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No Evidence of the Ego-Depletion Effect across Task Characteristics and Individual Differences: A Pre-Registered Study

PloS one, 2016-02, Vol.11 (2), p.e0147770-e0147770

2016

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Less-structured time in children's daily lives predicts self-directed executive functioning

Frontiers in psychology, 2014-06, Vol.5, p.593-593

2014

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Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors

Development (Cambridge), 2010-06, Vol.137 (11), p.1907-1917

2010

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Identification of a ferrireductase required for efficient transferrin-dependent iron uptake in erythroid cells

Nature genetics, 2005-11, Vol.37 (11), p.1264-1269

2005

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Getting ready to use control: Advances in the measurement of young children's use of proactive control

PloS one, 2017-04, Vol.12 (4), p.e0175072-e0175072

2017

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Chemotactic action of prostaglandin E₂ on mouse mast cells acting via the PGE₂ receptor 3

Proceedings of the National Academy of Sciences - PNAS, 2007-07, Vol.104 (28), p.11712-11717

2007

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Time Isn't of the Essence: Activating Goals Rather Than Imposing Delays Improves Inhibitory Control in Children

Psychological science, 2015-12, Vol.26 (12), p.1898-1908

2015

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Resolution of airway inflammation and hyperreactivity after in vivo transfer of CD4+CD25+ regulatory T cells is interleukin 10 dependent

The Journal of experimental medicine, 2005-12, Vol.202 (11), p.1539-1547

2005

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nm1054: a spontaneous, recessive, hypochromic, microcytic anemia mutation in the mouse

Blood, 2005-11, Vol.106 (10), p.3625-3631

2005

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Gender and Academic Promotion to Full Professor in Ontario

Canadian journal of sociology, 2020-01, Vol.45 (1), p.47-70

2020

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Lower General Executive Function Is Primarily Associated with Trait Worry: A Latent Variable Analysis of Negative Thought/Affect Measures

Emotion (Washington, D.C.), 2020-06, Vol.20 (4), p.557-571

2020

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Mutations in a NIMA-Related Kinase Gene, Nek1, Cause Pleiotropic Effects including a Progressive Polycystic Kidney Disease in Mice

Proceedings of the National Academy of Sciences - PNAS, 2000-01, Vol.97 (1), p.217-221

2000

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Reactive oxygen species mediate endothelium-dependent relaxations in tetrahydrobiopterin-deficient mice

Arteriosclerosis, thrombosis, and vascular biology, 2001-04, Vol.21 (4), p.496-502

2001

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Developing Self-Directed Executive Functioning: Recent Findings and Future Directions

Mind, brain and education, 2015-06, Vol.9 (2), p.92-99

2015

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Inducible nitric oxide synthase (iNOS) activity promotes ischaemic skin flap survival

British journal of pharmacology, 2001-04, Vol.132 (8), p.1631-1638

2001

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Reversal of pathology in murine mucopolysaccharidosis type VII by somatic cell gene transfer

Nature (London), 1992-12, Vol.360 (6406), p.749-753

1992

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Genetic Modifiers of Polycystic Kidney Disease in Intersubspecific KAT2J Mutants

Genomics (San Diego, Calif.), 1999-06, Vol.58 (2), p.129-137

1999

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T time

Haematologica (Roma), 2005-10, Vol.90 (10), p.1303A-1303A

Barker, Jane E

2005

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Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis

Blood, 2001-01, Vol.97 (2), p.543-550

2001

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Nitric oxide-mediated mitochondrial damage: A potential neuroprotective role for glutathione

Free radical biology & medicine, 1996, Vol.21 (7), p.995-1001

1996

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Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins

The Journal of pathology, 2004-11, Vol.204 (4), p.450-459

2004

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Donor cell expansion is delayed following nonablative in utero transplantation to treat murine mucopolysaccharidosis type VII

Experimental hematology, 2003-11, Vol.31 (11), p.1112-1118

2003

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Increased erythrocyte adhesion in mice and humans with hereditary spherocytosis and hereditary elliptocytosis

Blood, 2004-01, Vol.103 (2), p.710-716

2004

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Nitric oxide synthase II gene disruption : Implications for tumor growth and vascular endothelial growth factor production

Cancer research (Chicago, Ill.), 2001-04, Vol.61 (7), p.3182-3187

2001

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Enzyme replacement in murine mucopolysaccharidosis type VII : Neuronal and glial response to β-glucuronidase requires early initiation of enzyme replacement therapy

Pediatric research, 1999-06, Vol.45 (6), p.838-844

1999

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No Evidence of the Ego-Depletion Effect across Task Characteristics and Individual Differences: A Pre-Registered Study

Less-structured time in children's daily lives predicts self-directed executive functioning

Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors

Identification of a ferrireductase required for efficient transferrin-dependent iron uptake in erythroid cells

Getting ready to use control: Advances in the measurement of young children's use of proactive control

Chemotactic action of prostaglandin E₂ on mouse mast cells acting via the PGE₂ receptor 3

Time Isn't of the Essence: Activating Goals Rather Than Imposing Delays Improves Inhibitory Control in Children

Resolution of airway inflammation and hyperreactivity after in vivo transfer of CD4+CD25+ regulatory T cells is interleukin 10 dependent

nm1054: a spontaneous, recessive, hypochromic, microcytic anemia mutation in the mouse

Gender and Academic Promotion to Full Professor in Ontario

Lower General Executive Function Is Primarily Associated with Trait Worry: A Latent Variable Analysis of Negative Thought/Affect Measures

Mutations in a NIMA-Related Kinase Gene, Nek1, Cause Pleiotropic Effects including a Progressive Polycystic Kidney Disease in Mice

Reactive oxygen species mediate endothelium-dependent relaxations in tetrahydrobiopterin-deficient mice

Developing Self-Directed Executive Functioning: Recent Findings and Future Directions

Inducible nitric oxide synthase (iNOS) activity promotes ischaemic skin flap survival

Reversal of pathology in murine mucopolysaccharidosis type VII by somatic cell gene transfer

Genetic Modifiers of Polycystic Kidney Disease in Intersubspecific KAT2J Mutants

T time

Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis

Nitric oxide-mediated mitochondrial damage: A potential neuroprotective role for glutathione

Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins

Donor cell expansion is delayed following nonablative in utero transplantation to treat murine mucopolysaccharidosis type VII

Increased erythrocyte adhesion in mice and humans with hereditary spherocytosis and hereditary elliptocytosis

Nitric oxide synthase II gene disruption : Implications for tumor growth and vascular endothelial growth factor production

Enzyme replacement in murine mucopolysaccharidosis type VII : Neuronal and glial response to β-glucuronidase requires early initiation of enzyme replacement therapy

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