Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sule Altiner"'
Autor:
Atil Bisgin, Sebnem Ozemri Sag, Muhammet E. Dogan, Mahmut S. Yildirim, Aydeniz Aydin Gumus, Nejmiye Akkus, Ozgur Balasar, Ceren D. Durmaz, Recep Eroz, Sule Altiner, Adem Alemdar, Lamia Aliyeva, Ibrahim Boga, Fethi S. Cam, Berkcan Dogan, Onur Esbah, Abdullah Hanta, Cem Mujde, Cemre Ornek, Sinem Ozer, Cagla Rencuzogullari, Ozge Sonmezler, Sevcan Tug Bozdogan, Munis Dundar, Sehime G. Temel
Publikováno v:
Breast, Vol 65, Iss , Pp 15-22 (2022)
BRCA1/2 mutations play a significant role in cancer pathogenesis and predisposition particularly in breast, ovarian and prostate cancers. Thus, germline analysis of BRCA1 and BRCA2 is essential for clinical management strategies aiming at the identif
Externí odkaz:
https://doaj.org/article/e63eea3f85294bbebe3b5c247e16a423
Autor:
Hasan Fatih Cakmaklı, Hatice Mutlu, Şule Altıner, Fatma Aydın, Talia Ilerı, Elif Ince, Mehmet Ertem
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S23-S24 (2023)
Objective: Ghosal hematodiaphyseal dysplasia (GHDD) is a very rare autosomal recessive disease caused by prostaglandin metabolism disturbances due to biallelic mutations on chromosome 7q33-34 which lead to decrease in thromboxane synthase function. P
Externí odkaz:
https://doaj.org/article/ad8fb4f239984a5691344e40fd2e090e
Publikováno v:
Cukurova Medical Journal, Vol 45, Iss 3, Pp 933-939 (2020)
Amaç: Bu çalışmanın amacı, bcr-abl negatif kronik miyeloproliferatif hastalık tanısı alan hastaların tanı anında JAK2 V617F, kalretikulin (CALR tip-1 ve tip-2) ve MPL-W515K / L mutasyonların sıklığını ve bu mutasyonların klinik ön
Externí odkaz:
https://doaj.org/article/aae5d055c8fa4f4494cced8f21de591f
Autor:
Şule Altıner, Nüket Yürür Kutlay
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-10 (2019)
Abstract Background Etiology of developmental delay/intellectual disability is very heterogeneous. In recent years, genetic causes have been defined through the use of chromosomal microarray analysis as a first step genetic test. Results Samples from
Externí odkaz:
https://doaj.org/article/feb04f09508f4b119b9258ada1704e77
Publikováno v:
Cogent Medicine, Vol 4, Iss 1 (2017)
Type I plasminogen deficiency is a rare autosomal recessive systemic disorder. It usually starts in infancy and is clinically characterized by chronic mucosal pseudomembranous lesions which contain largely fibrin due to diminished extracellular plasm
Externí odkaz:
https://doaj.org/article/a430e192531a4d88969cb9d4f430fbb5