Feil Robert相关文献与解析，生知库 | 链接生命科学的每一步

Imaizumi Yui, Charon FranÃ§ois, Surcis Caroline, Picard Christel, Arnau-Romero Pol, Andrau Jean-Christophe, Noordermeer Daan, Moindrot Benoit, Cadoret Jean-Charles, Feil Robert

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lncRNA

DNA甲基化

发表日期：2026

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Activating PRKG1 Variant Enhances Smooth Muscle Cell Deformability to Cause Aortopathy.

激活 PRKG1 变体可增强平滑肌细胞变形能力，从而导致主动脉病变。

期刊:Jacc-Basic To Translational Science

影响因子:7.2

doi:10.1016/j.jacbts.2025.101452

Jost Marie E, Schweizer Moyra, Henning Philipp, Gorzelanny Christian, Lehners Moritz, Ellinger Bernhard, Boix-Campos Javier, Kux Johan-Moritz, Singh Shubhangi, Fachinger Alexandra, Martinez Pomier Karla, VanSchouwen Bryan, Billing Anja M, Biedenweg Doreen, Schweizer Michaela, Siegel Saskia, Reimer Rudolph, Brandt Mona, Priesmeier Laura, Fuchs Ulrike, Pflaumenbaum Julia, Nikolaev Viacheslav O, Newbury-Ecob Ruth, Wilsdon Anna, Rybczynski Meike, Gehle Petra, ZelarayÃ¡n Laura C, Stafforst Thorsten, Feil Robert, Rinschen Markus M, Pless Ole, Eaton Philip, SÃ¡ez Pablo J, Otto Oliver, Melacini Giuseppe, Demal Till J, Eschenhagen Thomas, Herberg Friedrich W, Cuello Friederike

细胞生物学

发表日期：2026

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CNP-induced cGMP signaling reduces growth cone stiffness and Ca(2+) levels in embryonic DRG neurons.

CNP诱导的cGMP信号传导降低胚胎DRG神经元的生长锥刚度和Ca(2+)水平。

期刊:Frontiers in Molecular Neuroscience

影响因子:3.8

doi:10.3389/fnmol.2026.1769175

Balmes Aylin, Schmidt Hannes, Peters Stefanie, Kenet Selin, Botezatu Adelina, Wen Lai, BÃ¶ttcher Alexandra, Benz Peter M, Feil Robert, SchÃ¤ffer Tilman E

神经科学

发表日期：2026

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A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations

与常染色体隐性COPZ1基因突变相关的新型严重先天性中性粒细胞减少症

期刊:Blood

影响因子:23.1

doi:10.1182/blood.2023022576

Borbaran Bravo, Natalia; Deordieva, Ekaterina; Doll, Larissa; ElGamacy, Mohammad; Dannenmann, Benjamin; Azevedo, Joana; Iannuzzo, Alberto; Delafontaine, Selket; Lehners, Moritz; Kolodziej, Marius; Hernandez Alvarez, Birte; Hellmuth, Anna-Sophia; Ritter, Malte; Findik, Betül; Zakharova, Viktoria; Bräuning, Sandro; Kandabarau, Sergey; Lengerke, Claudia; Feil, Robert; Meyts, Isabelle; Delon, Jérôme; Templin, Markus; Sturm, Marc; Rieß, Olaf; Zeidler, Cornelia; Welte, Karl; Shcherbina, Anna; Klimiankou, Maksim; Skokowa, Julia

Single-cell analysis identifies the CNP/GC-B/cGMP axis as marker and regulator of modulated VSMCs in atherosclerosis

单细胞分析确定 CNP/GC-B/cGMP 轴是动脉粥样硬化中调节 VSMC 的标志物和调节剂

期刊:Nature Communications

影响因子:14.7

doi:10.1038/s41467-024-55687-9

Moritz Lehners, Hannes Schmidt, Maria T K Zaldivia, Daniel Stehle, Michael Krämer, Andreas Peter, Julia Adler, Robert Lukowski, Susanne Feil, Robert Feil

Smooth Muscle Cell-Derived Fibronectin Promotes an Atheroprotective Smooth Muscle Cell Phenotype Associated With Altered NO-cGMP Signaling.

平滑肌细胞衍生的纤连蛋白促进与NO-cGMP信号改变相关的抗动脉粥样硬化平滑肌细胞表型

期刊:Journal of the American Heart Association

影响因子:5.3

doi:10.1161/JAHA.124.040395

Feil Susanne, Zaldivia Maria T K, Kiesel Jacek, Roessing Malte, Peter Andreas, Morales-Cano Daniel, Bentzon Jacob F, Lehners Moritz, Feil Robert

Pharmacological activation of NO-sensitive guanylyl cyclase ameliorates obesity-induced arterial stiffness.

药物激活NO敏感的鸟苷酸环化酶可改善肥胖引起的动脉僵硬

期刊:Vascular Pharmacology

影响因子:3.5

doi:10.1016/j.vph.2025.107503

Budbazar Enkhjargal, Balmes Aylin, Elliott Danielle, Peres Tintin Lisette, Kopp Timo, Feil Susanne, Feil Robert, SchÃ¤ffer Tilman E, Seta Francesca

Differential 3D genome architecture and imprinted gene expression: cause or consequence?

差异性三维基因组结构与印记基因表达：是原因还是结果？

期刊:Biochemical Society Transactions

影响因子:4.3

doi:10.1042/BST20230143

Moindrot, Benoit; Imaizumi, Yui; Feil, Robert

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发表日期：2024

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Real-time imaging of cGMP signaling shows pronounced differences between glomerular endothelial cells and podocytes

cGMP 信号的实时成像显示肾小球内皮细胞和足细胞之间存在明显差异

期刊:Scientific Reports

影响因子:3.8

doi:10.1038/s41598-024-76768-1

Nelli Rutkowski, Frederik Görlitz, Eva Wiesner, Julia Binz-Lotter, Susanne Feil, Robert Feil, Thomas Benzing, Matthias J Hackl

Noninvasive Detection of Smooth Muscle Cell-Derived Hot Spots to Study Atherosclerosis by PET/MRI in Mice

利用PET/MRI技术对小鼠平滑肌细胞衍生热点进行无创检测，以研究动脉粥样硬化

期刊:Circulation Research

影响因子:16.2

doi:10.1161/CIRCRESAHA.122.322296

Feil, Susanne; Stowbur, Dimitri; Schörg, Barbara F; Ehrlichmann, Walter; Reischl, Gerald; Kneilling, Manfred; Pichler, Bernd J; Feil, Robert

DNA methylation and lncRNA control asynchronous DNA replication at specific imprinted gene domains.

DNA甲基化和lncRNA控制特定印记基因区域的异步DNA复制。

Activating PRKG1 Variant Enhances Smooth Muscle Cell Deformability to Cause Aortopathy.

激活 PRKG1 变体可增强平滑肌细胞变形能力，从而导致主动脉病变。

CNP-induced cGMP signaling reduces growth cone stiffness and Ca(2+) levels in embryonic DRG neurons.

CNP诱导的cGMP信号传导降低胚胎DRG神经元的生长锥刚度和Ca(2+)水平。

A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations

与常染色体隐性COPZ1基因突变相关的新型严重先天性中性粒细胞减少症

Single-cell analysis identifies the CNP/GC-B/cGMP axis as marker and regulator of modulated VSMCs in atherosclerosis

单细胞分析确定 CNP/GC-B/cGMP 轴是动脉粥样硬化中调节 VSMC 的标志物和调节剂

Smooth Muscle Cell-Derived Fibronectin Promotes an Atheroprotective Smooth Muscle Cell Phenotype Associated With Altered NO-cGMP Signaling.

平滑肌细胞衍生的纤连蛋白促进与NO-cGMP信号改变相关的抗动脉粥样硬化平滑肌细胞表型

Pharmacological activation of NO-sensitive guanylyl cyclase ameliorates obesity-induced arterial stiffness.

药物激活NO敏感的鸟苷酸环化酶可改善肥胖引起的动脉僵硬

Differential 3D genome architecture and imprinted gene expression: cause or consequence?

差异性三维基因组结构与印记基因表达：是原因还是结果？

Real-time imaging of cGMP signaling shows pronounced differences between glomerular endothelial cells and podocytes

cGMP 信号的实时成像显示肾小球内皮细胞和足细胞之间存在明显差异

Noninvasive Detection of Smooth Muscle Cell-Derived Hot Spots to Study Atherosclerosis by PET/MRI in Mice

利用PET/MRI技术对小鼠平滑肌细胞衍生热点进行无创检测，以研究动脉粥样硬化