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J T Epplen

Showing results (261-270 of 365) with videos related to

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Behavior Genetics|January 1, 1994
Male polymorphism in Limia perugiae (Pisces: Poeciliidae)C Erbelding-Denk, J H Schröder, M Schartl, et al.
Human Molecular Genetics|September 1, 1993
Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German originC Zühlke, O Riess, K Schröder, et al.
Bone Marrow Transplantation|December 1, 1993
Rapid detection of engraftment using T cell receptor gene polymorphism after allogeneic bone marrow transplantation in an alloimmunized child with severe aplastic anemiaB Kremens, M Gomolka, H Ottinger, et al.
Tissue Antigens|June 26, 2003
TNFA promoter polymorphisms and narcolepsyS Wieczorek, M Gencik, D Rujescu, et al.
Journal of Autoimmunity|February 24, 2009
Variation in the IL7RA and IL2RA genes in German multiple sclerosis patientsD A Akkad, S Hoffjan, E Petrasch-Parwez, et al.
The Journal of Pathology|May 1, 1996
Genomic instability in colorectal carcinomas: comparison of different evaluation methods and their biological significanceT Bocker, J Schlegel, F Kullmann, et al.
Human Genetics|March 1, 1996
Geographic differences in the allele frequencies of the human Y-linked tetranucleotide polymorphism DYS19F R Santos, T Gerelsaikhan, B Munkhtuja, et al.
Human Molecular Genetics|July 1, 1995
Expression of the Huntington disease gene in rodents: cloning the rat homologue and evidence for downregulation in non-neuronal tissues during developmentI Schmitt, D Bächner, D Megow, et al.
Arthritis and Rheumatism|June 3, 2008
Functionally relevant variations of the interleukin-10 gene associated with antineutrophil cytoplasmic antibody-negative Churg-Strauss syndrome, but not with Wegener's granulomatosisS Wieczorek, B Hellmich, L Arning, et al.
Journal of Molecular Evolution|September 1, 1993
The paradox of MHC-DRB exon/intron evolution: alpha-helix and beta-sheet encoding regions diverge while hypervariable intronic simple repeats coevolve with beta-sheet codonsF W Schwaiger, E Weyers, C Epplen, et al.
Pageof 37

Showing results (261-270 of 365) with videos related to

Sort By:
Pageof 37
Behavior Genetics|January 1, 1994
Male polymorphism in Limia perugiae (Pisces: Poeciliidae)C Erbelding-Denk, J H Schröder, M Schartl, et al.
Human Molecular Genetics|September 1, 1993
Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German originC Zühlke, O Riess, K Schröder, et al.
Bone Marrow Transplantation|December 1, 1993
Rapid detection of engraftment using T cell receptor gene polymorphism after allogeneic bone marrow transplantation in an alloimmunized child with severe aplastic anemiaB Kremens, M Gomolka, H Ottinger, et al.
Tissue Antigens|June 26, 2003
TNFA promoter polymorphisms and narcolepsyS Wieczorek, M Gencik, D Rujescu, et al.
Journal of Autoimmunity|February 24, 2009
Variation in the IL7RA and IL2RA genes in German multiple sclerosis patientsD A Akkad, S Hoffjan, E Petrasch-Parwez, et al.
The Journal of Pathology|May 1, 1996
Genomic instability in colorectal carcinomas: comparison of different evaluation methods and their biological significanceT Bocker, J Schlegel, F Kullmann, et al.
Human Genetics|March 1, 1996
Geographic differences in the allele frequencies of the human Y-linked tetranucleotide polymorphism DYS19F R Santos, T Gerelsaikhan, B Munkhtuja, et al.
Human Molecular Genetics|July 1, 1995
Expression of the Huntington disease gene in rodents: cloning the rat homologue and evidence for downregulation in non-neuronal tissues during developmentI Schmitt, D Bächner, D Megow, et al.
Arthritis and Rheumatism|June 3, 2008
Functionally relevant variations of the interleukin-10 gene associated with antineutrophil cytoplasmic antibody-negative Churg-Strauss syndrome, but not with Wegener's granulomatosisS Wieczorek, B Hellmich, L Arning, et al.
Journal of Molecular Evolution|September 1, 1993
The paradox of MHC-DRB exon/intron evolution: alpha-helix and beta-sheet encoding regions diverge while hypervariable intronic simple repeats coevolve with beta-sheet codonsF W Schwaiger, E Weyers, C Epplen, et al.
Pageof 37