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E3 ubiquitin ligase Herc3 deficiency leads to accumulation of subretinal microglia and retinal neurodegeneration.
Zegeye Y, Aredo B, Yuksel S, Kirman DC, Kumar A, Chen B, Turpin E, Shresta S, He YG, Gautron L, Tang M, Li X, DiCesare SM, Hulleman JD, Xing C, Ludwig S, Moresco EMY, Beutler BA, Ufret-Vincenty RL. Zegeye Y, et al. Among authors: yuksel s. Sci Rep. 2024 Feb 6;14(1):3010. doi: 10.1038/s41598-024-53731-8. Sci Rep. 2024. PMID: 38321224 Free PMC article.
Adolescence-onset atypical hemolytic uremic syndrome: is it different from infant-onset?
Celegen K, Gulhan B, Fidan K, Yuksel S, Yilmaz N, Yılmaz AC, Demircioğlu Kılıç B, Gokce I, Kavaz Tufan A, Kalyoncu M, Nalcacıoglu H, Ozlu SG, Kurt Sukur ED, Canpolat N, K Bayazit A, Çomak E, Tabel Y, Tulpar S, Celakil M, Bek K, Zeybek C, Duzova A, Ozcakar B, Topaloglu R, Soylemezoglu O, Ozaltin F. Celegen K, et al. Among authors: yuksel s. Clin Exp Nephrol. 2024 May 5. doi: 10.1007/s10157-024-02505-7. Online ahead of print. Clin Exp Nephrol. 2024. PMID: 38704765
Variable phenotype and genotype of pediatric patients with HNF1B nephropathy.
Gülhan B, Ekici O, Dursun İ, Göknar N, Yüksel S, Alaygut D, Özçakar ZB, Nalçacıoğlu H, Demircioğlu Kılıç B, Söylemezoğlu O, Duzova A, Topaloglu R, Ozaltin F. Gülhan B, et al. Among authors: yuksel s. Clin Nephrol. 2024 May 3. doi: 10.5414/CN111310. Online ahead of print. Clin Nephrol. 2024. PMID: 38699986
654 results