Published in Gene on April 05, 2006
Directional and balancing selection in human beta-defensins. BMC Evol Biol (2008) 1.09
Antimicrobial peptides and proteins of the horse--insights into a well-armed organism. Vet Res (2011) 0.86
The repertoire of equine intestinal alpha-defensins. BMC Genomics (2009) 0.81
A novel horse alpha-defensin: gene transcription, recombinant expression and characterization of the structure and function. Biochem J (2007) 0.81
Dynamics of mammalian chromosome evolution inferred from multispecies comparative maps. Science (2005) 5.47
A mutation in hairless dogs implicates FOXI3 in ectodermal development. Science (2008) 2.06
Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis. PLoS Genet (2013) 1.69
A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta. PLoS Genet (2009) 1.68
A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies. PLoS Genet (2012) 1.66
Candidate genes for physical performance in the horse. Vet J (2010) 1.44
Analysis of sequence variability of the bovine prion protein gene (PRNP) in German cattle breeds. Neurogenetics (2004) 1.43
Bovine prion protein gene (PRNP) promoter polymorphisms modulate PRNP expression and may be responsible for differences in bovine spongiform encephalopathy susceptibility. J Biol Chem (2005) 1.40
A genome-wide association study reveals loci influencing height and other conformation traits in horses. PLoS One (2012) 1.39
Evolutionary movement of centromeres in horse, donkey, and zebra. Genomics (2006) 1.34
Genome-wide analysis reveals selection for important traits in domestic horse breeds. PLoS Genet (2013) 1.26
Novel gene acquisition on carnivore Y chromosomes. PLoS Genet (2006) 1.23
Fine mapping of the polled locus to a 1-Mb region on bovine chromosome 1q12. Mamm Genome (2005) 1.20
Genetic diversity in the modern horse illustrated from genome-wide SNP data. PLoS One (2013) 1.18
Spongiform encephalopathy in a miniature zebu. Emerg Infect Dis (2006) 1.17
Influence of priors in Bayesian estimation of genetic parameters for multivariate threshold models using Gibbs sampling. Genet Sel Evol (2007) 1.16
Serial translocation by means of circular intermediates underlies colour sidedness in cattle. Nature (2012) 1.16
LUPA: a European initiative taking advantage of the canine genome architecture for unravelling complex disorders in both human and dogs. Vet J (2011) 1.15
LGI2 truncation causes a remitting focal epilepsy in dogs. PLoS Genet (2011) 1.14
PRNP promoter polymorphisms are associated with BSE susceptibility in Swiss and German cattle. BMC Genet (2007) 1.13
Identification of the bovine Arachnomelia mutation by massively parallel sequencing implicates sulfite oxidase (SUOX) in bone development. PLoS Genet (2010) 1.13
A high-resolution cat radiation hybrid and integrated FISH mapping resource for phylogenomic studies across Felidae. Genomics (2008) 1.13
Pyrosequencing of 16S rRNA genes in fecal samples reveals high diversity of hindgut microflora in horses and potential links to chronic laminitis. BMC Vet Res (2012) 1.11
Mutations in MITF and PAX3 cause "splashed white" and other white spotting phenotypes in horses. PLoS Genet (2012) 1.11
Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency. Gastroenterology (2008) 1.07
Osteogenesis imperfecta in dachshunds. Vet Rec (2013) 1.07
Congenital syndactyly in cattle: four novel mutations in the low density lipoprotein receptor-related protein 4 gene (LRP4). BMC Genet (2007) 1.06
European domestic horses originated in two holocene refugia. PLoS One (2011) 1.06
Natural killer cell receptors in the horse: evidence for the existence of multiple transcribed LY49 genes. Eur J Immunol (2004) 1.05
An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle. PLoS One (2011) 1.05
A single point mutation within the ED1 gene disrupts correct splicing at two different splice sites and leads to anhidrotic ectodermal dysplasia in cattle. J Mol Med (Berl) (2002) 1.04
Signaling of human ciliary neurotrophic factor (CNTF) revisited. The interleukin-6 receptor can serve as an alpha-receptor for CTNF. J Biol Chem (2003) 1.04
Gene discovery and comparative analysis of X-degenerate genes from the domestic cat Y chromosome. Genomics (2008) 1.04
Mapping quantitative trait loci for canine hip dysplasia in German Shepherd dogs. Mamm Genome (2007) 1.04
Molecular basis for the action of the collagen-specific chaperone Hsp47/SERPINH1 and its structure-specific client recognition. Proc Natl Acad Sci U S A (2012) 1.04
Expression levels of LCORL are associated with body size in horses. PLoS One (2013) 1.03
A human-horse comparative map based on equine BAC end sequences. Genomics (2006) 1.02
A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier. PLoS Genet (2011) 1.02
A genome-wide association study to detect QTL for commercially important traits in Swiss Large White boars. PLoS One (2013) 1.02
Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption. Hum Mutat (2006) 1.01
Allelic heterogeneity at the equine KIT locus in dominant white (W) horses. PLoS Genet (2007) 1.01
Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses. Brief Funct Genomics (2010) 1.00
Exceptional conservation of horse-human gene order on X chromosome revealed by high-resolution radiation hybrid mapping. Proc Natl Acad Sci U S A (2004) 1.00
Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families. Genomics (2005) 0.99
A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism. PLoS One (2013) 0.99
The mutation causing the black-and-tan pigmentation phenotype of Mangalitza pigs maps to the porcine ASIP locus but does not affect its coding sequence. Mamm Genome (2006) 0.98
Unusual vascular ring anomaly associated with a persistent right aortic arch and an aberrant left subclavian artery in German pinschers. Vet J (2010) 0.98
Congenital sensorineural deafness in dogs: a molecular genetic approach toward unravelling the responsible genes. Vet J (2005) 0.98
Hereditary ataxia in the Jack Russell Terrier--clinical and genetic investigations. J Vet Intern Med (2004) 0.97
Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease. Genomics (2008) 0.95
Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse. PLoS One (2013) 0.95
Biochemical typing of pathological prion protein in aging cattle with BSE. Virol J (2009) 0.94
Conservation of gene order between horse and human X chromosomes as evidenced through radiation hybrid mapping. Genomics (2002) 0.94
A detailed physical map of the horse Y chromosome. Proc Natl Acad Sci U S A (2004) 0.94
A noncoding melanophilin gene (MLPH) SNP at the splice donor of exon 1 represents a candidate causal mutation for coat color dilution in dogs. J Hered (2007) 0.93
Identification of quantitative trait loci (QTL) for canine hip dysplasia and canine elbow dysplasia in Bernese mountain dogs. PLoS One (2012) 0.93
Functional relevance of DNA polymorphisms within the promoter region of the prion protein gene and their association to BSE infection. FASEB J (2007) 0.92
A Single Nucleotide Polymorphism within the Interferon Gamma Receptor 2 Gene Perfectly Coincides with Polledness in Holstein Cattle. PLoS One (2013) 0.92
Two loci on chromosome 5 are associated with serum IgE levels in Labrador retrievers. PLoS One (2012) 0.92
A gene catalogue of the euchromatic male-specific region of the horse Y chromosome: comparison with human and other mammals. PLoS One (2011) 0.91
Stallion sperm transcriptome comprises functionally coherent coding and regulatory RNAs as revealed by microarray analysis and RNA-seq. PLoS One (2013) 0.91
A frameshift mutation within LAMC2 is responsible for Herlitz type junctional epidermolysis bullosa (HJEB) in black headed mutton sheep. PLoS One (2011) 0.91
A MITF mutation associated with a dominant white phenotype and bilateral deafness in German Fleckvieh cattle. PLoS One (2011) 0.89
FISH for mapping single copy genes. Methods Mol Biol (2008) 0.89
Analysis of copy number variants by three detection algorithms and their association with body size in horses. BMC Genomics (2013) 0.89
Polymorphisms within the canine MLPH gene are associated with dilute coat color in dogs. BMC Genet (2005) 0.89
X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle. Genet Sel Evol (2003) 0.89
Congenital hypotrichosis with anodontia in cattle: a genetic, clinical and histological analysis. Vet Dermatol (2002) 0.89
[Review of literature and results from test matings of East Friesian milk sheep affected with brachygnathia inferior]. Berl Munch Tierarztl Wochenschr (2008) 0.89
[Congenital cardiac anomalies (pentalogy of Fallot) in a two year old ram with brachygnathia inferior]. Berl Munch Tierarztl Wochenschr (2013) 0.88
A high-resolution physical map of equine homologs of HSA19 shows divergent evolution compared with other mammals. Mamm Genome (2005) 0.88
Arachnomelia in Brown Swiss cattle maps to chromosome 5. Mamm Genome (2008) 0.88
Expression of Foxi3 is regulated by ectodysplasin in skin appendage placodes. Dev Dyn (2013) 0.88
[Reproducibility of bovine neonatal pancytopenia (BNP) via the application of colostrum]. Berl Munch Tierarztl Wochenschr (2011) 0.87
Epidermolysis bullosa in German black headed mutton sheep. Berl Munch Tierarztl Wochenschr (2010) 0.87
A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption). PLoS One (2013) 0.86
A 4 Mb high resolution BAC contig on bovine chromosome 1q12 and comparative analysis with human chromosome 21q22. Comp Funct Genomics (2005) 0.86
Genetic and phenotypic trends in canine hip dysplasia in the German population of German shepherd dogs. Berl Munch Tierarztl Wochenschr (2008) 0.86
Multiple Loci are associated with dilated cardiomyopathy in Irish wolfhounds. PLoS One (2012) 0.85
No bull: upholding community standards in public sharing of biological datasets. Proc Natl Acad Sci U S A (2013) 0.85
Total RNA isolation from stallion sperm and testis biopsies. Theriogenology (2010) 0.85
Remarkable synteny conservation of melanocortin receptors in chicken, human, and other vertebrates. Genomics (2003) 0.85
Classification of diet-modulated gene signatures at the colon cancer initiation and progression stages. Dig Dis Sci (2011) 0.84