CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis-Reference-Cited by-同舟云学术

CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis

Published:2023-04-17 Issue:8 Volume:133 Page:
ISSN:1558-8238
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Nuzhat Nafisa^ORCID,Van Schil Kristof^ORCID,Liakopoulos Sandra^ORCID,Bauwens Miriam,Rey Alfredo Dueñas,Käseberg Stephan^ORCID,Jäger Melanie,Willer Jason R.^ORCID,Winter Jennifer,Truong Hanh M.^ORCID,Gruartmoner Nuria,Van Heetvelde Mattias^ORCID,Wolf Joachim,Merget Robert,Grasshoff-Derr Sabine,Van Dorpe Jo^ORCID,Hoorens Anne^ORCID,Stöhr Heidi^ORCID,Mansard Luke^ORCID,Roux Anne-Françoise^ORCID,Langmann Thomas^ORCID,Dannhausen Katharina,Rosenkranz David,Wissing Karl M.^ORCID,Van Lint Michel,Rossmann Heidi^ORCID,Häuser Friederike^ORCID,Nürnberg Peter^ORCID,Thiele Holger^ORCID,Zechner Ulrich,Pearring Jillian N.^ORCID,De Baere Elfride^ORCID,Bolz Hanno J.^ORCID

Funder

NIH P30

NIH T32

PRO RETINA Deutschland

Dr. Senckenbergische Stiftung

University Hospital of Cologne

Deutsche Ophthalmologische Gesellschaft

Ghent University

Ghent University Hospital

John W. Mouton

H2020 MSCA ITN grant

Solve-RET

ERN-EYE

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://www.jci.org/articles/view/161156/files/pdf

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5. The centrosomal/basal body protein OFD1 is required for microtubule organization and cell cycle progression

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1. Cep131-Cep162 and Cby-Fam92 complexes cooperatively maintain Cep290 at the basal body and contribute to ciliogenesis initiation;PLOS Biology;2024-03-05

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