L. Murgiano

发表

Ellis–van Creveld Syndrome in Grey Alpine Cattle

C. Drögemüller, K. Dittmer, K. Thompson, 2015, Veterinary pathology.

Proteomics and transcriptomics investigation on longissimus muscles in Large White and Casertana pig breeds.

A. D’Alessandro, L. Zolla, A. Valentini, 2010, Journal of proteome research.

Fast-twitch skeletal muscle fiber adaptation to SERCA1 deficiency in a Dutch Improved Red and White calf pseudomyotonia case

C. Drögemüller, F. Mascarello, T. Dorotea, 2015, Neuromuscular Disorders.

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

T. Leeb, M. Penedo, V. Jagannathan, 2016, G3: Genes, Genomes, Genetics.

CCDC66 frameshift variant associated with a new form of early-onset progressive retinal atrophy in Portuguese Water Dogs

G. Aguirre, T. Leeb, V. Jagannathan, 2020, Scientific Reports.

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

G. Aguirre, T. Leeb, Fan Wang, 2018, G3: Genes, Genomes, Genetics.

Candidate Genetic Modifiers for RPGR Retinal Degeneration

G. Aguirre, D. Becker, Evelyn Santana, 2020, Investigative ophthalmology & visual science.

Canine reference genome accuracy impacts variant calling: Lessons learned from investigating embryonic lethal variants.

C. Mellersh, J. Mickelson, C. Drögemüller, 2022, Animal genetics.

Oligomeric characterization of the photosynthetic apparatus of Rhodobacter sphaeroides R26.1 by nondenaturing electrophoresis methods.

L. Zolla, S. Rinalducci, G. M. D'amici, 2010, Journal of proteome research.

KDM2B‐associated paunch calf syndrome in Marchigiana cattle

C. Drögemüller, M. Bolcato, A. Gentile, 2020, Journal of Veterinary Internal Medicine.

Epidermolysa bullosa in Danish Hereford calves is caused by a deletion in LAMC2 gene

C. Drögemüller, V. Jagannathan, L. K. Isling, 2015, BMC Veterinary Research.

Looking the Cow in the Eye: Deletion in the NID1 Gene Is Associated with Recessive Inherited Cataract in Romagnola Cattle

C. Drögemüller, V. Jagannathan, A. Gentile, 2014, PloS one.

Prevalence of paunch calf syndrome carriers in Italian Romagnola cattle.

C. Drögemüller, M. Bolcato, A. Gentile, 2014, Veterinary journal.

Frequency of bovine congenital pseudomyotonia carriers in selected Italian Chianina sires.

C. Drögemüller, M. Bolcato, S. Testoni, 2013, Veterinary journal.

Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations

C. Drögemüller, R. Liguori, F. Mascarello, 2012, BMC Veterinary Research.

Comparison of Milk Fat Globule Membrane (MFGM) proteins in milk samples of Chianina and Holstein cattle breeds across three lactation phases through 2D IEF SDS PAGE — A preliminary study

A. D’Alessandro, L. Zolla, L. Pariset, 2013 .

Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation

C. Drögemüller, M. Mikkola, V. Jagannathan, 2015, PLoS genetics.

X-Linked Duchenne-Type Muscular Dystrophy in Jack Russell Terrier Associated with a Partial Deletion of the Canine DMD Gene

C. Drögemüller, A. Letko, V. Jagannathan, 2020, Genes.

A de novo germline mutation in MYH7 causes a progressive dominant myopathy in pigs

C. Drögemüller, B. Harlizius, L. Murgiano, 2012, BMC Genetics.

Redox proteomics: basic principles and future perspectives for the detection of protein oxidation in plants.

L. Zolla, S. Rinalducci, L. Murgiano, 2008, Journal of experimental botany.

Short prolactin isoforms are expressed in photoreceptors of canine retinas undergoing retinal degeneration

G. Aguirre, Hsin-Yao Tang, T. Olsen, 2021, Scientific reports.

Correction: Deletion in the EVC2 Gene Causes Chondrodysplastic Dwarfism in Tyrolean Grey Cattle

K. Dittmer, C. Benazzi, M. Bolcato, 2014, PLoS ONE.

Deletion in the EVC2 Gene Causes Chondrodysplastic Dwarfism in Tyrolean Grey Cattle

C. Drögemüller, K. Dittmer, C. Benazzi, 2014, PloS one.

Comparison of Milk Fat Globule Membrane (MFGM) Proteins of Chianina and Holstein Cattle Breed Milk Samples Through Proteomics Methods

L. Zolla, L. Pariset, A. Valentini, 2009, Nutrients.

Improving the resolution of canine genome-wide association studies using genotype imputation: A study of two breeds

C. Wade, C. Mellersh, U. Giger, 2021, Animal Genetics.

A Nonsense Mutation in the IKBKG Gene in Mares with Incontinentia Pigmenti

J. Goodship, A. Clarke, C. Drögemüller, 2013, PloS one.

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.

A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle

C. Drögemüller, M. Bolcato, V. Jagannathan, 2016, BMC Veterinary Research.

De novo stop-lost germline mutation in FGFR3 causes severe chondrodysplasia in the progeny of a Holstein bull.

C. Drögemüller, I. Häfliger, A. Letko, 2020, Animal genetics.

Natural disease history of a canine model of oligogenic RPGRIP1-cone-rod dystrophy establishes variable effects of previously and newly mapped modifier loci.

G. Aguirre, N. Ziółkowska, K. Miyadera, 2023, Human molecular genetics.

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

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

Frameshift Variant in AMPD2 in Cirneco dell’Etna Dogs with Retinopathy and Tremors

W. Beltran, L. Murgiano, L. Benedicenti, 2024, Genes.