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Items: 6

1.
Oligogenic inheritance of a human heart disease involving a genetic modifier
Casey A. Gifford, Sanjeev S. Ranade, Ryan Samarakoon, Hazel T. Salunga, T. Yvanka de Soysa, Yu Huang, Ping Zhou, Aryé Elfenbein, Stacia K. Wyman, Yen Kim Bui, Kimberly R. Cordes Metzler, Philip Ursell, Kathryn N. Ivey, Deepak Srivastava
Science. Author manuscript; available in PMC 2019 Nov 30.
Published in final edited form as: Science. 2019 May 31; 364(6443): 865–870. Published online 2019 May 30. doi: 10.1126/science.aat5056
PMCID:
PMC6557373
AbstractArticlePDF–1.6M
2.
Association of NKX2‐5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children
Eman G. Behiry, Mahmoud A. Al‐Azzouny, Dina Sabry, Ola G. Behairy, Nessrine E. Salem
Mol Genet Genomic Med. 2019 May; 7(5): e612. Published online 2019 Mar 4. doi: 10.1002/mgg3.612
PMCID:
PMC6503026
AbstractArticlePDF–499K
3.
Analysis of NKX2-5 in 439 Chinese Patients with Sporadic Atrial Septal Defect
Hongshu Wang, Yong Liu, Yaxiong Li, Wenju Wang, Lin Li, Mingyao Meng, Yanhua Xie, Yayong Zhang, Yunfeng Zi, Shen Han, Jianying Zeng, ZongLiu Hou, Lihong Jiang
Med Sci Monit. 2019; 25: 2756–2763. Published online 2019 Apr 15. doi: 10.12659/MSM.916052
PMCID:
PMC6481236
AbstractArticlePDF–1.1M
4.
Molecular cloning, chromosomal mapping, and characterization of the human cardiac-specific homeobox gene hCsx.
D. Turbay, S. B. Wechsler, K. M. Blanchard, S. Izumo
Mol Med. 1996 Jan; 2(1): 86–96.
PMCID:
PMC2230031
SummaryPage BrowsePDF–2.3M
5.
The cardiac transcription factors Nkx2-5 and GATA-4 are mutual cofactors.
D Durocher, F Charron, R Warren, R J Schwartz, M Nemer
EMBO J. 1997 Sep 15; 16(18): 5687–5696. doi: 10.1093/emboj/16.18.5687
PMCID:
PMC1170200
SummaryPDF–437K
6.
Recruitment of the tinman homolog Nkx-2.5 by serum response factor activates cardiac alpha-actin gene transcription.
C Y Chen, R J Schwartz
Mol Cell Biol. 1996 Nov; 16(11): 6372–6384. doi: 10.1128/mcb.16.11.6372
PMCID:
PMC231639
SummaryPDF–1.8M

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