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

Cultural factors that affected the spatial and temporal epidemiology of kuru

影响库鲁病时空流行病学的文化因素

Whitfield, J T; Pako, W H; Collinge, J; Alpers, M P

Genome-wide association study of behavioural and psychiatric features in human prion disease

人类朊病毒病行为和精神特征的全基因组关联研究

Thompson, A G B; Uphill, J; Lowe, J; Porter, M-C; Lukic, A; Carswell, C; Rudge, P; MacKay, A; Collinge, J; Mead, S

Rapid cell-surface prion protein conversion revealed using a novel cell system

利用一种新型细胞系统揭示了细胞表面朊蛋白的快速转化。

Goold, R; Rabbanian, S; Sutton, L; Andre, R; Arora, P; Moonga, J; Clarke, A R; Schiavo, G; Jat, P; Collinge, J; Tabrizi, S J

PRION-1 scales analysis supports use of functional outcome measures in prion disease

PRION-1 量表分析支持在朊病毒病中使用功能性结局指标。

Mead, S; Ranopa, M; Gopalakrishnan, G S; Thompson, A G B; Rudge, P; Wroe, S; Kennedy, A; Hudson, F; MacKay, A; Darbyshire, J H; Collinge, J; Walker, A S

Brain-water diffusion coefficients reflect the severity of inherited prion disease

脑水扩散系数反映了遗传性朊病毒病的严重程度。

Hyare, H; Wroe, S; Siddique, D; Webb, T; Fox, N C; Stevens, J; Collinge, J; Yousry, T; Thornton, J S

High-b-value diffusion MR imaging and basal nuclei apparent diffusion coefficient measurements in variant and sporadic Creutzfeldt-Jakob disease

高b值扩散磁共振成像和基底核表观扩散系数测量在变异型和散发型克雅氏病中的应用

Hyare, H; Thornton, J; Stevens, J; Mead, S; Rudge, P; Collinge, J; Yousry, T A; Jäger, H R

Review: contribution of transgenic models to understanding human prion disease

综述:转基因模型对理解人类朊病毒病的贡献

Wadsworth, J D F; Asante, E A; Collinge, J

Crystal structure of human prion protein bound to a therapeutic antibody

人朊病毒蛋白与治疗性抗体结合的晶体结构

Antonyuk, S V; Trevitt, C R; Strange, R W; Jackson, G S; Sangar, D; Batchelor, M; Cooper, S; Fraser, C; Jones, S; Georgiou, T; Khalili-Shirazi, A; Clarke, A R; Hasnain, S S; Collinge, J

Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series

国际系列研究中P102L遗传性朊病毒病的表型异质性和基因修饰

Webb, T E F; Poulter, M; Beck, J; Uphill, J; Adamson, G; Campbell, T; Linehan, J; Powell, C; Brandner, S; Pal, S; Siddique, D; Wadsworth, J D; Joiner, S; Alner, K; Petersen, C; Hampson, S; Rhymes, C; Treacy, C; Storey, E; Geschwind, M D; Nemeth, A H; Wroe, S; Collinge, J; Mead, S

Association of a null allele of SPRN with variant Creutzfeldt-Jakob disease.

SPRN基因的无效等位基因与变异型克雅氏病相关

Beck J A, Campbell T A, Adamson G, Poulter M, Uphill J B, Molou E, Collinge J, Mead S