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

Differential regulation of gene co-expression modules in muscles and liver of preterm newborns

早产儿肌肉和肝脏中基因共表达模块的差异性调控

Janovska, Petra; Kobets, Tatyana; Steiner Mrazova, Lenka; Svobodova, Michaela; Tesarova, Marketa; Kopecky, Pavel; Zouhar, Petr; Rossmeisl, Martin; Stranecky, Viktor; Kmoch, Stanislav; Kopecky, Jan

Faster postnatal decline in hepatic erythropoiesis than granulopoiesis in human newborns.

人类新生儿出生后肝脏红细胞生成能力下降速度快于粒细胞生成能力下降速度

Janovska Petra, Bardova Kristina, Prouzova Zuzana, Irodenko Ilaria, Kobets Tatyana, Haasova Eliska, Steiner Mrazova Lenka, Stranecky Viktor, Kmoch Stanislav, Rossmeisl Martin, Zouhar Petr, Kopecky Jan

Sodium-glucose cotransporter 2 inhibitors induce anti-inflammatory and anti-ferroptotic shift in epicardial adipose tissue of subjects with severe heart failure

钠-葡萄糖协同转运蛋白 2 抑制剂可诱导严重心力衰竭患者心外膜脂肪组织发生抗炎和抗铁凋亡转变

Barbora Judita Kasperova, Milos Mraz, Petr Svoboda, Daniel Hlavacek, Helena Kratochvilova, Istvan Modos, Nikola Vrzackova, Peter Ivak, Petra Janovska, Tatyana Kobets, Jakub Mahrik, Martin Riecan, Lenka Steiner Mrazova, Viktor Stranecky, Ivan Netuka, Tomas Cajka, Ondrej Kuda, Vojtech Melenovsky, Sona

A deep intronic recurrent CHEK2 variant c.1009-118_1009-87delinsC affects pre-mRNA splicing and contributes to hereditary breast cancer predisposition

CHEK2基因深内含子复发性变异c.1009-118_1009-87delinsC影响前体mRNA剪接,并与遗传性乳腺癌易感性相关。

Zemankova, Petra; Cerna, Marta; Horackova, Klara; Ernst, Corinna; Soukupova, Jana; Borecka, Marianna; Blümcke, Britta; Cerna, Leona; Cerna, Monika; Curtisova, Vaclava; Dolezalova, Tatana; Duskova, Petra; Dvorakova, Lenka; Foretova, Lenka; Havranek, Ondrej; Hauke, Jan; Hahnen, Eric; Hodulova, Miloslava; Hovhannisyan, Milena; Hruskova, Lucie; Janatova, Marketa; Janikova, Maria; Jelinkova, Sandra; Just, Pavel; Kosarova, Marcela; Koudova, Monika; Krutilkova, Vera; Machackova, Eva; Matejkova, Katerina; Michalovska, Renata; Misove, Adela; Nehasil, Petr; Nemcova, Barbora; Novotny, Jan; Panczak, Ales; Pesek, Pavel; Scheinost, Ondrej; Springer, Drahomira; Stastna, Barbora; Stranecky, Viktor; Subrt, Ivan; Tavandzis, Spiros; Tureckova, Eva; Vesela, Kamila; Vlckova, Zdenka; Vocka, Michal; Wappenschmidt, Barbara; Zima, Tomas; Kleibl, Zdenek; Kleiblova, Petra

A comprehensive analysis of germline predisposition to early-onset ovarian cancer

对早发性卵巢癌的种系易感性进行全面分析

Horackova, Klara; Zemankova, Petra; Nehasil, Petr; Vocka, Michal; Hovhannisyan, Milena; Matejkova, Katerina; Janatova, Marketa; Cerna, Marta; Kleiblova, Petra; Jelinkova, Sandra; Stastna, Barbora; Just, Pavel; Dolezalova, Tatana; Nemcova, Barbora; Urbanova, Marketa; Koudova, Monika; Hazova, Jana; Machackova, Eva; Foretova, Lenka; Stranecky, Viktor; Zikan, Michal; Kleibl, Zdenek; Soukupova, Jana

Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy

OVOL2远端调控元件的破坏可能是角膜内皮营养不良的机制之一

Dudakova, Lubica; Noskova, Lenka; Kmoch, Stanislav; Filipec, Martin; Filous, Ales; Davidson, Alice E; Toulis, Vasileios; Jedlickova, Jana; Skalicka, Pavlina; Hartmannova, Hana; Stranecky, Viktor; Drabova, Jana; Novotna, Drahuse; Havlovicova, Marketa; Sedlacek, Zdenek; Liskova, Petra

Genotype is associated with left ventricular reverse remodelling and early events in recent-onset dilated cardiomyopathy

基因型与左心室逆向重塑和近期发作的扩张型心肌病早期事件相关

Kubanek, Milos; Binova, Jana; Piherova, Lenka; Krebsova, Alice; Kotrc, Martin; Hartmannova, Hana; Hodanova, Katerina; Musalkova, Dita; Stranecky, Viktor; Palecek, Tomas; Chaloupka, Anna; Grochova, Ilga; Krejci, Jan; Petrkova, Jana; Melenovsky, Vojtech; Kmoch, Stanislav; Kautzner, Josef

ATAD3A-related pontocerebellar hypoplasia: new patients and insights into phenotypic variability

ATAD3A 相关小脑桥脑发育不全:新患者和对表型变异性的见解

Martina Skopkova, Hana Stufkova, Vibhuti Rambani, Viktor Stranecky, Katarina Brennerova, Miriam Kolnikova, Michaela Pietrzykova, Miloslav Karhanek, Lenka Noskova, Marketa Tesarova, Hana Hansikova, Daniela Gasperikova

Germline multigene panel testing of patients with endometrial cancer

对子宫内膜癌患者进行种系多基因检测

Kral, Jan; Jelinkova, Sandra; Zemankova, Petra; Vocka, Michal; Borecka, Marianna; Cerna, Leona; Cerna, Marta; Dostalek, Lukas; Duskova, Petra; Foretova, Lenka; Havranek, Ondrej; Horackova, Klara; Hovhannisyan, Milena; Chvojka, Stepan; Kalousova, Marta; Kosarova, Marcela; Koudova, Monika; Krutilkova, Vera; Machackova, Eva; Nehasil, Petr; Novotny, Jan; Otahalova, Barbora; Puchmajerova, Alena; Safarikova, Marketa; Slama, Jiri; Stranecky, Viktor; Subrt, Ivan; Tavandzis, Spiros; Zikan, Michal; Zima, Tomas; Soukupova, Jana; Kleiblova, Petra; Kleibl, Zdenek; Janatova, Marketa

A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype-phenotype correlation

一例由SLC5A7复合杂合错义变异引起的先天性肌无力综合征20型新病例提示了基因型-表型相关性的趋势。

Vlckova, Marketa; Prchalova, Darina; Zimmermann, Pavel; Haberlova, Jana; Bendova, Sarka; Moslerova, Veronika; Stranecky, Viktor; Sedlacek, Zdenek; Hancarova, Miroslava