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

Severe Prenatal Presentation of Adenylosuccinate Lyase Deficiency Caused by a Synonymous ADSL Variant Inducing Aberrant Splicing

由同义ADSL变异引起的腺苷酸琥珀酸裂解酶缺乏症的严重产前表现,该变异导致异常剪接

Klapperich, Aysegül; Skopova, Vaclava; Karakaya, Mert; Velmans, Clara; Netzer, Christian; Strizek, Brigitte; Mrazova, Lenka Steiner; Zikanova, Marie

Expanding clinical spectrum of PAICS deficiency: Comprehensive analysis of two sibling cases.

PAICS 缺陷的临床谱系不断扩大:对两例同胞病例的综合分析

Weng Wen-Chin, Skopova Vaclava, Baresova Veronika, Liu Yao-Lin, Hsueh Hsueh-Wen, Chien Yin-Hsiu, Hwu Wuh-Liang, Souckova Olga, Hnizda Ales, Kmoch Stanislav, Lee Ni-Chung, Zikanova Marie

Phosphoribosylformylglycinamidine Synthase (PFAS) Deficiency: Clinical, Genetic and Metabolic Characterisation of a Novel Defect in Purine de Novo Synthesis

磷酸核糖甲酰甘氨酰胺合成酶(PFAS)缺乏症:嘌呤从头合成中一种新型缺陷的临床、遗传和代谢特征

Zikanova, Marie; Skopova, Vaclava; Stuurman, Kyra E; Baresova, Veronika; Souckova, Olga; Hnizda, Ales; Krijt, Matyas; Bleyer, Anthony J; Zeman, Jiri; Kmoch, Stanislav

Metabolites of De Novo Purine Synthesis: Metabolic Regulators and Cytotoxic Compounds

从头嘌呤合成的代谢产物:代谢调节剂和细胞毒性化合物

Souckova, Olga; Skopova, Vaclava; Baresova, Veronika; Sedlak, David; Bleyer, Anthony J; Kmoch, Stanislav; Zikanova, Marie

Study of purinosome assembly in cell-based model systems with de novo purine synthesis and salvage pathway deficiencies

在具有从头嘌呤合成和补救途径缺陷的细胞模型系统中研究嘌呤体组装

Veronika Baresova, Vaclava Skopova, Olga Souckova, Matyas Krijt, Stanislav Kmoch, Marie Zikanova

Adenylosuccinate lyase deficiency

腺苷酸琥珀酸裂解酶缺乏症

Jurecka, Agnieszka; Zikanova, Marie; Kmoch, Stanislav; Tylki-Szymańska, Anna

Genetic and metabolomic analysis of AdeD and AdeI mutants of de novo purine biosynthesis: cellular models of de novo purine biosynthesis deficiency disorders

嘌呤从头生物合成的 AdeD 和 AdeI 突变体的遗传和代谢组学分析:嘌呤从头生物合成缺陷症的细胞模型

Nathan Duval #, Kyleen Luhrs #, Terry G Wilkinson 2nd, Veronika Baresova, Vaclava Skopova, Stanislav Kmoch, Guido N Vacano, Marie Zikanova, David Patterson

Mutations of ATIC and ADSL affect purinosome assembly in cultured skin fibroblasts from patients with AICA-ribosiduria and ADSL deficiency

ATIC 和 ADSL 突变会影响患有 AICA-核糖苷尿症和 ADSL 缺乏症的患者培养皮肤成纤维细胞中的嘌呤体组装

Veronika Baresova, Vaclava Skopova, Jakub Sikora, David Patterson, Jana Sovova, Marie Zikanova, Stanislav Kmoch