PubMed (OMIM) for id: 21498

Year	Number of Results
1962	1
1972	1
1974	1
1976	1
1985	2
1988	1
1990	2
1991	2
1992	1
1993	3
1994	2
1995	6
1996	4
1997	9
1998	3
1999	12
2000	8
2001	17
2002	9
2003	10
2004	4
2005	4
2006	1
2024	0

1

Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome.

Guris DL, Duester G, Papaioannou VE, Imamoto A. Guris DL, et al. Dev Cell. 2006 Jan;10(1):81-92. doi: 10.1016/j.devcel.2005.12.002. Dev Cell. 2006. PMID: 16399080 Free article.

2

Low expression VEGF haplotype increases the risk for tetralogy of Fallot: a family based association study.

Lambrechts D, Devriendt K, Driscoll DA, Goldmuntz E, Gewillig M, Vlietinck R, Collen D, Carmeliet P. Lambrechts D, et al. J Med Genet. 2005 Jun;42(6):519-22. doi: 10.1136/jmg.2004.026443. J Med Genet. 2005. PMID: 15937089 Free PMC article. No abstract available.

3

Morphogenesis of the right ventricle requires myocardial expression of Gata4.

Zeisberg EM, Ma Q, Juraszek AL, Moses K, Schwartz RJ, Izumo S, Pu WT. Zeisberg EM, et al. J Clin Invest. 2005 Jun;115(6):1522-31. doi: 10.1172/JCI23769. Epub 2005 May 12. J Clin Invest. 2005. PMID: 15902305 Free PMC article.

4

Expression of mutant JAGGED1 alleles in patients with Alagille syndrome.

Boyer J, Crosnier C, Driancourt C, Raynaud N, Gonzales M, Hadchouel M, Meunier-Rotival M. Boyer J, et al. Hum Genet. 2005 May;116(6):445-53. doi: 10.1007/s00439-005-1262-7. Epub 2005 Mar 17. Hum Genet. 2005. PMID: 15772854

5

AML1-FOG2 fusion protein in myelodysplasia.

Chan EM, Comer EM, Brown FC, Richkind KE, Holmes ML, Chong BH, Shiffman R, Zhang DE, Slovak ML, Willman CL, Noguchi CT, Li Y, Heiber DJ, Kwan L, Chan RJ, Vance GH, Ramsey HC, Hromas RA. Chan EM, et al. Blood. 2005 Jun 1;105(11):4523-6. doi: 10.1182/blood-2004-07-2762. Epub 2005 Feb 10. Blood. 2005. PMID: 15705784 Free article.

6

Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease.

Reamon-Buettner SM, Borlak J. Reamon-Buettner SM, et al. J Med Genet. 2004 Sep;41(9):684-90. doi: 10.1136/jmg.2003.017483. J Med Genet. 2004. PMID: 15342699 Free PMC article.

7

GATA4 is essential for formation of the proepicardium and regulates cardiogenesis.

Watt AJ, Battle MA, Li J, Duncan SA. Watt AJ, et al. Proc Natl Acad Sci U S A. 2004 Aug 24;101(34):12573-8. doi: 10.1073/pnas.0400752101. Epub 2004 Aug 13. Proc Natl Acad Sci U S A. 2004. PMID: 15310850 Free PMC article.

8

Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block.

Pashmforoush M, Lu JT, Chen H, Amand TS, Kondo R, Pradervand S, Evans SM, Clark B, Feramisco JR, Giles W, Ho SY, Benson DW, Silberbach M, Shou W, Chien KR. Pashmforoush M, et al. Cell. 2004 Apr 30;117(3):373-86. doi: 10.1016/s0092-8674(04)00405-2. Cell. 2004. PMID: 15109497 Free article.

9

Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system.

Jay PY, Harris BS, Maguire CT, Buerger A, Wakimoto H, Tanaka M, Kupershmidt S, Roden DM, Schultheiss TM, O'Brien TX, Gourdie RG, Berul CI, Izumo S. Jay PY, et al. J Clin Invest. 2004 Apr;113(8):1130-7. doi: 10.1172/JCI19846. J Clin Invest. 2004. PMID: 15085192 Free PMC article.

10

Role of TBX1 in human del22q11.2 syndrome.

Yagi H, Furutani Y, Hamada H, Sasaki T, Asakawa S, Minoshima S, Ichida F, Joo K, Kimura M, Imamura S, Kamatani N, Momma K, Takao A, Nakazawa M, Shimizu N, Matsuoka R. Yagi H, et al. Lancet. 2003 Oct 25;362(9393):1366-73. doi: 10.1016/s0140-6736(03)14632-6. Lancet. 2003. PMID: 14585638

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