Alison Rigby

Mrs. Alison Rigby

University of California, San Diego, San Diego, California, USA
orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2010 in Neuropharmacology
Verified
Journal Article
Closed access
CWChristopher J. Winrow
Christopher J. Winrow
KTKeith Q. Tanis
Keith Q. Tanis
DRDuane R. Reiss
Duane R. Reiss
Alison RigbyAlison Rigby
Alison Rigby
JUJason M. Uslaner
Jason M. Uslaner
JRJohn J. Renger
John J. Renger

Barbara ColomboBarbara Colombo
Barbara Colombo
Alison RigbyAlison Rigby
Alison Rigby
MGMartina Gnerre
Martina Gnerre
Federica BiassoniFederica Biassoni
Federica Biassoni
Previous research has shown the positive effects of music and dance-based interventions on the physical and psychosocial symptoms of Parkinson’s disease (PD). The aims of this study were: (1) to investigate how PD patients subjectively perceive the emotional, cognitive, and social benefits of a music- and dance-based intervention; (2) to apply an innovative methodology for an interview analysis combining findings from a linguistic text with an analytic approach and conducted with the software LIWC and from the content analysis performed by human coders. Extensive, open-ended interviews were conducted with 13 patients with PD who had participated in a dance and music program. The interviews were analyzed using both human coders and the computer-based approach. The results show that emotional and social aspects are considered the most frequent perceived benefits of the dance program. The data confirm the positive impact of dance- and music-based programs on promoting participants’ emotional and social well-being. A combined approach to text analysis appears to be a promising way to achieve more in-depth insights into patients’ subjective perceptions.

19 May 2009 in Brain Research
Verified
Journal Article
Closed access
CWChristopher J. Winrow
Christopher J. Winrow
KTKeith Q. Tanis
Keith Q. Tanis
Alison RigbyAlison Rigby
Alison Rigby
RTRhonda R. Taylor
Rhonda R. Taylor
KSKyle Serikawa
Kyle Serikawa
JRJohn J. Renger
John J. Renger

18 April 2017 in SLEEP
Verified
Journal Article
Open access
PDF file
ENElena V. Nikonova
Elena V. Nikonova
JGJason DA Gilliland
Jason DA Gilliland
KTKeith Q. Tanis
Keith Q. Tanis
APAlexei A. Podtelezhnikov
Alexei A. Podtelezhnikov
Alison RigbyAlison Rigby
Alison Rigby
CWChristopher J. Winrow
Christopher J. Winrow
To assess differences in gene expression in cholinergic basal forebrain cells between sleeping and sleep-deprived mice sacrificed at the same time of day. Tg(ChAT-eGFP)86Gsat mice expressing enhanced green fluorescent protein (eGFP) under control of the choline acetyltransferase (Chat) promoter were utilized to guide laser capture of cholinergic cells in basal forebrain. Messenger RNA expression levels in these cells were profiled using microarrays. Gene expression in eGFP(+) neurons was compared (1) to that in eGFP(−) neurons and to adjacent white matter, (2) between 7:00 am (lights on) and 7:00 pm (lights off), (3) between sleep-deprived and sleeping animals at 0, 3, 6, and 9 hours from lights on. There was a marked enrichment of ChAT and other markers of cholinergic neurons in eGFP(+) cells. Comparison of gene expression in these eGFP(+) neurons between 7:00 am and 7:00 pm revealed expected differences in the expression of clock genes (Arntl2, Per1, Per2, Dbp, Nr1d1) as well as mGluR3. Comparison of expression between spontaneous sleep and sleep-deprived groups sacrificed at the same time of day revealed a number of transcripts (n = 55) that had higher expression in sleep deprivation compared to sleep. Genes upregulated in sleep deprivation predominantly were from the protein folding pathway (25 transcripts, including chaperones). Among 42 transcripts upregulated in sleep was the cold-inducible RNA-binding protein. Cholinergic cell signatures were characterized. Whether the identified genes are changing as a consequence of differences in behavioral state or as part of the molecular regulatory mechanism remains to be determined.