相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Coding variants in TREM2 increase risk for Alzheimer's disease
Sheng Chih Jin et al.
HUMAN MOLECULAR GENETICS (2014)
Triggering receptor expressed on myeloid cells 2 variants are rare in Parkinson's disease in a Han Chinese cohort
Shu-jun Feng et al.
NEUROBIOLOGY OF AGING (2014)
Triggering receptor expressed on myeloid cells 2 variant is rare in late-onset Alzheimer's disease in Han Chinese individuals
Jin-Tai Yu et al.
NEUROBIOLOGY OF AGING (2014)
Association study of TREM2 polymorphism rs75932628 with late-onset Alzheimer's disease in Chinese Han population
Jianfang Ma et al.
NEUROLOGICAL RESEARCH (2014)
TREM2 Variant p.R47H as a Risk Factor for Sporadic Amyotrophic Lateral Sclerosis
Janet Cady et al.
JAMA NEUROLOGY (2014)
TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease
Sruti Rayaprolu et al.
MOLECULAR NEURODEGENERATION (2013)
Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease
Margarita Giraldo et al.
NEUROBIOLOGY OF AGING (2013)
TREM2 is associated with the risk of Alzheimer's disease in Spanish population
Bruno A. Benitez et al.
NEUROBIOLOGY OF AGING (2013)
TREM2 and Neurodegenerative Disease
Christiane Reitz et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
Variant of TREM2 Associated with the Risk of Alzheimer's Disease
Thorlakur Jonsson et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
TREM2 Variants in Alzheimer's Disease
Rita Guerreiro et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
α-Synucleinopathy phenotypes
Heather McCann et al.
PARKINSONISM & RELATED DISORDERS (2013)
Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement
Rita Joao Guerreiro et al.
JAMA NEUROLOGY (2013)
Mutations in TREM2 Lead to Pure Early-Onset Dementia Without Bone Cysts
Eliane Chouery et al.
HUMAN MUTATION (2008)
Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype
J Paloneva et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
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