arrow
R

Rosmarie Friemann

Sahlgrenska University Hospital
H指数:25
被引数:1,985

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Structural and biophysical analysis of a Haemophilus influenzae tripartite ATP-independent periplasmic (TRAP) transporter
2024-02-135
OA
Structure and mechanism of a tripartite ATP-independent periplasmic TRAP transporter
2023-02-2711
OAAI
Sialic Acid Derivatives Inhibit SiaT Transporters and Delay Bacterial Growth
2022-06-083
OAAI
Hydroxyazole scaffold-based Plasmodium falciparum dihydroorotate dehydrogenase inhibitors: Synthesis, biological evaluation and X-ray structural studies
2019-02-0129
OAAI
Targeting Myeloid Differentiation Using Potent 2-Hydroxypyrazolo[1,5-a]pyridine Scaffold-Based Human Dihydroorotate Dehydrogenase Inhibitors (vol 61, pg 6034, 2018)
2019-01-290
OAAI
Targeting Myeloid Differentiation Using Potent 2-Hydroxypyrazolo[1,5-a]pyridine Scaffold-Based Human Dihydroorotate Dehydrogenase Inhibitors
2018-06-2571
OAAI
Substrate-bound outward-open structure of a Na+-coupled sialic acid symporter reveals a new Na+ site

Na偶联的唾液酸同向转运体的底物结合的外向开放结构揭示了一个新的Na位点

2018-05-0155
OAAI
Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid

基于苯并异恶唑部分的有效和选择性的醛酮还原酶1C3 (AKR1C3) 抑制剂: 生物等排支架跳跃方法在氟芬那酸中的应用

2018-04-0150
OAAI
Automation aided optimization of cloning, expression and purification of enzymes of the bacterial sialic acid catabolic and sialylation pathways enzymes for structural studies
2018-01-179
OAAI
Design, synthesis, biological evaluation and X-ray structural studies of potent human dihydroorotate dehydrogenase inhibitors based on hydroxylated azole scaffolds

基于羟化唑支架的强效人二氢乳清酸脱氢酶抑制剂的设计、合成、生物学评价及X-射线结构研究

2017-03-0153
PREAI