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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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Absolute quantification reveals the stable transmission of a high copy number variant linked to autoinflammatory disease

BMC genomics, 2016-04, Vol.17 (289), p.299-299, Article 299

2016

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Genome‐wide SNP association-based localization of a dwarfism gene in Friesian dwarf horses

Animal genetics, 2010-12, Vol.41 (s2), p.2-7

2010

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Heritabilities of copper-accumulating traits in Labrador retrievers

Animal genetics, 2008-08, Vol.39 (4), p.454-454

2008

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Severe combined immunodeficiency in Frisian Water Dogs caused by a RAG1 mutation

Genes and immunity, 2011-06, Vol.12 (4), p.310-313

2011

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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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Expression and mutation analysis of Tpit in the canine pituitary gland and corticotroph adenomas

Domestic animal endocrinology, 2008-04, Vol.34 (3), p.217-222

2008

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Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene

American journal of human genetics, 2000-11, Vol.67 (5), p.1306-1308

2000

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Clinical and genetic heterogeneity in megalencephalic leukoencephalopathy with subcortical cysts (MLC)

Neuropediatrics, 2003-08, Vol.34 (4), p.215-218

2003

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A novel susceptibility locus for Hirschsprung’s disease maps to 4q31.3–q32.3

Journal of medical genetics, 2006-07, Vol.43 (7), p.e35-e35

2006

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The leukemia inhibitory factor receptor gene is not involved in the etiology of pituitary dwarfism in German shepherd dogs

Research in veterinary science, 2006-12, Vol.81 (3), p.316-320

2006

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Inherited Congenital Extrahepatic Portosystemic Shunts in Cairn Terriers

Journal of veterinary internal medicine, 2005-05, Vol.19 (3), p.321

2005

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The Gene for Leukoencephalopathy with Vanishing White Matter Is Located on Chromosome 3q27

American journal of human genetics, 1999-09, Vol.65 (3), p.728-734

1999

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Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter

Nature genetics, 2001-12, Vol.29 (4), p.383-388

2001

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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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Analysis of the inheritance of white spotting and the evaluation of KIT and EDNRB as spotting loci in Dutch boxer dogs

The Journal of heredity, 2004-11, Vol.95 (6), p.526-531

2004

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Mutations of MLC1 ( KIAA0027), Encoding a Putative Membrane Protein, Cause Megalencephalic Leukoencephalopathy with Subcortical Cysts

American journal of human genetics, 2001-04, Vol.68 (4), p.831-838

2001

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Analysis of DNA methylation of the 5′ region of the deoxycytidine kinase gene in CCRF-CEM-sensitive and cladribine (CdA)- and 2-chloro-2′-arabino-fluoro-2′-deoxyadenosine (CAFdA)-resistant cells

Cancer letters, 1998-08, Vol.130 (1), p.169-174

1998

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The Fanconi Anemia Group E Gene, FANCE, Maps to Chromosome 6p

American journal of human genetics, 1999-05, Vol.64 (5), p.1400-1405

1999

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Association of WKL1/MLC1 with catatonic schizophrenia

Molecular psychiatry, 2002-01, Vol.7 (10), p.1037; author reply 1037-1037

2002

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A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia

American journal of human genetics, 2003-01, Vol.72 (1), p.191-199

2003

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Thorough investigation of a canine autoinflammatory disease (AID) confirms one main risk locus and suggests a modifier locus for amyloidosis

PloS one, 2013-10, Vol.8 (10), p.e75242-e75242

2013

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DNA methylation patterns in the calcitonin gene region at first diagnosis and at relapse of acute lymphoblastic leukemia (ALL)

Leukemia, 1997-07, Vol.11 (7), p.971-978

1997

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Evaluation of 15 Candidate Genes for Dilated Cardiomyopathy in the Newfoundland Dog

The Journal of heredity, 2008-01, Vol.99 (1), p.73-80

2008

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Inhibition of DNA methylation in malignant MOLT F4 lymphoblasts by 6-mercaptopurine

Clinical chemistry (Baltimore, Md.), 1998-03, Vol.44 (3), p.556-559

1998

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Phenotyping of aggressive behavior in golden retriever dogs with a questionnaire

Absolute quantification reveals the stable transmission of a high copy number variant linked to autoinflammatory disease

Genome‐wide SNP association-based localization of a dwarfism gene in Friesian dwarf horses

Heritabilities of copper-accumulating traits in Labrador retrievers

Severe combined immunodeficiency in Frisian Water Dogs caused by a RAG1 mutation

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)

Expression and mutation analysis of Tpit in the canine pituitary gland and corticotroph adenomas

Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene

Clinical and genetic heterogeneity in megalencephalic leukoencephalopathy with subcortical cysts (MLC)

A novel susceptibility locus for Hirschsprung’s disease maps to 4q31.3–q32.3

The leukemia inhibitory factor receptor gene is not involved in the etiology of pituitary dwarfism in German shepherd dogs

Inherited Congenital Extrahepatic Portosystemic Shunts in Cairn Terriers

The Gene for Leukoencephalopathy with Vanishing White Matter Is Located on Chromosome 3q27

Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter

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

Analysis of the inheritance of white spotting and the evaluation of KIT and EDNRB as spotting loci in Dutch boxer dogs

Mutations of MLC1 ( KIAA0027), Encoding a Putative Membrane Protein, Cause Megalencephalic Leukoencephalopathy with Subcortical Cysts

Analysis of DNA methylation of the 5′ region of the deoxycytidine kinase gene in CCRF-CEM-sensitive and cladribine (CdA)- and 2-chloro-2′-arabino-fluoro-2′-deoxyadenosine (CAFdA)-resistant cells

The Fanconi Anemia Group E Gene, FANCE, Maps to Chromosome 6p

Association of WKL1/MLC1 with catatonic schizophrenia

A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia

Thorough investigation of a canine autoinflammatory disease (AID) confirms one main risk locus and suggests a modifier locus for amyloidosis

DNA methylation patterns in the calcitonin gene region at first diagnosis and at relapse of acute lymphoblastic leukemia (ALL)

Evaluation of 15 Candidate Genes for Dilated Cardiomyopathy in the Newfoundland Dog

Inhibition of DNA methylation in malignant MOLT F4 lymphoblasts by 6-mercaptopurine

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