Abigail Lukowicz
Overview
Explore the profile of Abigail Lukowicz including associated specialties, affiliations and a list of published articles.
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Articles
4
Citations
80
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0
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Recent Articles
1.
Dias C, Issac B, Sun L, Lukowicz A, Talukdar M, Akula S, et al.
Proc Natl Acad Sci U S A
. 2023 May;
120(23):e2300052120.
PMID: 37252957
Short trinucleotide expansions at the FMR1 locus are associated with the late-onset condition fragile X-associated tremor/ataxia syndrome (FXTAS), which shows very different clinical and pathological features from fragile X syndrome...
2.
Kim J, Lukowicz A, Qu W, Johnson A, Cvetanovic M
Glia
. 2018 Jul;
66(9):1972-1987.
PMID: 30043530
Spinocerebellar ataxia type 1 (SCA1) is a fatal, dominantly inherited neurodegenerative disease caused by the expansion of CAG repeats in the Ataxin-1 (ATXN1) gene. SCA1 is characterized by balance and...
3.
Ferro A, Qu W, Lukowicz A, Svedberg D, Johnson A, Cvetanovic M
PLoS One
. 2018 Jul;
13(7):e0200013.
PMID: 29975753
Spinocerebellar Ataxia type 1 (SCA1) is a fatal neurodegenerative genetic disease that is characterized by pronounced neuronal loss and gliosis in the cerebellum. We have previously demonstrated microglial activation, measured...
4.
Qu W, Johnson A, Kim J, Lukowicz A, Svedberg D, Cvetanovic M
J Neuroinflammation
. 2017 May;
14(1):107.
PMID: 28545543
Background: Polyglutamine (polyQ) expansion in the protein Ataxin-1 (ATXN1) causes spinocerebellar ataxia type 1 (SCA1), a fatal dominantly inherited neurodegenerative disease characterized by motor deficits, cerebellar neurodegeneration, and gliosis. Currently,...