Erratum to "Multi-trait stability index for identification of stable green gram (Vigna radiata (L.) Wilczek) genotypes with MYMV resistance" [Heliyon Volume , Issue 12, June 2024, Article e32763].

[This corrects the article DOI: 10.1016/j.heliyon.

Age- And Gender-Based Predisposition Of MMP-9 -1562 C > T Genotype And Allele Frequencies With Serum MMP-9 Levels As Probable Risk Factors In Patients With Coronary Artery Disease.

Unlabelled: Coronary artery disease (CAD) is the third foremost reason of death worldwide in both men and women of different age groups, and is associated with 17.8 million mortalities annually due to unknown specific genetic background. Hence, we elucidated the age- and gender-based predisposition of MMP-9 -1562 C > T (rs3918242) genotype and allele frequencies along with serum MMP-9 levels as probable risk factors in the development of CAD.

Evaluation of Marginal Adaptation of a Self-Adhering Flowable Composite Resin Liner: A Scanning Electron Microscopic Study.

Background: "Self-adhering composite resins," are claimed to eliminate the need for a separate acid etching and bonding agent application step, thus simplifying the direct restorative procedure, both regarding the technique sensitivity and the duration of treatment.

Aim: The aim of this study is to evaluate the marginal adaptation of self-adhering flowable composite (Dyad flow) in comparison to the conventional flowable composite (Tetric N-flow) under scanning electron microscope (SEM).

Settings And Design: This study was conducted on 44 extracted human maxillary premolars.

Partial empty sella syndrome: a case report and review.

Empty sella syndrome is a damaged pituitary gland. Either the gland has shrunk or has been crushed and flattened making it look like an empty sella on MRI scan. The reported prevalence of primary empty sella in general population is 8-35 %.

End stage renal disease, differential diagnosis, a rare genetic disorder: bardet-biedl syndrome: case report and review.

End stage renal disease (ESRD) represents a clinical condition in which there is an irreversible loss of endogenous renal function. Both structural and functional abnormalities of the kidney are associated with increased morbidity, mortality. Bardet-Biedel syndrome (BBS) is one of the rare genetic disorders with prevalence of 1 in 1, 40,000-1 in 1,60,000 worldwide.