日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Five quantitative trait loci control radiation-induced adenoma multiplicity in Mom1R Apc Min/+ mice

五个数量性状基因座控制Mom1R Apc Min/+小鼠辐射诱导的腺瘤数量

Elahi, Eiram; Suraweera, Nirosha; Volikos, Emmanouil; Haines, Jackie; Brown, Natalie; Davidson, Gerovie; Churchman, Mike; Ilyas, Mohammed; Tomlinson, Ian; Silver, Andrew

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

LKB1基因外显子缺失和全基因缺失是Peutz-Jeghers综合征的常见病因。

Volikos, E; Robinson, J; Aittomäki, K; Mecklin, J-P; Järvinen, H; Westerman, A M; de Rooji, F W M; Vogel, T; Moeslein, G; Launonen, V; Tomlinson, I P M; Silver, A R J; Aaltonen, L A

Exon 3 beta-catenin mutations are specifically associated with colorectal carcinomas in hereditary non-polyposis colorectal cancer syndrome

外显子3 β-catenin突变与遗传性非息肉性结直肠癌综合征中的结直肠癌密切相关。

Johnson, V; Volikos, E; Halford, S E; Eftekhar Sadat, E T; Popat, S; Talbot, I; Truninger, K; Martin, J; Jass, J; Houlston, R; Atkin, W; Tomlinson, I P M; Silver, A R J