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内部出版物
在“
Elsevier电子期刊
”中,
命中:
8
条,耗时:小于0.01 秒
1.
TYROBP
genetic variants in early-onset Alzheimer's disease
作者:
Cyril Pottier
a
;
Thomas A. Ravenscroft
a
;
Patricia H. Brown
a
;
NiCole A. Finch
a
;
Matt Baker
a
;
Meeia Parsons
a
;
Yan W. Asmann
b
;
Yingxue Ren
a
;
Elizabeth Christopher
a
;
Denise Levitch
a
;
Marka van Blitterswijk
a
;
Carlos Cruchaga
c
;
Dominique Campion
d
;
e
;
f
;
Gaë
;
l Nicolas
d
;
e
;
g
;
Anne-Claire Richard
d
;
e
;
Rita Guerreiro
h
;
Jose T. Bras
h
;
Stephan Zuchner
i
;
Michael A. Gonzalez
j
;
Guojun Bu
a
;
Steven Younkin
a
;
David S. Knopman
k
;
Keith A. Josephs
k
;
Joseph E. Parisi
k
;
Ronald C. Petersen
k
;
Nilü
;
fer Ertekin-Taner
a
;
l
;
Neill R. Graff-Radford
l
;
Bradley F. Boeve
k
;
Dennis W. Dickson
a
;
Rosa Rademakers
a
;
Rademakers.rosa@mayo.edu" class="auth_mail" title="E-mail the corresponding author
关键词:
Alzheimer's disease
;
TYROBP
;
TREM2
;
Exome sequencing
;
Burden test
刊名:Neurobiology of Aging
出版年:2016
2.
The triggering receptor expressed on myeloid cells 2 (TREM2) is associated with enhanced inflammation, neuropathological lesions and increased risk for Alzheimer's dementia
作者:
Panos Roussos
a
;
b
;
c
;
1
;
Pavel Katsel
a
;
1
;
Peter Fam
d
;
Weilun Tan
a
;
Dushyant P. Purohit
a
;
e
;
Vahram Haroutunian
a
;
c
;
d
;
vahram.haroutunian@mssm.edu" class="auth_mail" title="E-mail the corresponding author
关键词:
Microglia
;
TYROBP
;
Mutation
;
Inflammation
;
Gene expression
;
Protein
刊名:Alzheimer's & Dementia
出版年:2015
3.
RNA-sequencing reveals transcriptional up-regulation of Trem2 in response to bexarotene treatment
作者:
Iliya Lefterov
a
;
iliyal@pitt.edu" class="auth_mail" title="E-mail the corresponding author
;
Jonathan Schug
b
;
c
;
Anais Mounier
a
;
Kyong Nyon Nam
a
;
Nicholas F. Fitz
a
;
Radosveta Koldamova
a
;
radak@pitt.edu" class="auth_mail" title="E-mail the corresponding author
关键词:
Alzheimer's disease
;
APP/PS1 transgenic mice
;
mRNA-seq
;
ChIP
;
RXR
;
Bexarotene
;
Trem2
;
Tyrobp
;
Aβ phagocytosis
刊名:Neurobiology of Disease
出版年:2015
4.
The C9ORF72 expansion does not affect the phenotype in Nasu-Hakola disease with the DAP12 mutation
作者:
Eino Solje
a
;
Pä
;
ivi Hartikainen
b
;
Miko Valori
c
;
Ritva Vanninen
d
;
e
;
Jari Tiihonen
f
;
g
;
h
;
Panu Hakola
g
;
Pentti J. Tienari
c
;
Anne M. Remes
a
;
b
;
anne.remes@uef.fi" class="auth_mail
关键词:
Polycystic lipomembranous osteodysplasia and sclerosing leukoencephalopathy
;
TYROBP
;
DAP12
;
TREM2
;
C9ORF72
;
Frontotemporal dementia
;
Epilepsy
刊名:Neurobiology of Aging
出版年:July, 2014
5.
Integrated Systems Approach Identifies Genetic Nodes and Networks in Late-Onset Alzheimer¡¯s Disease
作者:
Bin Zhang
1
;
2
;
3
;
4
;
14
;
bin.zhang@mssm.edu
;
Chris Gaiteri
4
;
14
;
Liviu-Gabriel Bodea
5
;
14
;
Zhi Wang
4
;
Joshua McElwee
6
;
Alexei A. Podtelezhnikov
7
;
Chunsheng Zhang
6
;
Tao Xie
6
;
Linh Tran
4
;
Radu Dobrin
6
;
Eugene Fluder
6
;
Bruce Clurman
8
;
Stacey Melquist
6
;
Manikandan Narayanan
6
;
Christine Suver
4
;
Hardik Shah
1
;
2
;
Milind Mahajan
1
;
2
;
3
;
Tammy Gillis
9
;
Jayalakshmi Mysore
9
;
Marcy E. MacDonald
9
;
John R. Lamb
10
;
David A. Bennett
11
;
Cliona Molony
6
;
David J. Stone
7
;
Vilmundur Gudnason
12
;
Amanda J. Myers
13
;
Eric E. Schadt
1
;
2
;
3
;
Harald Neumann
5
;
Jun Zhu
1
;
2
;
3
;
Valur Emilsson
12
;
valur@hjarta.is
刊名:Cell
出版年:2013
6.
Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy (PLOSL): A new report of an Italian woman and review of the literature
作者:
Veronika Bock
a
;
VeronikaBock@gmx.de
;
Andrea Botturi
a
;
Paola Gaviani
a
;
Elena Lamperti
a
;
Carmelo Maccagnano
b
;
Laura Piccio
c
;
Antonio Silvani
a
;
Andrea Salmaggi
a
;
salmaggi@istituto-besta.it
关键词:
PLOSL
;
Central nervous system diseases
;
Dementia
;
TREM
;
Nasu Hakola disease
;
Microglia
;
Bone
;
Fracture
;
Osteoclast
刊名:Journal of the Neurological Sciences
出版年:2013
7.
A novel compound heterozygous mutation in the DAP12 gene in a patient with Nasu-Hakola disease
关键词:
Compound heterozygote
;
DAP12
;
Loss of function mutations
;
TYROBP
;
Nasu-Hakola disease
刊名:Journal of the Neurological Sciences
出版年:2007
8.
Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype
作者:
Juha Paloneva
;
Tuula Manninen
;
Grant Christman
;
Karine Hovanes
;
Jami M
;
elin
;
Rolf Adolfsson
;
Marino Bianchin
;
Thomas Bird
;
Roxana Mir
a ;
Andrea Salmaggi
;
Lisbeth Tranebjæ
;
rg
;
Yrjö
;
Konttinen
;
Leena Peltonen
刊名:The American Journal of Human Genetics
出版年:2002
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