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

Multiomic analyses direct hypotheses for Creutzfeldt-Jakob disease risk genes

多组学分析为克雅氏病风险基因的假设提供直接依据

Küçükali, Fahri; Hill, Elizabeth; Watzeels, Tijs; Hummerich, Holger; Campbell, Tracy; Darwent, Lee; Collins, Steven; Stehmann, Christiane; Kovacs, Gabor G; Geschwind, Michael D; Frontzek, Karl; Budka, Herbert; Gelpi, Ellen; Aguzzi, Adriano; van der Lee, Sven J; van Duijn, Cornelia M; Liberski, Pawel P; Calero, Miguel; Sanchez-Juan, Pascual; Bouaziz-Amar, Elodie; Laplanche, Jean-Louis; Haïk, Stéphane; Brandel, Jean-Phillipe; Mammana, Angela; Capellari, Sabina; Poleggi, Anna; Ladogana, Anna; Tiple, Dorina; Zafar, Saima; Booth, Stephanie; Jansen, Gerard H; Areškevičiūtė, Aušrinė; Lund, Eva Løbner; Glisic, Katie; Parchi, Piero; Hermann, Peter; Zerr, Inga; Safar, Jiri; Gambetti, Pierluigi; Appleby, Brian S; Collinge, John; Sleegers, Kristel; Mead, Simon

PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker features.

PRNP E146G 突变遗传性朊病毒病:独特的临床、病理和体液生物标志物特征

Coysh Thomas, Jaunmuktane Zane, Hosszu Laszlo L P, Majbour Nour, Zhang Fuquan, Campbell Tracy, Darwent Lee, Matus Marcelo Barria, Chan Edgar, Holm-Mercer Leah, Mok Tze How, Wadsworth Jonathan D F, Bieschke Jan, Nithi Kannan, Brandner Sebastian, Smith Colin, Esiri Margaret, Collinge John, Mead Simon

Inherited prion disease caused by a novel frameshift mutation of PRNP resulting in protein truncation at codon 157

由PRNP基因新型移码突变引起的遗传性朊病毒病,导致第157位密码子处蛋白质截断。

Holm-Mercer, Leah; Mok, Tze How; Sequeira, Danielle; Coysh, Thomas; Rudge, Peter; Ramadan, Hawraman; Darwent, Lee; Campbell, Tracy; Murphy, Thomas; Smith, Colin; Ritchie, Diane; Brandner, Sebastian; Jaunmuktane, Zane; Collinge, John; Mead, Simon

Enhanced efficiency fertilizers, potato production, and nitrate leaching in the Wisconsin Central Sands

威斯康星州中部沙地高效肥料、马铃薯生产和硝酸盐淋溶

Campbell, Tracy; Ruark, Matthew; Boswell, Edward; Lowery, Birl

Population structure and migration in the Eastern Highlands of Papua New Guinea, a region impacted by the kuru epidemic

巴布亚新几内亚东部高地的人口结构和迁移情况,该地区受库鲁病疫情影响

Quinn, Liam; Whitfield, Jerome; Alpers, Michael P; Campbell, Tracy; Hummerich, Holger; Pomat, William; Siba, Peter; Koki, George; Moltke, Ida; Collinge, John; Hellenthal, Garrett; Mead, Simon

Genome wide association study of clinical duration and age at onset of sporadic CJD

散发性克雅氏病临床病程和发病年龄的全基因组关联研究

Hummerich, Holger; Speedy, Helen; Campbell, Tracy; Darwent, Lee; Hill, Elizabeth; Collins, Steven; Stehmann, Christiane; Kovacs, Gabor G; Geschwind, Michael D; Frontzek, Karl; Budka, Herbert; Gelpi, Ellen; Aguzzi, Adriano; van der Lee, Sven J; van Duijn, Cornelia M; Liberski, Pawel P; Calero, Miguel; Sanchez-Juan, Pascual; Bouaziz-Amar, Elodie; Laplanche, Jean-Louis; Haïk, Stéphane; Brandel, Jean-Phillipe; Mammana, Angela; Capellari, Sabina; Poleggi, Anna; Ladogana, Anna; Pocchiari, Maurizio; Zafar, Saima; Booth, Stephanie; Jansen, Gerard H; Areškevičiūtė, Aušrinė; Løbner Lund, Eva; Glisic, Katie; Parchi, Piero; Hermann, Peter; Zerr, Inga; Appleby, Brian S; Safar, Jiri; Gambetti, Pierluigi; Collinge, John; Mead, Simon

Estimation of the number of inherited prion disease mutation carriers in the UK

英国遗传性朊病毒病突变携带者人数估计

Corbie, Rosie; Campbell, Tracy; Darwent, Lee; Rudge, Peter; Collinge, John; Mead, Simon

Prion protein gene mutation detection using long-read Nanopore sequencing

利用长读长纳米孔测序检测朊病毒蛋白基因突变

Kroll, François; Dimitriadis, Athanasios; Campbell, Tracy; Darwent, Lee; Collinge, John; Mead, Simon; Vire, Emmanuelle

Academic and Community ICUs Participating in a Critical Care Randomized Trial: A Comparison of Patient Characteristics and Trial Metrics

参与重症监护随机试验的学术型和社区型ICU:患者特征和试验指标的比较

Tsang, Jennifer L Y; Binnie, Alexandra; Duan, Erick H; Johnstone, Jennie; Heels-Ansdell, Diane; Reeve, Brenda; Trop, Sebastien; Hosek, Paul; Dionne, Joanna C; Archambault, Patrick; Lysecki, Paul; Cirone, Robert; Zytaruk, Nicole L; Dechert, William; Camargo, Mercedes Peñuela; Jesso, Rebecca; McMillan, Elliot; Panchbhaya, Zaynab; Campbell, Tracy; Saunders, Lois; Copland, Mary; Kavikondala, Kanthi; Cook, Deborah J

Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease

一例散发性克雅氏病中PRNP基因E200D纯合突变的病例报告

Hassan, Ahamad; Campbell, Tracy; Darwent, Lee; Odd, Hans; Green, Alison; Collinge, John; Mead, Simon