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Elsevier电子期刊(13)
在“
Elsevier电子期刊
”中,
命中:
13
条,耗时:小于0.01 秒
在所有数据库中总计命中:
13
条
1.
Rare interstitial deletion of chromosome 2p11.2p12. Report of a new patient with developmental delay and unusual clinical features
作者:
Rosamaria Silipigni
a
;
rosamariasilipigni@gmail.com" class="auth_mail" title="E-mail the corresponding author
;
Elisa Cattaneo
b
;
Marco Baccarin
a
;
Monica Fumagalli
c
;
Maria Francesca Bedeschi
b
关键词:
Deletion 2p11.2p12
;
CGH array
;
Bilateral choanal atresia
;
Atrial septal defect
;
Developmental delay
;
Facial anomalies
;
CTNNA2
;
LRRTM1
;
REEP1
刊名:European Journal of Medical Genetics
出版年:2016
2.
The PSD protein ProSAP2/Shank3 displays synapto-nuclear shuttling which is deregulated in a schizophrenia-associated mutation
作者:
Stefanie Grabrucker
;
Christian Proepper
;
Katharina Mangus
;
Matti Eckert
;
Resham Chhabra
;
Michael J. Schmeisser
;
Tobias M. Boeckers
;
Andreas M. Grabrucker
关键词:
SCZ
;
Synapse
;
Shank3
;
hnRNP
;
Autism
;
PSD
;
Nuclear shuttling
;
LRRTM1
;
Synaptotagmin 1
刊名:Experimental Neurology
出版年:March, 2014
3.
LRRTM1
-deficient mice show a rare phenotype of avoiding small enclosures¡ªA tentative mouse model for claustrophobia-like behaviour
作者:
V. Voikar
a
;
c
;
1
;
vootele.voikar@gmail.com
;
N. Kulesskaya
a
;
c
;
1
;
T. Laakso
a
;
J. Lauren
d
;
S.M. Strittmatter
d
;
M.S. Airaksinen
a
;
b
;
matti.airaksinen@helsinki.fi
关键词:
Anxiety
;
Leucine-rich repeat
;
Neurexin
;
Species-typical behaviour
;
Social interaction
;
Claustrophobia
刊名:Behavioural Brain Research
出版年:2013
4.
Bidirectional transcription from human LRRTM2/CTNNA1 and
LRRTM1
/CTNNA2 gene loci leads to expression of N-terminally truncated CTNNA1 and CTNNA2 isoforms
作者:
Martin Kask
1
;
a
;
Priit Pruunsild
1
;
a
;
Tõ
;
nis Timmusk
;
a
;
tonis.timmusk@ttu.ee" rel="nofollow
关键词:
LRRTM family
;
CTNNA family
;
Alternative promoter
;
Schizophrenia
;
Handedness
刊名:Biochemical and Biophysical Research Communications
出版年:2011
5.
Bidirectional transcription from human LRRTM2/CTNNA1 and
LRRTM1
/CTNNA2 gene loci leads to expression of N-terminally truncated CTNNA1 and CTNNA2 isoforms
作者:
Martin Kask
1
;
a
;
Priit Pruunsild
1
;
a
;
Tõ
;
nis Timmusk
;
a
;
tonis.timmusk@ttu.ee"" rel=""nofollow
关键词:
LRRTM family
;
CTNNA family
;
Alternative promoter
;
Schizophrenia
;
Handedness
刊名:Biochemical and Biophysical Research Communications
出版年:2011
6.
Predicting protein-protein interactions in the post synaptic density
作者:
Ossnat Bar-shira
;
Gal Chechik
关键词:
Classification
;
Computational biology
;
Network reconstruction
;
Postsynaptic density
;
Protein&ndash
;
protein interactions
刊名:Molecular and Cellular Neuroscience
出版年:2013
7.
Leucine-Rich Repeat Transmembrane Proteins Are Essential for Maintenance of Long-Term Potentiation
作者:
Gilberto?J. Soler-Llavina
;
Pamela Arstikaitis
;
Wade Morishita
;
Mohiuddin Ahmad
;
Thomas?C. S¨¹dhof
;
Robert?C. Malenka
刊名:Neuron
出版年:2013
8.
Sequence analysis of CTNNA2 and
LRRTM1
for late-onset Alzheimer's disease in the Amish
作者:
Anna Cummings
;
Christian Shaffer
;
Lan Jiang
;
Renee Laux
;
Denise Fuzzell
;
Clare Knebusch
;
Lori Reinhart-Mercer
;
Laura Caywood
;
Charles Jackson
;
William Scott
;
Margaret Pericak-Vance
;
Jonathan Haines
刊名:Alzheimer's Dementia
出版年:2012
9.
Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12
作者:
Maria Santa Rocca
a
;
uisius@libero.it
;
Antonella Fabretto
a
;
Flavio Faletra
a
;
Ombretta Carlet
b
;
Aldo Skabar
a
;
Paolo Gasparini
a
;
Vanna Pecile
a
关键词:
SPG31
;
Spastic paraplegia 31
;
HSP
;
Hereditary Spastic Paraplegia
刊名:Gene
出版年:2012
10.
Executive dysfunction in novel environment and altered hippocampal synapse morphology in mice lacking
Lrrtm1
作者:
Noriko Takashima
1
;
Yuri Odaka
1
;
Kazuto Sakoori
1
;
Takumi Akagi
2
;
Tsutomu Hashikawa
2
;
Naoko Morimura
1
;
Kazuyuki Yamada
3
;
Jun Aruga
1
刊名:Neuroscience Research
出版年:2011
1
2
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