S. Tamm

发表

Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test

T. Welte, F. Stanke, B. Tümmler, 2020, BMJ open respiratory research.

Effect of Alpha-1 Antitrypsin on CFTR Levels in Primary Human Airway Epithelial Cells Grown at the Air-Liquid-Interface

F. Stanke, D. Jonigk, P. Braubach, 2021, Molecules.

Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia

T. Wienker, T. Becker, M. Macek, 2010, Journal of Medical Genetics.

Mechanism of allele specific assembly and disruption of master regulator transcription factor complexes of NF-KBp50, NF-KBp65 and HIF1a on a non-coding FAS SNP.

D. Steinemann, F. Stanke, B. Tümmler, 2016, Biochimica et biophysica acta.

Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1B

T. Becker, F. Stanke, B. Tümmler, 2020, Scientific Reports.

Functional analysis of F508del CFTR in native human colon.

F. Stanke, B. Tümmler, N. Derichs, 2010, Biochimica et biophysica acta.

Genes that determine immunology and inﬂammation modify the basic defect of impaired ion conductance in cystic ﬁbrosis epithelia

T. Wienker, T. Becker, M. Macek, 2022 .

Changes in cystic fibrosis transmembrane conductance regulator protein expression prior to and during elexacaftor-tezacaftor-ivacaftor therapy

T. Welte, F. Stanke, B. Tümmler, 2023, Frontiers in Pharmacology.

Molecular Epidemiology of Chronic Pseudomonas aeruginosa Airway Infections in Cystic Fibrosis

B. Tümmler, N. Høiby, L. Wiehlmann, 2012, PloS one.

CLCA4 variants determine the manifestation of the cystic fibrosis basic defect in the intestine

T. Becker, F. Stanke, B. Tümmler, 2012, European Journal of Human Genetics.

Hierarchical fine mapping of the cystic fibrosis modifier locus on 19q13 identifies an association with two elements near the genes CEACAM3 and CEACAM6

T. Wienker, T. Becker, F. Stanke, 2010, Human Genetics.

Transmission ratio distortion and maternal effects confound the analysis of modulators of cystic fibrosis disease severity on 19q13

T. Wienker, T. Becker, F. Stanke, 2007, European Journal of Human Genetics.

Functional analysis of the p.[Arg74Trp;Val201Met;Asp1270Asn]/p.Phe508del CFTR mutation genotype in human native colon

F. Stanke, B. Tümmler, J. Reiss, 2019, Molecular genetics & genomic medicine.

Genes that determine immunology and inﬂammation modify the basic defect of impaired ion conductance in cystic ﬁbrosis epithelia

T. Wienker, F. Stanke, B. Tümmler, 2022 .

A Fast Scoring of Human Primary Respiratory Epithelia Grown at Air–Liquid Interface (ALI) to Assess Epithelial Morphology in Research and Personalized Medicine Settings

F. Stanke, S. Tamm, Anna-Maria Dittrich, 2024, Journal of Personalized Medicine.

Analysis of CFTR mRNA and Protein in Peripheral Blood Mononuclear Cells via Quantitative Real-Time PCR and Western Blot

F. Stanke, A. Munder, Silke Hedtfeld, 2024, International journal of molecular sciences.