Molecular Structural Analysis of Porcine CMAH–Native Ligand Complex and High Throughput Virtual Screening to Identify Novel Inhibitors

por Ogun, Oluwamayowa Joshua, Thaller, Georg, Becker, Doreen
Publicado 2023

An Overview of the Importance and Value of Porcine Species in Sialic Acid Research

por Ogun, Oluwamayowa Joshua, Thaller, Georg, Becker, Doreen
Publicado 2022

Coat Color Roan Shows Association with KIT Variants and No Evidence of Lethality in Icelandic Horses

por Voß, Katharina, Tetens, Julia, Thaller, Georg, Becker, Doreen
Publicado 2020

Single-cell RNA sequencing of freshly isolated bovine milk cells and cultured primary mammary epithelial cells

por Becker, Doreen, Weikard, Rosemarie, Hadlich, Frieder, Kühn, Christa
Publicado 2021

An In Silico Functional Analysis of Non-Synonymous Single-Nucleotide Polymorphisms of Bovine CMAH Gene and Potential Implication in Pathogenesis

por Ogun, Oluwamayowa Joshua, Soremekun, Opeyemi S., Thaller, Georg, Becker, Doreen
Publicado 2023

Molecular studies of phenotype variation in canine RPGR-XLPRA1

por Appelbaum, Tatyana, Becker, Doreen, Santana, Evelyn, Aguirre, Gustavo D.
Publicado 2016

A Genome-Wide Association Study to Detect QTL for Commercially Important Traits in Swiss Large White Boars

por Becker, Doreen, Wimmers, Klaus, Luther, Henning, Hofer, Andreas, Leeb, Tosso
Publicado 2013

A 50-kb deletion disrupting the RSPO2 gene is associated with tetradysmelia in Holstein Friesian cattle

por Becker, Doreen, Weikard, Rosemarie, Schulze, Christoph, Wohlsein, Peter, Kühn, Christa
Publicado 2020

Candidate Genetic Modifiers for RPGR Retinal Degeneration

por Appelbaum, Tatyana, Murgiano, Leonardo, Becker, Doreen, Santana, Evelyn, Aguirre, Gustavo D.
Publicado 2020

Exploring the Origin and Relatedness of Maternal Lineages Through Analysis of Mitochondrial DNA in the Holstein Horse

por Engel, Laura, Becker, Doreen, Nissen, Thomas, Russ, Ingolf, Thaller, Georg, Krattenmacher, Nina
Publicado 2021

Mitochondrial DNA Variation Contributes to the Aptitude for Dressage and Show Jumping Ability in the Holstein Horse Breed

por Engel, Laura, Becker, Doreen, Nissen, Thomas, Russ, Ingolf, Thaller, Georg, Krattenmacher, Nina
Publicado 2022

Microphthalmia in Texel Sheep Is Associated with a Missense Mutation in the Paired-Like Homeodomain 3 (PITX3) Gene

por Becker, Doreen, Tetens, Jens, Brunner, Adrian, Bürstel, Daniela, Ganter, Martin, Kijas, James, Drögemüller, Cord
Publicado 2010

Improving the annotation of the cattle genome by annotating transcription start sites in a diverse set of tissues and populations using Cap Analysis Gene Expression sequencing

por Salavati, Mazdak, Clark, Richard, Becker, Doreen, Kühn, Christa, Plastow, Graham, Dupont, Sébastien, Moreira, Gabriel Costa Monteiro, Charlier, Carole, Clark, Emily Louise
Publicado 2023

A Missense Mutation in the SERPINH1 Gene in Dachshunds with Osteogenesis Imperfecta

por Drögemüller, Cord, Becker, Doreen, Brunner, Adrian, Haase, Bianca, Kircher, Patrick, Seeliger, Frank, Fehr, Michael, Baumann, Ulrich, Lindblad-Toh, Kerstin, Leeb, Tosso
Publicado 2009

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs

por Becker, Doreen, Minor, Katie M., Letko, Anna, Ekenstedt, Kari J., Jagannathan, Vidhya, Leeb, Tosso, Shelton, G. Diane, Mickelson, James R., Drögemüller, Cord
Publicado 2017

A Deletion in the N-Myc Downstream Regulated Gene 1 (NDRG1) Gene in Greyhounds with Polyneuropathy

por Drögemüller, Cord, Becker, Doreen, Kessler, Barbara, Kemter, Elisabeth, Tetens, Jens, Jurina, Konrad, Hultin Jäderlund, Karin, Flagstad, Annette, Perloski, Michele, Lindblad-Toh, Kerstin, Matiasek, Kaspar
Publicado 2010

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

por Murgiano, Leonardo, Becker, Doreen, Spector, Courtney, Carlin, Kendall, Santana, Evelyn, Niggel, Jessica K., Jagannathan, Vidhya, Leeb, Tosso, Pearce-Kelling, Sue, Aguirre, Gustavo D., Miyadera, Keiko
Publicado 2020

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

por Das, Rueben G., Becker, Doreen, Jagannathan, Vidhya, Goldstein, Orly, Santana, Evelyn, Carlin, Kendall, Sudharsan, Raghavi, Leeb, Tosso, Nishizawa, Yuji, Kondo, Mineo, Aguirre, Gustavo D., Miyadera, Keiko
Publicado 2019

An ARHGEF10 Deletion Is Highly Associated with a Juvenile-Onset Inherited Polyneuropathy in Leonberger and Saint Bernard Dogs

por Ekenstedt, Kari J., Becker, Doreen, Minor, Katie M., Shelton, G. Diane, Patterson, Edward E., Bley, Tim, Oevermann, Anna, Bilzer, Thomas, Leeb, Tosso, Drögemüller, Cord, Mickelson, James R.
Publicado 2014

Allele-biased expression of the bovine APOB gene associated with the cholesterol deficiency defect suggests cis-regulatory enhancer effects of the LTR retrotransposon insertion

por Becker, Doreen, Weikard, Rosemarie, Heimes, Annika, Hadlich, Frieder, Hammon, Harald M., Meyerholz, Marie M., Petzl, Wolfram, Zerbe, Holm, Schuberth, Hans-Joachim, Hoedemaker, Martina, Schmicke, Marion, Engelmann, Susanne, Kühn, Christa
Publicado 2022