[HTML][HTML] TALPID3 and ANKRD26 selectively orchestrate FBF1 localization and cilia gating

H Yan, C Chen, H Chen, H Hong, Y Huang… - Nature …, 2020 - nature.com
Transition fibers (TFs) regulate cilia gating and make the primary cilium a distinct functional
entity. However, molecular insights into the biogenesis of a functional cilia gate remain …

Centriole splitting caused by loss of the centrosomal linker protein C-NAP1 reduces centriolar satellite density and impedes centrosome amplification

AM Flanagan, E Stavenschi, S Basavaraju… - Molecular biology of …, 2017 - Am Soc Cell Biol
Duplication of the centrosomes is a tightly regulated process. Abnormal centrosome
numbers can impair cell division and cause changes in how cells migrate. Duplicated …

[HTML][HTML] Genome-wide screen identifies novel machineries required for both ciliogenesis and cell cycle arrest upon serum starvation

JH Kim, SM Ki, JG Joung, E Scott… - … et Biophysica Acta (BBA …, 2016 - Elsevier
Biogenesis of the primary cilium, a cellular organelle mediating various signaling pathways,
is generally coordinated with cell cycle exit/re-entry. Although the dynamic cell cycle …

Mice with a conditional deletion of Talpid3 (KIAA0586) – a model for Joubert syndrome

AL Bashford, V Subramanian - The Journal of Pathology, 2019 - Wiley Online Library
Joubert syndrome (JS) is a ciliopathy associated with mutations in numerous genes
encoding cilia components. TALPID3 encoded by KIAA0856 in man (2700049A03Rik in …

The complexity of the cilium: spatiotemporal diversity of an ancient organelle

W Heydeck, L Fievet, EE Davis, N Katsanis - Current opinion in cell biology, 2018 - Elsevier
Cilia are microtubule-based appendages present on almost all vertebrate cell types where
they mediate a myriad of cellular processes critical for development and homeostasis. In …

[HTML][HTML] Utilizing the chicken as an animal model for human craniofacial ciliopathies

EN Schock, CF Chang, IA Youngworth, MG Davey… - Developmental …, 2016 - Elsevier
The chicken has been a particularly useful model for the study of craniofacial development
and disease for over a century due to their relatively large size, accessibility, and …

Emerging insights into CP110 removal during early steps of ciliogenesis

S Xie, N Naslavsky, S Caplan - Journal of cell science, 2024 - journals.biologists.com
The primary cilium is an antenna-like projection from the plasma membrane that serves as a
sensor of the extracellular environment and a crucial signaling hub. Primary cilia are …

Proteolytic control in ciliogenesis: Temporal restriction or early initiation?

G Habeck, J Schweiggert - Bioessays, 2022 - Wiley Online Library
Cellular processes are highly dependent on a dynamic proteome that undergoes structural
and functional rearrangements to allow swift conversion between different cellular states. By …

Adeno-Associated Virus-Mediated Gene Therapy in the Mashlool, Atp1a3Mashl/+, Mouse Model of Alternating Hemiplegia of Childhood

AS Hunanyan, B Kantor, RS Puranam, C Elliott… - Human Gene …, 2021 - liebertpub.com
Alternating Hemiplegia of Childhood (AHC) is a devastating autosomal dominant disorder
caused by ATP1A3 mutations, resulting in severe hemiplegia and dystonia spells, ataxia …

[HTML][HTML] The ciliopathy protein TALPID3/KIAA0586 acts upstream of Rab8 activation in zebrafish photoreceptor outer segment formation and maintenance

I Ojeda Naharros, FB Cristian, J Zang, M Gesemann… - Scientific reports, 2018 - nature.com
Ciliopathies are human disorders caused by dysfunction of primary cilia, ubiquitous
microtubule-based organelles involved in signal transduction. Cilia are anchored inside the …