E-LIB Suche - Ergebnisse für: Wallmeier, Julia

1

Ciliopathy patient variants reveal organelle-specific funct..:

Dodd, Daniel O. ; Mechaussier, Sabrina ; Yeyati, Patricia L....
Science. 384 (2024) 6694 - p. , 2024

Link: https://doi.org/10.1126/..

2

Primary ciliary dyskinesia:

Raidt, Johanna ; Loges, Niki Tomas ; Olbrich, Heike...
La Presse Médicale. 52 (2023) 3 - p. 104171 , 2023

Link: https://doi.org/10.1016/..

3

The role of cilia for hydrocephalus formation:

Wallmeier, Julia ; Dallmayer, Marlene ; Omran, Heymut
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 190 (2022) 1 - p. 47-56 , 2022

Link: https://doi.org/10.1002/..

4

miR449 Protects Airway Regeneration by Controlling AURKA/HD..:

Wildung, Merit ; Herr, Christian ; Riedel, Dietmar...
International Journal of Molecular Sciences. 23 (2022) 14 - p. 7749 , 2022

Link: https://doi.org/10.3390/..

5

Motility of efferent duct cilia aids passage of sperm cells..:

Aprea, Isabella ; Nöthe-Menchen, Tabea ; Dougherty, Gerard W...
Molecular Human Reproduction. 27 (2021) 3 - p. , 2021

Link: https://doi.org/10.1093/..

6

CFAP45 deficiency causes situs abnormalities and asthenospe..:

Dougherty, Gerard W. ; Mizuno, Katsutoshi ; Nöthe-Menchen, Tabea...
Nature Communications. 11 (2020) 1 - p. , 2020

Link: https://doi.org/10.1038/..

7

Loss of CBY1 results in a ciliopathy characterized by featu..:

Epting, Daniel ; Senaratne, Lokuliyange D. S. ; Ott, Elisabeth...
Human Mutation. 41 (2020) 12 - p. 2179-2194 , 2020

Link: https://doi.org/10.1002/..

8

DYNC2H1 mutation causes Jeune syndrome and recurrent lung i..:

Emiralioglu, Nagehan ; Wallmeier, Julia ; Olbrich, Heike..
The Clinical Respiratory Journal. 12 (2017) 3 - p. 1017-1020 , 2017

Link: https://doi.org/10.1111/..

9

Mutation ofserine/threonine protein kinase 36(STK36) causes..:

Edelbusch, Christine ; Cindrić, Sandra ; Dougherty, Gerard W....
Human Mutation. 38 (2017) 8 - p. 964-969 , 2017

Link: https://doi.org/10.1002/..

10

Systematic Analysis ofCCNOVariants in a Defined Population:..:

Amirav, Israel ; Wallmeier, Julia ; Loges, Niki T....
Human Mutation. 37 (2016) 4 - p. 396-405 , 2016

Link: https://doi.org/10.1002/..

11

TTC25 Deficiency Results in Defects of the Outer Dynein Arm..:

Wallmeier, Julia ; Shiratori, Hidetaka ; Dougherty, Gerard W....
The American Journal of Human Genetics. 99 (2016) 2 - p. 460-469 , 2016

Link: https://doi.org/10.1016/..

12

Mutations in CCDC11, which Encodes a Coiled-Coil Containing..:

Narasimhan, Vijayashankaranarayanan ; Hjeij, Rim ; Vij, Shubha...
Human Mutation. 36 (2015) 3 - p. 307-318 , 2015

Link: https://doi.org/10.1002/..

13

Mutations in CCNO result in congenital mucociliary clearanc..:

Wallmeier, Julia ; Al-Mutairi, Dalal A ; Chen, Chun-Ting...
Nature Genetics. 46 (2014) 6 - p. 646-651 , 2014

Link: https://doi.org/10.1038/..

14

ENT manifestations in patients with primary ciliary dyskine..:

Sommer, J. Ulrich ; Schäfer, Kerstin ; Omran, Heymut...
European Archives of Oto-Rhino-Laryngology. 268 (2010) 3 - p. 383-388 , 2010

Link: https://doi.org/10.1007/..

15

miR449 Protects Airway Regeneration by Controlling AURKA/HD..:

Wildung, Merit ; Herr, Christian ; Riedel, Dietmar...
https://research.rug.nl/en/publications/a7e4299c-6527-4d17-bee9-684574a07e97. , 2022

Link: https://hdl.handle.net/1..