T. Leeb

发表

The Sixth Transmembrane Domains of the Human B1 and B2 Bradykinin Receptors Are Structurally Compatible and Involved in Discriminating between Subtype-selective Agonists*

L. M. Leeb-Lundberg, S. A. Mathis, T. Leeb, 1997, The Journal of Biological Chemistry.

Regulation of Tissue-specific Expression of the Skeletal Muscle Ryanodine Receptor Gene (*)

G. Brem, B. Brenig, H. Brinkmeier, 1996, The Journal of Biological Chemistry.

Translational veterinary epilepsy: A win-win situation for human and veterinary neurology.

R. Raedt, M. Walker, W. Löscher, 2023, Veterinary journal.

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

B. Brenig, T. Leeb, 1998, FEBS letters.

Methemoglobinemia, Increased Deformability and Reduced Membrane Stability of Red Blood Cells in a Cat with a CYB5R3 Splice Defect

R. Hofmann-Lehmann, A. Bogdanova, V. Jagannathan, 2023, Cells.

A novel missense variant in the L2HGDH gene in a cat with L‐2‐hydroxyglutaric aciduria and multicystic cerebral lesions

V. Jagannathan, J. Guevar, R. Gutierrez‐Quintana, 2023, Journal of veterinary internal medicine.

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*

L. M. Leeb-Lundberg, S. A. Mathis, T. Leeb, 1998, The Journal of Biological Chemistry.

Case report: Sacral agenesis in two boxer dogs: clinical presentation, diagnostic investigations, and outcome

V. Jagannathan, A. Volta, M. Fumeo, 2023, Frontiers in Veterinary Science.

A TNR Frameshift Variant in Weimaraner Dogs with an Exercise‐Induced Paroxysmal Movement Disorder

C. Mellersh, H. Lohi, V. Jagannathan, 2023, Movement disorders : official journal of the Movement Disorder Society.

Effects of whole body vibration on spinal proprioception in healthy individuals

T. Leeb, D. H. K. Chowa, M. H. Popec, 2018 .

Ancient segmentally duplicated LCORL retrocopies in equids

V. Jagannathan, T. Raudsepp, D. Bannasch, 2023, PloS one.

Genomic Diversity and Runs of Homozygosity in Bernese Mountain Dogs

E. Ostrander, P. Quignon, C. André, 2023, Genes.

Heterozygous KRT10 missense variant in a Chihuahua with severe epidermolytic ichthyosis.

V. Jagannathan, S. Soto, S. Åhman, 2023, Animal genetics.

RALGAPA1 Deletion in Belgian Shepherd Dogs with Cerebellar Ataxia

V. Jagannathan, M. Kleiter, M. Leschnik, 2023, Genes.

PKD1 Nonsense Variant in a Lagotto Romagnolo Family with Polycystic Kidney Disease

V. Jagannathan, T. Leeb, M. Keiner, 2023, Genes.

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

T. Leeb, S. Rieder, M. Neuditschko, 2017, Animal genetics.

Genome Sequence, Comparative Analysis, and Population Genetics of the Domestic Horse

J. N. MacLeod, M. M. Binns, J. R. Mickelson, 2009, Science.

Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture

K. Lindblad-Toh, J. Kidd, E. Ostrander, 2023, Genome Biology.

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

C. Wade, C. Mellersh, G. Aguirre, 2019, Animal genetics.

PUBLISHED VERSION

M. Hofreiter, D. Adelson, A. Ludwig, 2013 .

SDR9C7 missense variant in a Chihuahua with non-epidermolytic ichthyosis.

V. Jagannathan, M. Welle, S. Kiener, 2023, Animal genetics.

Biallelic variants in DNA2 cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome

M. Passos-Bueno, M. Warman, Philippe M. Campeau, 2023, Journal of Medical Genetics.

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

S. Menet, H. Simianer, T. Leeb, 2011, Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie.

Autosomal recessive hyposegmentation of granulocytes in Australian Shepherd Dogs indicates a role for LMBR1L in myeloid leukocytes

A. Kipar, V. Jagannathan, B. Riond, 2023, PLoS Genetics.

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

T. Leeb, T. Leeb, 2007, Reproduction in domestic animals = Zuchthygiene.

First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data

Holly C. Beale, G. Barsh, N. Pedersen, 2018, BMC Genomics.

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

C. Drögemüller, T. Leeb, F. Seefried, 2018, Animal genetics.

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

T. Leeb, V. Jagannathan, M. De Lucia, 2019, Animal genetics.

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

O. Distl, T. Leeb, C. Lassnig, 2004, Cytogenetic and Genome Research.

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

C. Drögemüller, O. Distl, T. Leeb, 2001, Genome research.

FEELnc: A tool for Long non-coding RNAs annotation and its application to the dog transcriptome

V Wucher, F Legeai, B Hédan, 2016, bioRxiv.

A novel MLPH variant in dogs with coat colour dilution.

T. Leeb, V. Jagannathan, A. Kehl, 2018, Animal genetics.

Generation of an equine biobank to be used for Functional Annotation of Animal Genomes project

T. Kalbfleisch, J. MacLeod, J. Petersen, 2018, Animal genetics.

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

C. Drögemüller, T. Leeb, S. Rieder, 2010, Animal genetics.

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

B. Brenig, C. Drögemüller, O. Distl, 2002, Animal Genetics.

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

T. Leeb, V. Jagannathan, M. Welle, 2019, Animal genetics.

Osteogenesis Imperfecta in Two Litters of Dachshunds

M. Hewicker-Trautwein, F. Seeliger, M. Fehr, 2003, Veterinary pathology.

Animal Cytogenetics and Comparative Mapping

P. Quignon, C. Drögemüller, A. Scott, 2003 .

Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human

C. Mellersh, S. Katayama, K. Krjutškov, 2023, Genome Medicine.

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

T. Leeb, A. Fischer, Lisa Alves, 2011, Journal of veterinary internal medicine.

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

T. Sonstegard, O. Hanotte, H. Simianer, 2010, Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie.

Spontaneous Human B2 Bradykinin Receptor Activity Determines the Action of Partial Agonists as Agonists or Inverse Agonists

S. A. Mathis, D B Fathy, T Leeb, 1999, The Journal of Biological Chemistry.

A FAS-ligand variant associated with autoimmune lymphoproliferative syndrome in cats

R. Todhunter, K. Dittmer, R. Malik, 2016, Mammalian Genome.

Current Classification of Canine Muscular Dystrophies and Identification of New Variants

Jonah N Cullen, J. Mickelson, Ling T Guo, 2023, Genes.

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

R. Agarwala, A. Schäffer, J. MacLeod, 2008, Cytogenetic and Genome Research.

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

B. Brenig, C. Drögemüller, O. Distl, 2003, Cytogenetic and Genome Research.

Characterization of the porcine transferrin gene (TF) and its association with disease severity following an experimental Actinobacillus pleuropneumoniae infection.

F. Stanke, R. Martínez-Arias, D. Höltig, 2009, Animal genetics.

PBMC Treatment Significantly Changes Gene Expression Regulation in Horses

T. Leeb, V. Gerber, Victor C. Mason, 2019, bioRxiv.

Naturally occurring canine laminopathy leading to a dilated and fibrosing cardiomyopathy in the Nova Scotia Duck Tolling Retriever

D. Bannasch, M. Christen, T. Leeb, 2023, Scientific reports.

Identification of an ADAMTS2 frameshift variant in a cat family with Ehlers–Danlos syndrome

G. Lühken, U. Gärtner, C. Herden, 2023, G3.

Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture

K. Lindblad-Toh, J. Kidd, E. Ostrander, 2023, Genome Biology.

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

T. Leeb, V. Jagannathan, S. Brooks, 2019, Animal genetics.

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

T. Leeb, V. Gerber, E. Słota, 2007, Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie.

Insights into post-translational processing of β-galactosidase in an animal model resembling late infantile human GM1-gangliosidosis

R. Kreutzer, M. Kreutzer, A. Sewell, 2007, Journal of cellular and molecular medicine.

PCYT2 deficiency in Saarlooswolfdogs with progressive retinal, central, and peripheral neurodegeneration.

V. Jagannathan, A. Oevermann, M. Hytönen, 2024, Molecular genetics and metabolism.

Heterozygous ATP2A2 missense variant identified in a Shih Tzu with Darier disease.

V. Jagannathan, E. Mauldin, S. Kiener, 2023, Animal genetics.

Evidence for a Retroviral Insertion in TRPM1 as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse

Arne Ludwig, David L. Adelson, Padmanabhan Mahadevan, 2013, PloS one.

DNA Testing in Neurologic Diseases

T. Leeb, D. O'brien, T. Leeb, 2014, Journal of veterinary internal medicine.

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

C. Drögemüller, T. Leeb, C. Gurtner, 2013, Veterinary dermatology.

Single-cell profiling of bronchoalveolar cells reveals a Th17 signature in neutrophilic severe equine asthma

V. Jagannathan, V. Gerber, S. Sage, 2023, bioRxiv.

A FAS-ligand variant associated with autoimmune lymphoproliferative syndrome in cats

R. Todhunter, K. Dittmer, R. Malik, 2016, Mammalian Genome.

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

B. Brenig, T. Leeb, B. Kriegesmann, 2000, Animal genetics.

EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia

V. Jagannathan, L. Chevallier, Noelle Cochet-Faivre, 2024, Genes.

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

C. Drögemüller, T. Leeb, J. Tetens, 2018, Animal genetics.

Breeding German sheep for resistance to scrapie

C. Drögemüller, O. Distl, T. Leeb, 2004, Veterinary Record.

Polioencephalopathy in Eurasier dogs

M. Christen, T. Leeb, Emilie Paran, 2023, Journal of veterinary internal medicine.

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

E. Wolf, O. Distl, T. Leeb, 2005, Cytogenetic and Genome Research.

Translational veterinary epilepsy – a win-win situation between human and veterinary neurology

R. Raedt, K. Vonck, A. Galanopoulou, 2022 .

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

T. Leeb, B. Haase, S. Rieder, 2009, Animal genetics.

Degenerative axonopathy in a Tyrolean grey calf.

C. Drögemüller, T. Leeb, J. Sölkner, 2010, Journal of veterinary internal medicine.

Genetic variability of the equine casein genes.

C. Drögemüller, T. Leeb, J. Tetens, 2016, Journal of dairy science.

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

T. Leeb, V. Jagannathan, H. Holl, 2022 .

Polycystic Kidneys and GM2 Gangliosidosis-Like Disease in Neonatal Springboks (Antidorcas marsupialis)

M. Kummrow, F. Hansmann, V. Herder, 2015, Veterinary pathology.