نتائج البحث

1

Ift88, but not Kif3a, is required for establishment of the periciliary membrane compartment

المؤلفون: Amandine Viau, Gerd Walz, Esben Lorentzen, Heike Janusch, Athina Ganner, Fruzsina Kotsis, Albrecht Kramer-Zucker, Christopher Boehlke, Roland Nitschke, Daniel Epting, Yujie Li, Elke Neumann-Haefelin, E. Wolfgang Kuehn

المصدر: Kotsis, F, Janusch, H, Li, Y, Viau, A, Epting, D, Kramer-Zucker, A, Walz, G, Nitschke, R, Lorentzen, E, Ganner, A, Neumann-Haefelin, E, Kuehn, E W & Boehlke, C 2021, ' Ift88, but not Kif3a, is required for establishment of the periciliary membrane compartment ', Biochemical and Biophysical Research Communications, vol. 584, pp. 19-25 . https://doi.org/10.1016/j.bbrc.2021.10.075Test

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73bd892c18036ca5cadf7a4f5379a30bTest
https://doi.org/10.1016/j.bbrc.2021.10.075Test

2

Heterotrimeric Kinesin II is required for flagellar assembly and elongation of nuclear morphology during spermiogenesis in Schmidtea mediterranea

المؤلفون: Labib Rouhana, Donovan A. Christman, Haley N. Curry

المصدر: Dev Biol

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::550077ef1a034033f01d92b288eea4c2Test
https://doi.org/10.1016/j.ydbio.2021.05.018Test

3

Phosphosite T674A mutation in kinesin family member 3A fails to reproduce tissue and ciliary defects characteristic of CILK1 loss of function

المؤلفون: Xudong Li, Sean Ahmadi, Eric J. Wang, Michael Scott, David L. Brautigan, Li Jin, Zheng Fu, Wenhao Xu, Casey D. Gailey

المصدر: Dev Dyn

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c77343d955fb51366f02c5f77da0c885Test
https://doi.org/10.1002/dvdy.252Test

4

Hedgehog-induced ciliary trafficking of kinesin-4 motor KIF7 requires intraflagellar transport but not KIF7's microtubule binding

المؤلفون: T. Lynne Blasius, Yang Yue, Kristen J. Verhey, Martin F Engelke

المصدر: Molecular biology of the cell. 33(1)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84a2ce618d70d953a4b8c225b71ef3d9Test
https://pubmed.ncbi.nlm.nih.gov/34705483Test

5

Kinesin-2 heterodimerization alters entry into a processive run along the microtubule but not stepping within the run

المؤلفون: Juergen Hahn, Sean M. Quinn, Susan P. Gilbert, Daniel P. Howsmon

المصدر: Journal of Biological Chemistry. 293:13389-13400

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::566adfb2c1bff1f95071c6de3aedf3d6Test
https://doi.org/10.1074/jbc.ra118.002767Test

6

Phosphosite T674A mutation in kinesin family member 3A fails to reproduce tissue and ciliary defects characteristic of CILK1 loss of function

المؤلفون: David L. Brautigan, Eric J. Wang, Xudong Li, Sean Ahmadi, Li Jin, Zheng Fu, Casey D. Gailey, Wenhao Xu

مصطلحات موضوعية: Intraflagellar transport, Ciliogenesis, Cilium, Kinesin, Phosphorylation, KIF3A, Biology, Ciliopathies, Loss function, Cell biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::60cf3057c04750fb77830143453c31d2Test
https://doi.org/10.1101/2020.06.30.180307Test

7

Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy

المؤلفون: Julia H. Wildschutte, Marta G. Castelhano, Max F. Rothschild, Maria Kaukonen, Georgios Kellaris, Joshua A. Stern, Stéphane Bézieau, Laurence Legeai-Mallet, Shrinivas P. Mane, Dominique Debray, Hannes Lohi, Ottmar Distl, Laurence M. Occelli, Kinga M. Bujakowska, Marjo K. Hytönen, Oliver P. Forman, Elizabeth A. Wilcox, Richard Malik, Tosso Leeb, Ronald H.L. Li, Elizabeth L. Cadena, William F. Swanson, Teri L. Lear, Yoshihiko Yu, Robert J. Harvey, Dominique Caldari, Erica E. Davis, Bianca Haase, Eric A. Pierce, Reuben M. Buckley, Stephen P. Daiger, L. Martin, D. Aberdein, Clare Rusbridge, Simon M. Petersen-Jones, Edward I. Ginns, Daniel C. Koboldt, Benjamin Cogné, Lokuliyanage Dona Samudita Senaratne, Michael B. Gorin, Niels C Pedersen, Margret L. Casal, Xenia Latypova, Adam R. Boyko, Isabel Hernandez, Tomoki Kosho, Sara J. Bowne, Nicholas H. Dodman, Tomas F. Bergström, Nicholas Katsanis, Rebecca R. Bellone, Guylène Le Meur, Bertrand Isidor, Daisuke Hasegawa, Christopher B. Kaelin, Mathilde Nizon, Karen A. Terio, Paulo C. Alves, Leslie A. Lyons, Christopher R Helps, Eirik Frengen, Emilie Leclerc, William J. Murphy, Beth Shapiro, Mark A. Magnuson, Lorraine Fievet, Maria Longeri, Rory J. Todhunter, Jeffrey A. Brockman, Lori S. Sullivan, Dorian J. Garrick, Jens Häggström, Jonathan E. Fogle, N. Matthew Ellinwood, Wesley C. Warren, John S. Munday, Gregory S. Barsh

المساهمون: Université Paris Cité (UPC), Imagine - Institut des maladies génétiques (IHU) (Imagine - U1163), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPC), CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Université de Paris (UP), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP)

المصدر: American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2020, 106, pp.893-904. ⟨10.1016/j.ajhg.2020.04.005⟩
Am J Hum Genet