|
1
|
Roger VL, Go AS, Lloyd-Jones DM, et al:
American Heart Association Statistics Committee and Stroke
Statistics Subcommittee: Heart disease and stroke statistics - 2011
update: a report from the American Heart Association. Circulation.
123:e18–e209. 2011. View Article : Google Scholar
|
|
2
|
Hoffman JI: Incidence of congenital heart
disease: II. Prenata incidence. Pediatr Cardiol. 16:155–165. 1995.
View Article : Google Scholar : PubMed/NCBI
|
|
3
|
Mitchell SC, Korones SB, Berendes HW, et
al: Congenital heart disease in 56,109 births. Incidence and
natural history. Circulation. 43:323–332. 1971. View Article : Google Scholar : PubMed/NCBI
|
|
4
|
Ferencz C, Rubin JD, McCarter RJ, et al:
Congenital heart disease: prevalence in live birth. The
Baltimore-Washington Infant Study. Am J Epidemiol. 121:31–36.
1981.
|
|
5
|
Kola S, Koneti NR, Golla JP, et al:
Mutational analysis of JAG1 gene in non-syndromic Tetralogy of
Fallot children. Clin Chim Acta. 412:2232–2236. 2011. View Article : Google Scholar : PubMed/NCBI
|
|
6
|
Kaynak B, von Heydebreck A, Mebus S, et
al: Genome-wide array analysis of normal and malformed human
hearts. Circulation. 107:2467–2474. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
7
|
Schott JJ, Benson DW, Basson CT, et al:
Congenital heart disease caused by mutations in the transcription
factor NKX2-5. Science. 281:108–111. 1998. View Article : Google Scholar : PubMed/NCBI
|
|
8
|
Okubo A, Miyoshi O, Baba K, Takagi M, et
al: A novel GATA4 mutation completely segregated with atrial septal
defect in a large Japanese family. J Med Genet. 41:e972004.
View Article : Google Scholar : PubMed/NCBI
|
|
9
|
Basson CT, Huang T, Lin RC, et al:
Different TBX5 interactions in heart and limb defined by Holt-Oram
syndrome mutations. Proc Natl Acad Sci USA. 96:2919–2924. 1999.
View Article : Google Scholar : PubMed/NCBI
|
|
10
|
Reese DE, Zavaljevski M, Streiff NL and
Bader D: bves: a novel gene expressed during coronary blood vessel
development. Dev Biol. 209:159–171. 1999. View Article : Google Scholar : PubMed/NCBI
|
|
11
|
Andree B, Hillemann T, Kessler-Icekson G,
et al: Isolation and characterization of the novel popeye gene
family expressed in skeletal muscle and heart. Dev Biol.
223:371–382. 2000. View Article : Google Scholar : PubMed/NCBI
|
|
12
|
Russ PK, Kupperman AI, Presley SH, et al:
Inhibition of RhoA signaling with increased Bves in trabecular
meshwork cells. Invest Ophthalmol Vis Sci. 51:223–230. 2010.
View Article : Google Scholar : PubMed/NCBI
|
|
13
|
Wilson P and Keller R: Cell rearrangement
during gastrulation of Xenopus: direct observation of
cultured explants. Development. 112:289–300. 1991.
|
|
14
|
Russ PK, Pino CJ, Williams CS, et al: Bves
modulates tight junction associated signaling. PLoS One.
6:e145632011. View Article : Google Scholar : PubMed/NCBI
|
|
15
|
Hager HA and Bader DM: Bves: ten years
after. Histol Histopathol. 24:777–787. 2009.PubMed/NCBI
|
|
16
|
Hager HA, Roberts RJ, Cross EE, et al:
Identification of a novel Bves function: regulation of vesicular
transport. EMBO J. 29:532–545. 2010. View Article : Google Scholar : PubMed/NCBI
|
|
17
|
Boukens BJ and Christoffels VM: Popeye
proteins: muscle for the aging sinus node. J Clin Invest.
122:810–813. 2012. View
Article : Google Scholar : PubMed/NCBI
|
|
18
|
Gingold-Belfer R, Bergman M, Alcalay Y, et
al: Popeye domain-containing 1 is down-regulated in failing human
hearts. Int J Mol Med. 27:25–31. 2011.
|
|
19
|
Zhang H, Zhou L, Yang R, et al:
Identification of differentially expressed genes in human heart
with ventricular septal defect using suppression subtractive
hybridization. Biochem Biophys Res Commun. 342:135–144. 2006.
View Article : Google Scholar
|
|
20
|
Tian XL and Wang QK: Generation of
transgenic mice for cardiovascular research. Methods Mol Med.
129:69–81. 2006.PubMed/NCBI
|
|
21
|
Warnes CA: The adult with congenital heart
disease: born to be bad? J Am Coll Cardiol. 46:1–8. 2005.
View Article : Google Scholar : PubMed/NCBI
|
|
22
|
Giannopoulos NM, Chatzis AC, Bobos DP, et
al: Tetralogy of Fallot: influence of right ventricular outflow
tract reconstruction on late outcome. Int J Cardiol. 97(Suppl 1):
87–90. 2004. View Article : Google Scholar : PubMed/NCBI
|
|
23
|
Jain R, Rentschler S and Epstein JA: Notch
and cardiac outflow tract development. Ann NY Acad Sci.
1188:184–190. 2010. View Article : Google Scholar : PubMed/NCBI
|
|
24
|
Hein S, Kostin S, Heling A, et al: The
role of the cytoskeleton in heart failure. Cardiovasc Res.
45:273–278. 2000. View Article : Google Scholar : PubMed/NCBI
|
|
25
|
Maslen CL: Molecular genetics of
atrioventricular septal defects. Curr Opin Cardiol. 19:205–210.
2004. View Article : Google Scholar : PubMed/NCBI
|
|
26
|
Marino B and Digilio MC: Congenital heart
disease and genetic syndromes: specific correlation between cardiac
phenotype and genotype. Cardiovasc Pathol. 9:303–315. 2000.
View Article : Google Scholar : PubMed/NCBI
|
|
27
|
Wada AM, Reese DE and Bader DM: Bves:
prototype of a new class of cell adhesion molecules expressed
during coronary artery development. Development. 128:2085–2093.
2001.PubMed/NCBI
|
|
28
|
Andree B, Fleige A, Arnold HH, et al:
Mouse Pop1 is required for muscle regeneration in adult skeletal
muscle. Mol Cell Biol. 22:1504–1512. 2002. View Article : Google Scholar : PubMed/NCBI
|
|
29
|
Parnes D, Jacoby V, Sharabi A, et al: The
Popdc gene family in the rat: molecular cloning, characterization
and expression analysis in the heart and cultured cardiomyocytes.
Biochim Biophys Acta. 1769:586–592. 2007. View Article : Google Scholar : PubMed/NCBI
|
