Latest papers

Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies.

Ectopic pregnancy in primary ciliary dyskinesia.

Functional recovery of rabbit maxillary sinus mucosa in two different experimental injury models.

The cell biological basis of ciliary disease.

[Mucociliary transport and motility of the ciliary system of the nasal mucosa in patients with chronic polypous rhinosinusitis]

Bronchiectasis and sino-nasal disease: a review.

Ciliary syndromes and treatment.

Bronchiectasis in children with recurrent pneumonia: an immunopathological damage associated with secondary ciliary dysmotility.

A recombinant turkey herpesvirus expressing chicken interleukin-2 increases the protection provided by in ovo vaccination with infectious bursal disease and infectious bronchitis virus.

Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia.

When cilia go bad: cilia defects and ciliopathies.

Change of nasal function with aging in Korean.

Pulmonary radioaerosol mucociliary clearance in diagnosis of primary ciliary dyskinesia.

Birth after intracytoplasmic sperm injection with use of testicular sperm from men with Kartagener or immotile cilia syndrome.

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.

Clinical variability in ciliary disorders.

Heterotaxia, congenital heart disease, and primary ciliary dyskinesia.

Exhaled nitric oxide in infants--what is a nice test like FENO doing in a place like this?

Biosynthesis of Wdr16, a marker protein for kinocilia-bearing cells, starts at the time of kinocilia formation in rat, and wdr16 gene knockdown causes hydrocephalus in zebrafish.