DOI: 10.26355/eurrev_202305_32480
Genetics
DOI: 10.26355/eurrev_202305_32480
DOI: 10.26355/eurrev_202305_32315
Novel implication of the prolactin (PRL) gene in the comorbidity of type 2 diabetes and depression
DOI: 10.26355/eurrev_202303_31800
Oxytocin receptor (OXTR) is a risk gene for polycystic ovarian syndrome
DOI: 10.26355/eurrev_202302_31380
MTHFR C677T polymorphism, homocysteine, burden, and location of AMI and ACI
DOI: 10.26355/eurrev_202302_31201
The promoter methylations of the autoimmune regulator (AIRE) gene and matrix metalloproteinase-3 (MMP-3) gene may have a role in gestational diabetes mellitus
DOI: 10.26355/eurrev_202302_31187
The mineralocorticoid receptor gene (NR3C2) is linked to and associated with polycystic ovarian syndrome in Italian families
DOI: 10.26355/eurrev_202301_31072
Novel TCF7L2 familial linkage and association with Type 2 diabetes, depression, and their comorbidity
DOI: 10.26355/eurrev_202301_31071
22q11.2 deletion syndrome complicated with pulmonary alveolar proteinosis in a child: a case report
DOI: 10.26355/eurrev_202301_30893
The effect of hereditary thrombotic factors and comorbidities on the severity of COVID-19 disease
DOI: 10.26355/eurrev_202301_30868
Association of MTHFR gene C677T polymorphism with pregnancy outcome
DOI: 10.26355/eurrev_202212_30559
PSMD9 is linked to T2D age of onset, years of isolated and combined insulin therapy, irregular menses, and hot flashes
DOI: 10.26355/eurrev_202212_30549
IFNG and IFNGR1 polymorphisms are associated with tuberculosis: a case-control study
DOI: 10.26355/eurrev_202211_30372
Linkage and association of novel DRD2 variants to the comorbidity of type 2 diabetes and depression
DOI: 10.26355/eurrev_202211_30161
A novel nomogram associated with regulatory T cells infiltration by weighted gene co-expression network analysis for predicting survival in patients with colon cancer
DOI: 10.26355/eurrev_202211_30138
The correlation between copy number variation in Chromosome 14 and DNA methylation in Saudi autistic children
DOI: 10.26355/eurrev_202211_30130
Aberrantly high DEPDC1B expression leads to poor prognosis in patients with lower-grade gliomas
DOI: 10.26355/eurrev_202209_29774
Identification of ferroptosis-related genes for the prediction of prognosis and chemotherapy benefit of gastric cancer
DOI: 10.26355/eurrev_202209_29771
EMMPRIN is an emerging protein capable of regulating cancer hallmarks
DOI: 10.26355/eurrev_202209_29759
DNA repair gene (XRCC1 and XPD) polymorphism and risk of primary ovarian failure
DOI: 10.26355/eurrev_202208_29540