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

The class II myosin MYH4 safeguards genome integrity and suppresses tumor progression

II类肌球蛋白MYH4可保护基因组完整性并抑制肿瘤进展。

Jayashree Thatte ,Ana Moisés da Silva ,Judit Börcsök ,Thorkell Gudjónsson ,Jan Benada ,Xin Li ,Muthiah Bose ,Hanneke van der Gulden ,Ji-Ying Song ,Renée Menezes ,Elena Martín-Doncel ,Luis Toledo ,Valdemaras Petrosius ,Cord Brakebusch ,Jos Jonkers ,Finn Cilius Nielsen ,Maria Rossing ,Claus S Sørensen

Nuclear N-WASP Induces Actin Polymerization in the Nucleus with Cortactin as an Essential Factor

核 N-WASP 诱导细胞核内肌动蛋白聚合,其中 Cortactin 是必需因素

Xin Jiang, Purusottam Mohapatra, Maria Rossing, Wenqian Zheng, Olga Zbodakova, Jayashree Vijay Thatte, Claus Storgaard Sørensen, Thu Han Le Phan, Cord Brakebusch

Assessing expression patterns of PTGR1, a potential biomarker for acylfulven sensitivity in urothelial carcinoma

评估 PTGR1 的表达模式,PTGR1 是尿路上皮癌中酰基氟戊酸敏感性的潜在生物标志物

Dag Rune Stormoen, Signe Lehn, Kent W Mouw, Zoltan Szallasi, Linea Cecilie Melchior, Line Hammer Dohn, Judit Börcsok, Maria Rossing, Birgitte Grønkaer Toft, Helle Pappot

Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points-based ACMG/AMP approach

临床、剪接和功能分析对 BRCA2 外显子 3 变异进行分类:基于点的 ACMG/AMP 方法的应用

Mads Thomassen, Romy L S Mesman, Thomas V O Hansen, Mireia Menendez, Maria Rossing, Ada Esteban-Sánchez, Emma Tudini, Therese Törngren, Michael T Parsons, Inge S Pedersen, Soo H Teo, Torben A Kruse, Pål Møller, Åke Borg, Uffe B Jensen, Lise L Christensen, Christian F Singer, Daniela Muhr, Marta Sant

Severe Congenital Thrombocytopenia Characterized by Decreased Platelet Sialylation and Moderate Complement Activation Caused by Novel Compound Heterozygous Variants in GNE

严重先天性血小板减少症,特征为血小板唾液酸化降低和中度补体活化,由 GNE 中的新型复合杂合变异引起

Karolina I Smolag, Marcus Fager Ferrari, Eva Zetterberg, Eva Leinoe, Torben Ek, Anna M Blom, Maria Rossing, Myriam Martin

Germline RBBP8 variants associated with early-onset breast cancer compromise replication fork stability

与早发性乳腺癌相关的种系 RBBP8 变异损害了复制叉的稳定性

Reihaneh Zarrizi, Martin R Higgs, Karolin Voßgröne, Maria Rossing, Birgitte Bertelsen, Muthiah Bose, Arne Nedergaard Kousholt, Heike Rösner, The Complexo Network, Bent Ejlertsen, Grant S Stewart, Finn Cilius Nielsen, Claus S Sørensen

Genotype-phenotype associations in PPGLs in 59 patients with variants in SDHX genes

59例携带SDHX基因变异的嗜铬细胞瘤/副神经节瘤患者的基因型-表型关联分析

Main, Ailsa Maria; Rossing, Maria; Borgwardt, Line; Grønkær Toft, Birgitte; Rasmussen, Åse Krogh; Feldt-Rasmussen, Ulla

MicroRNA Changes in Cerebrospinal Fluid After Subarachnoid Hemorrhage

蛛网膜下腔出血后脑脊液中的microRNA变化

Søren Bache, Rune Rasmussen, Maria Rossing, Finn Pedersen Laigaard, Finn Cilius Nielsen, Kirsten Møller

Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia

应用全外显子组测序指导对斯堪的纳维亚半岛厄勒海峡地区患者进行罕见遗传性出血性疾病的特定功能检测和诊断

Eva Leinøe, Eva Zetterberg, Savvas Kinalis, Olga Østrup, Peter Kampmann, Eva Norström, Nadine Andersson, Jenny Klintman, Klaus Qvortrup, Finn Cilius Nielsen, Maria Rossing

A new NFIA:RAF1 fusion activating the MAPK pathway in pilocytic astrocytoma

新的 NFIA:RAF1 融合激活毛细胞星形细胞瘤中的 MAPK 通路

Christina Westmose Yde, Astrid Sehested, Àngels Mateu-Regué, Olga Østrup, David Scheie, Karsten Nysom, Finn Cilius Nielsen, Maria Rossing