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P Guldberg

Showing results (11-20 of 101) with videos related to

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Biotechniques|May 1, 1994
Constant denaturant gel electrophoresis without formamideP Guldberg, K F Henriksen, F Güttler
Genomics|July 1, 1993
Molecular analysis of phenylketonuria in Denmark: 99% of the mutations detected by denaturing gradient gel electrophoresisP Guldberg, K F Henriksen, F Güttler
International Journal of Cancer|May 2, 1997
A one-step DGGE scanning method for detection of mutations in the K-, N-, and H-ras oncogenes: mutations at codons 12, 13 and 61 are rare in B-cell non-Hodgkin's lymphomaT Nedergaard, P Guldberg, E Ralfkiaer, et al.
Cancer Research|February 2, 1999
Extensive intra- and interindividual heterogeneity of p15INK4B methylation in acute myeloid leukemiaA Aggerholm, P Guldberg, M Hokland, et al.
Clinical Chemistry|December 10, 1999
Single-step mutation scanning of the 6-pyruvoyltetrahydropterin synthase gene in patients with hyperphenylalaninemiaA Romstad, P Guldberg, N Blau, et al.
European Journal of Haematology|August 31, 2000
Mutational analysis of the tumour suppressor gene MMAC1/PTEN in malignant myeloid disordersA Aggerholm, K Grønbaek, P Guldberg, et al.
Molecular Genetics and Metabolism|February 13, 2001
In vitro expression of 34 naturally occurring mutant variants of phenylalanine hydroxylase: correlation with metabolic phenotypes and susceptibility toward protein aggregationT Gjetting, M Petersen, P Guldberg, et al.
American Journal of Human Genetics|April 28, 2001
Missense mutations in the N-terminal domain of human phenylalanine hydroxylase interfere with binding of regulatory phenylalanineT Gjetting, M Petersen, P Guldberg, et al.
Molecular Genetics and Metabolism|May 1, 1998
Mild hyperphenylalaninemia and heterozygosity of the phenylalanine hydroxylase geneR Koch, F Güttler, P Guldberg, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Genotype-phenotype correlation in 11 Romanian PKU familiesA Popescu, T Andrian, F Güttler, et al.
Pageof 11

Showing results (11-20 of 101) with videos related to

Sort By:
Pageof 11
Biotechniques|May 1, 1994
Constant denaturant gel electrophoresis without formamideP Guldberg, K F Henriksen, F Güttler
Genomics|July 1, 1993
Molecular analysis of phenylketonuria in Denmark: 99% of the mutations detected by denaturing gradient gel electrophoresisP Guldberg, K F Henriksen, F Güttler
International Journal of Cancer|May 2, 1997
A one-step DGGE scanning method for detection of mutations in the K-, N-, and H-ras oncogenes: mutations at codons 12, 13 and 61 are rare in B-cell non-Hodgkin's lymphomaT Nedergaard, P Guldberg, E Ralfkiaer, et al.
Cancer Research|February 2, 1999
Extensive intra- and interindividual heterogeneity of p15INK4B methylation in acute myeloid leukemiaA Aggerholm, P Guldberg, M Hokland, et al.
Clinical Chemistry|December 10, 1999
Single-step mutation scanning of the 6-pyruvoyltetrahydropterin synthase gene in patients with hyperphenylalaninemiaA Romstad, P Guldberg, N Blau, et al.
European Journal of Haematology|August 31, 2000
Mutational analysis of the tumour suppressor gene MMAC1/PTEN in malignant myeloid disordersA Aggerholm, K Grønbaek, P Guldberg, et al.
Molecular Genetics and Metabolism|February 13, 2001
In vitro expression of 34 naturally occurring mutant variants of phenylalanine hydroxylase: correlation with metabolic phenotypes and susceptibility toward protein aggregationT Gjetting, M Petersen, P Guldberg, et al.
American Journal of Human Genetics|April 28, 2001
Missense mutations in the N-terminal domain of human phenylalanine hydroxylase interfere with binding of regulatory phenylalanineT Gjetting, M Petersen, P Guldberg, et al.
Molecular Genetics and Metabolism|May 1, 1998
Mild hyperphenylalaninemia and heterozygosity of the phenylalanine hydroxylase geneR Koch, F Güttler, P Guldberg, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Genotype-phenotype correlation in 11 Romanian PKU familiesA Popescu, T Andrian, F Güttler, et al.
Pageof 11