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Expression of receptors for insulin and leptin in the ventral tegmental area/substantia nigra (VTA/SN) of the rat

Brain research, 2003-02, Vol.964 (1), p.107-115

2003

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Adiposity signals and food reward: expanding the CNS roles of insulin and leptin

American journal of physiology. Regulatory, integrative and comparative physiology, 2003-04, Vol.284 (4), p.882-R892

Figlewicz, Dianne P

2003

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Effect of moderate intake of sweeteners on metabolic health in the rat

Physiology & behavior, 2009-12, Vol.98 (5), p.618-624

2009

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Effect of recurrent yohimbine on immediate and post-hoc behaviors, stress hormones, and energy homeostatic parameters

Physiology & behavior, 2014-04, Vol.129, p.186-193

2014

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Intraventricular Insulin and Leptin Reverse Place Preference Conditioned With High-Fat Diet in Rats

Behavioral neuroscience, 2004-06, Vol.118 (3), p.479-487

2004

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Aggregation of Mutant Cu/Zn Superoxide Dismutase Proteins in a Culture Model of ALS

Journal of neuropathology and experimental neurology, 1997-05, Vol.56 (5), p.523-530

1997

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Loss of islet sympathetic nerves and impairment of glucagon secretion in the NOD mouse: relationship to invasive insulitis

Diabetologia, 2009-12, Vol.52 (12), p.2602-2611

2009

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Paraoxonase gene polymorphisms and sporadic ALS

Neurology, 2006-09, Vol.67 (5), p.766

2006

Volltextzugriff (PDF)

Up‐Regulation of Protein Chaperones Preserves Viability of Cells Expressing Toxic Cu/Zn‐Superoxide Dismutase Mutants Associated with Amyotrophic Lateral Sclerosis

Journal of neurochemistry, 1999-02, Vol.72 (2), p.693-699

1999

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DD genotype of ACE gene is a risk factor for intracerebral hemorrhage

Neurology, 2004-07, Vol.63 (2), p.359

2004

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A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

Nature genetics, 2001-10, Vol.29 (2), p.166-173

2001

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Obesity, diabetes and the central nervous system

Diabetologia, 1998-08, Vol.41 (8), p.863-881

1998

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Leptin reverses sucrose-conditioned place preference in food-restricted rats

Physiology & behavior, 2001-05, Vol.73 (1), p.229-234

2001

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Intramuscular grafts of myoblasts genetically modified to secrete glial cell line-derived neurotrophic factor prevent motoneuron loss and disease progression in a mouse model of familial amyotrophic lateral sclerosis

Human gene therapy, 1999-07, Vol.10 (11), p.1853-1866

1999

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Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis

Human molecular genetics, 1994-10, Vol.3 (10), p.1757-1761

1994

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Insulin in the brain : a hormonal regulator of energy balance

Endocrine reviews, 1992-08, Vol.13 (3), p.387-414

1992

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Glutamate Potentiates the Toxicity of Mutant Cu/Zn-Superoxide Dismutase in Motor Neurons by Postsynaptic Calcium-Dependent Mechanisms

The Journal of neuroscience, 1998-12, Vol.18 (23), p.9673-9684

1998

Volltextzugriff (PDF)

Central insulin enhances sensitivity to cholecystokinin

Physiology & behavior, 1995-10, Vol.58 (4), p.755-760

1995

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PVN activation is suppressed by repeated hypoglycemia but not antecedent corticosterone in the rat

American journal of physiology. Regulatory, integrative and comparative physiology, 2001-11, Vol.281 (5), p.1426-R1436

2001

Volltextzugriff (PDF)

Spinobulbar muscular atrophy can mimic ALS: the importance of genetic testing in male patients with atypical ALS

Neurology, 1997-08, Vol.49 (2), p.568

1997

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Definitive molecular diagnosis of facioscapulohumeral dystrophy

Neurology, 1999-06, Vol.52 (9), p.1822

1999

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Intraventricular insulin decreases kappa opioid-mediated sucrose intake in rats

Peptides (New York, N.Y. : 1980), 2002-12, Vol.23 (12), p.2181-2187

2002

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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35

Nature genetics, 1994-07, Vol.7 (3), p.425-428

1994

Volltextzugriff (PDF)

FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients

Journal of medical genetics, 2004-11, Vol.41 (11), p.826-836

2004

Volltextzugriff (PDF)

Establishing a Canadian Registry of Patients with Amyotrophic Lateral Sclerosis

Canadian journal of neurological sciences, 2013-01, Vol.40 (1), p.29-35

2013

Volltextzugriff (PDF)

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Expression of receptors for insulin and leptin in the ventral tegmental area/substantia nigra (VTA/SN) of the rat

Adiposity signals and food reward: expanding the CNS roles of insulin and leptin

Effect of moderate intake of sweeteners on metabolic health in the rat

Effect of recurrent yohimbine on immediate and post-hoc behaviors, stress hormones, and energy homeostatic parameters

Intraventricular Insulin and Leptin Reverse Place Preference Conditioned With High-Fat Diet in Rats

Aggregation of Mutant Cu/Zn Superoxide Dismutase Proteins in a Culture Model of ALS

Loss of islet sympathetic nerves and impairment of glucagon secretion in the NOD mouse: relationship to invasive insulitis

Paraoxonase gene polymorphisms and sporadic ALS

Up‐Regulation of Protein Chaperones Preserves Viability of Cells Expressing Toxic Cu/Zn‐Superoxide Dismutase Mutants Associated with Amyotrophic Lateral Sclerosis

DD genotype of ACE gene is a risk factor for intracerebral hemorrhage

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

Obesity, diabetes and the central nervous system

Leptin reverses sucrose-conditioned place preference in food-restricted rats

Intramuscular grafts of myoblasts genetically modified to secrete glial cell line-derived neurotrophic factor prevent motoneuron loss and disease progression in a mouse model of familial amyotrophic lateral sclerosis

Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis

Insulin in the brain : a hormonal regulator of energy balance

Glutamate Potentiates the Toxicity of Mutant Cu/Zn-Superoxide Dismutase in Motor Neurons by Postsynaptic Calcium-Dependent Mechanisms

Central insulin enhances sensitivity to cholecystokinin

PVN activation is suppressed by repeated hypoglycemia but not antecedent corticosterone in the rat

Spinobulbar muscular atrophy can mimic ALS: the importance of genetic testing in male patients with atypical ALS

Definitive molecular diagnosis of facioscapulohumeral dystrophy

Intraventricular insulin decreases kappa opioid-mediated sucrose intake in rats

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35

FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients

Establishing a Canadian Registry of Patients with Amyotrophic Lateral Sclerosis

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