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

Rare germline variants contribute to glioma predisposition: Whole-genome analysis of a regional cohort of glioma patients

罕见种系变异与胶质瘤易感性相关:对区域性胶质瘤患者队列的全基因组分析

Rosenbaum, Adam; Wibom, Carl; Hammermeister Suger, Austin; Pensch, Raphaela; Roy, Ananya; Brännström, Thomas; Rentoft, Matilda; Forsberg-Nilsson, Karin; Lindblad-Toh, Kerstin; Lindström, Sara; Dahlin, Anna Margareta; Melin, Beatrice

Person-centered care at population scale: The Swedish registry for behavioral and psychological symptoms of dementia

以人为本的大规模人群护理:瑞典痴呆症行为和心理症状登记处

Jönsson, Linus; Wibom, Moa; Londos, Elisabet; Nägga, Katarina

Tissue-specific responses to TFAM and mtDNA copy number manipulation in prematurely ageing mice.

TFAM 和 mtDNA 拷贝数操纵对早衰小鼠的组织特异性反应

Kremer Laura Sophie, Gao Guanbin, Rigoni Giovanni, Filograna Roberta, Mennuni Mara, Wibom Rolf, Végvári Ákos, Koolmeister Camilla, Larsson Nils-Göran

Factors related to identification and treatment of pain underlying neuropsychiatric symptoms: a prospective study using data from a multi-component dementia care programme

识别和治疗神经精神症状相关疼痛的因素:一项利用多组分痴呆症护理计划数据的前瞻性研究

Nakanishi, Miharu; Shindo, Yumi; Miyamoto, Yuki; Toya, Junichiro; Ogawa, Asao; Nägga, Katarina; Wibom, Moa; Achterberg, Wilco P; van der Steen, Jenny T; Nishida, Atsushi

Prediagnostic Serum Immune Marker Levels and Multiple Myeloma: A Prospective Longitudinal Study Using Samples from the Janus Serum Bank in Norway

诊断前血清免疫标志物水平与多发性骨髓瘤:一项使用挪威 Janus 血清库样本的前瞻性纵向研究

Herdenberg, Simona; Wibom, Carl; Krop, Esmeralda J M; Langseth, Hilde; Vermeulen, Roel; Harlid, Sophia; Wu, Wendy Yi-Ying; Späth, Florentin

PARKIN is not required to sustain OXPHOS function in adult mammalian tissues

在成年哺乳动物组织中,PARKIN 不是维持 OXPHOS 功能所必需的

Roberta Filograna, Jule Gerlach, Hae-Na Choi, Giovanni Rigoni, Michela Barbaro, Mikael Oscarson, Seungmin Lee, Katarina Tiklova, Markus Ringnér, Camilla Koolmeister, Rolf Wibom, Sara Riggare, Inger Nennesmo, Thomas Perlmann, Anna Wredenberg, Anna Wedell, Elisa Motori, Per Svenningsson, Nils-Göran La

Quantitative proteomics of patient fibroblasts reveal biomarkers and diagnostic signatures of mitochondrial disease

患者成纤维细胞的定量蛋白质组学揭示了线粒体疾病的生物标志物和诊断特征

Sandrina P Correia, Marco F Moedas, Lucie S Taylor, Karin Naess, Albert Z Lim, Robert McFarland, Zuzanna Kazior, Anastasia Rumyantseva, Rolf Wibom, Martin Engvall, Helene Bruhn, Nicole Lesko, Ákos Végvári, Lukas Käll, Matthias Trost, Charlotte L Alston, Christoph Freyer, Robert W Taylor, Anna Wedell

Novel Synonymous and Deep Intronic Variants Causing Primary and Secondary Pyruvate Dehydrogenase Complex Deficiency

导致原发性和继发性丙酮酸脱氢酶复合物缺乏症的新型同义突变和深内含子突变

Bruhn, Helene; Naess, Karin; Ygberg, Sofia; Peña-Pérez, Lucía; Lesko, Nicole; Wibom, Rolf; Freyer, Christoph; Stranneheim, Henrik; Wedell, Anna; Wredenberg, Anna

Human mitochondria require mtRF1 for translation termination at non-canonical stop codons

人类线粒体需要mtRF1在非规范终止密码子处终止翻译

Annika Krüger, Cristina Remes, Dmitrii Igorevich Shiriaev, Yong Liu, Henrik Spåhr, Rolf Wibom, Ilian Atanassov, Minh Duc Nguyen, Barry S Cooperman, Joanna Rorbach

Low-grade glioma risk SNP rs11706832 is associated with type I interferon response pathway genes in cell lines

低级别胶质瘤风险 SNP rs11706832 与细胞系中的 I 型干扰素反应通路基因相关

Adam Rosenbaum, Anna M Dahlin, Ulrika Andersson, Benny Björkblom, Wendy Yi-Ying Wu, Håkan Hedman, Carl Wibom, Beatrice Melin