Results
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A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta. [electronic resource] by
- Drögemüller, Cord
- Becker, Doreen
- Brunner, Adrian
- Haase, Bianca
- Kircher, Patrick
- Seeliger, Frank
- Fehr, Michael
- Baumann, Ulrich
- Lindblad-Toh, Kerstin
- Leeb, Tosso
Producer: 20090917
In:
PLoS genetics vol. 5
Availability: No items available.
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Lack of association of delta-aminolevulinate dehydratase polymorphisms with blood lead levels and hemoglobin in Romanian women from a lead-contaminated region. [electronic resource] by
- Rabstein, Sylvia
- Unfried, Klaus
- Ranft, Ulrich
- Illig, Thomas
- Kolz, Melanie
- Mambetova, Chinara
- Vlad, Mariana
- Roman, Cecilia
- Weiss, Tobias
- Becker, Doreen
- Brüning, Thomas
- Pesch, Beate
Producer: 20080711
In:
Journal of toxicology and environmental health. Part A vol. 71
Availability: No items available.
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11.
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A deletion in the N-myc downstream regulated gene 1 (NDRG1) gene in Greyhounds with polyneuropathy. [electronic resource] by
- Drögemüller, Cord
- Becker, Doreen
- Kessler, Barbara
- Kemter, Elisabeth
- Tetens, Jens
- Jurina, Konrad
- Jäderlund, Karin Hultin
- Flagstad, Annette
- Perloski, Michele
- Lindblad-Toh, Kerstin
- Matiasek, Kaspar
Producer: 20100901
In:
PloS one vol. 5
Availability: No items available.
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Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness. [electronic resource] by
- 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
Producer: 20201028
In:
Scientific reports vol. 9
Availability: No items available.
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An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs. [electronic resource] by
- 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
Producer: 20160427
In:
PLoS genetics vol. 10
Availability: No items available.
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A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH). [electronic resource] by
- Drögemüller, Michaela
- Jagannathan, Vidhya
- Becker, Doreen
- Drögemüller, Cord
- Schelling, Claude
- Plassais, Jocelyn
- Kaerle, Cécile
- Dufaure de Citres, Caroline
- Thomas, Anne
- Müller, Eliane J
- Welle, Monika M
- Roosje, Petra
- Leeb, Tosso
Producer: 20141215
In:
PLoS genetics vol. 10
Availability: No items available.
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Complex Structural [electronic resource] by
- Murgiano, Leonardo
- Becker, Doreen
- Torjman, Dina
- Niggel, Jessica K
- Milano, Ausra
- Cullen, Cheryl
- Feng, Rui
- Wang, Fan
- Jagannathan, Vidhya
- Pearce-Kelling, Sue
- Katz, Martin L
- Leeb, Tosso
- Aguirre, Gustavo D
Producer: 20190604
In:
G3 (Bethesda, Md.) vol. 9
Availability: No items available.
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A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease. [electronic resource] by
- Kyöstilä, Kaisa
- Syrjä, Pernilla
- Jagannathan, Vidhya
- Chandrasekar, Gayathri
- Jokinen, Tarja S
- Seppälä, Eija H
- Becker, Doreen
- Drögemüller, Michaela
- Dietschi, Elisabeth
- Drögemüller, Cord
- Lang, Johann
- Steffen, Frank
- Rohdin, Cecilia
- Jäderlund, Karin H
- Lappalainen, Anu K
- Hahn, Kerstin
- Wohlsein, Peter
- Baumgärtner, Wolfgang
- Henke, Diana
- Oevermann, Anna
- Kere, Juha
- Lohi, Hannes
- Leeb, Tosso
Producer: 20160324
In:
PLoS genetics vol. 11
Availability: No items available.
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