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J Apold

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Human Mutation|January 1, 1992
A de novo phenylketonuria mutation: ATG (Met) to ATA (Ile) in the start codon of the phenylalanine hydroxylase geneH G Eiken, P M Knappskog, J Apold, et al.
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1991
The structural requirements of epitopes with IgE binding capacity demonstrated by three major allergens from fish, egg and tree pollenS Elsayed, J Apold, E Holen, et al.
International Archives of Allergy and Applied Immunology|January 1, 1986
Antigenic and allergenic determinants of ovalbumin. I. Peptide mapping, cleavage at the methionyl peptide bonds and enzymic hydrolysis of native and carboxymethyl OAS Elsayed, A S Hammer, M B Kalvenes, et al.
Human Genetics|March 1, 1992
PKU mutations R408Q and F299C in Norway: haplotype associations, geographic distributions and phenotype characteristicsH G Eiken, K Stangeland, L Skjelkvåle, et al.
Nucleic Acids Research|April 11, 1991
Application of natural and amplification created restriction sites for the diagnosis of PKU mutationsH G Eiken, E Odland, H Boman, et al.
Progress in Clinical and Biological Research|January 1, 1990
Screening for base mutations in the PAH and HPRT loci using the polymerase chain reaction (PCR) in combination with denaturing gradient gel electrophoresis (DGGE)A L Børresen, E Hovig, B Smith-Sørensen, et al.
Human Mutation|January 1, 1996
PKU mutation (D143G) associated with an apparent high residual enzyme activity: expression of a kinetic variant form of phenylalanine hydroxylase in three different systemsP M Knappskog, H G Eiken, A Martínez, et al.
Advances in Experimental Medicine and Biology|January 1, 1993
Expression of wild type and mutant forms of human phenylalanine hydroxylase in E. coliM Knappskog, H G Eiken, A Martinez, et al.
European Journal of Cancer (Oxford, England : 1990)|May 4, 2001
The BRCA1 syndrome and other inherited breast or breast-ovarian cancers in a Norwegian prospective seriesP Møller, A Borg, K Heimdal, et al.
American Journal of Human Genetics|December 1, 1990
A termination mutant prevalent in Norwegian haplotype 7 phenylketonuria genesJ Apold, H G Eiken, E Odland, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Human Mutation|January 1, 1992
A de novo phenylketonuria mutation: ATG (Met) to ATA (Ile) in the start codon of the phenylalanine hydroxylase geneH G Eiken, P M Knappskog, J Apold, et al.
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1991
The structural requirements of epitopes with IgE binding capacity demonstrated by three major allergens from fish, egg and tree pollenS Elsayed, J Apold, E Holen, et al.
International Archives of Allergy and Applied Immunology|January 1, 1986
Antigenic and allergenic determinants of ovalbumin. I. Peptide mapping, cleavage at the methionyl peptide bonds and enzymic hydrolysis of native and carboxymethyl OAS Elsayed, A S Hammer, M B Kalvenes, et al.
Human Genetics|March 1, 1992
PKU mutations R408Q and F299C in Norway: haplotype associations, geographic distributions and phenotype characteristicsH G Eiken, K Stangeland, L Skjelkvåle, et al.
Nucleic Acids Research|April 11, 1991
Application of natural and amplification created restriction sites for the diagnosis of PKU mutationsH G Eiken, E Odland, H Boman, et al.
Progress in Clinical and Biological Research|January 1, 1990
Screening for base mutations in the PAH and HPRT loci using the polymerase chain reaction (PCR) in combination with denaturing gradient gel electrophoresis (DGGE)A L Børresen, E Hovig, B Smith-Sørensen, et al.
Human Mutation|January 1, 1996
PKU mutation (D143G) associated with an apparent high residual enzyme activity: expression of a kinetic variant form of phenylalanine hydroxylase in three different systemsP M Knappskog, H G Eiken, A Martínez, et al.
Advances in Experimental Medicine and Biology|January 1, 1993
Expression of wild type and mutant forms of human phenylalanine hydroxylase in E. coliM Knappskog, H G Eiken, A Martinez, et al.
European Journal of Cancer (Oxford, England : 1990)|May 4, 2001
The BRCA1 syndrome and other inherited breast or breast-ovarian cancers in a Norwegian prospective seriesP Møller, A Borg, K Heimdal, et al.
American Journal of Human Genetics|December 1, 1990
A termination mutant prevalent in Norwegian haplotype 7 phenylketonuria genesJ Apold, H G Eiken, E Odland, et al.
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