Aortic aneurysm and craniosynostosis in a family with Cantu syndrome-Reference-Cited by-同舟云学术

Aortic aneurysm and craniosynostosis in a family with Cantu syndrome

Published:2013-11-25 Issue:1 Volume:164 Page:231-236
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Hiraki Yoko¹,Miyatake Satoko²,Hayashidani Michiko³,Nishimura Yutaka³,Matsuura Hiroo⁴,Kamada Masahiro⁵,Kawagoe Takuji⁶,Yunoki Keiji⁷,Okamoto Nobuhiko⁸,Yofune Hiroko⁹,Nakashima Mitsuko²,Tsurusaki Yoshinori²,Satisu Hirotomo²,Murakami Akira²,Miyake Noriko²,Nishimura Gen¹⁰,Matsumoto Naomichi²

Affiliation:

1. Hiroshima Municipal Center for Child Health and Development; Hiroshima Japan

2. Yokohama City University Graduate School of Medicine; Yokohama Japan

3. Medical Center for Premature and Neonatal Infants; Hiroshima City Hospital; Hiroshima Japan

4. Department of Pathology; Hiroshima City Hospital; Hiroshima Japan

5. Division of Pediatric Cardiology; Hiroshima City Hospital; Hiroshima Japan

6. Department of Cardiology; Hiroshima City Hospital; Hiroshima Japan

7. Department of Cardiovascular Surgery; Hiroshima City Hospital; Hiroshima Japan

8. Department of Medical Genetics; Osaka Medical Center and Research Institute for Maternal and Child Health; Osaka Japan

9. Hiroshima City Hokubu Center for Children's Treatment and Guidance; Hiroshima Japan

10. Department of Pediatric Imaging; Tokyo Metropolitan Children's Medical Center; Tokyo Japan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36228/fullpdf

Reference17 articles.

1. ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating;Bienengraeber;Nat Genet,2004

2. A distinct osteochondrodysplasia with hypertrichosis-Individualization of a probable autosomal recessive entity;Cantu;Hum Genet,1982

3. A framework for variation discovery and genotyping using next-generation DNA sequencing data;DePristo;Nat Genet,2011

4. A transmembrane domain of the sulfonylurea receptor mediates activation of ATP-sensitive K(+) channels by K(+) channel openers;D'Hahan;Mol Pharmacol,1999

5. Overexpression of SUR2A generates a cardiac phenotype resistant to ischemia;Du;FASEB J,2006

Cited by 31 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Innovation in pathogenesis and management of aortic aneurysm;World Journal of Experimental Medicine;2024-06-20

2. Aging as a loss of morphostatic information: A developmental bioelectricity perspective;Ageing Research Reviews;2024-06

3. Electrophysiology of Human iPSC-derived Vascular Smooth Muscle Cells and Cell-autonomous Consequences of Cantú Syndrome Mutations;Function;2024

4. Personalized Therapeutics for K_ATP-Dependent Pathologies;Annual Review of Pharmacology and Toxicology;2023-01-20

5. A Unique High‐Output Cardiac Hypertrophy Phenotype Arising From Low Systemic Vascular Resistance in Cantu Syndrome;Journal of the American Heart Association;2022-12-20