✦ LIBER ✦

Analysis of the human folate receptor β gene for an association with neural tube defects

✍ Scribed by Valerie B O’Leary; James L Mills; Peadar N Kirke; Anne Parle-McDermott; Deborah A Swanson; Andrea Weiler; Faith Pangilinan; Mary Conley; Anne M Molloy; Miriam Lynch; Christopher Cox; John M Scott; Lawrence C Brody

Book ID: 117735523
Publisher: Elsevier Science
Year: 2003
Tongue: English
Weight: 121 KB
Volume: 79
Category: Article
ISSN: 1096-7192
DOI: 10.1016/s1096-7192(03)00075-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Promoter haplotype combinations for the

Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects

✍ Huiping Zhu; Ned J Wicker; Kelly Volcik; Jing Zhang; Gary M Shaw; Edward J Lamme 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 217 KB

Novel polymorphisms of the human cholecy

Novel polymorphisms of the human cholecystokinin a receptor gene: An association analysis with schizophrenia

✍ Tachikawa, Hirokazu; Harada, Shoji; Kawanishi, Yoichi; Okubo, Takehito; Shiraish 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 15 KB 👁 3 views

The cholecystokinin A receptor (CCK-AR) modulates CCK-stimulated dopamine release in the posterior nucleus accumbens, and its gene is mapped to 4p15.2-15.1 with the dopamine receptor 5 (DR5) gene. We speculated that alterations in the CCK-AR lead to an increase in dopamine release, which may in turn

A Second Common Mutation in the Methylen

A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects?

✍ Nathalie M.J. van der Put; Fons Gabreëls; Erik M.B. Stevens; Jan A.M. Smeitink; 📂 Article 📅 1998 🏛 American Society of Human Genetics 🌐 English ⚖ 300 KB

Testing for genetic associations in a sp

Testing for genetic associations in a spina bifida population: Analysis of theHOX gene family and human candidate gene regions implicated by mouse models of neural tube defects

✍ Volcik, K.A. ;Blanton, S.H. ;Kruzel, M.C. ;Townsend, I.T. ;Tyerman, G.H. ;Mier, 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 57 KB 👁 3 views

Novel polymorphism in the promoter and c

Novel polymorphism in the promoter and coding regions of the human cholecystokinin B receptor gene: An association analysis with schizophrenia

✍ Tachikawa, Hirokazu; Harada, Shoji; Kawanishi, Yoichi; Okubo, Takehito; Shiraish 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 38 KB 👁 3 views

Genetic variations in the 5-untranslated region and the coding region of the CCK-B receptor (CCK-BR) gene were investigated in healthy controls. Novel variants (-215 C→A, Leu37Phe, Arg319Glu) were found in addition to the mutations (Val125Iso, His207His, Arg215His, 2491 C→A) reported previously. In

Expression of the gene encoding the high

Expression of the gene encoding the high-Kmglucose transporter 2 by the early postimplantation mouse embryo is essential for neural tube defects associated with diabetic embryopathy

✍ R. Li; B. Thorens; M. R. Loeken 📂 Article 📅 2007 🏛 Springer 🌐 English ⚖ 196 KB