𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Molecular genetic analysis of human folate receptors in neural tube defects

✍ Scribed by Heil, Sandra G; van der Put, Nathalie MJ; Trijbels, Frans JM; Gabreëls, Fons JM; Blom, Henk J


Book ID
110024812
Publisher
Nature Publishing Group
Year
1999
Tongue
English
Weight
95 KB
Volume
7
Category
Article
ISSN
1018-4813

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Molecular genetic analysis of human homo
✍ Elisa Merello; Patrizia De Marco; Anna Moroni; Alessandro Raso; Maria Grazia Cal 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 209 KB 👁 2 views

## Abstract ## BACKGROUND Neural tube defects (NTDs) are complex embryological malformations, affecting 1 in 1,000 live births. Antisense studies have implicated murine __Mab21__ genes as having an important role in neural tube development. We investigated whether __MAB21L1__/__L2__ genes could be

The search for genetic polymorphisms in
✍ Anne M. Molloy; Lawrence C. Brody; James L. Mills; John M. Scott; Peadar N. Kirk 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 175 KB 👁 3 views

## Abstract In this paper, we trace the history of current research into the genetic and biochemical mechanisms that underlie folate‐preventable neural tube defects (NTDs). The inspired suggestion by Smithells that common vitamins might prevent NTDs ignited a decade of biochemical investigations—fi

Abnormal folate metabolism and genetic p
✍ Al-Gazali, L.I. ;Padmanabhan, R. ;Melnyk, S. ;Yi, P. ;Pogribny, I.P. ;Pogribna, 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 86 KB 👁 2 views

The association of neural tube defects (NTDs) with Down syndrome (trisomy 21) and altered folate metabolism in both mother and affected offspring provide a unique opportunity for insight into the etiologic role of folate deficiency in these congenital anomalies. We describe here the case of a male c