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Cardiac resynchronisation therapy in paediatric and congenital heart disease: differential effects in various anatomical and functional substrates

Heart (British Cardiac Society), 2009-07, Vol.95 (14), p.1165-1171

2009

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Daytime spikes in dopaminergic activity drive rapid mood-cycling in mice

Molecular psychiatry, 2015-11, Vol.20 (11), p.1406-1419

2015

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High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease

Journal of medical genetics, 2008-11, Vol.45 (11), p.704-709

2008

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Relationship between cumulative anthracycline dose and late cardiotoxicity in childhood acute lymphoblastic leukemia

Journal of clinical oncology, 1998-02, Vol.16 (2), p.545-550

1998

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Daytime spikes in dopaminergic activity drive rapid mood-cycling in mice

Molecular psychiatry, 2015-11, Vol.20 (11), p.1479-1480

2015

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Selective cognitive deficits and reduced hippocampal brain-derived neurotrophic factor mRNA expression in small-conductance calcium-activated K+ channel deficient mice

Neuroscience, 2009-09, Vol.163 (1), p.73-81

2009

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Deficient serotonin neurotransmission and depression-like serotonin biomarker alterations in tryptophan hydroxylase 2 (Tph2) loss-of-function mice

Molecular psychiatry, 2012-07, Vol.17 (7), p.694-704

2012

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Evidence for a Multivalent Interaction of Symmetrical, N-Linked, Lidocaine Dimers with Voltage-Gated Na+ Channels

Molecular pharmacology, 2006-03, Vol.69 (3), p.921-931

2006

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Precursor-Directed Biosynthesis of Erythromycin Analogs by an Engineered Polyketide Synthase

Science (American Association for the Advancement of Science), 1997-07, Vol.277 (5324), p.367-369

1997

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SK3 K+ channel‐deficient mice have enhanced dopamine and serotonin release and altered emotional behaviors

Genes, brain and behavior, 2008-11, Vol.7 (8), p.836-848

2008

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The effects of congenital brain serotonin deficiency on responses to chronic fluoxetine

Translational psychiatry, 2013-08, Vol.3 (8), p.e291-e291

2013

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Differential psychostimulant-induced activation of neural circuits in dopamine transporter knockout and wild type mice

Neuroscience, 2003-01, Vol.118 (2), p.297-310

2003

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Monoaminergic dysregulation in glutathione-deficient mice: Possible relevance to schizophrenia?

Neuroscience, 2005, Vol.132 (4), p.1055-1072

2005

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TOLERANCE AND SPECIFICITY OF POLYKETIDE SYNTHASES

Annual review of biochemistry, 1999-01, Vol.68 (1), p.219-253

1999

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Is the arterial switch operation still a challenge in small centers?

European journal of cardio-thoracic surgery, 1997-04, Vol.11 (4), p.682-686

1997

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A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome

Clinica chimica acta, 1999-02, Vol.280 (1), p.113-125

1999

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Antibody Catalysis of Peptide Bond Formation

Proceedings of the National Academy of Sciences - PNAS, 1994-06, Vol.91 (13), p.5888-5892

1994

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An Efficient Antibody-Catalyzed Aminoacylation Reaction

Science (American Association for the Advancement of Science), 1992-04, Vol.256 (5055), p.365-367

1992

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Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2

Clinical genetics, 2000-02, Vol.57 (2), p.125-130

2000

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One-Stage Repair of Truncus Arteriosus, CAVC, and TAPVC

The Annals of thoracic surgery, 1997-06, Vol.63 (6), p.1781-1783

1997

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ACUTE MYELOBLASTIC LEUKAEMIA AND t(8;21) TRANSLOCATION

British journal of haematology, 1984-07, Vol.57 (3), p.539-540

1984

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Erratum: Daytime spikes in dopaminergic activity drive rapid mood-cycling in mice

Molecular psychiatry, 2015-11, Vol.20 (11), p.1479-1480

2015

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Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRPI ion channel: Implications for acquired and congenital long Q-T syndrome

Clinical chemistry (Baltimore, Md.), 2001-08, Vol.47 (8), p.1390-1395

2001

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Mutations in the HERG K +-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

The American journal of cardiology, 2005-02, Vol.95 (3), p.433-434

2005

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Double-homograft Repair of Truncus Arteriosus with Severe Truncal Valve Dysfunction

Scandinavian cardiovascular journal : SCJ, 1997, Vol.31 (4), p.245-247

1997

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Cardiac resynchronisation therapy in paediatric and congenital heart disease: differential effects in various anatomical and functional substrates

Daytime spikes in dopaminergic activity drive rapid mood-cycling in mice

High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease

Relationship between cumulative anthracycline dose and late cardiotoxicity in childhood acute lymphoblastic leukemia

Daytime spikes in dopaminergic activity drive rapid mood-cycling in mice

Selective cognitive deficits and reduced hippocampal brain-derived neurotrophic factor mRNA expression in small-conductance calcium-activated K+ channel deficient mice

Deficient serotonin neurotransmission and depression-like serotonin biomarker alterations in tryptophan hydroxylase 2 (Tph2) loss-of-function mice

Evidence for a Multivalent Interaction of Symmetrical, N-Linked, Lidocaine Dimers with Voltage-Gated Na+ Channels

Precursor-Directed Biosynthesis of Erythromycin Analogs by an Engineered Polyketide Synthase

SK3 K+ channel‐deficient mice have enhanced dopamine and serotonin release and altered emotional behaviors

The effects of congenital brain serotonin deficiency on responses to chronic fluoxetine

Differential psychostimulant-induced activation of neural circuits in dopamine transporter knockout and wild type mice

Monoaminergic dysregulation in glutathione-deficient mice: Possible relevance to schizophrenia?

TOLERANCE AND SPECIFICITY OF POLYKETIDE SYNTHASES

Is the arterial switch operation still a challenge in small centers?

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome

Antibody Catalysis of Peptide Bond Formation

An Efficient Antibody-Catalyzed Aminoacylation Reaction

Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2

One-Stage Repair of Truncus Arteriosus, CAVC, and TAPVC

ACUTE MYELOBLASTIC LEUKAEMIA AND t(8;21) TRANSLOCATION

Erratum: Daytime spikes in dopaminergic activity drive rapid mood-cycling in mice

Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRPI ion channel: Implications for acquired and congenital long Q-T syndrome

Mutations in the HERG K +-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

Double-homograft Repair of Truncus Arteriosus with Severe Truncal Valve Dysfunction

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