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

LGG-13. UNRAVELING THE SPATIAL TUMOR MICROENVIRONMENT OF PEDIATRIC LOW-GRADE GLIOMAS USING IMAGING MASS CYTOMETRY

LGG-13. 利用成像质谱流式细胞术揭示儿童低级别胶质瘤的空间肿瘤微环境

Swain, E; Poulton, J E; Faria Andrade*, Augusto; Sigaud*, Romain; Puligandla*, Evan; Liu, Bridget; Karimi, Elham; Schmid, Simone; Selt, Florian; Driever, Pablo Hernáiz; Koch, Arend; Sahm, Felix; Sievers, Philipp; Pfister, Stefan M; Witt, Olaf; Jones, David T W; Capper, David; Walsh*, Logan; Jabado*, Nada; Milde*, Till

Correction to: Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease

更正:儿童POLG疾病的运动障碍谱和神经递质异常

Papandreou, A; Rahman, S; Fratter, C; Ng, J; Meyer, E; Carr, L J; Champion, M; Clarke, A; Gissen, P; Hemingway, C; Hussain, N; Jayawant, S; King, M D; Lynch, B J; Mewasingh, L; Patel, J; Prabhakar, P; Neergheen, V; Pope, S; Heales, S J R; Poulton, J; Kurian, Manju A

Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease

儿童POLG疾病的运动障碍谱和神经递质异常

Papandreou, A; Rahman, S; Fratter, C; Ng, J; Meyer, E; Carr, L J; Champion, M; Clarke, A; Gissen, P; Hemingway, C; Hussain, N; Jayawant, S; King, M D; Lynch, B J; Mewasingh, L; Patel, J; Prabhakar, P; Neergheen, V; Pope, S; Heales, S J R; Poulton, J; Kurian, Manju A

RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions

RRM2B基因突变在伴有多处线粒体DNA缺失的家族性进行性眼外肌麻痹症(PEO)中较为常见。

Fratter, C; Raman, P; Alston, C L; Blakely, E L; Craig, K; Smith, C; Evans, J; Seller, A; Czermin, B; Hanna, M G; Poulton, J; Brierley, C; Staunton, T G; Turnpenny, P D; Schaefer, A M; Chinnery, P F; Horvath, R; Turnbull, D M; Gorman, G S; Taylor, R W

The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading

线粒体DNA的16189变异体在患有血色素沉着症的C282Y纯合子中比在无铁过载者中更常见。

Livesey, K J; Wimhurst, V L C; Carter, K; Worwood, M; Cadet, E; Rochette, J; Roberts, A G; Pointon, J J; Merryweather-Clarke, A T; Bassett, M L; Jouanolle, A-M; Mosser, A; David, V; Poulton, J; Robson, K J H

Synthesis of mitochondrial DNA in permeabilised human cultured cells.

在透化人类培养细胞中合成线粒体DNA

Emmerson C F, Brown G K, Poulton J

The mitochondrial genome in Wolfram syndrome

沃尔夫拉姆综合征中的线粒体基因组

Barrett, T G; Scott-Brown, M; Seller, A; Bednarz, A; Poulton, K; Poulton, J

Molecular analysis of (R)-(+)-mandelonitrile lyase microheterogeneity in black cherry

黑樱桃中(R)-(+)-扁桃腈裂解酶微异质性的分子分析

Hu, Z; Poulton, J E

Vincristine treatment revealing asymptomatic hereditary motor sensory neuropathy type 1A

长春新碱治疗揭示了无症状遗传性运动感觉神经病1A型

Mercuri, E; Poulton, J; Buck, J; Broadbent, V; Bamford, M; Jungbluth, H; Manzur, A Y; Muntoni, F

Reply to Hofmann et al

回复 Hofmann 等人

Mackey, D; Oostra, R J; Rosenberg, T; Nikoskelainen, E; Poulton, J; Barratt, T; Bolhuis, P; Norby, S; Savontaus, M L; Chan, C; Howell, N