Standard

A standard model of Alzheimer's disease? / Walker, Lary C; Lynn, David G; Chernoff, Yury O.

в: Prion, Том 12, № 5-6, 02.11.2018, стр. 261-265.

Результаты исследований: Научные публикации в периодических изданияхкомментарий, выступлениеРецензирование

Harvard

Walker, LC, Lynn, DG & Chernoff, YO 2018, 'A standard model of Alzheimer's disease?', Prion, Том. 12, № 5-6, стр. 261-265. https://doi.org/10.1080/19336896.2018.1525256

APA

Walker, L. C., Lynn, D. G., & Chernoff, Y. O. (2018). A standard model of Alzheimer's disease? Prion, 12(5-6), 261-265. https://doi.org/10.1080/19336896.2018.1525256

Vancouver

Walker LC, Lynn DG, Chernoff YO. A standard model of Alzheimer's disease? Prion. 2018 Нояб. 2;12(5-6):261-265. https://doi.org/10.1080/19336896.2018.1525256

Author

Walker, Lary C ; Lynn, David G ; Chernoff, Yury O. / A standard model of Alzheimer's disease?. в: Prion. 2018 ; Том 12, № 5-6. стр. 261-265.

BibTeX

@article{6f92dd378f0840eaa5e736ed9857bc8b,
title = "A standard model of Alzheimer's disease?",
abstract = "The recent Research Framework proposed by the US National Institute on Aging and the Alzheimer's Association (NIA-AA) recommends that Alzheimer's disease be defined by its specific biology rather than by non-specific neurodegenerative and syndromal features. By affirming markers of abnormal Aβ and tau proteins as the essential pathobiological signature of Alzheimer's disease, the Framework tacitly reinforces the amyloid (Aβ) cascade as the leading theory of Alzheimer pathogenesis. In light of recent evidence that the cascade is driven by the misfolding and templated aggregation of Aβ and tau, we believe that an empirically grounded Standard Model of Alzheimer's pathogenesis is within reach. A Standard Model can clarify and consolidate existing information, contextualize risk factors and the complex disease phenotype, identify testable hypotheses for future research, and pave the most direct path to effective prevention and treatment.",
keywords = "Abeta, Alzheimer, aging, amyloid, dementia, neurodegeneration, prion, proteopathy, seeding, tau",
author = "Walker, {Lary C} and Lynn, {David G} and Chernoff, {Yury O}",
year = "2018",
month = nov,
day = "2",
doi = "10.1080/19336896.2018.1525256",
language = "English",
volume = "12",
pages = "261--265",
journal = "Prion",
issn = "1933-6896",
publisher = "Landes Bioscience",
number = "5-6",

}

RIS

TY - JOUR

T1 - A standard model of Alzheimer's disease?

AU - Walker, Lary C

AU - Lynn, David G

AU - Chernoff, Yury O

PY - 2018/11/2

Y1 - 2018/11/2

N2 - The recent Research Framework proposed by the US National Institute on Aging and the Alzheimer's Association (NIA-AA) recommends that Alzheimer's disease be defined by its specific biology rather than by non-specific neurodegenerative and syndromal features. By affirming markers of abnormal Aβ and tau proteins as the essential pathobiological signature of Alzheimer's disease, the Framework tacitly reinforces the amyloid (Aβ) cascade as the leading theory of Alzheimer pathogenesis. In light of recent evidence that the cascade is driven by the misfolding and templated aggregation of Aβ and tau, we believe that an empirically grounded Standard Model of Alzheimer's pathogenesis is within reach. A Standard Model can clarify and consolidate existing information, contextualize risk factors and the complex disease phenotype, identify testable hypotheses for future research, and pave the most direct path to effective prevention and treatment.

AB - The recent Research Framework proposed by the US National Institute on Aging and the Alzheimer's Association (NIA-AA) recommends that Alzheimer's disease be defined by its specific biology rather than by non-specific neurodegenerative and syndromal features. By affirming markers of abnormal Aβ and tau proteins as the essential pathobiological signature of Alzheimer's disease, the Framework tacitly reinforces the amyloid (Aβ) cascade as the leading theory of Alzheimer pathogenesis. In light of recent evidence that the cascade is driven by the misfolding and templated aggregation of Aβ and tau, we believe that an empirically grounded Standard Model of Alzheimer's pathogenesis is within reach. A Standard Model can clarify and consolidate existing information, contextualize risk factors and the complex disease phenotype, identify testable hypotheses for future research, and pave the most direct path to effective prevention and treatment.

KW - Abeta

KW - Alzheimer

KW - aging

KW - amyloid

KW - dementia

KW - neurodegeneration

KW - prion

KW - proteopathy

KW - seeding

KW - tau

UR - http://www.scopus.com/inward/record.url?scp=85054745803&partnerID=8YFLogxK

UR - http://www.mendeley.com/research/standard-model-alzheimers-disease

U2 - 10.1080/19336896.2018.1525256

DO - 10.1080/19336896.2018.1525256

M3 - Comment/debate

C2 - 30220236

VL - 12

SP - 261

EP - 265

JO - Prion

JF - Prion

SN - 1933-6896

IS - 5-6

ER -

ID: 36219963