A. Schmidt

发表

In vitro radiosensitivity of human leukemia cell lines.

R. Weichselbaum, J. Little, J. Greenberger, 1981, Radiology.

Revertant mutants G550E and 4RK rescue cystic fibrosis mutants in the first nucleotide-binding domain of CFTR by different mechanisms

C. Soares, M. Amaral, D. Sheppard, 2006, Proceedings of the National Academy of Sciences.

An Extract from the Medicinal Plant Phyllanthus acidus and Its Isolated Compounds Induce Airway Chloride Secretion: A Potential Treatment for Cystic Fibrosis

Tiago Grego, M. Amaral, J. Ousingsawat, 2007, Molecular Pharmacology.

Analysis of Wilms Tumor Gene (WT1) Expression in Acute Leukemia Patients with Special Reference to the Differential Diagnosis between Eosinophilic Leukemia and Idiopathic Hypereosinophilic Syndromes

S. Bartelt, H. Menssen, R. Leben, 2000, Leukemia & lymphoma.

Mononuclear Cell Preparations from Patients with Idiopathic Hypereosinophilic Syndromes Do Not Express the Wilms’ Tumor Gene

H. Menssen, A. Schmidt, E. Thiel, 2004 .

Characterization of an intramolecular protein-protein interaction in c-Ets1 and its viral homologue v-Ets.

Mélanie Schmidt, J. Dietl, A. Schmidt, 2007, Oncology reports.

A novel breast cancer cell line initially established from pleural effusion: evolution towards a more aggressive phenotype.

R. Kreienberg, Mélanie Schmidt, J. Waltenberger, 2007, International journal of oncology.

Vaccination strategy to target lysyl oxidase-like 4 in dendritic cell based immunotherapy for head and neck cancer.

K. Csiszȧr, D. Kabelitz, A. Heiser, 2008, International journal of oncology.

Requirements for Efficient Correction of ΔF508 CFTR Revealed by Analyses of Evolved Sequences

Philip J. Thomas, Robert J. Bridges, André Schmidt, 2012, Cell.

The Primary Folding Defect and Rescue of ΔF508 CFTR Emerge during Translation of the Mutant Domain

Philip J. Thomas, P. Thomas, I. Braakman, 2010, PloS one.

Strategies to investigate the mechanism of action of CFTR modulators.

D. Sheppard, Z. Cai, Hongyu Li, 2004, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Direct block of the cystic fibrosis transmembrane conductance regulator Cl− channel by niflumic acid

Z. Cai, Hongyu Li, A. Schmidt, 2004, Molecular membrane biology.

Restoration of cystic fibrosis transmembrane conductance regulator function to CF mutants by enhancing protein processing and channel activity

A. Schmidt, 2008 .

Increased efficacy of VX-809 in different cellular systems results from an early stabilization effect of F508del-CFTR

M. Amaral, C. Farinha, M. Sousa, 2015, Pharmacology research & perspectives.

Reduced histone deacetylase 7 activity restores function to misfolded CFTR in cystic fibrosis.

John R Yates, Gerard Manning, Yoshihiro Matsumura, 2010, Nature chemical biology.

Biochemical and biophysical approaches to probe CFTR structure.

P. Thomas, J. Mendoza, A. Schmidt, 2011, Methods in molecular biology.

Epigenetic regulation of transcription factor binding motifs promotes Th1 response in Chagas disease cardiomyopathy

E. Donadi, M. Hirata, J. Marin-Neto, 2022, Frontiers in Immunology.

Solubilizing mutations used to crystallize one CFTR domain attenuate the trafficking and channel defects caused by the major cystic fibrosis mutation.

M. Amaral, P. Thomas, C. Farinha, 2008, Chemistry & biology.

Introduction to section IV: biophysical methods to approach CFTR structure.

P. Thomas, J. Mendoza, A. Schmidt, 2011, Methods in molecular biology.

Prolonged treatment of cells with genistein modulates the expression and function of the cystic fibrosis transmembrane conductance regulator

M. Amaral, D. Sheppard, Z. Cai, 2008, British journal of pharmacology.

Role of microRNAs in B cell leukemias and lymphomas.

R. Küppers, A. Schmidt, 2014, Current molecular medicine.