Publications by authors named "Thomas A Ravenscroft"

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Live imaging of the extracellular matrix with a glycan-binding fluorophore.
Antonio Fiore, Guoqiang Yu, Jason J Northey, Ronak Patel, Thomas A Ravenscroft

Nat Methods· May 2025

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Imaging the extracellular matrix in live tissues and organisms with a glycan-binding fluorophore.
Antonio Fiore, Guoqiang Yu, Jason J Northey, Ronak Patel, Thomas A Ravenscroft

bioRxiv· May 2024

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Tissue-specific transcriptome analyses in Drosophila provide novel insights into the mode of action of the insecticide spinosad and the function of its target, nAChRα6.
Felipe Martelli, Thomas A Ravenscroft, William Hutchison, Philip Batterham

Pest Manag Sci· October 2023

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The Voltage-Gated Sodium Channel in , Para, Localizes to Dendrites As Well As Axons in Mechanosensitive Chordotonal Neurons.
Thomas A Ravenscroft, Ashleigh Jacobs, Mingxue Gu, Daniel F Eberl, Hugo J Bellen

eNeuro· June 2023

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Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling.
Paul C Marcogliese, Debdeep Dutta, Shrestha Sinha Ray, Nghi D P Dang, Zhongyuan Zuo, Thomas A Ravenscroft

Sci Adv· January 2022

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Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11.
Thomas A Ravenscroft, Jennifer B Phillips, Elizabeth Fieg, Sameer S Bajikar, Judy Peirce

Genet Med· October 2021

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TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.
Lindsey D Goodman, Heidi Cope, Zelha Nil, Thomas A Ravenscroft, Wu-Lin Charng

Am J Hum Genet· September 2021

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Voltage-Gated Sodium Channels Are Only Expressed in Active Neurons and Are Localized to Distal Axonal Initial Segment-like Domains.
Thomas A Ravenscroft, Jasper Janssens, Pei-Tseng Lee, Burak Tepe, Paul C Marcogliese

J Neurosci· October 2020

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Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms.
Hyung-Lok Chung, Michael F Wangler, Paul C Marcogliese, Juyeon Jo, Thomas A Ravenscroft

Neuron· May 2020

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Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature.
Muhammad Ansar, Hyung-Lok Chung, Ali Al-Otaibi, Mohammad Nael Elagabani, Thomas A Ravenscroft

Am J Hum Genet· November 2019

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Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency.
Bret M Evers, Carlos Rodriguez-Navas, Rachel J Tesla, Janine Prange-Kiel, Catherine R Wasser, Thomas A Ravenscroft

Cell Rep· September 2017

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TYROBP genetic variants in early-onset Alzheimer's disease.
Cyril Pottier, Thomas A Ravenscroft, Patricia H Brown, NiCole A Finch, Matt Baker

Neurobiol Aging· December 2016

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Genetics of FTLD: overview and what else we can expect from genetic studies.
Cyril Pottier, Thomas A Ravenscroft, Monica Sanchez-Contreras, Rosa Rademakers

J Neurochem· August 2016

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The presenilin 1 p.Gly206Ala mutation is a frequent cause of early-onset Alzheimer's disease in Hispanics in Florida.
Thomas A Ravenscroft, Cyril Pottier, Melissa E Murray, Matt Baker, Elizabeth Christopher

Am J Neurodegener Dis· April 2016

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Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS.
Thomas A Ravenscroft, Matt C Baker, Nicola J Rutherford, Manuela Neumann, Ian R Mackenzie

Neurobiol Aging· September 2013

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