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Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A

Science (American Association for the Advancement of Science), 1993-10, Vol.262 (5133), p.578-580

1993

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Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine

Science (American Association for the Advancement of Science), 1994-04, Vol.264 (5155), p.92-95

1994

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High‐resolution genetic mapping of mammalian motor activity levels in mice

Genes, brain and behavior, 2009-02, Vol.8 (1), p.13-22

2009

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X-linked borderline mental retardation with prominent behavioral disturbance : phenotype, genetic localization, and evidence for disturbed monoamine metabolism

American journal of human genetics, 1993-06, Vol.52 (6), p.1032-1039

1993

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Identification of a premature stop codon in the melanocyte-stimulating hormone receptor gene (MC1R) in Labrador and Golden retrievers with yellow coat colour

Animal genetics, 2000-06, Vol.31 (3), p.194-199

2000

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Structure and Variation of Three Canine Genes Involved in Serotonin Binding and Transport: The Serotonin Receptor 1A Gene (htr1A), Serotonin Receptor 2A Gene (htr2A), and Serotonin Transporter Gene (slc6A4)

The Journal of heredity, 2005, Vol.96 (7), p.786-796

2005

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Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

American journal of human genetics, 1996-01, Vol.58 (1), p.35-41

1996

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Evaluation of the Serotonergic Genes htr1A, htr1B, htr2A, and slc6A4 in Aggressive Behavior of Golden Retriever Dogs

Behavior genetics, 2008-01, Vol.38 (1), p.55-66

2008

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A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome

Annals of neurology, 1999-01, Vol.45 (1), p.130-133

1999

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Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriers

Animal genetics, 2005-12, Vol.36 (6), p.497-501

2005

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Evaluation of Canine COL4A3 and COL4A4 as Candidates for Familial Renal Disease in the Norwegian Elkhound

The Journal of heredity, 2005-11, Vol.96 (7), p.739-744

2005

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A novel VWF variant associated with type 2 von Willebrand disease in German Wirehaired Pointers and German Shorthaired Pointers

Animal genetics, 2017-08, Vol.48 (4), p.493-496

2017

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Duplication of the proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease

Neurology, 1998-06, Vol.50 (6), p.1749

1998

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A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch family

Human genetics, 1996-03, Vol.97 (3), p.337-339

1996

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Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia

American journal of human genetics, 1996-04, Vol.58 (4), p.703-711

1996

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Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene

American journal of human genetics, 1994-10, Vol.55 (4), p.648-652

1994

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Chicken single nucleotide polymorphism identification and selection for genetic mapping

Poultry science, 2004-12, Vol.83 (12), p.1925-1931

2004

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Genetic Mapping of the Copper Toxicosis Locus in Bedlington Terriers to Dog Chromosome 10, in a Region Syntenic to Human Chromosome Region 2p13–p16

Human molecular genetics, 1999-03, Vol.8 (3), p.501-507

1999

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Cloning, characterization, and physical mapping of the canine Prop-1 gene (PROP1): exclusion as a candidate for combined pituitary hormone deficiency in German shepherd dogs

Cytogenetics and cell genetics, 2000, Vol.88 (1-2), p.140

2000

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Mapping of rabbit microsatellite markers using chromosome-specific libraries

The Journal of heredity, 2003-03, Vol.94 (2), p.161-169

2003

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A radiation hybrid map of the X-chromosome of the dog (Canis familiaris)

Cytogenetic and genome research, 2002-01, Vol.98 (1), p.86-92

2002

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Non‐pruritic granuloma in Norwegian forest cats

Veterinary record, 2005-04, Vol.156 (18), p.575-577

2005

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Complete cDNA Sequence of Human Preceruloplasmin

Proceedings of the National Academy of Sciences - PNAS, 1986-07, Vol.83 (14), p.5086-5090

1986

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The canine sarcoglycan delta gene: BAC clone contig assembly, chromosome assignment and interrogation as a candidate gene for dilated cardiomyopathy in Dobermann dogs

Cytogenetic and genome research, 2005-01, Vol.111 (2), p.140-146

2005

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Phenotyping of aggressive behavior in golden retriever dogs with a questionnaire

Behavior genetics, 2006-11, Vol.36 (6), p.882-902

2006

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Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A

Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine

High‐resolution genetic mapping of mammalian motor activity levels in mice

X-linked borderline mental retardation with prominent behavioral disturbance : phenotype, genetic localization, and evidence for disturbed monoamine metabolism

Identification of a premature stop codon in the melanocyte-stimulating hormone receptor gene (MC1R) in Labrador and Golden retrievers with yellow coat colour

Structure and Variation of Three Canine Genes Involved in Serotonin Binding and Transport: The Serotonin Receptor 1A Gene (htr1A), Serotonin Receptor 2A Gene (htr2A), and Serotonin Transporter Gene (slc6A4)

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

Evaluation of the Serotonergic Genes htr1A, htr1B, htr2A, and slc6A4 in Aggressive Behavior of Golden Retriever Dogs

A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome

Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriers

Evaluation of Canine COL4A3 and COL4A4 as Candidates for Familial Renal Disease in the Norwegian Elkhound

A novel VWF variant associated with type 2 von Willebrand disease in German Wirehaired Pointers and German Shorthaired Pointers

Duplication of the proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease

A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch family

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia

Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene

Chicken single nucleotide polymorphism identification and selection for genetic mapping

Genetic Mapping of the Copper Toxicosis Locus in Bedlington Terriers to Dog Chromosome 10, in a Region Syntenic to Human Chromosome Region 2p13–p16

Cloning, characterization, and physical mapping of the canine Prop-1 gene (PROP1): exclusion as a candidate for combined pituitary hormone deficiency in German shepherd dogs

Mapping of rabbit microsatellite markers using chromosome-specific libraries

A radiation hybrid map of the X-chromosome of the dog (Canis familiaris)

Non‐pruritic granuloma in Norwegian forest cats

Complete cDNA Sequence of Human Preceruloplasmin

The canine sarcoglycan delta gene: BAC clone contig assembly, chromosome assignment and interrogation as a candidate gene for dilated cardiomyopathy in Dobermann dogs

Phenotyping of aggressive behavior in golden retriever dogs with a questionnaire

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