Ara
Toplam kayıt 5, listelenen: 1-5
Identification of candidate genes in a family with cancer overload by whole-exome sequencing
(Turkish National Pediatric Society, 2022)
Background. Approximately 120 out of every 1 million children in the world develop cancer each year. In Turkey, 2500-3000 children are diagnosed with new cancer each year. The causes of childhood cancer have been studied ...
SARKOM PATOGENEZİNDE ETKİLİ OLABİLECEK YENİ ADAY GENLERİN ARAŞTIRILMASI
(İstanbul Üniversitesi, 2023)
Amaç: Nükleer tıpta radyonüklit tedavilerde çalışan radyasyon görevlilerinin uzun dönemde maruz kaldığı radyasyon dozlarının belirlenmesi ve
rutin olarak yapılan her bir tedavi prosedürünün bu dozlara katkısının
belirlenmesi ...
RB1 gene mutations and genetic spectrum in retinoblastoma cases
(LIPPINCOTT WILLIAMS & WILKINS, 2023)
The aim of the study was to investigate the frequency and types of mutations on the retinoblastoma gene (RB1 gene) in Turkish population. RB1 gene mutation analysis was performed in a total of 219 individuals (122 probands ...
RB1 GENE MUTATIONS IN TURKISH PATIENTS WITH RETINOBLASTOMA
(WILEY, 2022)
RB1 GENE MUTATIONS IN TURKISH PATIENTS WITH RETINOBLASTOMA
Investigation of the methylation changes in the promoter region of RB1 gene in retinoblastoma
(Elsevier GmbH, 2024)
Retinoblastoma is an infrequent neoplasm that arises during childhood from retinal nerve cells and is attributed to the biallelic inactivation of the RB1 gene. In conjunction with anatomical anomalies, it is widely ...