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

Clinical Value of MLPA for Prognostic Assessment of Chromosomal Rearrangements and DNA Methylation in Uveal Melanoma.

MLPA在葡萄膜黑色素瘤染色体重排和DNA甲基化预后评估中的临床价值

Soltysova Andrea, Dvorska Dana, Ficek Andrej, Pecimonova Martina, Samec Marek, Kasubova Ivana, Horvathova Kajabova Viera, Demkova Lucia, Babal Pavel, Valaskova Jela, Dankova Zuzana, Smolkova Bozena, Furdova Alena

Characterization of CTNND2-related neurodevelopmental disease, phenotype-genotype spectrum and WNT dynamics in early neurogenesis

CTNND2相关神经发育疾病的特征、表型-基因型谱以及早期神经发生过程中WNT信号通路的动态变化

Shahsavani, Mansoureh; Wincent, Josephine; Reiter, Ricarda; Soltysova, Andrea; Schuy, Jakob; Helgadottir, Hafdis T; Eisfeldt, Jesper; Ek, Marlene; Ficek, Andrej; Druschke, Lotta; Kusikova, Katarina; Hsieh, Tzung-Chien; Krichhoff, Aron; Krawitz, Peter; Li, Jing-Mei; Webersinke, Gerald; Gorokhova, Svetlana; Missirian, Chantal; Riccardi, Florence; Pavinato, Lisa; Brusco, Alfredo; Mandrile, Giorgia; Trajkova, Slavica; Pintus, Francesco; Gagachovska, Biljana; Waisfisz, Quinten; van Hagen, Annet; Bedoukian, Emma; Izumi, Kosuke; Granger, Leslie; Petersen, Andrea; Oegema, Renske; Huibers, Manon; Demurger, Florence; Brischoux-Boucher, Elise; Julia, Sophie; Banneau, Guillaume; Zavala, M Jesus; Lagos, Catalina; Repetto, Gabriela M; Jouret, Guillaume; Kentros, Catherine; Ganapathi, Mythily; Chung, Wendy K; May, Halie; Hiatt, Susan M; Kelley, Whitley V; Förster, Alisa; Olfe, Lisa; Shillington, Amelle; Dauriat, Benjamin; Mercier, Sandra; Cogné, Benjamin; Engel, Camille; Dahlen, Eric; Rosenberger, Georg; Sauvigny, Thomas; Abdallah, Hamza Hadj; Courtin, Thomas; Stray-Pedersen, Asbjørg; Bernat, John A; Paolillo, Vitoria K; Viso, Florencia Del; Alaimo, Joseph T; Thiffault, Isabelle; Farrow, Emily G; Cohen, Ana S A; Weis, Serge; Duba, Hans-Christoph; Nordgren, Ann; Falk, Anna; Weis, Denisa; Lindstrand, Anna

Biallelic Cys141Tyr variant of SEL1L is associated with neurodevelopmental disorders, agammaglobulinemia, and premature death

SEL1L 的双等位基因 Cys141Tyr 变体与神经发育障碍、无丙种球蛋白血症和过早死亡有关

Denisa Weis, Liangguang L Lin, Huilun H Wang, Zexin Jason Li, Katarina Kusikova, Peter Ciznar, Hermann M Wolf, Alexander Leiss-Piller, Zhihong Wang, Xiaoqiong Wei, Serge Weis, Katarina Skalicka, Gabriela Hrckova, Lubos Danisovic, Andrea Soltysova, Tingxuan T Yang, René Günther Feichtinger, Johannes

Epigenomic and phenotypic characterization of DEGCAGS syndrome

DEGCAGS综合征的表观基因组学和表型特征分析

Karimi, Karim; Weis, Denisa; Aukrust, Ingvild; Hsieh, Tzung-Chien; Horackova, Marie; Paulsen, Julie; Mendoza Londono, Roberto; Dupuis, Lucie; Dickson, Megan; Lesman, Hellen; Lau, Tracy; Murphy, David; Hama Salih, Khalid; Al-Musawi, Bassam M S; Al-Obaidi, Ruqayah G Y; Rydzanicz, Malgorzata; Biela, Mateus; Santos, Mafalda Saraiva; Aldeeri, Abdulrahman; Gazda, Hanna T; Pais, Lynn; Shril, Shirlee; Døllner, Henrik; Bartakke, Sandip; Laccone, Franco; Soltysova, Andrea; Kitzler, Thomas; Soliman, Neveen A; Relator, Raissa; Levy, Michael A; Kerkhof, Jennifer; Rzasa, Jessica; Houlden, Henry; Pilshofer, Gabriela V; Jobst-Schwan, Tilman; Hildebrandt, Friedhelm; Sousa, Sergio B; Maroofian, Reza; Yu, Timothy W; Krawitz, Peter; Sadikovic, Bekim; Douzgou Houge, Sofia

Requirements and Barriers for Human-Centered SMEs

以人为本的中小企业的要求和障碍

Nazarejova, Julia; Soltysova, Zuzana; Rudeichuk, Tetiana

Uncovering accurate prognostic markers for high-risk uveal melanoma through DNA methylation profiling

通过DNA甲基化谱分析揭示高危葡萄膜黑色素瘤的准确预后标志物

Soltysova, Andrea; Dvorska, Dana; Kajabova, Viera Horvathova; Pecimonova, Martina; Cepcekova, Klaudia; Ficek, Andrej; Demkova, Lucia; Buocikova, Verona; Babal, Pavel; Juras, Ivan; Janikova, Katarina; Kasubova, Ivana; Samec, Marek; Brany, Dusan; Lyskova, Darina; Valaskova, Jela; Dankova, Zuzana; Smolkova, Bozena; Furdova, Alena

Genome-wide DNA methylome and transcriptome changes induced by inorganic nanoparticles in human kidney cells after chronic exposure

长期暴露于无机纳米颗粒后,人肾细胞中全基因组DNA甲基化组和转录组发生改变。

Soltysova, Andrea; Begerova, Patricia; Jakic, Kristina; Kozics, Katarina; Sramkova, Monika; Meese, Eckart; Smolkova, Bozena; Gabelova, Alena

Breakpoints characterisation of the genomic deletions identified by MLPA in alkaptonuria patients

对通过MLPA鉴定的尿黑酸症患者基因组缺失进行断点表征

Soltysova, Andrea; Sekelska, Martina; Zatkova, Andrea

Assessment of Product Variety Complexity

产品多样性复杂性评估

Modrak, Vladimir; Soltysova, Zuzana

Alkaptonuria in Russia

俄罗斯的尿黑酸症

Soltysova, Andrea; Kuzin, Alexandr; Samarkina, Elena; Zatkova, Andrea