Research Article

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02/19/2013
Cleft lip; Cleft palate; Folic acid; Nonsyndromic; Registry-based cases; Turkey

Oral clefts are one of the most common birth defects in humans. However, few population-based studies of these defects have been carried out in Turkey. Our objective was to determine the registries of cases of cleft lip and palate. All cases of cleft lip and palate referred to central state hospitals in Denizli between January 2000 and May 2010 were investigated retrospectively. Anomalies ... more

A.G. Tomatir; I. Acikbas; B. Akdag; A. Köksal
03/26/2014
bifida; Diabetes; Folic acid; MTHFR; Neural tube defects

Abnormalities in maternal folate and carbohydrate metabolism have both been shown to induce neural tube defects (NTD) in humans and animal models. However, the relationship between these two factors in the development of NTDs remains unclear. Data from mothers of children with spina bifida seen at the Unidad de Espina Bífida del Hospital Infantil Virgen del Rocío (case group) were ... more

N.M. Cadenas-Benitez; F. Yanes-Sosa; A. Gonzalez-Meneses; L. Cerrillos; D. Acosta; J.M. Praena-Fernandez; O. Neth; G. de Terreros; P. Ybot-González
01/03/2014
Differentially expressed genes; Endothelial progenitor cells; Folic acid; Immune response; Type 1 diabetes mellitus

We investigated the effects of type 1 diabetes mellitus (T1DM) on endothelial progenitor cells (EPCs) at the molecular level and assessed the therapeutic potential of folic acid (FA) in DM. We downloaded the gene expression profile of the EPCs from T1DM patients before and after treatment with FA and from healthy controls. We identified the differentially expressed genes (DEGs) in the ... more

D.N. Fang; X.D. He; X.H. Li; H. Jia; P.Y. Li; Q. Lu; Z. Quan; Q.L. Wang
10/25/2011
Congenital heart defect; Folic acid; Homocysteine; Methionine synthase reductase; Polymorphisms

Congenital heart defects (CHDs) are the most common birth defects; genes involved in homocysteine/folate metabolism may play important roles in CHDs. Methionine synthase reductase (MTRR) is one of the key regulatory enzymes involved in the metabolic pathway of homocysteine. We investigated whether two polymorphisms (A66G and C524T) of the MTRR gene are associated with ... more

W. Zeng; L. Liu; Y. Tong; H.M. Liu; L. Dai; M. Mao
02/02/2015
Folate metabolism; Folic acid; Preterm birth; Single nucleotide polymorphism

We investigated the association between 12 single nucleotide polymorphisms (SNPs) in 11 genes involved in folate metabolic and preterm birth. A subset of SNPs selected from 11 genes/loci involved in the folic acid metabolism pathway were subjected to SNaPshot analysis in a case-control study. Twelve SNPs (CBS-C699T, DHFR-c594+59del19, GST01-C428T, MTHFD- ... more

B.J. Wang; M.J. Liu; Y. Wang; J.R. Dai; J.Y. Tao; S.N. Wang; N. Zhong; Y. Chen
05/03/2011
Agribusiness; Plant breeding; Protection; Public-private partnership; Registry

During the last 20 years, the national production of grains has increased 156.1%; productivity increased 93.8% and there has been an increase of 29.1% in cultivated area. Currently, agribusiness is responsible for 40% of Brazilian exports. Nevertheless, there is little quantitative information on the main plant species of economic interest that have been registered and protected in the ... more

C.D. Marinho; F.J.O. Martins; S.C.S. Amaral; A.T.Amaral Júnior; L.S.A. Gonçalves; M.P. de Mello
08/21/2013
Loop-tail; N-ethyl-N-nitrosourea; Neural tube defect; Vangl2

N-ethyl-N-nitrosourea (ENU) is a powerful point mutagen that can generate random mutations. It has been used to generate mouse mutations to produce phenotypic models of human disease. Neural tube defects (NTD) are common birth defects in which the brain and/or spinal cord can be exposed; however, the mechanisms of these defects are poorly understood. Craniorachischisis ... more

B. Chen; H.H. Mao; L. Chen; F.L. Zhang; K. Li; Z.F. Xue
02/20/2014
Anencephaly; Bioinformatics; MAPK signaling pathway; Microarray; MicroRNA; Neural tube defect

Anencephaly is one of the most serious forms of neural tube defects (NTDs), a group of congenital central nervous system (CNS) malformations. MicroRNAs (miRNAs) are involved in diverse biological processes via the post-transcriptional regulation of target mRNAs. Although miRNAs play important roles in the development of mammalian CNS, their function in human NTDs remains unknown. Using a ... more

W.D. Zhang; X. Yu; X. Fu; S. Huang; S.J. Jin; Q. Ning; X.P. Luo
04/14/2009
Genetic diversity; Malus; Random amplified polymorphic DNA; Rootstocks; Turkey; UPOV

Two local (Vezir-1 and Vezir-2) and two standard (M9 and MM106) clonal apple rootstocks were compared using both morphological and molecular markers. International Union for the Protection of New Varieties of Plants criteria were used for morphological evaluation, which did not clearly separate these rootstocks. We tested 47 random decamer primers for random amplified polymorphic DNA analysis ... more

A. Koc; M. Akbulut; E. Orhan; Z. Celik; S. Bilgener; S. Ercisli
12/08/2011
FMF; Haplotype; MDR1; Polymorphism; Turkey

The multidrug resistance (MDR1) gene encodes a P-glycoprotein that plays a key role in drug bioavailability and response to drugs in different human populations. More than 50 SNPs have been described for the MDR1 gene. Familial Mediterranean fever (FMF) is considered an autosomal recessive hereditary disease, associated with a single gene named the Mediterranean fever gene (MEFV). However ... more

A. Rüstemoglu; G. Gümüş-Akay; S. Yigit; T. Tasliyurt

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