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Biochemical Genetics
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April 8, 2004
Characterization of two SNPs (single nucleotide polymorphisms) in the porcine INSL3 gene and their exclusion as a common genetic basis of hernia inguinalis in pigs
Christoph Knorr, Helge Täubert, Ulrike Peters, et al.
Journal of Veterinary Internal Medicine
|
December 10, 1999
Analysis of blood clotting factor activities in canine Legg-Calvé-Perthes' disease
B Brenig, T Leeb, S Jansen, et al.
Animal Genetics
|
January 12, 1999
Characterisation and mapping of a highly polymorphic microsatellite within the porcine skeletal muscle triadin gene
S Duscher, I Pfeiffer, T Leeb, et al.
Analytical Biochemistry
|
June 10, 1995
Ultraviolet shadowing of proteins in preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresis
S Jansen, B Kriegesmann, R Jones, et al.
Animal Genetics
|
December 6, 2000
Genomic structure and nucleotide polymorphisms of the porcine agouti signalling protein gene (ASIP)
T Leeb, A Doppe, B Kriegesmann, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping
|
July 21, 2000
Genomic structure of the 5' end of the porcine ryanodine receptor 3 gene (RYR3)
A Giese, A Deppe, B Brenig, et al.
Cytogenetics and Cell Genetics
|
November 4, 2000
Isolation and characterization of a new FHL1 variant (FHL1C) from porcine skeletal muscle
A Krempler, S Kollers, R Fries, et al.
Animal Genetics
|
July 20, 2005
Identification of a mutation in the ovine uroporphyrinogen decarboxylase (UROD) gene associated with a type of porphyria
R Nezamzadeh, A Seubert, J Pohlenz, et al.
Plos One
|
May 29, 2025
Findings from transcriptomics and immunohistochemistry indicate an autoimmune disease targeting brainstem inhibitory interneurons in bovine spastic paresis
Frederik Krull, Shahrbanou Hosseini, Martina Bleyer, et al.
Plos One
|
January 22, 2024
A missense mutation in the highly conserved TNF-like domain of Ectodysplasin A is the candidate causative variant for X-linked hypohidrotic ectodermal dysplasia in Limousin cattle: Clinical, histological, and molecular analyses
Frederik Krull, Martina Bleyer, Jana Schäfer, et al.
Page
of 47
Search research articles
Search
Showing results (101-110 of 463) with videos related to
Sort By:
Page
of 47
Biochemical Genetics
|
April 8, 2004
Characterization of two SNPs (single nucleotide polymorphisms) in the porcine INSL3 gene and their exclusion as a common genetic basis of hernia inguinalis in pigs
Christoph Knorr, Helge Täubert, Ulrike Peters, et al.
Journal of Veterinary Internal Medicine
|
December 10, 1999
Analysis of blood clotting factor activities in canine Legg-Calvé-Perthes' disease
B Brenig, T Leeb, S Jansen, et al.
Animal Genetics
|
January 12, 1999
Characterisation and mapping of a highly polymorphic microsatellite within the porcine skeletal muscle triadin gene
S Duscher, I Pfeiffer, T Leeb, et al.
Analytical Biochemistry
|
June 10, 1995
Ultraviolet shadowing of proteins in preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresis
S Jansen, B Kriegesmann, R Jones, et al.
Animal Genetics
|
December 6, 2000
Genomic structure and nucleotide polymorphisms of the porcine agouti signalling protein gene (ASIP)
T Leeb, A Doppe, B Kriegesmann, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping
|
July 21, 2000
Genomic structure of the 5' end of the porcine ryanodine receptor 3 gene (RYR3)
A Giese, A Deppe, B Brenig, et al.
Cytogenetics and Cell Genetics
|
November 4, 2000
Isolation and characterization of a new FHL1 variant (FHL1C) from porcine skeletal muscle
A Krempler, S Kollers, R Fries, et al.
Animal Genetics
|
July 20, 2005
Identification of a mutation in the ovine uroporphyrinogen decarboxylase (UROD) gene associated with a type of porphyria
R Nezamzadeh, A Seubert, J Pohlenz, et al.
Plos One
|
May 29, 2025
Findings from transcriptomics and immunohistochemistry indicate an autoimmune disease targeting brainstem inhibitory interneurons in bovine spastic paresis
Frederik Krull, Shahrbanou Hosseini, Martina Bleyer, et al.
Plos One
|
January 22, 2024
A missense mutation in the highly conserved TNF-like domain of Ectodysplasin A is the candidate causative variant for X-linked hypohidrotic ectodermal dysplasia in Limousin cattle: Clinical, histological, and molecular analyses
Frederik Krull, Martina Bleyer, Jana Schäfer, et al.
Page
of 47