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Sandra Ammann

medical center university of freiburg
H指数:23
被引数:2,229

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ERCC6L2 ensures repair fidelity for staggered-end DNA double-strand breaks

ERCC6L2 确保错位末端DNA双链断裂的修复保真度

2026-02-250
OAAI
Base edited skin equivalents with clinical potential for ex vivo correction of Recessive Dystrophic Epidermolysis Bullosa

具有临床潜力的碱基编辑皮肤替代物,用于体外修复隐性营养不良型大疱性表皮松解症

2025-11-170
PRE
Targeted Inhibition of ELANE Expression Using Adenine Base Editing to Treat Severe Congenital Neutropenia

利用腺嘌呤碱基编辑靶向抑制ELANE表达以治疗重症先天性中性粒细胞减少症

2025-11-050
OAAI
Prime editing as a promising therapeutic strategy for junctional epidermolysis bullosa

连接性表皮松解症的潜在治疗策略:碱基编辑

2025-10-300
OAAI
Targeted gene editing and near-universal cDNA insertion of CYBA and CYBB as a treatment for chronic granulomatous disease

靶向基因编辑和近全基因组cDNA插入CYBA和CYBB作为慢性肉芽肿病的治疗方法

2025-08-120
OAAI
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect (vol 221, e20221122, 2024)
2024-05-210
OAAI
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect
2024-05-091
OAAI
Gene editing of hematopoietic stem cells restores T-cell response in familial hemophagocytic lymphohistiocytosis
2024-01-015
PRE
IFNγ binding to extracellular matrix prevents fatal systemic toxicity

Ifn γ 与细胞外基质结合可预防致命的全身毒性

2023-02-0214
OAAI
Definition and validation of serum biomarkers for optimal differentiation of hyperferritinaemic cytokine storm conditions in children: a retrospective cohort study
2021-08-0118
OAAI
Functional flow cytometry of monocytes for routine diagnosis of innate primary immunodeficiencies
2020-01-016
OAAI
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
2019-03-19110
OAAI