Petra Pennekamp
Muenster, NW 48149, Germany
Last Updated: 09/26/2026
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Found 51 publications
Caffeine citrate increases ciliary beat frequency in human respiratory epithelial cells.
Journal: Molecular and cellular pediatrics
Published: August 13, 2025
mRNA therapy improves the composition and motility in CCDC40-deficient cilia in vitro and in vivo.
Journal: American journal of respiratory cell and molecular biology
Published: July 30, 2025
mRNA therapy improves the composition and motility in CCDC40-deficient cilia in vitro and in vivo.
Journal: American journal of respiratory cell and molecular biology
Published: July 30, 2025
Urinary Dickkopf-3 Reflects Disease Severity and Predicts Short-Term Kidney Function Decline in Renal Ciliopathies.
Journal: Kidney international reports
Published: June 17, 2024
Pathogenic variants in CFAP46, CFAP54, CFAP74 and CFAP221 cause primary ciliary dyskinesia with a defective C1d projection of the central apparatus.
Journal: The European respiratory journal
Published: April 25, 2024
Novel pathogenic variants of DNAH5 associated with clinical and genetic spectra of primary ciliary dyskinesia in an Arab population.
Journal: Frontiers in genetics
Published: March 06, 2024
Immunofluorescence analyses of respiratory epithelial cells aid the diagnosis of nephronophthisis.
Journal: Pediatric nephrology (Berlin, Germany)
Published: February 26, 2024
Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype-phenotype correlations.
Journal: The European respiratory journal
Published: October 17, 2023
Mapping the Most Common Founder Variant in RSPH9 That Causes Primary Ciliary Dyskinesia in Multiple Consanguineous Families of Bedouin Arabs.
Journal: Journal of clinical medicine
Published: September 12, 2023
A range of 30-62% of functioning multiciliated airway cells is sufficient to maintain ciliary airway clearance.
Journal: The European respiratory journal
Published: August 25, 2023
Identification of a novel founder variant in DNAI2 cause primary ciliary dyskinesia in five consanguineous families derived from a single tribe descendant of Arabian Peninsula.
Journal: Frontiers in genetics
Published: August 11, 2022
Last Updated: 09/26/2026