To elucidate the genetic factors causing clinical differences in the children with Down syndrome and evaluate possible maternal risk factors, the researchers have investigated GSTM1, GSTT1, GSTP1 gene polymorphisms. Four groups were defined: group I (n = 52), children with Down syndrome; group II (n = 70), healthy children; group III (n = 52), mothers of the children with Down syndrome; and group IV (n = 69), mothers of the healthy children. Genomic DNA was extracted from the white blood cells and GenID (R) GmbH kit used for GST MI, T1 and PI gene amplification to determine polymorphisms. The researchers did not detect any significant difference in the allele frequencies between groups I and II, nor groups III and IV. The data indicated no ...
CONTEXT AND OBJECTIVE: Polymorphisms in genes involved in folate metabolism may modulate the materna...
A common polymorphism (c.80A>G) in the gene coding for the reduced folate carrier (SLC19A1, commo...
Background: Down syndrome (DS) is one of the most common chromosomal abnormalities among live-born b...
To elucidate the genetic factors causing clinical differences in the children with Down syndrome and...
Down syndrome is a complex genetic and metabolic disorder attributed to the presence of three copies...
Background: Polymorphisms of genes encoding enzymes involved in folate metabolism have long been hyp...
CONTEXT AND OBJECTIVE: There is evidence that polymorphisms of genes involved in folate metabolism m...
This study aimed to investigate the role of maternal polymorphisms, as well as their risk genotypes ...
Recent researches have investigated the factors that determine the maternal risk for Down syndrome (...
Associations between specific alleles of genes encoding enzymes in the methionine/homocysteine pathw...
Inconclusive results of the association between genetic polymorphisms involved in folate metabolism ...
Studies investigating the association between gene polymorphisms involved in homocysteine/folate met...
We recently observed an association between combinations of polymorphisms in the methylenetetrahydro...
The origin of nondisjunction in trisomy 21 has so far been studied using cytogenetic heteromorphisms...
Several variants have been identified for genes encoding Glutathione S-transferase (GST) enzymes; so...
CONTEXT AND OBJECTIVE: Polymorphisms in genes involved in folate metabolism may modulate the materna...
A common polymorphism (c.80A>G) in the gene coding for the reduced folate carrier (SLC19A1, commo...
Background: Down syndrome (DS) is one of the most common chromosomal abnormalities among live-born b...
To elucidate the genetic factors causing clinical differences in the children with Down syndrome and...
Down syndrome is a complex genetic and metabolic disorder attributed to the presence of three copies...
Background: Polymorphisms of genes encoding enzymes involved in folate metabolism have long been hyp...
CONTEXT AND OBJECTIVE: There is evidence that polymorphisms of genes involved in folate metabolism m...
This study aimed to investigate the role of maternal polymorphisms, as well as their risk genotypes ...
Recent researches have investigated the factors that determine the maternal risk for Down syndrome (...
Associations between specific alleles of genes encoding enzymes in the methionine/homocysteine pathw...
Inconclusive results of the association between genetic polymorphisms involved in folate metabolism ...
Studies investigating the association between gene polymorphisms involved in homocysteine/folate met...
We recently observed an association between combinations of polymorphisms in the methylenetetrahydro...
The origin of nondisjunction in trisomy 21 has so far been studied using cytogenetic heteromorphisms...
Several variants have been identified for genes encoding Glutathione S-transferase (GST) enzymes; so...
CONTEXT AND OBJECTIVE: Polymorphisms in genes involved in folate metabolism may modulate the materna...
A common polymorphism (c.80A>G) in the gene coding for the reduced folate carrier (SLC19A1, commo...
Background: Down syndrome (DS) is one of the most common chromosomal abnormalities among live-born b...