Differences in genetic and epigenetic alterations between von Hippel–Lindau disease–related and sporadic hemangioblastomas of the central nervous system

BACKGROUND: Although inactivation of the von Hippel–Lindau gene (VHL), located on chromosome 3p25, is considered to be a major cause of hemangioblastomas (HBs), the incidence of biallelic inactivation of VHL is reportedly low. The aim of this study was to determine the prevalence of VHL alterations...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Neuro Oncol
Asıl Yazarlar: Takayanagi, Shunsaku, Mukasa, Akitake, Tanaka, Shota, Nomura, Masashi, Omata, Mayu, Yanagisawa, Shunsuke, Yamamoto, Shogo, Ichimura, Koichi, Nakatomi, Hirofumi, Ueki, Keisuke, Aburatani, Hiroyuki, Saito, Nobuhito
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2017
Konular:
Basic and Translational Investigations
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5570160/
https://ncbi.nlm.nih.gov/pubmed/28379443
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/nox034
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller