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Phenotypic effects of maternal immune activation and early postnatal milieu in mice mutant for the schizophrenia risk gene neuregulin-1

Neuroscience, 2014-09, Vol.277, p.294-305

2014

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Schizophrenia-related endophenotypes in heterozygous neuregulin-1 'knockout' mice

The European journal of neuroscience, 2010-01, Vol.31 (2), p.349-358

2010

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Phenotypic characterization of spatial cognition and social behavior in mice with ‘knockout’ of the schizophrenia risk gene neuregulin 1

Neuroscience, 2007-06, Vol.147 (1), p.18-27

2007

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Phenotypic characterization of cognition and social behavior in mice with heterozygous versus homozygous deletion of catechol- O -methyltransferase

Neuroscience, 2008-09, Vol.155 (4), p.1021-1029

2008

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Associations between single-nucleotide polymorphisms of ADIPOQ, serum adiponectin and increased type 2 diabetes mellitus risk in Bahraini individuals

Eastern Mediterranean health journal, 2016-11, Vol.22 (8), p.611-618

2016

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Disruption of thermal nociceptive behaviour in mice mutant for the schizophrenia-associated genes NRG1, COMT and DISC1

Brain research, 2010-08, Vol.1348, p.114-119

2010

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The role of human demographic history in determining the distribution and frequency of transferase-deficient galactosaemia mutations

Heredity, 2010-02, Vol.104 (2), p.148-154

2010

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P.3.b.010 Examination of nociceptive behaviour and stress reactivity in susceptibility gene mutant models of schizophrenia

European neuropsychopharmacology, 2010, Vol.20, p.S457-S458

2010

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Serial analysis of gene expression identifies putative metastasis-associated transcripts in colon tumour cell lines

British journal of cancer, 2000-09, Vol.83 (6), p.725-728

2000

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P.3.b.010 Structural brain abnormalities and altered sensitivity to psychotomimetic drugs in neuregulin-1 knockout mice

European neuropsychopharmacology, 2009, Vol.19, p.S508-S509

2009

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Phenotypic resolution of spontaneous and D1-like agonist-induced orofacial movement topographies in congenic dopamine D1A receptor knockout' mice

Neuropharmacology, 2002-04, Vol.42 (5), p.644-652

2002

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Replication error phenotype, clinicopathological variables, and patient outcome in Dukes' B stage II (T3,N0,M0) colorectal cancer

Gut, 2000-02, Vol.46 (2), p.200-204

2000

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Phenotypic resolution of spontaneous and D 1-like agonist-induced orofacial movement topographies in congenic dopamine D 1A receptor ‘knockout’ mice

Neuropharmacology, 2002-04, Vol.42 (5), p.644-652

2002

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Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA array hybridization

Oncogene, 2002-05, Vol.21 (20), p.3253-3257

2002

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Associations between single-nucleotide polymorphisms of ADIPOQ, serum adiponectin and increased type 2 diabetes mellitus risk in Bahraini individuals/Associations entre les polymorphismes mononucleotidiques du gene ADIPOQ, l'adiponectine serique et le risque accru de diabete de type 2 dans la population Bahreinienne

Eastern Mediterranean health journal, 2016-08, p.611

2016

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Sexually dimorphic changes in the exploratory and habituation profiles of heterozygous neuregulin-1 knockout mice

Neuroreport, 2006-01, Vol.17 (1), p.79-83

2006

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Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA array hybridization

Oncogene, 2002-05, Vol.21 (20), p.3253-3257

2002

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Exploratory and habituation phenotype of heterozygous and homozygous COMT knockout mice

Behavioural brain research, 2007-11, Vol.183 (2), p.236-239

2007

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Rapid detection of the R408W and I65T mutations in phenylketonuria by glycosylase mediated polymorphism detection

Human mutation, 2001-05, Vol.17 (5), p.432-432

2001

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Replication error phenotype in colorectal cancer

Gut, 2000-10, Vol.47 (4), p.597-598

JASS, J R

2000

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Ethological resolution of behavioural topography and D 1 ‐like versus D 2 ‐like agonist responses in congenic D 5 dopamine receptor mutants: Identification of D 5 :D 2 ‐like interactions

Synapse (New York, N.Y.), 2005-03, Vol.55 (4), p.201-211

2005

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Topographical evaluation of the phenotype of spontaneous behaviour in mice with targeted gene deletion of the D 1A dopamine receptor: paradoxical elevation of grooming syntax

Neuropharmacology, 1998-12, Vol.37 (12), p.1595-1602

1998

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Corrigendum to the Article Herpetological Diversity of Timor-Leste： Updates and a Review of Species Distributions by O＇Shea et aL （2015）

亚洲两栖爬行动物研究：英文版, 2015 (3), p.I0001-I0001

Hinrich Kaiser Kenneth A. Tighe Mark O＇ Shea

2015

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Genetic basis of transferase-deficient galactosaemia in Ireland and the population history of the Irish Travellers

European journal of human genetics : EJHG, 1999-07, Vol.7 (5), p.549-554

1999

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Topographical Assessment of Ethological and Dopamine Receptor Agonist-Induced Behavioral Phenotype in Mutants with Congenic DARPP-32 'Knockout'

Neuropsychopharmacology, 2003-12, Vol.28 (12), p.2055-2063

2003

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Phenotypic effects of maternal immune activation and early postnatal milieu in mice mutant for the schizophrenia risk gene neuregulin-1

Schizophrenia-related endophenotypes in heterozygous neuregulin-1 'knockout' mice

Phenotypic characterization of spatial cognition and social behavior in mice with ‘knockout’ of the schizophrenia risk gene neuregulin 1

Phenotypic characterization of cognition and social behavior in mice with heterozygous versus homozygous deletion of catechol- O -methyltransferase

Associations between single-nucleotide polymorphisms of ADIPOQ, serum adiponectin and increased type 2 diabetes mellitus risk in Bahraini individuals

Disruption of thermal nociceptive behaviour in mice mutant for the schizophrenia-associated genes NRG1, COMT and DISC1

The role of human demographic history in determining the distribution and frequency of transferase-deficient galactosaemia mutations

P.3.b.010 Examination of nociceptive behaviour and stress reactivity in susceptibility gene mutant models of schizophrenia

Serial analysis of gene expression identifies putative metastasis-associated transcripts in colon tumour cell lines

P.3.b.010 Structural brain abnormalities and altered sensitivity to psychotomimetic drugs in neuregulin-1 knockout mice

Phenotypic resolution of spontaneous and D1-like agonist-induced orofacial movement topographies in congenic dopamine D1A receptor knockout' mice

Replication error phenotype, clinicopathological variables, and patient outcome in Dukes' B stage II (T3,N0,M0) colorectal cancer

Phenotypic resolution of spontaneous and D 1-like agonist-induced orofacial movement topographies in congenic dopamine D 1A receptor ‘knockout’ mice

Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA array hybridization

Sexually dimorphic changes in the exploratory and habituation profiles of heterozygous neuregulin-1 knockout mice

Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA array hybridization

Exploratory and habituation phenotype of heterozygous and homozygous COMT knockout mice

Rapid detection of the R408W and I65T mutations in phenylketonuria by glycosylase mediated polymorphism detection

Replication error phenotype in colorectal cancer

Ethological resolution of behavioural topography and D 1 ‐like versus D 2 ‐like agonist responses in congenic D 5 dopamine receptor mutants: Identification of D 5 :D 2 ‐like interactions

Topographical evaluation of the phenotype of spontaneous behaviour in mice with targeted gene deletion of the D 1A dopamine receptor: paradoxical elevation of grooming syntax

Corrigendum to the Article Herpetological Diversity of Timor-Leste： Updates and a Review of Species Distributions by O＇Shea et aL （2015）

Genetic basis of transferase-deficient galactosaemia in Ireland and the population history of the Irish Travellers

Topographical Assessment of Ethological and Dopamine Receptor Agonist-Induced Behavioral Phenotype in Mutants with Congenic DARPP-32 'Knockout'

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