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

High pretreatment disease burden as a risk factor for infectious complications following CD19 chimeric antigen receptor T-cell therapy for large B-cell lymphoma

治疗前疾病负担高是CD19嵌合抗原受体T细胞疗法治疗大B细胞淋巴瘤后发生感染并发症的危险因素

O'Reilly, Maeve A; Neill, Lorna; Collin, Simon M; Stone, Neil; Springell, Deborah; Mensah, Jeremy; Cheok, Kathleen P L; Jalowiec, Katarzyna; Benjamin, Reuben; Kuhnl, Andrea; Roddie, Claire; Sanderson, Robin

Single-centre experience of implementing physiotherapist-led prehabilitation for chimeric antigen receptor T cell therapy

单中心实施理疗师主导的嵌合抗原受体T细胞疗法术前康复的经验

McCourt, Orla; Maciocia, Paul; Roddie, Claire; Hwang, Angela; Wood, Leigh; Panopoulou, Aikaterini; Springell, Deborah Ann; Al Bakir, Maise; O'Reilly, Maeve

Acquired thrombotic thrombocytopenic purpura: A rare disease associated with BNT162b2 vaccine: Comment from Doyle et al

获得性血栓性血小板减少性紫癜:一种与BNT162b2疫苗相关的罕见疾病:Doyle等人的评论

Doyle, Andrew J; Springell, Deborah; Dutt, Tina; Kenworthy, Jessica; Ling, Gavin; Desborough, Michael; Thomas, William; Hermans, Joannes; Vanveen, Joost; Cranfield, Tanya; Belsham, Edward; Hill, Quentin A; Lester, Will; Scully, Marie

The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis

中心体NDE1在人类大脑皮层神经发生中的重要作用

Mehmet Bakircioglu, Ofélia P Carvalho, Maryam Khurshid, James J Cox, Beyhan Tuysuz, Tanyeri Barak, Saliha Yilmaz, Okay Caglayan, Alp Dincer, Adeline K Nicholas, Oliver Quarrell, Kelly Springell, Gulshan Karbani, Saghira Malik, Caroline Gannon, Eamonn Sheridan, Moira Crosier, Steve N Lisgo, Susan Lin

Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice

金属蛋白酶ADAM9的缺失会导致人类视锥细胞-视杆细胞营养不良和小鼠视网膜退化。

Parry, David A; Toomes, Carmel; Bida, Lina; Danciger, Michael; Towns, Katherine V; McKibbin, Martin; Jacobson, Samuel G; Logan, Clare V; Ali, Manir; Bond, Jacquelyn; Chance, Rebecca; Swendeman, Steven; Daniele, Lauren L; Springell, Kelly; Adams, Matthew; Johnson, Colin A; Booth, Adam P; Jafri, Hussain; Rashid, Yasmin; Banin, Eyal; Strom, Tim M; Farber, Debora B; Sharon, Dror; Blobel, Carl P; Pugh, Edward N Jr; Pierce, Eric A; Inglehearn, Chris F

Mutation of the variant alpha-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia

变异型α-微管蛋白TUBA8的突变会导致多小脑回畸形伴视神经发育不全

Abdollahi, Mohammad R; Morrison, Ewan; Sirey, Tamara; Molnar, Zoltan; Hayward, Bruce E; Carr, Ian M; Springell, Kelly; Woods, C Geoff; Ahmed, Mushtaq; Hattingh, Louise; Corry, Peter; Pilz, Daniela T; Stoodley, Neil; Crow, Yanick; Taylor, Graham R; Bonthron, David T; Sheridan, Eamonn

Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome

WNT7A基因突变会导致一系列肢体畸形,包括福尔曼综合征和阿瓦迪/拉斯-罗斯柴尔德/辛泽尔海豹肢畸形综合征。

Woods, C G; Stricker, S; Seemann, P; Stern, R; Cox, J; Sherridan, E; Roberts, E; Springell, K; Scott, S; Karbani, G; Sharif, S M; Toomes, C; Bond, J; Kumar, D; Al-Gazali, L; Mundlos, S

The enzymic reaction of amino acids with glutathione

氨基酸与谷胱甘肽的酶促反应

HIRD, F J; SPRINGELL, P H