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Lista de obras de Tosso Leeb

A 16-bp deletion in the canine PDK4 gene is not associated with dilated cardiomyopathy in a European cohort of Doberman Pinschers.

artículo científico publicado en 2012

A 4 Mb high resolution BAC contig on bovine chromosome 1q12 and comparative analysis with human chromosome 21q22

artículo científico publicado en 2005

A 4,103 marker integrated physical and comparative map of the horse genome.

artículo científico publicado en 2008

A <i>COL7A1</i> Variant in a Litter of Neonatal Basset Hounds with Dystrophic Epidermolysis Bullosa

scientific article published on 04 December 2020

A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism

artículo científico publicado en 2013

A DSG1 Frameshift Variant in a Rottweiler Dog with Footpad Hyperkeratosis

artículo científico publicado en 2020

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs

artículo científico publicado en 2017

A Genome-Wide Association Analysis in Noriker Horses Identifies a SNP Associated With Roan Coat Color

scientific article published on 05 February 2020

A Large Deletion in the NSDHL Gene in Labrador Retrievers with a Congenital Cornification Disorder.

artículo científico publicado en 2017

A Missense Variant Affecting the C-Terminal Tail of UNC93B1 in Dogs with Exfoliative Cutaneous Lupus Erythematosus (ECLE)

artículo científico publicado en 2020

A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1).

artículo científico publicado en 2016

A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy

artículo científico publicado en 2015

A Nonsense Variant in the ACADVL Gene in German Hunting Terrier Dogs with Exercise Induced Metabolic Myopathy

artículo científico publicado en 2018

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome.

scientific article published on 24 February 2017

A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities, and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1).

artículo científico publicado en 2015

A RAPGEF6 variant constitutes a major risk factor for laryngeal paralysis in dogs

artículo científico publicado en 2019

A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2).

artículo científico publicado en 2017

A SIX6 Nonsense Variant in Golden Retrievers with Congenital Eye Malformations

artículo científico publicado en 2019

A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype

artículo científico publicado en 2016

A TAC3 Missense Variant in a Domestic Shorthair Cat with Testicular Hypoplasia and Persistent Primary Dentition

artículo científico publicado en 2019

A breeding experiment confirms the dominant mode of inheritance of the brown coat colour associated with the (496) Asp TYRP1 allele in goats

artículo científico publicado en 2015

A comparative radiation hybrid map of sheep chromosome 10.

artículo científico publicado en 2008

A complex structural variant at the KIT locus in cattle with the Pinzgauer spotting pattern

scientific article published on 11 July 2019

A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves

artículo científico publicado en 2019

A de novo variant in the ASPRV1 gene in a dog with ichthyosis.

artículo científico publicado en 2017

A deletion spanning the promoter and first exon of the hair cycle-specific ASIP transcript isoform in black and tan rabbits

scientific article published on 15 November 2019

A duplication in the canine beta-galactosidase gene GLB1 causes exon skipping and GM1-gangliosidosis in Alaskan huskies

artículo científico publicado en 2005

A frameshift variant in the COL5A1 gene in a cat with Ehlers-Danlos syndrome

scientific article published on 23 September 2018

A frameshift variant in the EDA gene in Dachshunds with X-linked hypohidrotic ectodermal dysplasia

article

A genome-wide association study for equine recurrent airway obstruction in European Warmblood horses reveals a suggestive new quantitative trait locus on chromosome 13.

artículo científico publicado en 2017

A genome-wide association study reveals loci influencing height and other conformation traits in horses

artículo científico publicado en 2012

A genome-wide association study to detect QTL for commercially important traits in Swiss Large White boars

artículo científico publicado en 2013

A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies

artículo científico publicado en 2012

A high resolution physical and RH map of pig chromosome 6q1.2 and comparative analysis with human chromosome 19q13.1

artículo científico publicado en 2003

A high-resolution comparative RH map of the proximal part of bovine chromosome 1.

artículo científico publicado en 2002

A high-resolution comparative radiation hybrid map of equine chromosome 4q12-q22

scientific article published on 01 October 2006

A human-horse comparative map based on equine BAC end sequences

artículo científico publicado en 2006

A locus on chromosome 5 is associated with dilated cardiomyopathy in Doberman Pinschers

artículo científico publicado en 2011

A major facilitator superfamily domain 8 frameshift variant in a cat with suspected neuronal ceroid lipofuscinosis

artículo científico publicado en 2019

A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease

artículo científico publicado en 2015

A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta

artículo científico publicado en 2009

A missense variant in the NSDHL gene in a Chihuahua with a congenital cornification disorder resembling inflammatory linear verrucous epidermal nevi

scientific article published on 01 October 2019

A mola hydatidosa coexistent with a foetus in a bovine freemartin pregnancy

artículo científico publicado en 2003

A mutation in hairless dogs implicates FOXI3 in ectodermal development

artículo científico publicado en 2008

A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH)

artículo científico publicado en 2014

A non-coding regulatory variant in the 5'-region of the MITF gene is associated with white-spotted coat in Brown Swiss cattle

scientific article published on 02 December 2018

A noncoding melanophilin gene (MLPH) SNP at the splice donor of exon 1 represents a candidate causal mutation for coat color dilution in dogs

artículo científico publicado en 2007

A nonsense variant in the KRT14 gene in a domestic shorthair cat with epidermolysis bullosa simplex

artículo científico publicado en 2020

A novel KIT deletion variant in a German Riding Pony with white-spotting coat colour phenotype

scientific article published on 28 August 2019

A novel KIT variant in an Icelandic horse with white-spotted coat colour

artículo científico publicado en 2015

A polymorphism within the equine CRISP3 gene is associated with stallion fertility in Hanoverian warmblood horses

artículo científico publicado en 2007

A radiation hybrid map of sheep chromosome 23 based on ovine BAC-end sequences.

artículo científico publicado en 2007

A second KRT71 allele in curly coated dogs

scientific article published on 15 November 2018

A shared 336 kb haplotype associated with the belt pattern in three divergent cattle breeds

artículo científico publicado en 2009

A single base deletion in the SLC45A2 gene in a Bullmastiff with oculocutaneous albinism

artículo científico publicado en 2017

A single point mutation within the ED1 gene disrupts correct splicing at two different splice sites and leads to anhidrotic ectodermal dysplasia in cattle

scientific article published on 20 February 2002

A single position in the third transmembrane domains of the human B1 and B2 bradykinin receptors is adjacent to and discriminates between the C-terminal residues of subtype-selective ligands

scientific article published on 01 May 1998

A splice site variant in the SUV39H2 gene in Greyhounds with nasal parakeratosis

artículo científico publicado en 2018

A structural variant in the 5'-flanking region of the TWIST2 gene affects melanocyte development in belted cattle

artículo científico publicado en 2017

A variant in MYO10 is associated with hind limb conformation in Swiss Large White boars

artículo científico publicado en 2013

A whole-genome scan for recurrent airway obstruction in Warmblood sport horses indicates two positional candidate regions

artículo científico publicado en 2009

ATP2A2 SINE Insertion in an Irish Terrier with Darier Disease and Associated Infundibular Cyst Formation

artículo científico publicado en 2020

Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK)

artículo científico publicado en 2020

Albinism in the American mink (Neovison vison) is associated with a tyrosinase nonsense mutation

artículo científico publicado en 2008

Allele-specific polymerase chain reaction diagnostic test for the functional MDR1 polymorphism in dogs

artículo científico publicado en 2007

Allelic heterogeneity at the equine KIT locus in dominant white (W) horses

artículo científico publicado en 2007

An ABCA12 missense variant in a Shorthorn calf with ichthyosis fetalis

artículo científico publicado en 2019

An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome

scientific article published on 16 May 2019

An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs

artículo científico publicado en 2014

An Integrative miRNA-mRNA Expression Analysis Reveals Striking Transcriptomic Similarities between Severe Equine Asthma and Specific Asthma Endotypes in Humans

scientific article published on 28 September 2020

An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat Texture

artículo científico publicado en 2016

An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds

artículo científico publicado en 2008

An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle

artículo científico publicado en 2011

Analysis of blood clotting factor activities in canine Legg-Calvé-Perthes' disease

artículo científico publicado en 1999

Analysis of sequence variability of the bovine prion protein gene (PRNP) in German cattle breeds

artículo científico publicado en 2004

Analysis of the canine EDAR gene and exclusion as a candidate for the hairless phenotype in the Chinese Crested dog

artículo científico publicado en 2005

Ancient genomic changes associated with domestication of the horse

artículo científico publicado en 2017

Animal models of ectodermal dysplasia.

artículo científico publicado en 2012

Arachnomelia in Brown Swiss cattle maps to chromosome 5.

artículo científico publicado en 2008

Asian horses deepen the MSY phylogeny

artículo científico publicado en 2018

Assignment of the bovine TYK2 and PDE4A genes to bovine chromosome 7q15 by fluorescence in situ hybridization and radiation hybrid mapping.

artículo científico publicado en 2005

Assignment of the canine cadherin related 23 gene (CDH23) to chromosome 4q12-->q13 by fluorescence in situ hybridization and radiation hybrid mapping

artículo científico publicado en 2002

Assignment of the canine myosin Va gene (MYO5A) to chromosome 30q14 by fluorescence in situ hybridization and radiation hybrid mapping

artículo científico publicado en 2003

Assignment of the canine potassium voltage-gated channel, KQT-like subfamily, member 3 (KCNQ3) gene to CFA 13 by radiation hybrid mapping

artículo científico publicado en 2002

Assignment of the canine tectorin alpha gene (TECTA) to CFA5q12-->q13 by FISH and confirmation by radiation hybrid mapping

artículo científico publicado en 2002

Assignment of the equine S100A7 gene (psoriasin 1) to chromosome 5p12-->p13 by fluorescence in situ hybridization and radiation hybrid mapping

artículo científico publicado en 2005

Assignment of the porcine epidermal growth factor (EGF) gene to SSC8q2.3-q2.4 by fluorescence in situ hybridization and radiation hybrid mapping

artículo científico publicado en 2002

Association analysis of SNPs in the IL21R gene with recurrent airway obstruction (RAO) in Swiss Warmblood horses

artículo científico publicado en 2011

Association analysis of candidate SNPs in TRPM1 with leopard complex spotting (LP ) and congenital stationary night blindness (CSNB) in horses

article

Biochemical typing of pathological prion protein in aging cattle with BSE.

artículo científico publicado en 2009

Black hair follicular dysplasia in Large Münsterländer dogs: clinical, histological and ultrastructural features

artículo científico publicado en 2006

Bovine prion protein gene (PRNP) promoter polymorphisms modulate PRNP expression and may be responsible for differences in bovine spongiform encephalopathy susceptibility

scientific article published on 01 September 2005

Characterization and RH mapping of six gene-associated equine microsatellite markers

artículo científico publicado en 2006

Characterization and chromosome assignment of the porcine AHCY gene for S-adenosylhomocysteine hydrolase

artículo científico publicado en 2002

Characterization and linkage mapping of four gene-associated porcine microsatellites

artículo científico publicado en 2005

Characterization of the equine ITGAX gene and its association with recurrent airway obstruction in European Warmblood horses

artículo científico publicado en 2010

Christmas disease in a Hovawart family resembling human hemophilia B Leyden is caused by a single nucleotide deletion in a highly conserved transcription factor binding site of the F9 gene promoter

artículo científico publicado en 2019

Chromosomal assignment of 20 candidate genes for canine congenital sensorineural deafness by FISH and RH mapping

artículo científico publicado en 2003

Chromosomal assignment of five equine HTR genes by FISH and RH mapping

artículo científico publicado en 2007

Chromosomal assignment of the canine melanophilin gene (MLPH): a candidate gene for coat color dilution in Pinschers.

artículo científico publicado en 2005

Chromosomal assignment of the two candidate genes (EGFR, CLCA1) for equine recurrent airway obstruction (RAO) by FISH and RH mapping

scientific article published on 01 December 2006

Clinical and histological characterization of hair coat and glandular tissue of Chinese crested dogs

artículo científico publicado en 2013

Cloning and characterization of the mammalian-specific nicolin 1 gene (NICN1) encoding a nuclear 24 kDa protein

artículo científico publicado en 2002

Cloning and chromosomal localization of MYO15A to chromosome 5 of the dog (Canis familiaris).

artículo científico publicado en 2002

Comparative human-horse sequence analysis of the CYP3A subfamily gene cluster

scientific article published on 01 December 2010

Comparative human–mouse–rat sequence analysis of the ICAM gene cluster on HSA 19p13.2 and a 185-kb porcine region from SSC 2q

article

Comparative mapping of the canine diaphanous homologue 1 (Drosophila) gene (DIAPH1 ) to CFA2q23-q24.2.

artículo científico publicado en 2002

Comparison against 186 canid whole-genome sequences reveals survival strategies of an ancient clonally transmissible canine tumor

artículo científico publicado en 2015

Complex Structural PPT1 Variant Associated with Non-syndromic Canine Retinal Degeneration

scientific article published on 07 February 2019

Compound heterozygosity for TNXB genetic variants in a mixed-breed dog with Ehlers-Danlos syndrome

artículo científico publicado en 2019

Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency

artículo científico publicado en 2009

Comprehensive characterization of horse genome variation by whole-genome sequencing of 88 horses

artículo científico publicado en 2018

Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion

artículo científico publicado en 2015

Congenital hypotrichosis with anodontia in cattle: a genetic, clinical and histological analysis

artículo científico publicado en 2002

Congenital syndactyly in cattle: four novel mutations in the low density lipoprotein receptor-related protein 4 gene (LRP4)

artículo científico publicado en 2007

Construction of a 1.2-Mb BAC/PAC contig of the porcine gene RYR1 region on SSC 6q1.2 and comparative analysis with HSA 19q13.13.

artículo científico publicado en 2002

Cytogenetic localization of genetic markers on porcine chromosome 7q

artículo científico publicado en 1998

DNA testing in neurologic diseases

artículo científico publicado en 2014

Degenerative Axonopathy in a Tyrolean Grey Calf

article

Degenerative liver disease in young Beagles with hereditary cobalamin malabsorption because of a mutation in the cubilin gene

artículo científico publicado en 2014

Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds

artículo científico publicado en 2017

Dog colour patterns explained by modular promoters of ancient canid origin

artículo científico publicado en 2021

Ectodysplasin-1 deficiency in a German Holstein bull associated with loss of respiratory mucous glands and chronic rhinotracheitis

artículo científico publicado en 2005

Effective population size of an indigenous Swiss cattle breed estimated from linkage disequilibrium.

artículo científico publicado en 2010

Equine cytochrome P450 2B6--genomic identification, expression and functional characterization with ketamine

artículo científico publicado en 2012

Equine keratinocytes in the pathogenesis of insect bite hypersensitivity: Just another brick in the wall?

artículo científico publicado en 2022

Evaluation of the CTSL2 gene as a candidate gene for alopecia X in Pomeranians and Keeshonden

artículo científico publicado en 2007

Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse

artículo científico publicado en 2013

Evolution of the spermadhesin gene family

artículo científico publicado en 2005

Evolutionary Genomics and Conservation of the Endangered Przewalski's Horse

artículo científico publicado en 2015

Exclusion of adrenoceptor alpha 2 variants in a horse insensitive to medetomidine.

artículo científico publicado en 2018

Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses

article

Five novel KIT mutations in horses with white coat colour phenotypes.

artículo científico publicado en 2011

Fluorescent in situ hybridization mapping of the epidermal growth factor receptor gene in donkey

artículo científico publicado en 2007

Frame-shift variant in the CHRNE gene in a juvenile dog with suspected myasthenia gravis-like disease.

artículo científico publicado en 2017

Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland Ponies

artículo científico publicado en 2019

Functional relevance of DNA polymorphisms within the promoter region of the prion protein gene and their association to BSE infection

artículo científico publicado en 2007

Generation of a 5.5-Mb BAC/PAC contig of pig chromosome 6q1.2 and its integration with existing RH, genetic and comparative maps.

artículo científico publicado en 2003

Genetic analysis of white facial and leg markings in the Swiss Franches-Montagnes Horse Breed

artículo científico publicado en 2008

Genetic diversity in an indigenous horse breed: implications for mating strategies and the control of future inbreeding

artículo científico publicado en 2011

Genetic diversity in the modern horse illustrated from genome-wide SNP data

artículo científico publicado en 2013

Genetic evidence of subaortic stenosis in the Newfoundland dog.

artículo científico publicado en 2012

Genetic mapping of the belt pattern in Brown Swiss cattle to BTA3

artículo científico publicado en 2009

Genetic markers for stallion fertility--lessons from humans and mice

artículo científico publicado en 2005

Genetic testing in veterinary dermatology

artículo científico publicado en 2016

Genetic variability of the equine casein genes

artículo científico publicado en 2016

Genome sequence, comparative analysis, and population genetics of the domestic horse

artículo científico publicado en 2009

Genome-Wide Analyses Suggest Mechanisms Involving Early B-Cell Development in Canine IgA Deficiency

artículo científico publicado en 2015

Genome-Wide Association Studies Based on Equine Joint Angle Measurements Reveal New QTL Affecting the Conformation of Horses.

artículo científico publicado en 2019

Genome-wide analysis reveals selection for important traits in domestic horse breeds.

artículo científico publicado en 2013

Genome-wide association studies based on sequence-derived genotypes reveal new QTL associated with conformation and performance traits in the Franches-Montagnes horse breed

artículo científico publicado en 2016

Genome-wide association study and heritability estimate for ectopic ureters in Entlebucher mountain dogs

article

Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness

artículo científico publicado en 2019

Genomic organization of the dog dystroglycan gene DAG1 locus on chromosome 20q15.1-q15.2.

artículo científico publicado en 2000

Genomic organization of the murine aminomethyltransferase gene (Amt).

artículo científico publicado en 2002

Genomic organization of the porcine skeletal muscle ryanodine receptor (RYR1) gene coding region 4624 to 7929.

artículo científico publicado en 1993

Genomic structure and nucleotide polymorphisms of the porcine agouti signalling protein gene (ASIP)

scientific article published on 01 October 2000

Genomic structure of the 5' end of the porcine ryanodine receptor 3 gene (RYR3).

artículo científico publicado en 2000

Haematological parameters are normal in dominant white Franches-Montagnes horses carrying a KIT mutation

artículo científico publicado en 2009

IL26 gene inactivation in Equidae ⬇️

artículo científico publicado el 28 de junio de 2013

Identification of Two Independent COL5A1 Variants in Dogs with Ehlers-Danlos Syndrome

artículo científico publicado en 2019

Identification of a Missense Variant in MFSD12 Involved in Dilution of Phaeomelanin Leading to White or Cream Coat Color in Dogs

scientific article published on 21 May 2019

Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease.

artículo científico publicado en 2008

Identification of key contributors in complex population structures.

artículo científico publicado en 2017

Identification of the bovine Arachnomelia mutation by massively parallel sequencing implicates sulfite oxidase (SUOX) in bone development

artículo científico publicado en 2010

Impact of beta-galactosidase mutations on the expression of the canine lysosomal multienzyme complex

artículo científico publicado en 2009

In silico and in vitro analysis of genetic variants of the equine CYP3A94, CYP3A95 and CYP3A97 isoenzymes

artículo científico publicado en 2019

Insights into post-translational processing of beta-galactosidase in an animal model resembling late infantile human G-gangliosidosis

artículo científico publicado en 2007

Isolation and characterization of the porcine c-myc proto-oncogene and chromosomal assignment to SSC 4p13.

artículo científico publicado en 1999

LAMB3 Missense Variant in Australian Shepherd Dogs with Junctional Epidermolysis Bullosa

artículo científico publicado en 2020

LGI2 truncation causes a remitting focal epilepsy in dogs

artículo científico publicado en 2011

LUPA: a European initiative taking advantage of the canine genome architecture for unravelling complex disorders in both human and dogs

artículo científico publicado en 2011

MFSD8single-base pair deletion in a Chihuahua with neuronal ceroid lipofuscinosis

article published in 2016

MKLN1 splicing defect in dogs with lethal acrodermatitis.

artículo científico publicado en 2018

Mapping and microsatellite marker development for the porcine leukemia inhibitory factor receptor (LIFR) and epidermal growth factor receptor (EGFR) genes

artículo científico publicado en 2002

Mapping of the porcine urate oxidase and transforming growth factor beta 2 genes by fluorescence in situ hybridization

artículo científico publicado en 1996

Mitochondrial PCK2 Missense Variant in Shetland Sheepdogs with Paroxysmal Exercise-Induced Dyskinesia (PED)

artículo científico publicado en 2020

Molecular analysis of carbohydrate N-acetylgalactosamine 4-O sulfotransferase 8 (CHST8) as a candidate gene for bovine spongiform encephalopathy susceptibility

artículo científico publicado en 2009

Molecular analysis of the porcine proteolipid protein (PLP) gene

artículo científico publicado en 1999

Molecular characterization and SNP development for the porcine IL6 and IL10 genes.

artículo científico publicado en 2008

Molecular characterization and chromosomal assignment of the bovine glycinamide ribonucleotide formyltransferase (GART) gene on cattle chromosome 1q12.1-q12.2.

artículo científico publicado en 2005

Molecular characterization and chromosomal assignment of the canine protein C gene

artículo científico publicado en 1999

Molecular characterization of five porcine candidate genes for drip loss in pork

artículo científico publicado en 2010

Molecular characterization of the equine AEG1 locus

artículo científico publicado en 2002

Molecular characterization of the equine testis-specific protein 1 (TPX1) and acidic epididymal glycoprotein 2 (AEG2) genes encoding members of the cysteine-rich secretory protein (CRISP) family

artículo científico publicado en 2002

Molecular characterization of the porcine TYK2 gene on SSC 2q1.3-->q2.1.

artículo científico publicado en 2004

Molecular characterization of the porcine deleted in malignant brain tumors 1 gene (DMBT1).

artículo científico publicado en 2006

Molecular characterization of the porcine gene CAPNS1 encoding the small subunit 1 of calpain on SSC6q1.1-->q1.2.

artículo científico publicado en 2002

Molecular cloning and characterization of equine thymic stromal lymphopoietin.

artículo científico publicado en 2010

Molecular cloning and chromosomal assignment of the porcine 54 and 56 kDa vacuolar H(+)-ATPase subunit gene (V-ATPase).

artículo científico publicado en 1999

Molecular cloning of the porcine beta-1,2-N-acetylglucosaminyltransferase II gene and assignment to chromosome 1q23-q27.

artículo científico publicado en 1997

Molecular cloning, expression analysis and assignment of the porcine tumor necrosis factor superfamily member 10 gene (TNFSF10) to SSC13q34-->q36 by fluorescence in situ hybridization and radiation hybrid mapping

artículo científico publicado en 2005

Mosaic pattern of sucrase isomaltase deficiency in two brothers

artículo científico publicado en 2008

Multiple FGF4 Retrocopies Recently Derived within Canids

artículo científico publicado en 2020

Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd dogs

artículo científico publicado en 2016

Mutations in MITF and PAX3 cause "splashed white" and other white spotting phenotypes in horses

artículo científico publicado en 2012

Mutations within the FGF5 gene are associated with hair length in cats

artículo científico publicado en 2007

NHLRC1 dodecamer repeat expansion demonstrated by whole genome sequencing in a Chihuahua with Lafora disease

scientific article published on 07 December 2018

NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia

scientific article published on 03 September 2019

NSDHL Frameshift Deletion in a Mixed Breed Dog with Progressive Epidermal Nevi

artículo científico publicado en 2020

Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: intrafamilial overlap of phenotypes in patients with the same KRT14 frameshift variant

artículo científico publicado en 2019

Novel Brown Coat Color (Cocoa) in French Bulldogs Results from a Nonsense Variant in HPS3

scientific article published on 09 June 2020

Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X.

artículo científico publicado en 2017

Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption

artículo científico publicado en 2006

OCA2 splice site variant in German Spitz dogs with oculocutaneous albinism

artículo científico publicado en 2017

Osteogenesis imperfecta in two litters of dachshunds.

artículo científico publicado en 2003

PRNP promoter polymorphisms are associated with BSE susceptibility in Swiss and German cattle

artículo científico publicado en 2007

Partial deletion of the bovine ED1 gene causes anhidrotic ectodermal dysplasia in cattle

artículo científico publicado en 2001

Phenotypic Effects of FGF4 Retrogenes on Intervertebral Disc Disease in Dogs

scientific article published on 07 June 2019

Phylogeny of horse chromosome 5q in the genus Equus and centromere repositioning

artículo científico publicado en 2009

Polycystic kidneys and GM2 gangliosidosis-like disease in neonatal springboks (Antidorcas marsupialis).

artículo científico publicado en 2014

Polymorphic variants of the multidrug resistance gene Mdr1a and response to antiepileptic drug treatment in the kindling model of epilepsy

artículo científico

Polymorphisms in the ABCB1 gene in phenobarbital responsive and resistant idiopathic epileptic Border Collies

artículo científico publicado en 2011

Polymorphisms within the canine MLPH gene are associated with dilute coat color in dogs

artículo científico publicado en 2005

Rapid and accurate G M1-gangliosidosis diagnosis using a parentage testing microsatellite

artículo científico publicado en 2008

Regulation of tissue-specific expression of the skeletal muscle ryanodine receptor gene

artículo científico publicado en 1996

Replication and fine-mapping of a QTL for recurrent airway obstruction in European Warmblood horses

scientific article published on 26 January 2012

Role of the environment in the development of canine atopic dermatitis in Labrador and golden retrievers

artículo científico publicado en 2011

Selection signatures in Shetland ponies

artículo científico publicado en 2016

Selection signatures in goats reveal copy number variants underlying breed-defining coat color phenotypes

scientific article published on 16 December 2019

Sequence analysis of a 212 kb defensin gene cluster on ECA 27q17.

artículo científico publicado en 2006

Sequence analysis of the porcine IFNAR1 and IFNGR2 genes

artículo científico publicado en 2006

Serial translocation by means of circular intermediates underlies colour sidedness in cattle

artículo científico publicado en 2012

Seven novel KIT mutations in horses with white coat colour phenotypes.

artículo científico publicado en 2009

Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families.

artículo científico publicado en 2005

Sperm-binding fibronectin type II-module proteins are genetically linked and functionally related

artículo científico publicado en 2007

Spongiform encephalopathy in a miniature zebu

artículo científico publicado en 2006

Spontaneous human B2 bradykinin receptor activity determines the action of partial agonists as agonists or inverse agonists. Effect of basal desensitization

artículo científico publicado en 1999

Structural and functional analysis of the porcine secretory carrier membrane protein 1 gene (SCAMP1).

artículo científico publicado en 1998

Structure and function of secretory proteins of the male genital tract

artículo científico publicado en 2005

TSEN54 missense variant in Standard Schnauzers with leukodystrophy

artículo científico publicado en 2019

The LCORL Locus is under Selection in Large-Sized Pakistani Goat Breeds

scientific article published on 05 February 2020

The Spanish Riding School and the Haute Ecole of complex trait genetics ⬇️

artículo científico publicado el 30 de mayo de 2013

The bovine dilated cardiomyopathy locus maps to a 1.0-Mb interval on chromosome 18.

artículo científico publicado en 2009

The brown coat colour of Coppernecked goats is associated with a non-synonymous variant at the TYRP1 locus on chromosome 8.

artículo científico publicado en 2014

The canine FRDA gene maps to CFA 1q31.1-->q31.3.

artículo científico publicado en 2002

The horse Y chromosome as an informative marker for tracing sire lines

artículo científico publicado en 2019

The horse genome project--sequence based insights into male reproductive mechanisms

artículo científico publicado en 2007

The interleukin 4 receptor gene and its role in recurrent airway obstruction in Swiss Warmblood horses

artículo científico publicado en 2011

The locus for bovine dilated cardiomyopathy maps to chromosome 18

artículo científico publicado en 2007

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

artículo científico publicado en 2006

The role of stallion seminal proteins in fertilisation.

artículo científico publicado en 2005

The sixth transmembrane domains of the human B1 and B2 bradykinin receptors are structurally compatible and involved in discriminating between subtype-selective agonists

artículo científico publicado en 1997

Total IgE and allergen-specific IgE and IgG antibody levels in sera of atopic dermatitis affected and non-affected Labrador- and Golden retrievers

artículo científico publicado en 2012

Tracking the origins of Yakutian horses and the genetic basis for their fast adaptation to subarctic environments

artículo científico publicado en 2015

Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis

scientific article published on 04 August 2020

Two MC1R loss-of-function alleles in cream-coloured Australian Cattle Dogs and white Huskies

artículo científico publicado en 2018

Two highly polymorphic microsatellites between the canine DAG1 and BSN genes on CFA20q15.1-15.2.

scientific article published on 01 October 2000

Two loci on chromosome 5 are associated with serum IgE levels in Labrador retrievers

artículo científico publicado en 2012

Two variants in the KIT gene as candidate causative mutations for a dominant white and a white spotting phenotype in the donkey.

artículo científico publicado en 2015

Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs

artículo científico publicado en 2020

Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration.

artículo científico publicado en 2019

Whole genome sequencing confirms KIT insertions in a white cat.

artículo científico publicado en 2014

Whole genome sequencing reveals a novel deletion variant in the KIT gene in horses with white spotted coat colour phenotypes

artículo científico publicado en 2017

Whole-Genome Sequencing of a Canine Family Trio Reveals a FAM83G Variant Associated with Hereditary Footpad Hyperkeratosis

artículo científico publicado en 2016

Whole-genome sequencing reveals a large deletion in the MITF gene in horses with white spotted coat colour and increased risk of deafness

scientific article published on 15 January 2019

X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle

artículo científico publicado en 2003

X-linked cutaneous mosaicism in a dog

scientific article published on 22 April 2019

YARS2 Missense Variant in Belgian Shepherd Dogs with Cardiomyopathy and Juvenile Mortality

scientific article published on 14 March 2020

[Frequency of gene defects in selected European retriever populations].

artículo científico publicado en 2011

[Hereditary diseases in the horse: I. Monogenetic diseases]

scientific article published on 01 April 2008

cDNA cloning and sequencing of the human ryanodine receptor type 3 (RYR3) reveals a novel alternative splice site in the RYR3 gene

artículo científico publicado en 1998

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