define ANKRD1 as a candidate gene for total anomalous pulmonary venous return.

Cinquetti R, Badi I, Campione M, Bortoletto E, Chiesa G, Parolini C, Camesasca C, Russo A, Taramelli R, Acquati F.

Hum Mutat. 2008 Apr;29(4):468-74. doi: 10.1002/humu.20711.

PMID:
18273862
11.

Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome.

Taylor Clelland CL, Levy B, McKie JM, Duncan AM, Hirschhorn K, Bancroft C.

Mamm Genome. 2000 Aug;11(8):675-81.

PMID:
10920239
12.

Characterization of Nfatc1 regulation identifies an enhancer required for gene expression that is specific to pro-valve endocardial cells in the developing heart.

Zhou B, Wu B, Tompkins KL, Boyer KL, Grindley JC, Baldwin HS.

Development. 2005 Mar;132(5):1137-46. Epub 2005 Feb 2.

13.

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease.

Bruneau BG, Nemer G, Schmitt JP, Charron F, Robitaille L, Caron S, Conner DA, Gessler M, Nemer M, Seidman CE, Seidman JG.

Cell. 2001 Sep 21;106(6):709-21.

14.

Activation of Notch1 signaling in cardiogenic mesoderm induces abnormal heart morphogenesis in mouse.

Watanabe Y, Kokubo H, Miyagawa-Tomita S, Endo M, Igarashi K, Aisaki Ki, Kanno J, Saga Y.

Development. 2006 May;133(9):1625-34. Epub 2006 Mar 22.

15.

Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome.

Bruneau BG, Logan M, Davis N, Levi T, Tabin CJ, Seidman JG, Seidman CE.

Dev Biol. 1999 Jul 1;211(1):100-8.

16.

Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome.

Chrast R, Scott HS, Madani R, Huber L, Wolfer DP, Prinz M, Aguzzi A, Lipp HP, Antonarakis SE.

Hum Mol Genet. 2000 Jul 22;9(12):1853-64.

17.

The mammalian Tolloid-like 1 gene, Tll1, is necessary for normal septation and positioning of the heart.

Clark TG, Conway SJ, Scott IC, Labosky PA, Winnier G, Bundy J, Hogan BL, Greenspan DS.

Development. 1999 Jun;126(12):2631-42.

18.

Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency.

MacDonald ST, Bamforth SD, Chen CM, Farthing CR, Franklyn A, Broadbent C, Schneider JE, Saga Y, Lewandoski M, Bhattacharya S.

Cardiovasc Res. 2008 Aug 1;79(3):448-57. doi: 10.1093/cvr/cvn101. Epub 2008 Apr 25.

19.

Transcription factor Sp3 knockout mice display serious cardiac malformations.

van Loo PF, Mahtab EA, Wisse LJ, Hou J, Grosveld F, Suske G, Philipsen S, Gittenberger-de Groot AC.

Mol Cell Biol. 2007 Dec;27(24):8571-82. Epub 2007 Oct 8.

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