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Brenig

Showing results (101-110 of 463) with videos related to

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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 pigsChristoph 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' diseaseB 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 geneS Duscher, I Pfeiffer, T Leeb, et al.
Analytical Biochemistry|June 10, 1995
Ultraviolet shadowing of proteins in preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresisS 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 muscleA 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 porphyriaR 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 paresisFrederik 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 analysesFrederik Krull, Martina Bleyer, Jana Schäfer, et al.
Pageof 47

Showing results (101-110 of 463) with videos related to

Sort By:
Pageof 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 pigsChristoph 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' diseaseB 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 geneS Duscher, I Pfeiffer, T Leeb, et al.
Analytical Biochemistry|June 10, 1995
Ultraviolet shadowing of proteins in preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresisS 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 muscleA 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 porphyriaR 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 paresisFrederik 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 analysesFrederik Krull, Martina Bleyer, Jana Schäfer, et al.
Pageof 47