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1
5-HT release in nucleus accumbens rescues social deficits in mouse autism model
Springer US
Jessica J. Walsh & Daniel J. Christoffel & Boris D. Heifets & Gabriel A. Ben-Dor & Aslihan Selimbeyoglu & Lin W. Hung & Karl Deisseroth & Robert C. Malenka
mice
sert
interaction
sociability
chamber
assay
juvenile
16p11.2flx
eyfp
chr2
neurons
extended
quantification
stimulation
16p11.2
novel
activation
deletion
behaviours
expressing
deficits
mouse
preference
neuron
activity
optogenetic
experiments
springer
assays
ht1b
reserved
locomotion
vehicle
behaviour
proximity
dorsal
anova
brain
effects
schematic
terminals
behavioural
fibre
autism
nphr
terminal
tukey’s
raphe
s.e.m
session
年:
2018
語言:
english
文件:
PDF, 10.32 MB
你的標籤:
0
/
0
english, 2018
2
Multiple Autisms: Spectrums of Advocacy and Genomic Science
University of Minnesota Press
Jennifer S Singh
autism
genetics
genomic
scientists
scientific
parent
diagnosis
advocacy
diagnostic
autistic
genes
gene
agre
clinical
ssc
genome
disorder
genomics
spectrum
studies
funding
understanding
groups
citizenship
analysis
national
cnvs
complex
disorders
dsm
biological
speaks
agp
styles
diagnosed
specific
asperger’s
simons
range
technologies
biomedical
advocates
focus
journal
simplex
involved
researchers
network
expertise
individuals
年:
2016
語言:
english
文件:
PDF, 2.25 MB
你的標籤:
0
/
0
english, 2016
3
The Genetics of Obesity
Springer-Verlag New York
Struan F.A. Grant
,
(ed.)
obesity
fto
gene
association
bmi
variants
genet
studies
genome
loci
leptin
risk
gwas
receptor
increased
genes
mass
weight
childhood
diabetes
cnvs
syndrome
insulin
obese
mutations
mc4r
analysis
locus
onset
identified
individuals
protein
levels
severe
effects
mouse
mice
related
metabolic
traits
complex
adult
regulation
genetics
reported
heritability
function
deletion
analyses
population
年:
2014
語言:
english
文件:
PDF, 2.37 MB
你的標籤:
0
/
0
english, 2014
4
Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome
American College of Medical Genetics and Genomics
Cora M. Taylor & Brenda M. Finucane & Andres Moreno-De-Luca & Lauren K. Walsh & Christa Lese Martin & David H. Ledbetter
16p11.2
cnv
probands
duplication
scores
deletion
individuals
negative
background
shift
duplications
functioning
phenotypic
simons
srs
clinical
disorders
doi.org
effect
familial
npd
relatives
bmi
traits
analysis
cnvs
controls
deleterious
icc
inherited
vip
c.m.t
cognition
expressivity
genomic
outcomes
quantitative
recurrent
related
scale
significant
22q11.2
ascertained
autism
biparental
c.l.m
cognitive
d.h.l
deletions
fsiq
語言:
english
文件:
PDF, 619 KB
你的標籤:
0
/
4.5
english
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