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1
Behavioural phenotyping assays for mouse models of autism
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Behavioural phenotyping assays for mouse models of autism

Nature reviews. Neuroscience, 2010-07, Vol.11 (7), p.490-502 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2010 Nature Publishing Group ;Copyright Nature Publishing Group Jul 2010 ;2010 Macmillan Publishers Limited. All rights reserved 2010 ;ISSN: 1471-003X ;EISSN: 1471-0048 ;DOI: 10.1038/nrn2851 ;PMID: 20559336

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2
Molecular mechanisms of memory reconsolidation
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Molecular mechanisms of memory reconsolidation

Nature reviews. Neuroscience, 2007-04, Vol.8 (4), p.262-275 [Peer Reviewed Journal]

2007 INIST-CNRS ;COPYRIGHT 2007 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2007 ;ISSN: 1471-003X ;ISSN: 1471-0048 ;EISSN: 1471-0048 ;DOI: 10.1038/nrn2090 ;PMID: 17342174

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3
The honeybee as a model for understanding the basis of cognition
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The honeybee as a model for understanding the basis of cognition

Nature reviews. Neuroscience, 2012-11, Vol.13 (11), p.758-768 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Nov 2012 ;ISSN: 1471-003X ;EISSN: 1471-0048 ;DOI: 10.1038/nrn3357 ;PMID: 23080415

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4
Prenatal screening for Down syndrome: a survey of willingness in women and family physicians to engage in shared decision-making
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Prenatal screening for Down syndrome: a survey of willingness in women and family physicians to engage in shared decision-making

Prenatal diagnosis, 2011-04, Vol.31 (4), p.319-326 [Peer Reviewed Journal]

Copyright © 2011 John Wiley & Sons, Ltd. ;2015 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2624 ;PMID: 21268046 ;CODEN: PRDIDM

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5
Separated at birth? The functional and molecular divergence of OLIG1 and OLIG2
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Article
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Separated at birth? The functional and molecular divergence of OLIG1 and OLIG2

Nature reviews. Neuroscience, 2012-12, Vol.13 (12), p.819-831 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Dec 2012 ;ISSN: 1471-003X ;EISSN: 1471-0048 ;DOI: 10.1038/nrn3386 ;PMID: 23165259

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6
A pilot open label, single dose trial of fenobam in adults with fragile X syndrome
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Article
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A pilot open label, single dose trial of fenobam in adults with fragile X syndrome

Journal of medical genetics, 2009-04, Vol.46 (4), p.266-271 [Peer Reviewed Journal]

Berry-Kravis et al 2009 ;2009 INIST-CNRS ;Copyright: 2009 (c) Berry-Kravis et al 2009 ;Berry-Kravis et al 2009 2009 ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.2008.063701 ;PMID: 19126569 ;CODEN: JMDGAE

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7
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
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Article
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Individual common variants exert weak effects on the risk for autism spectrum disorderspi

Human molecular genetics, 2012-11, Vol.21 (21), p.4781-4792 [Peer Reviewed Journal]

2015 INIST-CNRS ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/dds301

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8
High fat diet increases hippocampal oxidative stress and cognitive impairment in aged mice: implications for decreased Nrf2 signaling
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High fat diet increases hippocampal oxidative stress and cognitive impairment in aged mice: implications for decreased Nrf2 signaling

Journal of neurochemistry, 2010-09, Vol.114 (6), p.1581-1589 [Peer Reviewed Journal]

2010 The Authors. Journal Compilation © 2010 International Society for Neurochemistry ;2015 INIST-CNRS ;2010 The Authors. Journal Compilation © 2010 International Society for Neurochemistry. ;Journal compilation © 2010 International Society for Neurochemistry ;ISSN: 0022-3042 ;EISSN: 1471-4159 ;DOI: 10.1111/j.1471-4159.2010.06865.x ;PMID: 20557430 ;CODEN: JONRA9

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9
Parents' and children's communication about genetic risk: a qualitative study, learning from families' experiences
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Parents' and children's communication about genetic risk: a qualitative study, learning from families' experiences

European journal of human genetics : EJHG, 2011-06, Vol.19 (6), p.640-646 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Jun 2011 ;Distributed under a Creative Commons Attribution 4.0 International License ;Copyright © 2011 Macmillan Publishers Limited 2011 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2010.258 ;PMID: 21326287

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10
Structural Variation of Chromosomes in Autism Spectrum Disorder
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Structural Variation of Chromosomes in Autism Spectrum Disorder

American journal of human genetics, 2008-02, Vol.82 (2), p.477-488 [Peer Reviewed Journal]

2008 The American Society of Human Genetics ;2008 INIST-CNRS ;2008 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved.. 2008 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2007.12.009 ;PMID: 18252227 ;CODEN: AJHGAG

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11
The complexity of reproductive decision-making in asymptomatic carriers of the Huntington mutation
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The complexity of reproductive decision-making in asymptomatic carriers of the Huntington mutation

European journal of human genetics : EJHG, 2007-04, Vol.15 (4), p.453-462 [Peer Reviewed Journal]

2007 INIST-CNRS ;Copyright Nature Publishing Group Apr 2007 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5201774 ;PMID: 17245406

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12
Sorting of the Alzheimer's Disease Amyloid Precursor Protein Mediated by the AP-4 Complex
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Article
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Sorting of the Alzheimer's Disease Amyloid Precursor Protein Mediated by the AP-4 Complex

Developmental cell, 2010-03, Vol.18 (3), p.425-436 [Peer Reviewed Journal]

2010 Elsevier Inc. ;2015 INIST-CNRS ;Copyright 2010 Elsevier Inc. All rights reserved. ;ISSN: 1534-5807 ;EISSN: 1878-1551 ;DOI: 10.1016/j.devcel.2010.01.015 ;PMID: 20230749

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13
A prospective study on parental coping 4 months after termination of pregnancy for fetal anomalies
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Article
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A prospective study on parental coping 4 months after termination of pregnancy for fetal anomalies

Prenatal diagnosis, 2007-08, Vol.27 (8), p.709-716 [Peer Reviewed Journal]

Copyright © 2007 John Wiley & Sons, Ltd. ;2007 INIST-CNRS ;Copyright (c) 2007 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1763 ;PMID: 17533631 ;CODEN: PRDIDM

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14
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
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Article
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Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder

Human molecular genetics, 2011-12, Vol.20 (24), p.4786-4796 [Peer Reviewed Journal]

The Author 2011. Published by Oxford University Press 2011 ;2015 INIST-CNRS ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddr416 ;PMID: 21908516

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15
Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits
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Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits

Human molecular genetics, 2012-07, Vol.21 (14), p.3083-3096 [Peer Reviewed Journal]

2015 INIST-CNRS ;The Author 2012. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2012 ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/dds124 ;PMID: 22492990

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16
The genetics of panic disorder
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Article
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The genetics of panic disorder

Journal of Medical Genetics, 2011-06, Vol.48 (6), p.361-368 [Peer Reviewed Journal]

2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;2015 INIST-CNRS ;Copyright: 2011 (c) 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.2010.086876 ;PMID: 21493958 ;CODEN: JMDGAE

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17
Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study
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Article
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Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study

Clinical genetics, 2007-01, Vol.71 (1), p.35-42 [Peer Reviewed Journal]

2007 Blackwell Munksgaard ;2007 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.2007.00731.x ;PMID: 17204044 ;CODEN: CLGNAY

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18
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
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Article
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Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

American journal of human genetics, 2012-05, Vol.90 (5), p.847-855 [Peer Reviewed Journal]

2012 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press May 4, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.03.021 ;PMID: 22541559 ;CODEN: AJHGAG

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19
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
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Article
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Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

Nature genetics, 2008-09, Vol.40 (9), p.1056-1058 [Peer Reviewed Journal]

2008 INIST-CNRS ;COPYRIGHT 2008 Nature Publishing Group ;Copyright Nature Publishing Group Sep 2008 ;2008 Nature Publishing Group 2008 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.209 ;PMID: 18711365 ;CODEN: NGENEC

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20
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders
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Article
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Key role for gene dosage and synaptic homeostasis in autism spectrum disorders

Trends in genetics, 2010-08, Vol.26 (8), p.363-372 [Peer Reviewed Journal]

Attribution ;ISSN: 0168-9525 ;DOI: 10.1016/j.tig.2010.05.007 ;PMID: 20609491

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