August 2013 Fetal Cardiology Articles

1. Recent advances in understanding the genetics of congenital heart defects.

Gelb BD.

Curr Opin Pediatr. 2013 Aug 29. [Epub ahead of print]

PMID: 23995429 [PubMed – as supplied by publisher]

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2. Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice.

Freyer L, Nowotschin S, Pirity MK, Baldini A, Morrow BE.

BMC Dev Biol. 2013 Aug 23;13(1):33. [Epub ahead of print]

PMID: 23971992 [PubMed – as supplied by publisher] Free PMC Article

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3. Misregulation of SDF1-CXCR4 signaling impairs early cardiac neural crest cell migration leading to conotruncal defects.

Escot S, Blavet C, Härtle S, Duband JL, Fournier-Thibault C.

Circ Res. 2013 Aug 16;113(5):505-16. doi: 10.1161/CIRCRESAHA.113.301333. Epub 2013 Jul 9.

PMID: 23838132 [PubMed – indexed for MEDLINE]

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4. Unchanged mitochondrial organization and compartmentation of high-energy phosphates in creatine-deficient GAMT-/- mouse hearts.

Branovets J, Sepp M, Kotlyarova S, Jepihhina N, Sokolova N, Aksentijevic D, Lygate CA, Neubauer S, Vendelin M, Birkedal R.

Am J Physiol Heart Circ Physiol. 2013 Aug 15;305(4):H506-20. doi: 10.1152/ajpheart.00919.2012. Epub 2013 Jun 21.

PMID: 23792673 [PubMed – indexed for MEDLINE] Free PMC Article

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5. Altered ubiquitin-proteasome signaling in right ventricular hypertrophy and failure.

Rajagopalan V, Zhao M, Reddy S, Fajardo G, Wang X, Dewey S, Gomes AV, Bernstein D.

Am J Physiol Heart Circ Physiol. 2013 Aug 15;305(4):H551-62. doi: 10.1152/ajpheart.00771.2012. Epub 2013 May 31.

PMID: 23729213 [PubMed – indexed for MEDLINE]

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6. Single-nucleotide polymorphism of the pri-miR-34b/c gene is not associated with susceptibility to congenital heart disease in the Han Chinese population.

Liu YM, Wang Y, Peng W, Wu Z, Wang XH, Wang ML, Wang W, Sun J, Zhang ZD, Mo XM.

Genet Mol Res. 2013 Aug 12;12(3):2937-44. doi: 10.4238/2013.August.12.9.

PMID: 24065649 [PubMed – in process] Free Article

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7. Associations between two genetic variants in NKX2-5 and risk of congenital heart disease in Chinese population: a meta-analysis.

Wang Z, Zou L, Zhong R, Zhu B, Chen W, Shen N, Ke J, Lou J, Song R, Miao XP.

PLoS One. 2013 Aug 2;8(8):e70979. doi: 10.1371/journal.pone.0070979. Print 2013.

PMID: 23936479 [PubMed – in process] Free PMC Article

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8. Non-trisomic homeobox gene expression during craniofacial development in the Ts65Dn mouse model of Down syndrome.

Billingsley CN, Allen JR, Baumann DD, Deitz SL, Blazek JD, Newbauer A, Darrah A, Long BC, Young B, Clement M, Doerge RW, Roper RJ.

Am J Med Genet A. 2013 Aug;161A(8):1866-74. doi: 10.1002/ajmg.a.36006. Epub 2013 Jul 10.

PMID: 23843306 [PubMed – indexed for MEDLINE]

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9. Embryonic cardiac chamber maturation: Trabeculation, conduction, and cardiomyocyte proliferation.

Samsa LA, Yang B, Liu J.

Am J Med Genet C Semin Med Genet. 2013 Aug;163C(3):157-68. doi: 10.1002/ajmg.c.31366. Epub 2013 May 29. Review.

PMID: 23720419 [PubMed – in process]

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10. Impact of late preterm birth on neonatal intensive care resources in a tertiary perinatal center.

Jefferies AL, Lyons ER, Shah PS, Shah V.

Am J Perinatol. 2013 Aug;30(7):573-8. doi: 10.1055/s-0032-1329685. Epub 2012 Dec 19.

PMID: 23254383 [PubMed – indexed for MEDLINE]

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11. Neural crest cells are required for correct positioning of the developing outflow cushions and pattern the arterial valve leaflets.

Phillips HM, Mahendran P, Singh E, Anderson RH, Chaudhry B, Henderson DJ.

Cardiovasc Res. 2013 Aug 1;99(3):452-60. doi: 10.1093/cvr/cvt132. Epub 2013 May 30.

PMID: 23723064 [PubMed – indexed for MEDLINE] Free PMC Article

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12. Co-ordinating Notch, BMP, and TGF-β signaling during heart valve development.

Garside VC, Chang AC, Karsan A, Hoodless PA.

Cell Mol Life Sci. 2013 Aug;70(16):2899-917. doi: 10.1007/s00018-012-1197-9. Epub 2012 Nov 16. Review.

PMID: 23161060 [PubMed – indexed for MEDLINE]

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13. Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls.

Mamasoula C, Prentice RR, Pierscionek T, Pangilinan F, Mills JL, Druschel C, Pass K, Russell MW, Hall D, Töpf A, Brown DL, Zelenika D, Bentham J, Cosgrove C, Bhattacharya S, Riveron JG, Setchfield K, Brook JD, Bu’Lock FA, Thornborough C, Rahman TJ, Doza JP, Tan HL, O’Sullivan J, Stuart AG, Blue G, Winlaw D, Postma AV, Mulder BJ, Zwinderman AH, van Engelen K, Moorman AF, Rauch A, Gewillig M, Breckpot J, Devriendt K, Lathrop GM, Farrall M, Goodship JA, Cordell HJ, Brody LC, Keavney BD.

Circ Cardiovasc Genet. 2013 Aug;6(4):347-53. doi: 10.1161/CIRCGENETICS.113.000191. Epub 2013 Jul 22.

PMID: 23876493 [PubMed – in process] Free PMC Article

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14. microRNAs in cardiac development and regeneration.

Porrello ER.

Clin Sci (Lond). 2013 Aug;125(4):151-66. doi: 10.1042/CS20130011. Review.

PMID: 23634935 [PubMed – indexed for MEDLINE]

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15. Bmp signaling represses Vegfa to promote outflow tract cushion development.

Bai Y, Wang J, Morikawa Y, Bonilla-Claudio M, Klysik E, Martin JF.

Development. 2013 Aug;140(16):3395-402. doi: 10.1242/dev.097360. Epub 2013 Jul 17.

PMID: 23863481 [PubMed – indexed for MEDLINE] Free Article

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16. Tbx20 acts upstream of Wnt signaling to regulate endocardial cushion formation and valve remodeling during mouse cardiogenesis.

Cai X, Zhang W, Hu J, Zhang L, Sultana N, Wu B, Cai W, Zhou B, Cai CL.

Development. 2013 Aug;140(15):3176-87. doi: 10.1242/dev.092502. Epub 2013 Jul 3.

PMID: 23824573 [PubMed – indexed for MEDLINE] Free Article

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17. A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring.

Rump A, Hildebrand L, Tzschach A, Ullmann R, Schrock E, Mitter D.

Eur J Hum Genet. 2013 Aug;21(8):887-90. doi: 10.1038/ejhg.2012.267. Epub 2012 Dec 12.

PMID: 23232695 [PubMed – indexed for MEDLINE]

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18. Cardiac anomalies in individuals with the 18q deletion syndrome; report of a child with Ebstein anomaly and review of the literature.

van Trier DC, Feenstra I, Bot P, de Leeuw N, Draaisma JM.

Eur J Med Genet. 2013 Aug;56(8):426-31. doi: 10.1016/j.ejmg.2013.05.002. Epub 2013 May 22. Review.

PMID: 23707655 [PubMed – indexed for MEDLINE]

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19. Identification of microRNAs present in congenital heart disease associated copy number variants.

Xing HJ, Li YJ, Ma QM, Wang AM, Wang JL, Sun M, Jian Q, Hu JH, Li D, Wang L.

Eur Rev Med Pharmacol Sci. 2013 Aug;17(15):2114-20.

PMID: 23884835 [PubMed – in process] Free Article

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20. R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease.

Beffagna G, Cecchetto A, Dal Bianco L, Lorenzon A, Angelini A, Padalino M, Vida V, Bhattacharya S, Stellin G, Rampazzo A, Daliento L.

J Cardiovasc Med (Hagerstown). 2013 Aug;14(8):582-6. doi: 10.2459/JCM.0b013e328356a326.

PMID: 22964646 [PubMed – indexed for MEDLINE]

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21. Fetal diagnosis of left-ventricular noncompaction cardiomyopathy in identical twins with discordant congenital heart disease.

Vinograd CA, Srivastava S, Panesar LE.

Pediatr Cardiol. 2013 Aug;34(6):1503-7. doi: 10.1007/s00246-012-0406-5. Epub 2012 Jun 15.

PMID: 22695766 [PubMed – indexed for MEDLINE]

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22. Three-dimensional HDlive rendering images of the fetal heart.

Hata T, Mashima M, Ito M, Uketa E, Mori N, Ishimura M.

Ultrasound Med Biol. 2013 Aug;39(8):1513-7. doi: 10.1016/j.ultrasmedbio.2013.03.027. Epub 2013 Jun 4.

PMID: 23743102 [PubMed – indexed for MEDLINE]

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23. The occurrence and suspected mode of inheritance of congenital subaortic stenosis and tricuspid valve dysplasia in Dogue de Bordeaux dogs.

Ohad DG, Avrahami A, Waner T, David L.

Vet J. 2013 Aug;197(2):351-7. doi: 10.1016/j.tvjl.2013.01.012. Epub 2013 Feb 20.

PMID: 23434219 [PubMed – indexed for MEDLINE]

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24. The HHEX gene is not related to congenital heart disease in 296 Chinese patients.

Deng XP, Zhao LX, Wang BB, Wang J, Cheng LF, Cheng Z, Suo PS, Li H, Ma X.

World J Pediatr. 2013 Aug;9(3):278-80. doi: 10.1007/s12519-013-0430-4. Epub 2013 Aug 9.

PMID: 23929257 [PubMed – in process]

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25. [Risk factors of congenital heart defects in fetal and infants born from 2004 to 2011 in Guangdong].

Nie ZQ, Ou YQ, Chen JM, Liu XQ, Mai JZ, Gao XM, Wu Y, Zhuang J.

Zhonghua Xin Xue Guan Bing Za Zhi. 2013 Aug;41(8):704-8. Chinese.

PMID: 24225245 [PubMed – in process]

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