Results
|
1.
|
|
|
2.
|
|
|
3.
|
|
|
4.
|
|
|
5.
|
|
|
6.
|
|
|
7.
|
Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defect. [electronic resource] by
- Edelbusch, Christine
- Cindrić, Sandra
- Dougherty, Gerard W
- Loges, Niki T
- Olbrich, Heike
- Rivlin, Joseph
- Wallmeier, Julia
- Pennekamp, Petra
- Amirav, Israel
- Omran, Heymut
Producer: 20180430
In:
Human mutation vol. 38
Availability: No items available.
|
|
8.
|
A mutation in the zebrafish Na,K-ATPase subunit atp1a1a.1 provides genetic evidence that the sodium potassium pump contributes to left-right asymmetry downstream or in parallel to nodal flow. [electronic resource] by
- Ellertsdottir, Elin
- Ganz, Julia
- Dürr, Katrin
- Loges, Niki
- Biemar, Frederic
- Seifert, Franziska
- Ettl, Anne-Katrin
- Kramer-Zucker, Albrecht K
- Nitschke, Roland
- Driever, Wolfgang
Producer: 20061024
In:
Developmental dynamics : an official publication of the American Association of Anatomists vol. 235
Availability: No items available.
|
|
9.
|
Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia. [electronic resource] by
- Raidt, Johanna
- Wallmeier, Julia
- Hjeij, Rim
- Onnebrink, Jörg Große
- Pennekamp, Petra
- Loges, Niki T
- Olbrich, Heike
- Häffner, Karsten
- Dougherty, Gerard W
- Omran, Heymut
- Werner, Claudius
Producer: 20150720
In:
The European respiratory journal vol. 44
Availability: No items available.
|
|
10.
|
Mutations in CCDC11, which encodes a coiled-coil containing ciliary protein, causes situs inversus due to dysmotility of monocilia in the left-right organizer. [electronic resource] by
- Narasimhan, Vijayashankaranarayanan
- Hjeij, Rim
- Vij, Shubha
- Loges, Niki Tomas
- Wallmeier, Julia
- Koerner-Rettberg, Cordula
- Werner, Claudius
- Thamilselvam, Surin Kumar
- Boey, Adrian
- Choksi, Semil P
- Pennekamp, Petra
- Roy, Sudipto
- Omran, Heymut
Producer: 20151125
In:
Human mutation vol. 36
Availability: No items available.
|
|
11.
|
The Rac1 regulator ELMO controls basal body migration and docking in multiciliated cells through interaction with Ezrin. [electronic resource] by
- Epting, Daniel
- Slanchev, Krasimir
- Boehlke, Christopher
- Hoff, Sylvia
- Loges, Niki T
- Yasunaga, Takayuki
- Indorf, Lara
- Nestel, Sigrun
- Lienkamp, Soeren S
- Omran, Heymut
- Kuehn, E Wolfgang
- Ronneberger, Olaf
- Walz, Gerd
- Kramer-Zucker, Albrecht
Producer: 20150220
In:
Development (Cambridge, England) vol. 142
Availability: No items available.
|
|
12.
|
The Rac1 regulator ELMO controls basal body migration and docking in multiciliated cells through interaction with Ezrin. [electronic resource] by
- Epting, Daniel
- Slanchev, Krasimir
- Boehlke, Christopher
- Hoff, Sylvia
- Loges, Niki T
- Yasunaga, Takayuki
- Indorf, Lara
- Nestel, Sigrun
- Lienkamp, Soeren S
- Omran, Heymut
- Kuehn, E Wolfgang
- Ronneberger, Olaf
- Walz, Gerd
- Kramer-Zucker, Albrecht
Producer: 20150601
In:
Development (Cambridge, England) vol. 142
Availability: No items available.
|
|
13.
|
Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism. [electronic resource] by
- Sass, Jorn Oliver
- Mohr, Verena
- Olbrich, Heike
- Engelke, Udo
- Horvath, Judit
- Fliegauf, Manfred
- Loges, Niki Tomas
- Schweitzer-Krantz, Susanne
- Moebus, Ralf
- Weiler, Polly
- Kispert, Andreas
- Superti-Furga, Andrea
- Wevers, Ron A
- Omran, Heymut
Producer: 20060425
In:
American journal of human genetics vol. 78
Availability: No items available.
|
|
14.
|
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis. [electronic resource] by
- Amirav, Israel
- Wallmeier, Julia
- Loges, Niki T
- Menchen, Tabea
- Pennekamp, Petra
- Mussaffi, Huda
- Abitbul, Revital
- Avital, Avraham
- Bentur, Lea
- Dougherty, Gerard W
- Nael, Elias
- Lavie, Moran
- Olbrich, Heike
- Werner, Claudius
- Kintner, Chris
- Omran, Heymut
Producer: 20161213
In:
Human mutation vol. 37
Availability: No items available.
|
|
15.
|
None [electronic resource] by
- Cindrić, Sandra
- Dougherty, Gerard W
- Olbrich, Heike
- Hjeij, Rim
- Loges, Niki Tomas
- Amirav, Israel
- Philipsen, Maria C
- Marthin, June K
- Nielsen, Kim G
- Sutharsan, Sivagurunathan
- Raidt, Johanna
- Werner, Claudius
- Pennekamp, Petra
- Dworniczak, Bernd
- Omran, Heymut
Producer: 20200727
In:
American journal of respiratory cell and molecular biology vol. 62
Availability: No items available.
|
|
16.
|
RPGR mutations might cause reduced orientation of respiratory cilia. [electronic resource] by
- Bukowy-Bieryłło, Zuzanna
- Ziętkiewicz, Ewa
- Loges, Niki Tomas
- Wittmer, Mariana
- Geremek, Maciej
- Olbrich, Heike
- Fliegauf, Manfred
- Voelkel, Katarzyna
- Rutkiewicz, Ewa
- Rutland, Jonathan
- Morgan, Lucy
- Pogorzelski, Andrzej
- Martin, James
- Haan, Eric
- Berger, Wolfgang
- Omran, Heymut
- Witt, Michał
Producer: 20130913
In:
Pediatric pulmonology vol. 48
Availability: No items available.
|
|
17.
|
The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans. [electronic resource] by
- Wirschell, Maureen
- Olbrich, Heike
- Werner, Claudius
- Tritschler, Douglas
- Bower, Raqual
- Sale, Winfield S
- Loges, Niki T
- Pennekamp, Petra
- Lindberg, Sven
- Stenram, Unne
- Carlén, Birgitta
- Horak, Elisabeth
- Köhler, Gabriele
- Nürnberg, Peter
- Nürnberg, Gudrun
- Porter, Mary E
- Omran, Heymut
Producer: 20130530
In:
Nature genetics vol. 45
Availability: No items available.
|
|
18.
|
Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex. [electronic resource] by
- Olbrich, Heike
- Cremers, Carolin
- Loges, Niki T
- Werner, Claudius
- Nielsen, Kim G
- Marthin, June K
- Philipsen, Maria
- Wallmeier, Julia
- Pennekamp, Petra
- Menchen, Tabea
- Edelbusch, Christine
- Dougherty, Gerard W
- Schwartz, Oliver
- Thiele, Holger
- Altmüller, Janine
- Rommelmann, Frank
- Omran, Heymut
Producer: 20160105
In:
American journal of human genetics vol. 97
Availability: No items available.
|
|
19.
|
Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects. [electronic resource] by
- Loges, Niki Tomas
- Olbrich, Heike
- Becker-Heck, Anita
- Häffner, Karsten
- Heer, Angelina
- Reinhard, Christina
- Schmidts, Miriam
- Kispert, Andreas
- Zariwala, Maimoona A
- Leigh, Margaret W
- Knowles, Michael R
- Zentgraf, Hanswalter
- Seithe, Horst
- Nürnberg, Gudrun
- Nürnberg, Peter
- Reinhardt, Richard
- Omran, Heymut
Producer: 20100114
In:
American journal of human genetics vol. 85
Availability: No items available.
|
|
20.
|
Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia. [electronic resource] by
- Mitchison, Hannah M
- Schmidts, Miriam
- Loges, Niki T
- Freshour, Judy
- Dritsoula, Athina
- Hirst, Rob A
- O'Callaghan, Christopher
- Blau, Hannah
- Al Dabbagh, Maha
- Olbrich, Heike
- Beales, Philip L
- Yagi, Toshiki
- Mussaffi, Huda
- Chung, Eddie M K
- Omran, Heymut
- Mitchell, David R
Producer: 20120530
In:
Nature genetics vol. 44
Availability: No items available.
|