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Polymorphism of XRCC1, XRCC3, and XPD Genes and Risk of Chronic Myeloid Leukemia
TLDR
The results suggest that the XPD Lys751Gln variant genotype increases the risk of CML.
XRCC1 Arg194Trp and Arg399Gln polymorphisms are significantly associated with shorter survival in acute myeloid leukemia
TLDR
The study suggests the involvement of XRCC1 Arg194Trp and Arg399Gln polymorphisms in the genetic predisposition to AML as they were significantly associated with overall survival.
CAT, GPX1, MnSOD, GSTM1, GSTT1, and GSTP1 Genetic Polymorphisms in Chronic Myeloid Leukemia: A Case-Control Study
TLDR
The aim of the study was to investigate the relationships between CAT C262T, GPX1 Pro198Leu, MnSOD Ala16Val, GSTM1, GSTT1, and GSTP1 Ile105Val polymorphisms and the risk of CML.
A Rare Case of Double-System With Ectopic Ureteral Openings Into Vagina
TLDR
The reported case does not represent just a typical presentation of a single ectopic ureter, as the duplex kidney system had ectopic both ipsilateral ureters (with insertion into the vagina).
Angiotensin-converting enzyme gene insertion/deletion polymorphism in nutritional disorders in children
TLDR
BMI, MUAC, TST and serum protein levels are correlated with D allele carriers of ACE genes in children with moderate undernutrition and moderate obesity, whereas II genotype is an unfavorable prognostic factor corresponding to severe obesity and severe undernutrition.
Vascular Endothelial Growth Factor Insertion/Deletion gene polymorphism in patients with type 2 diabetes and diabetic peripheral polyneuropathy
TLDR
It is suggested that D allele of VEGF gene is a risk factor for the occurrence of DPN, and there is a positive association between I/D polymorphism of V EGF gene and the presence of diabetic peripheral polyneuropathy.
Implications of visfatin genetic variants in the metabolic profile of the Romanian pediatric population
TLDR
NAMPT rs2302559 and rs4730153 polymorphisms do not seem to have a major impact in the development of obesity in children, however there may be an association with lipid profile, but further studies are needed.
FTO rs 9939609 SNP Is Associated With Adiponectin and Leptin Levels and the Risk of Obesity in a Cohort of Romanian Children Population
TLDR
Combined variant genotypes (AA/GG) of FTO rs9939609 /rs17817449 are strongly associated with several measures of adiposity and are also associated with total cholesterol, triglyceride, and LDL-cholesterol levels.
Influence of XPC, XPD, XPF, and XPG gene polymorphisms on the risk and the outcome of acute myeloid leukemia in a Romanian population
TLDR
XPC, XPD, XPF, and XPG genes are implicated in the nucleotide excision repair (NER) system, and variant genotypes were found to be associated with the risk of developing acute myeloid leukemia (AML), while other gene polymorphisms are not associated with AML.
Correlations Between Leptin Gene Polymorphisms 223 A/G, 1019 G/A, 492 G/C, 976 C/A, and Anthropometrical and Biochemical Parameters in Children With Obesity
TLDR
It is observed that obesity is more frequent in children with LEPR 223 AG+GG and LEPR 1019 GA+AA genotypes, and in obese children LE PR 223/492/1019 AG/GG/GA, GG/ GG/GA and AA/GG /GA combined genotypes are more frequent.
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