BHD-associated kidney cancer exhibits unique molecular characteristics and a wide variety of variants in chromatin remodeling genes

Birt–Hogg–Dubé (BHD) syndrome is a hereditary kidney cancer syndrome, which predisposes patients to develop kidney cancer, cutaneous fibrofolliculomas and pulmonary cysts. The responsible gene FLCN is a tumor suppressor for kidney cancer, which plays an important role in energy homeostasis through t...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Hasumi, Hisashi, Furuya, Mitsuko, Tatsuno, Kenji, Yamamoto, Shogo, Baba, Masaya, Hasumi, Yukiko, Isono, Yasuhiro, Suzuki, Kae, Jikuya, Ryosuke, Otake, Shinji, Muraoka, Kentaro, Osaka, Kimito, Hayashi, Narihiko, Makiyama, Kazuhide, Miyoshi, Yasuhide, Kondo, Keiichi, Nakaigawa, Noboru, Kawahara, Takashi, Izumi, Koji, Teranishi, Junichi, Yumura, Yasushi, Uemura, Hiroji, Nagashima, Yoji, Metwalli, Adam R, Schmidt, Laura S, Aburatani, Hiroyuki, Linehan, W Marston, Yao, Masahiro
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6048985/
https://ncbi.nlm.nih.gov/pubmed/29767721
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy181
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