Emma A. Hall

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TALPID 3 controls centrosome and cell polarity and the human ortholog KIAA 0586 is 1 mutated in Joubert syndrome ( JBTS 23 ) 2 3

Peter Nürnberg, Arif B Ekici, André Reis, 2015 .

A cell/cilia cycle biosensor for single cell kinetics reveals persistence of cilia after the G1/ S transition is a general property in cells and mice

A. Miyawaki, Asako Sakaue-Sawano, I. Jackson, 2022 .

PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins

Mark T. Handley, I. Jackson, R. Ribchester, 2017, American journal of human genetics.

Mutations in PLAA cause a lethal infantile epileptic encephalopathy by disrupting ubiquitin-mediated endolysosomal degradation of synaptic proteins

Mark T. Handley, R. Ribchester, C. Woods, 2017 .

Wt1 is required for cardiovascular progenitor cell formation through transcriptional control of Snail and E-cadherin

Abdelkader Essafi, N. Hosen, P. Hohenstein, 2009, Nature Genetics.

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis.

Martin A. M. Reijns, P. Lockhart, I. Jackson, 2011, American journal of human genetics.

Explorer Acute Versus Chronic Loss of Mammalian Azi 1 / Cep 131 Results in Distinct Ciliary Phenotypes

Lee B. Smith, I. Jackson, A. Jarman, 2017 .

Acute Versus Chronic Loss of Mammalian Azi1/Cep131 Results in Distinct Ciliary Phenotypes

Lee B. Smith, I. Jackson, A. Jarman, 2013, PLoS genetics.

Correction: Mutation of the Mouse Syce1 Gene Disrupts Synapsis and Suggests a Link between Synaptonemal Complex Structural Components and DNA Repair

R. Benavente, Ewelina Bolcun-Filas, C. Grey, 2009, PLoS Genetics.

A conserved role for Notch signaling in priming the cellular response to Shh through ciliary localisation of the key Shh transducer Smo

P. Serup, J. Dale, J. C. Silva, 2015, Development.

A conserved role for Notch in priming the cellular response to Shh through ciliary localisation of the key Shh transducer , Smoothened

P. Serup, J. Dale, J. C. Silva, 2015 .

Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis

Ahmed E. Fetit, A. Wood, C. Wise, 2016, Genes & development.

A WDR35-dependent coat protein complex transports ciliary membrane cargo vesicles to cilia

E. Lorentzen, Weihua Leng, G. Pigino, 2021, eLife.

A WDR 35-dependent coat protein complex 1 transports ciliary membrane cargo vesicles to cilia 2

J. Marsh, E. Lorentzen, Weihua Leng, 2022 .

TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23)

Peter Nürnberg, Arif B Ekici, André Reis, 2015, eLife.

Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis

L. Pelletier, J. Reiter, P. Yeyati, 2022, bioRxiv.

Manuscript submitted to eLife

J. Marsh, Weihua Leng, G. Pigino, 2020 .

A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice

Asako Sakaue-Sawano, I. Jackson, R. Meehan, 2018, Developmental cell.

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis.

Martin A. M. Reijns, P. Lockhart, I. Jackson, 2011, American journal of human genetics.

Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules

A. Fulton, E. Jabs, H. Omran, 2024, Science.

A WDR35-dependent coatomer transports ciliary membrane proteins from the Golgi to the cilia

J. Marsh, Weihua Leng, G. Pigino, 2020, bioRxiv.

Newcastle University Eprints Date Deposited: 3 This Work Is Licensed under a Creative Commons Attribution 4.0 International License Acute versus Chronic Loss of Mammalian Azi1/cep131 Results in Distinct Ciliary Phenotypes

Lee B. Smith, I. Jackson, A. Jarman, 2022 .