Sandra Cindric
Muenster, NW 48149, Germany
Last Updated: 09/26/2026
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Found 15 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
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
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
Recessive Mutations in CFAP74 Cause Primary Ciliary Dyskinesia with Normal Ciliary Ultrastructure.
Journal: American journal of respiratory cell and molecular biology
Published: September 01, 2022
Correction: A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice.
Journal: Disease models & mechanisms
Published: June 11, 2021
Mutations in TP73 cause impaired mucociliary clearance and lissencephaly.
Journal: American journal of human genetics
Published: January 15, 2021
A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice.
Journal: Disease models & mechanisms
Published: April 21, 2020
CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module.
Journal: Nature communications
Published: November 03, 2019
SPEF2- and HYDIN-Mutant Cilia Lack the Central Pair-associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia Diagnostics.
Journal: American journal of respiratory cell and molecular biology
Published: September 24, 2019
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry.
Journal: American journal of human genetics
Published: April 05, 2019
Last Updated: 09/26/2026