A Novel Variation of PLAGL1 in Chinese Patients with Isolated Ventricular Septal Defect-Reference-Cited by-同舟云学术

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A Novel Variation of PLAGL1 in Chinese Patients with Isolated Ventricular Septal Defect

Published:2012-08 Issue:8 Volume:16 Page:984-987
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Xuan Chao¹,Wang Bin-Bin²,Gao Ge¹,Bai Xiao-Yan¹,Yang Qin¹³,Liu Xiao-Cheng¹,Jing Wen-Bin¹,Ma Xu²,He Guo-Wei¹⁴

Affiliation:

1. TEDA International Cardiovascular Hospital, Medical College, Nankai University, Tianjin, PR China.

2. Center for Genetics, National Research Institute for Family Planning, Beijing, PR China.

3. The Chinese University of Hong Kong, Hong Kong, PR China.

4. Department of Surgery, Oregon Health and Science University, Portland, Oregon.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2012.0003

Reference28 articles.

1. ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome

2. Establishment of the primary imprint of the HYMAI/PLAGL1 imprint control region during oogenesis

3. Alternative splicing of the imprinted candidate tumor suppressor gene ZAC regulates its antiproliferative and DNA binding activities

4. Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome

5. Congenital ventricular septal defects and prenatal exposure to cyclooxygenase inhibitors

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