Cmarko相关文献与解析，生知库 | 链接生命科学的每一步

Electrophysiological classification of CACNA1G gene variants associated with neurodevelopmental and neurological disorders

CACNA1G基因变异与神经发育和神经系统疾病相关的电生理分类

doi:10.3389/fphar.2025.1613072

Davakan, Amaël; Cmarko, Leos; Ribeiro Oliveira-Mendes, Barbara; Bernat, Claire; Boulali, Najlae; Montnach, Jérôme; Vallee, Stephanie E; Dinulos, Mary B; Burglen, Lydie; Cantagrel, Vincent; Weiss, Norbert; Nicole, Sophie; Monteil, Arnaud; De Waard, Michel; Lory, Philippe

Deletions in (CCCT)(n) repeat regions belonging to the human pRNA gene inhibit its expression

人类pRNA基因中(CCCT)(n)重复序列区域的缺失会抑制其表达。

期刊:Human Genomics

影响因子:4.3

doi:10.1186/s40246-025-00830-w

Chmúrčiaková, Nikola; Nógell, Adam; Smirnov, Evgeny; Cmarko, Dušan

发表日期：2025

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Homocysteine enhances the excitability of cultured hippocampal neurons without altering the gene expression of voltage-gated ion channels

同型半胱氨酸可增强培养的海马神经元的兴奋性，而不改变电压门控离子通道的基因表达。

期刊:Molecular Brain

影响因子:2.9

doi:10.1186/s13041-025-01205-x

Filipova, Alzbeta; Tomko, Matus; Ondacova, Katarina; Dubiel-Hoppanova, Lucia; Chmúrčiaková, Nikola; Cmarko, Leoš; Stringer, Robin N; Weiss, Norbert; Lacinova, Lubica

神经科学

发表日期：2025

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The Proteomic Composition and Organization of Constitutive Heterochromatin in Mouse Tissues

小鼠组织中组成异染色质的蛋白质组组成和组织

期刊:Cells

影响因子:5.1

doi:10.3390/cells13020139

Annika Schmidt, Hui Zhang, Stephanie Schmitt, Cathia Rausch, Oliver Popp, Jiaxuan Chen, Dusan Cmarko, Falk Butter, Gunnar Dittmar, Frederik Lermyte, M Cristina Cardoso

Lysine Demethylase KDM2A Promotes Proteasomal Degradation of TCF/LEF Transcription Factors in a Neddylation-Dependent Manner

赖氨酸脱甲基酶 KDM2A 以 Neddylation 依赖的方式促进 TCF/LEF 转录因子的蛋白酶体降解

期刊:Cells

影响因子:5.1

doi:10.3390/cells12222620

Tijana Šopin 34wwq3,František Liška, Tomáš Kučera, Dušan Cmarko, Tomáš Vacík

Electrophysiological characterization of a Ca(v)3.2 calcium channel missense variant associated with epilepsy and hearing loss

对与癫痫和听力损失相关的Ca(v)3.2钙通道错义变异进行电生理学表征

期刊:Molecular Brain

影响因子:2.9

doi:10.1186/s13041-023-01058-2

Stringer, Robin N; Cmarko, Leos; Zamponi, Gerald W; De Waard, Michel; Weiss, Norbert

Screening an In-House Isoquinoline Alkaloids Library for New Blockers of Voltage-Gated Na+ Channels Using Voltage Sensor Fluorescent Probes: Hits and Biases

使用电压传感器荧光探针筛选内部异喹啉生物碱库以寻找新的电压门控 Na+ 通道阻滞剂：命中和偏差

期刊:Molecules

影响因子:4.2

doi:10.3390/molecules27134133

Quentin Coquerel, Claire Legendre, Jacinthe Frangieh, Stephan De Waard, Jérôme Montnach, Leos Cmarko, Joseph Khoury, Charifat Said Hassane, Dimitri Bréard, Benjamin Siegler, Ziad Fajloun, Harold De Pomyers, Kamel Mabrouk, Norbert Weiss, Daniel Henrion, Pascal Richomme, César Mattei, Michel De Waard,

AROS

发表日期：2022

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Secretory carrier-associated membrane protein 2 (SCAMP2) regulates cell surface expression of T-type calcium channels

分泌载体相关膜蛋白2 (SCAMP2) 调节T型钙通道的细胞表面表达

期刊:Molecular Brain

影响因子:2.9

doi:10.1186/s13041-021-00891-7

Cmarko, Leos; Stringer, Robin N; Jurkovicova-Tarabova, Bohumila; Vacik, Tomas; Lacinova, Lubica; Weiss, Norbert

Variability of Human rDNA

人类rDNA的变异性

期刊:Cells

影响因子:5.2

doi:10.3390/cells10020196

Smirnov, Evgeny; Chmúrčiaková, Nikola; Liška, František; Bažantová, Pavla; Cmarko, Dušan

Human

发表日期：2021

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Pathophysiology of homocysteine: insights into ion channel dysfunction

同型半胱氨酸的病理生理学：离子通道功能障碍的深入研究

Electrophysiological classification of CACNA1G gene variants associated with neurodevelopmental and neurological disorders

CACNA1G基因变异与神经发育和神经系统疾病相关的电生理分类

Deletions in (CCCT)(n) repeat regions belonging to the human pRNA gene inhibit its expression

人类pRNA基因中(CCCT)(n)重复序列区域的缺失会抑制其表达。

Homocysteine enhances the excitability of cultured hippocampal neurons without altering the gene expression of voltage-gated ion channels

同型半胱氨酸可增强培养的海马神经元的兴奋性，而不改变电压门控离子通道的基因表达。

The Proteomic Composition and Organization of Constitutive Heterochromatin in Mouse Tissues

小鼠组织中组成异染色质的蛋白质组组成和组织

Lysine Demethylase KDM2A Promotes Proteasomal Degradation of TCF/LEF Transcription Factors in a Neddylation-Dependent Manner

赖氨酸脱甲基酶 KDM2A 以 Neddylation 依赖的方式促进 TCF/LEF 转录因子的蛋白酶体降解

Electrophysiological characterization of a Ca(v)3.2 calcium channel missense variant associated with epilepsy and hearing loss

对与癫痫和听力损失相关的Ca(v)3.2钙通道错义变异进行电生理学表征

Screening an In-House Isoquinoline Alkaloids Library for New Blockers of Voltage-Gated Na+ Channels Using Voltage Sensor Fluorescent Probes: Hits and Biases

使用电压传感器荧光探针筛选内部异喹啉生物碱库以寻找新的电压门控 Na+ 通道阻滞剂：命中和偏差

Secretory carrier-associated membrane protein 2 (SCAMP2) regulates cell surface expression of T-type calcium channels

分泌载体相关膜蛋白2 (SCAMP2) 调节T型钙通道的细胞表面表达

Variability of Human rDNA

人类rDNA的变异性