Emma A. Hall

Edinburgh, SCT EH42XU, United Kingdom

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications

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

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

Journal: Science (New York, N.Y.)
Published: April 25, 2024

Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis.

Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis.

Journal: eLife
Published: April 06, 2022

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

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

Journal: eLife
Published: April 26, 2021

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.

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.

Journal: Developmental cell
Published: March 22, 2018

Corrigendum: Mutations in genes encoding condensins cause microcephaly through decatenation failure at mitosis.

Corrigendum: Mutations in genes encoding condensins cause microcephaly through decatenation failure at mitosis.

Journal: Genes & development
Published: June 02, 2017

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

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

Journal: American journal of human genetics
Published: January 01, 2017

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

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

Journal: Genes & development
Published: June 29, 2016

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

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

Journal: Development (Cambridge, England)
Published: April 14, 2015

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

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

Journal: eLife
Published: April 13, 2015

Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes.

Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes.

Journal: PLoS genetics
Published: June 26, 2013
Showing 1-10 of 10

Last Updated: 09/26/2026