Publications by authors named "M Y Mutlu"

Objective: To investigate the association between clinical factors and post-tonsillectomy hemorrhage (PTH) including rebleeding episodes.

Methods: The medical records of 1,082 patients who underwent tonsillectomy between May 2018 and April 2019 were reviewed. The entire study cohort included 431 (39.

View Article and Find Full Text PDF

This study aimed to evaluate the effects of different dietary supplementation levels with jujube fruit powder on the performance, biochemical parameters, and egg quality characteristics of laying quails. A total of 60 quails (45 days old) were randomly assigned to treatments with different levels of jujube fruit powder: a basal diet (control) and diets supplemented with 5 g/kg (T1), 10 g/kg (T2), with five replicates per treatment (20 quails/treatment and four quails/replicate). The differences between 1-15 and 16-30 days for feed intake (p<0.

View Article and Find Full Text PDF

Broad-complex, tramtrack, and bric-à-brac domain (BTB) and CNC homolog 1 (BACH1) is a key regulator of the cellular oxidative stress response and an oncogene that undergoes tight post-translational control by two distinct F-box ubiquitin ligases, SCF and SCF. However, how both ligases recognize BACH1 under oxidative stress is unclear. In our study, we elucidate the mechanism by which FBXO22 recognizes a quaternary degron in a domain-swapped β-sheet of the BACH1 BTB dimer.

View Article and Find Full Text PDF

Detailed literature search and writing is very important for the success of long research projects, publications and theses. Search engines provide significant convenience in research processes. However, conducting a comprehensive and systematic research on the web requires a long working process.

View Article and Find Full Text PDF
Article Synopsis
  • * Results showed that 3.7% of patients had structural chromosomal anomalies, while 18.52% exhibited CNVs, with 27.3% of those being pathogenic.
  • * A novel pathogenic CNV linked to a specific gene region was discovered, potentially offering insights into ASD’s genetic causes and aiding clinical predictions about prognosis and recurrence risk.
View Article and Find Full Text PDF