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Advanced Search Results For "Zane NW"

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 "Zane NW"
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Genomic prediction of switchgrass winter survivorship across diverse lowland populations.

Publication Type: Academic Journal

Source(s): G3 (Bethesda, Md.) [G3 (Bethesda)] 2023 Jan 17. Date of Electronic Publication: 2023 Jan 17.

Abstract: In the North-Central United States lowland ecotype switchgrass can increase yield by up to 50% compared to locally adapted but early-flowering cultivars. However, lowland ecotypes are not winter tolerant. The mechanism for winter damage is unknown but ...

Examining risk and protective predictors of substance use among low-income Native Hawaiian and Pacific Islander adolescents.

Publication Type: Academic Journal

Source(s): The American journal of orthopsychiatry [Am J Orthopsychiatry] 2022; Vol. 92 (1), pp. 18-24. Date of Electronic Publication: 2021 Sep 13.

Abstract: Substance use (SU) among adolescents is a critical public health concern that increases the risk for negative outcomes. Although Asian American (AA) adolescents tend to report low rates of SU, Native Hawaiian and Pacific Islander (NH/PI) adolescents of...

Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism.

Publication Type: Academic Journal

Source(s): Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2022 Jan; Vol. 37 (1), pp. 148-161. Date of Electronic Publication: 2021 Oct 08.

Abstract: Background: Complex parkinsonism is the commonest phenotype in late-onset PLA2G6-associated neurodegeneration.Objectives: The aim of this study was to deeply characterize phenogenotypically PLA2G6-related parkinsonism in the largest cohort ever reporte...

Epigenetic Small Molecules Rescue Nucleocytoplasmic Transport and DNA Damage Phenotypes in C9ORF72 ALS/FTD.

Publication Type: Academic Journal

Source(s): Brain sciences [Brain Sci] 2021 Nov 20; Vol. 11 (11). Date of Electronic Publication: 2021 Nov 20.

Abstract: Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurodegenerative disease with available treatments only marginally slowing progression or improving survival. A hexanucleotide repeat expansion mutation in the C9ORF72 gene is the most com...

Reducing mental health disparities by increasing the personal relevance of interventions.

Publication Type: Academic Journal

Source(s): The American psychologist [Am Psychol] 2021 Jan; Vol. 76 (1), pp. 91-103. Date of Electronic Publication: 2020 Mar 02.

Abstract: One of the most persistent health disparities is the underutilization of mental health services by people of color. Neither evidence-based treatments (universal focus) nor culturally adapted treatments (group focus) have reduced these disparities. We p...

Low Prevalence of NOTCH2NLC GGC Repeat Expansion in White Patients with Movement Disorders.

Publication Type: Academic Journal

Source(s): Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2021 Jan; Vol. 36 (1), pp. 251-255. Date of Electronic Publication: 2020 Oct 07.

Abstract: Background: The objective of this study was to determine the prevalence of the GGC-repeat expansion in NOTCH2NLC in whites presenting with movement disorders.Methods: We searched for the GGC-repeat expansion in NOTCH2NLC using repeat-primed polymerase ...

Neuronal intranuclear inclusion disease is genetically heterogeneous.

Publication Type: Academic Journal

Source(s): Annals of clinical and translational neurology [Ann Clin Transl Neurol] 2020 Sep; Vol. 7 (9), pp. 1716-1725. Date of Electronic Publication: 2020 Aug 10.

Abstract: Neuronal intranuclear inclusion disease (NIID) is a clinically heterogeneous neurodegenerative condition characterized by pathological intranuclear eosinophilic inclusions. A CGG repeat expansion in NOTCH2NLC was recently identified to be associated wi...

Dipeptide repeat proteins inhibit homology-directed DNA double strand break repair in C9ORF72 ALS/FTD.

Publication Type: Academic Journal

Source(s): Molecular neurodegeneration [Mol Neurodegener] 2020 Feb 24; Vol. 15 (1), pp. 13. Date of Electronic Publication: 2020 Feb 24.

Abstract: Background: The C9ORF72 hexanucleotide repeat expansion is the most common known genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), two fatal age-related neurodegenerative diseases. The C9ORF72 expansion encodes fiv...

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion.

Publication Type: Academic Journal

Source(s): Brain : a journal of neurology [Brain] 2020 Feb 01; Vol. 143 (2), pp. 480-490.

Abstract: Ataxia, causing imbalance, dizziness and falls, is a leading cause of neurological disability. We have recently identified a biallelic intronic AAGGG repeat expansion in replication factor complex subunit 1 (RFC1) as the cause of cerebellar ataxia, neu...

Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia.

Publication Type: Academic Journal

Source(s): Nature genetics [Nat Genet] 2019 May; Vol. 51 (5), pp. 920.

Abstract: In the version of this article initially published, the name of author Wai Yan Yau was misspelled. The error has been corrected in the HTML and PDF versions of the article.

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