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CRISPR/Cas9 Editing of the Mutant Huntingtin Allele In Vitro and In Vivo

Molecular therapy, 2017-01, Vol.25 (1), p.12-23

2017

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Gene suppression strategies for dominantly inherited neurodegenerative diseases: lessons from Huntington's disease and spinocerebellar ataxia

Human molecular genetics, 2016-04, Vol.25 (R1), p.R53-R64

2016

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Viral Vectors for Gene Transfer

Current protocols in mouse biology, 2018-12, Vol.8 (4), p.e58-n/a

2018

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Responding to COVID-19: Developing a Virtual “On-Campus” Experience for Adult-Geriatric Acute Care Nurse Practitioner Students

The Journal of nursing education, 2021-10, Vol.60 (10), p.586-589

2021

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Broad Therapeutic Benefit After RNAi Expression Vector Delivery to Deep Cerebellar Nuclei: Implications for Spinocerebellar Ataxia Type 1 Therapy

Molecular therapy, 2014-03, Vol.22 (3), p.588-595

2014

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RNAi prevents and reverses phenotypes induced by mutant human ataxin-1

Annals of neurology, 2016-11, Vol.80 (5), p.754-765

2016

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Using Simulation to Evaluate Clinical Performance and Reasoning in Adult-Geriatric Acute Care Nurse Practitioner Students

The Journal of nursing education, 2019-10, Vol.58 (10), p.599-603

2019

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Toxicity after AAV delivery of RNAi expression constructs into nonhuman primate brain

Nature medicine, 2021-11, Vol.27 (11), p.1982-1989

2021

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Cochlear transduction via cerebrospinal fluid delivery of AAV in non-human primates

Molecular therapy, 2023-03, Vol.31 (3), p.609-612

2023

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The long non-coding RNA NEAT1 is elevated in polyglutamine repeat expansion diseases and protects from disease gene-dependent toxicities

Human molecular genetics, 2018-12, Vol.27 (24), p.4303-4314

2018

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Report and Prevent: A Quality Improvement Project to Protect Nurses From Violence in the Emergency Department

Journal of emergency nursing, 2020-05, Vol.46 (3), p.338-344.e7

2020

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RNAi or overexpression: Alternative therapies for Spinocerebellar Ataxia Type 1

Neurobiology of disease, 2013-08, Vol.56, p.6-13

2013

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Autopsy Observation as Experiential Learning for Nurse Practitioner Students in an Online Advanced Pathophysiology Course

Nurse educator, 2020-03, Vol.45 (2), p.111-113

2020

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APOE2 gene therapy reduces amyloid deposition and improves markers of neuroinflammation and neurodegeneration in a mouse model of Alzheimer disease

Molecular therapy, 2024-05, Vol.32 (5), p.1373-1386

2024

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Implementing a Delirium Admission Protocol in the Emergency Department

International Journal of Gerontology, 2021-04, Vol.15 (2), p.150-153

2021

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Broad distribution of ataxin 1 silencing in rhesus cerebella for spinocerebellar ataxia type 1 therapy

Brain (London, England : 1878), 2015-12, Vol.138 (Pt 12), p.3555-3566

2015

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VWA3A-derived ependyma promoter drives increased therapeutic protein secretion into the CSF

Molecular therapy. Nucleic acids, 2023-09, Vol.33, p.296-304

2023

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Combined overexpression of ATXN1L and mutant ATXN1 knockdown by AAV rescue motor phenotypes and gene signatures in SCA1 mice

Molecular therapy. Methods & clinical development, 2022-06, Vol.25, p.333-343

2022

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Using Interprofessional Simulation with Telehealth to Enhance Teamwork and Communication in Home Care

Home healthcare now, 2022-05, Vol.40 (3), p.139-145

2022

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Techniques for Intracranial Stereotaxic Injections of Adeno‐Associated Viral Vectors in Adult Mice

Current protocols in mouse biology, 2018-12, Vol.8 (4), p.e57-n/a

2018

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Altered Purkinje cell miRNA expression and SCA1 pathogenesis

Neurobiology of disease, 2013-06, Vol.54, p.456-463

2013

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Adeno‐Associated Virus Production, Purification, and Titering

Current protocols in mouse biology, 2018-12, Vol.8 (4), p.e56-n/a

2018

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Recent Advances in RNA Interference Therapeutics for CNS Diseases

Neurotherapeutics, 2013-07, Vol.10 (3), p.473-485

2013

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Haplotyping SNPs for allele-specific gene editing of the expanded huntingtin allele using long-read sequencing

HGG advances, 2023-01, Vol.4 (1), p.100146-100146, Article 100146

2023

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Use of Care Guides to Reduce Emergency Department Visits by High-Frequency Utilizers

Journal of emergency nursing, 2023-11, Vol.49 (6), p.863-869

2023

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CRISPR/Cas9 Editing of the Mutant Huntingtin Allele In Vitro and In Vivo

Gene suppression strategies for dominantly inherited neurodegenerative diseases: lessons from Huntington's disease and spinocerebellar ataxia

Viral Vectors for Gene Transfer

Responding to COVID-19: Developing a Virtual “On-Campus” Experience for Adult-Geriatric Acute Care Nurse Practitioner Students

Broad Therapeutic Benefit After RNAi Expression Vector Delivery to Deep Cerebellar Nuclei: Implications for Spinocerebellar Ataxia Type 1 Therapy

RNAi prevents and reverses phenotypes induced by mutant human ataxin-1

Using Simulation to Evaluate Clinical Performance and Reasoning in Adult-Geriatric Acute Care Nurse Practitioner Students

Toxicity after AAV delivery of RNAi expression constructs into nonhuman primate brain

Cochlear transduction via cerebrospinal fluid delivery of AAV in non-human primates

The long non-coding RNA NEAT1 is elevated in polyglutamine repeat expansion diseases and protects from disease gene-dependent toxicities

Report and Prevent: A Quality Improvement Project to Protect Nurses From Violence in the Emergency Department

RNAi or overexpression: Alternative therapies for Spinocerebellar Ataxia Type 1

Autopsy Observation as Experiential Learning for Nurse Practitioner Students in an Online Advanced Pathophysiology Course

APOE2 gene therapy reduces amyloid deposition and improves markers of neuroinflammation and neurodegeneration in a mouse model of Alzheimer disease

Implementing a Delirium Admission Protocol in the Emergency Department

Broad distribution of ataxin 1 silencing in rhesus cerebella for spinocerebellar ataxia type 1 therapy

VWA3A-derived ependyma promoter drives increased therapeutic protein secretion into the CSF

Combined overexpression of ATXN1L and mutant ATXN1 knockdown by AAV rescue motor phenotypes and gene signatures in SCA1 mice

Using Interprofessional Simulation with Telehealth to Enhance Teamwork and Communication in Home Care

Techniques for Intracranial Stereotaxic Injections of Adeno‐Associated Viral Vectors in Adult Mice

Altered Purkinje cell miRNA expression and SCA1 pathogenesis

Adeno‐Associated Virus Production, Purification, and Titering

Recent Advances in RNA Interference Therapeutics for CNS Diseases

Haplotyping SNPs for allele-specific gene editing of the expanded huntingtin allele using long-read sequencing

Use of Care Guides to Reduce Emergency Department Visits by High-Frequency Utilizers

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