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。Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence
Gabe Haller et al.
HUMAN MOLECULAR GENETICS (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)
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)
The PSEN1, p.E318G Variant Increases the Risk of Alzheimer's Disease in APOE-ε4 Carriers
Bruno A. Benitez et al.
PLOS GENETICS (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)
Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence
Gabe Haller et al.
HUMAN MOLECULAR GENETICS (2012)
Cerebrospinal fluid APOE levels: an endophenotype for genetic studies for Alzheimers disease
Carlos Cruchaga et al.
HUMAN MOLECULAR GENETICS (2012)
A mutation in APP protects against Alzheimer's disease and age-related cognitive decline
Thorlakur Jonsson et al.
NATURE (2012)
Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families
Carlos Cruchaga et al.
PLOS ONE (2012)
Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American cohort
Sheng Chih Jin et al.
ALZHEIMERS RESEARCH & THERAPY (2012)
Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
Michael C. Wu et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Nasu-Hakola disease with a splicing mutation of TREM2 in a Japanese family
Y. Numasawa et al.
EUROPEAN JOURNAL OF NEUROLOGY (2011)
High-throughput discovery of rare insertions and deletions in large cohorts
Francesco L. M. Vallania et al.
GENOME RESEARCH (2010)
Identification of soluble TREM-2 in the cerebrospinal fluid and its association with multiple sclerosis and CNS inflammation
Laura Piccio et al.
BRAIN (2008)
TREM2 is upregulated in amyloid plaque-associated microglia in aged APP23 transgenic mice
Stefanie Frank et al.
GLIA (2008)
Mutations in TREM2 Lead to Pure Early-Onset Dementia Without Bone Cysts
Eliane Chouery et al.
HUMAN MUTATION (2008)
Metalloproteinases shed TREM-1 ectodomain from lipopolysaccharide-stimulated human monocytes
Vanesa Gomez-Pina et al.
JOURNAL OF IMMUNOLOGY (2007)
PLINK: A tool set for whole-genome association and population-based linkage analyses
Shaun Purcell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
TREM2-transduced myeloid precursors mediate nervous tissue debris clearance and facilitate recovery in an animal model of multiple sclerosis
Kazuya Takahashi et al.
PLOS MEDICINE (2007)
Essential role of the microglial triggering receptor expressed on myeloid cells-2 (TREM2) for central nervous tissue immune homeostasis
Harald Neumann et al.
JOURNAL OF NEUROIMMUNOLOGY (2007)
Cutting edge: TREM-2 attenuates macrophage activation
Isaiah R. Turnbull et al.
JOURNAL OF IMMUNOLOGY (2006)
Principal components analysis corrects for stratification in genome-wide association studies
Alkes L. Price et al.
NATURE GENETICS (2006)
The structure of the extracellular domain of triggering receptor expressed on myeloid cells like transcript-1 and evidence for a naturally occurring soluble fragment
JL Gattis et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
The genetic causes of basal ganglia calcification, dementia, and bone cysts DAP12 and TREM2
HH Klünemann et al.
NEUROLOGY (2005)
Distribution and signaling of TREM2/DAP12, the receptor system mutated in human polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy dementia
G Sessa et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2004)
DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features
J Paloneva et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2003)
Heterogeneous expression of the triggering receptor expressed on myeloid cells-2 on adult murine microglia
CD Schmid et al.
JOURNAL OF NEUROCHEMISTRY (2002)
A DAP12-mediated pathway regulates expression of CC chemokine receptor 7 and maturation of human dendritic cells
A Bouchon et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2001)
Cutting edge: Inflammatory responses can be triggered by TREM-1, a novel receptor expressed on neutrophils and monocytes
A Bouchon et al.
JOURNAL OF IMMUNOLOGY (2000)