Tabea Menchen-Nothe

Muenster, NW, Germany

Last Updated: 09/26/2026

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Found 13 publications

Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis.

Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis.

Journal: American journal of respiratory and critical care medicine

Published: April 16, 2024

Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype-phenotype correlations.

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

Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility.

Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility.

Journal: Frontiers in genetics

Published: December 06, 2022

Pathogenic variants in CLXN encoding the outer dynein arm docking-associated calcium-binding protein calaxin cause primary ciliary dyskinesia.

Pathogenic variants in CLXN encoding the outer dynein arm docking-associated calcium-binding protein calaxin cause primary ciliary dyskinesia.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 20, 2022

miR449 Protects Airway Regeneration by Controlling AURKA/HDAC6-Mediated Ciliary Disassembly.

miR449 Protects Airway Regeneration by Controlling AURKA/HDAC6-Mediated Ciliary Disassembly.

Journal: International journal of molecular sciences

Published: June 23, 2022

Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility.

Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility.

Journal: PLoS genetics

Published: May 06, 2020

Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system.

Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system.

Journal: Molecular human reproduction

Published: April 28, 2020

CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module.

CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module.

Journal: Nature communications

Published: November 03, 2019

Randomization of Left-right Asymmetry and Congenital Heart Defects: The Role of DNAH5 in Humans and Mice.

Randomization of Left-right Asymmetry and Congenital Heart Defects: The Role of DNAH5 in Humans and Mice.

Journal: Circulation. Genomic and precision medicine

Published: October 23, 2019

De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry.

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

Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects.

Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects.

Journal: American journal of human genetics

Published: May 29, 2018

Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.

Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.

Journal: PLoS genetics

Published: March 23, 2018

Showing 1-12 of 13

Last Updated: 09/26/2026