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

Computational variant predictors for pharmacogenomics: from evaluation of single alleles to assessment of adverse drug reactions to antidepressants

药物基因组学中的计算变异预测器:从单个等位基因的评估到抗抑郁药不良反应的评估

Hajto, Jacek; Piechota, Marcin; Krätschmer, Ilse; Konowalska, Paula; Boyle, Gabriel E; Fowler, Douglas M; Borczyk, Malgorzata; Korostynski, Michal

Separating the genetics of disease, treatment, and treatment response using graphical modeling and large-scale electronic health records

利用图形建模和大规模电子健康记录,将疾病、治疗和治疗反应的遗传因素区分开来。

Borczyk, Malgorzata; Machnik, Nick; Hajto, Jacek; Krätschmer, Ilse; Konowalska, Paula; Baszkiewicz, Bartosz; Korostynski, Michal; Robinson, Matthew R

Spatiotemporal diversity in molecular and functional abnormalities in the mdx dystrophic brain.

mdx营养不良脑中分子和功能异常的时空多样性

Pomeroy Joanna, Borczyk Malgorzata, Kawalec Maria, Hajto Jacek, Carlson Emma, Svärd Samuel, Verma Suraj, Bareke Eric, Boratyńska-Jasińska Anna, Dymkowska Dorota, Mellado-Ibáñez Alvaro, Laight David, Zabłocki Krzysztof, Occhipinti Annalisa, Majewska Loydie, Angione Claudio, Majewski Jacek, Yegutkin Gennady G, Korostynski Michal, Zabłocka Barbara, Górecki Dariusz C

A cross-tissue transcriptomic approach decodes glucocorticoid receptor-dependent links to human metabolic phenotypes

跨组织转录组学方法揭示糖皮质激素受体依赖性与人类代谢表型的联系

Piechota, Marcin; Zieba, Mateusz; Borczyk, Małgorzata; Golda, Slawomir; Hajto, Jacek; Skupio, Urszula; Slezak, Michal; Parkitna, Jan Rodriguez; Korostynski, Michal

NFκB and JNK pathways mediate metabolic adaptation upon ESCRT-I deficiency

NFκB 和 JNK 通路介导 ESCRT-I 缺乏时的代谢适应

Jaroslaw Cendrowski, Marta Wrobel, Michal Mazur, Bartosz Jary, Ranjana Maurya, Surui Wang, Michal Korostynski, Anna Dziewulska, Maria Rohm, Patryk Kuropka, Natalia Pudelko-Malik, Piotr Mlynarz, Agnieszka Dobrzyn, Anja Zeigerer, Marta Miaczynska1

Genomic variants and inferred biological processes in multiplex families with Tourette syndrome

图雷特综合征多重家族的基因组变异及推断的生物学过程

Fichna, Jakub P; Borczyk, Małgorzata; Piechota, Marcin; Korostynski, Michał; Zekanowski, Cezary; Janik, Piotr

The First Potentially Causal Genetic Variant Documented in a Polish Woman with Multiple Cavernous Malformations of the Brain

首例在波兰女性脑部多发性海绵状血管畸形患者中发现的潜在致病基因变异

Szczygieł-Pilut, Elżbieta; Pilut, Daniel; Korostynski, Michal; Kopiński, Piotr; Potaczek, Daniel P; Wypasek, Ewa

Room-temperature valence transition in a strain-tuned perovskite oxide

应变调控钙钛矿氧化物中的室温价态转变

Chaturvedi, Vipul; Ghosh, Supriya; Gautreau, Dominique; Postiglione, William M; Dewey, John E; Quarterman, Patrick; Balakrishnan, Purnima P; Kirby, Brian J; Zhou, Hua; Cheng, Huikai; Huon, Amanda; Charlton, Timothy; Fitzsimmons, Michael R; Korostynski, Caroline; Jacobson, Andrew; Figari, Lucca; Barriocanal, Javier Garcia; Birol, Turan; Mkhoyan, K Andre; Leighton, Chris

Loss of full-length dystrophin expression results in major cell-autonomous abnormalities in proliferating myoblasts

全长肌营养不良蛋白表达的丧失导致增殖成肌细胞出现主要细胞自主异常

Maxime R F Gosselin, Virginie Mournetas, Malgorzata Borczyk, Suraj Verma, Annalisa Occhipinti, Justyna Róg, Lukasz Bozycki, Michal Korostynski, Samuel C Robson, Claudio Angione, Christian Pinset, Dariusz C Gorecki

Genetic Profiling in Children With Acute Lymphoblastic Leukemia Referred for Allogeneic Hematopoietic Stem Cell Transplantation

对接受异基因造血干细胞移植的急性淋巴细胞白血病患儿进行基因谱分析

Kwiecinska, Kinga; Strojny, Wojciech; Bik-Multanowski, Miroslaw; Michal Korostynski; Piechota, Marcin; Balwierz, Walentyna; Szymon Skoczen