Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ceren Hangül"'
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 4, Pp 306-307 (2020)
Externí odkaz:
https://doaj.org/article/40badc230b8f4969ae00ab89aa6e05e9
Publikováno v:
Turkish Journal of Hematology, Vol 36, Iss 2, Pp 124-125 (2019)
Externí odkaz:
https://doaj.org/article/68ddc59f2da6490999575ad11033a079
Autor:
Ceren HANGUL, Oznur TOKTA, Sibel BERKER KARAUZUM, Bahar AKKAYA, Hulya YILDIRIM, Funda TAYFUN KUPESIZ, Ayse Nur AKINEL
Publikováno v:
Türk Patoloji Dergisi, Vol 38, Iss 3, Pp 219-226 (2022)
Objective: DUX4 is an embryonic transcription factor (TF) later silenced in somatic tissues, while active in germline testis cells. Re-expression in somatic cells has been revealed to be present in pathologic conditions such as dystrophy, leukemia, a
Externí odkaz:
https://doaj.org/article/9dd030aa2e41481dbdeb8a17568f588f
Autor:
Ceren Hangul, Selen Bozkurt, Ugur Bilge, Sebahat Ozdem, Hasan Altunbas, Hilmi Uysal, Filiz Koc, Sibel Berker Karauzum
Publikováno v:
Neurological Sciences and Neurophysiology, Vol 37, Iss 4, Pp 190-196 (2020)
Background: Facioscapulohumeral muscular dystrophy (FSHD) occurs as a consequence of genetic deletion of D4Z4 repeats on chromosome 4q35. Onset of FSHD is earlier in males, suggesting that testosterone may trigger the disease. In accordance, the rapi
Externí odkaz:
https://doaj.org/article/0e800389d5bb4b67ae1e402e4729601e