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Transglutaminase 1-deficient recessive lamellar ichthyosis associated with a LINE-1 insertion in Jack Russell terrier dogs

British journal of dermatology (1951), 2009-08, Vol.161 (2), p.265-272

2009

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Selective Intestinal Cobalamin Malabsorption with Proteinuria (Imerslund‐Gräsbeck Syndrome) in Juvenile Beagles

Journal of veterinary internal medicine, 2014-03, Vol.28 (2), p.356-362

2014

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SCID in Jack Russell Terriers: A New Animal Model of DNA-PKcs Deficiency

The Journal of immunology (1950), 2001-08, Vol.167 (4), p.2142-2150

2001

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The long and the short of it: evidence that FGF5 is a major determinant of canine 'hair'-itability

Animal genetics, 2006-08, Vol.37 (4), p.309-315

2006

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Inducible nitric oxide expression in equine articular chondrocytes: effects of antiinflammatory compounds

Osteoarthritis and cartilage, 2002-01, Vol.10 (1), p.5-12

2002

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Congenital ureteral ectopia in continent and incontinent-related Entlebucher Mountain Dogs: 13 cases (2006-2009)

Journal of veterinary internal medicine, 2010-09, Vol.24 (5), p.1055-1062

2010

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Molecular Basis of Human Carbonic Anhydrase II Deficiency

Proceedings of the National Academy of Sciences - PNAS, 1992-03, Vol.89 (5), p.1804-1808

1992

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A von Willebrand's factor genomic nucleotide variant and polymerase chain reaction diagnostic test associated with inheritable type-2 von Willebrand's disease in a line of german shorthaired pointer dogs

Veterinary pathology, 2004-05, Vol.41 (3), p.221-228

2004

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N-Ethyl-N-nitrosourea-Induced Null Mutation at the Mouse Car-2 Locus: An Animal Model for Human Carbonic Anhydrase II Deficiency Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1988-03, Vol.85 (6), p.1962-1966

1988

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Within-breed heterozygosity of canine single nucleotide polymorphisms identified by across-breed comparison

Animal genetics, 2002-12, Vol.33 (6), p.464-467

2002

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Carbonic anhydrase II deficiency : single-base deletion in Exon 7 is the predominant mutation in Caribbean hispanic patients

American journal of human genetics, 1994-04, Vol.54 (4), p.602-608

1994

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DNA sequence and physical mapping of the canine transglutaminase 1 gene

Cytogenetic and genome research, 2001-01, Vol.93 (1-2), p.73-76

2001

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Comparative mapping of genes flanking the human chromosome 12 evolutionary breakpoint in the pig

Cytogenetic and Genome Research, 2003-01, Vol.102 (1-4), p.139-144

2003

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Polymorphism identification within 50 equine gene-specific sequence tagged sites

Animal genetics, 2001-04, Vol.32 (2), p.78-88

2001

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Expression of toll-like receptor 2 mRNA in bronchial epithelial cells is not induced in RAO-affected horses

Equine veterinary journal, 2009, Vol.41 (1), p.76-81

2009

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Mapping of the FES and FURIN genes to porcine chromosome 7

Animal genetics, 2004-04, Vol.35 (2), p.142-143

2004

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Nucleotide sequence of human liver carbonic anhydrase II cDNA

Nucleic acids research, 1987-06, Vol.15 (11), p.4687-4687

1987

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A PCR‐RSP Csp6I site in the canine DLA‐DQA1 gene

Animal genetics, 1999-02, Vol.30 (1), p.67-67

1999

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MspI RSP in exon 42 of the canine von Willebrand factor (VWF) gene

Animal genetics, 1999-06, Vol.30 (3), p.229-229

1999

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Digging up the canine genome – a tale to wag about

Cytogenetic and Genome Research, 2003-01, Vol.102 (1-4), p.244-248

2003

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AIRS-PCR for the canine DLA-DQA1 F141L polymorphism

Animal genetics, 1998-12, Vol.29 (6), p.475-475

1998

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Mucin genes in horse airways: MUC5AC, but not MUC2, may play a role in recurrent airway obstruction

Equine veterinary journal, 2003-05, Vol.35 (3), p.252-257

2003

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Localization of the mitochondrial carbonic anhydrase V gene, Car5, on mouse chromosome 8

Mammalian genome, 1997-03, Vol.8 (3), p.225-226

1997

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Characterization of the human gene for a newly discovered carbonic anhydrase, CA VII, and its localization to chromosome 16

Genomics (San Diego, Calif.), 1991-12, Vol.11 (4), p.835-848

1991

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Chromosomal assignment of seven genes on canine chromosomes by fluorescence in situ hybridization

Mammalian genome, 1996-04, Vol.7 (4), p.268-270, Article 268

1996

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Transglutaminase 1-deficient recessive lamellar ichthyosis associated with a LINE-1 insertion in Jack Russell terrier dogs

Selective Intestinal Cobalamin Malabsorption with Proteinuria (Imerslund‐Gräsbeck Syndrome) in Juvenile Beagles

SCID in Jack Russell Terriers: A New Animal Model of DNA-PKcs Deficiency

The long and the short of it: evidence that FGF5 is a major determinant of canine 'hair'-itability

Inducible nitric oxide expression in equine articular chondrocytes: effects of antiinflammatory compounds

Congenital ureteral ectopia in continent and incontinent-related Entlebucher Mountain Dogs: 13 cases (2006-2009)

Molecular Basis of Human Carbonic Anhydrase II Deficiency

A von Willebrand's factor genomic nucleotide variant and polymerase chain reaction diagnostic test associated with inheritable type-2 von Willebrand's disease in a line of german shorthaired pointer dogs

N-Ethyl-N-nitrosourea-Induced Null Mutation at the Mouse Car-2 Locus: An Animal Model for Human Carbonic Anhydrase II Deficiency Syndrome

Within-breed heterozygosity of canine single nucleotide polymorphisms identified by across-breed comparison

Carbonic anhydrase II deficiency : single-base deletion in Exon 7 is the predominant mutation in Caribbean hispanic patients

DNA sequence and physical mapping of the canine transglutaminase 1 gene

Comparative mapping of genes flanking the human chromosome 12 evolutionary breakpoint in the pig

Polymorphism identification within 50 equine gene-specific sequence tagged sites

Expression of toll-like receptor 2 mRNA in bronchial epithelial cells is not induced in RAO-affected horses

Mapping of the FES and FURIN genes to porcine chromosome 7

Nucleotide sequence of human liver carbonic anhydrase II cDNA

A PCR‐RSP Csp6I site in the canine DLA‐DQA1 gene

MspI RSP in exon 42 of the canine von Willebrand factor (VWF) gene

Digging up the canine genome – a tale to wag about

AIRS-PCR for the canine DLA-DQA1 F141L polymorphism

Mucin genes in horse airways: MUC5AC, but not MUC2, may play a role in recurrent airway obstruction

Localization of the mitochondrial carbonic anhydrase V gene, Car5, on mouse chromosome 8

Characterization of the human gene for a newly discovered carbonic anhydrase, CA VII, and its localization to chromosome 16

Chromosomal assignment of seven genes on canine chromosomes by fluorescence in situ hybridization

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