Table 1 Poster titles presented by authors (country of first author) at the 3rd BEAT-PCD Conference
From: Proceedings of the 3rd BEAT-PCD Conference and 4th PCD Training School
Poster title | Authors (country of first author) |
|---|---|
Is there a defect in ENaC activity in the nasal epithelium of patients with PCD? | Harman K, Alton EWFW, Davies JC, Waller MD, Crowley S (UK) |
Ciliary functional analysis using videomicroscopy: time for a standardisation | Kempeneers C, Seaton C, Espinosa BG, Chilvers (Belgium) |
Loss-of-function mutations in PIHD3 cause X-linked PCD with outer and inner dynein arm defects | Hoben I, Paff T, Loges NT, Aprea I, Wu K, Bakey Z, Haarman EG, Daniels JMA, Sistemaans EA, Bogunovic N, Dougherty GW, Große-Onnebrink J, Matter A, Olbrich H, Werner C, Pals G, Schmidts M, Omran H, Micha D (Germany) |
Increased plasma ceramide and sphingomyelin levels in the plasma of PCD patients | Topcu DB, Tugcu G, Ozcan F, Aslan M, Esref S, Hizal M, Yalcin E, Ersoz D, Ozcelik U, Kiper N, Lay I, Oztas Y (Turkey) |
The role of laterality signals from the left-right organiser in zebrafish gut patterning | Bota C, Lopes S (Portugal) |
Downstream target of Pkd2 affects nodal signalling regulator in left-right development. | Jacinto R, Lopes S (Portugal) |
ENKUR- a novel heterotaxy gene | Menchen T, Sigg MA, Lee C, Jungnickel MK, Dougherty GW, Pennekamp P, Florman HM, Wallingford JB, Reiter JF, Omran H (Germany) |
Successful pregnancies for six women with PCD | Sivaramakrishnan H, Cottee A, Coon C, Morgan L (Australia) |
Two siblings with PCD and hepatic involvement | Hizal MG, Bilgic E, Taskiran E, Atilla P, Akcoren Z, Gunaydin O, Ozen H, Esref S, Emiralioǧlu N, Yalcin E, Ersoz D, Kiper N, Yuce A, Ozcelik U (Turkey) |
Homozygous loss-of-function mutations in MNS1 cause laterality defects and male infertility | Hjeij R, Ta-Shma A, Perles Z, Dougherty GW, Abu Zahira I, Letteboer SJF, Antony D, Darwish A, Mans DA, Spittler S, Edelbusch C, Cindric S, Menchen T, Olbrich H, Stuhlmann F, Aprea I, Pennekamp P, Loges NT, Breuer O, Shaag A, Rein AJJT, Gulec EY, Gezdirci A, Abitbul R, Elias N, Amirav I, Schmidts M, Roepman R, Elpeleg O, Omran H (Germany) |
Creation of a Danio rerio mutant using CRISPR-Cas9 as a model system to study PCD. | Rasteiro M, Lopes S (Portugal) |
Continence assessment in paediatric patients with PCD | Wilkins H, Friend A, Harris A, Keenan V (UK) |
A new possible role of V-ATPase in the left-right development | Pestana S, Lopes S (Portugal) |
Immunofluorescence is a useful adjunct to TEM for diagnosis of PCD | Canoy I,MacKenney K, Clarke C, Morgan L, Buddle L, Hughes L (Australia) |
A four-year experience of a PCD diagnostic centre in Greece | Chatzipirasidis G, Douros K, Mpoutopoulou B, Papadopoulos M, Grammeniatis V, Dimakou K, Priftis KN (Greece) |