𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Identification of novel rare mutations of DACT1 in human neural tube defects

✍ Scribed by Yan Shi; Yi Ding; Yun-Ping Lei; Xue-Yan Yang; Guo-Ming Xie; Jun Wen; Chun-Quan Cai; Hong Li; Ying Chen; Ting Zhang; Bai-Lin Wu; Li Jin; Ye-Guang Chen; Hong-Yan Wang

Book ID
112099782
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
364 KB
Volume
33
Category
Article
ISSN
1059-7794

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Identification and characterization of n
Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defects
✍ Ciprian M. Bosoi; Valeria Capra; Redouane Allache; Vincent Quoc-Huy Trinh; Patri πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 227 KB

The planar cell polarity (PCP) pathway controls the process of convergent extension (CE) during gastrulation and neural tube closure, and has been implicated in the pathogenesis of neural tube defects (NTDs) in animal models and human cohorts. In this study, we analyzed the role of one core PCP gene

Novel mutations in VANGL1 in neural tube
Novel mutations in VANGL1 in neural tube defects
✍ Zoha Kibar; Ciprian M. Bosoi; Megan Kooistra; Sandra Salem; Richard H. Finnell; πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 142 KB

Neural tube defects (NTDs) are severe congenital malformations caused by failure of the neural tube to close during neurulation. Their etiology is complex involving both environmental and genetic factors. We have recently reported three mutations in the planar cell polarity gene VANGL1 associated wi