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P Guldberg

Showing results (41-50 of 101) with videos related to

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European Journal of Pediatrics|July 1, 1995
In vivo assessment of mutations in the phenylalanine hydroxylase gene by phenylalanine loading: characterization of seven common mutationsP Guldberg, I Mikkelsen, K F Henriksen, et al.
Experimental Cell Research|April 25, 2000
Cell cycle arrest by the PTEN tumor suppressor is target cell specific and may require protein phosphatase activityA Hlobilkova, P Guldberg, M Thullberg, et al.
Human Mutation|January 1, 1996
Clinically applicable mutation screening in familial hypercholesterolemiaH Nissen, P Guldberg, A B Hansen, et al.
The Journal of Investigative Dermatology|December 14, 1999
Accumulation of identical T cells in melanoma and vitiligo-like leukodermaJ C Becker, P Guldberg, J Zeuthen, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
Large deletions in the phenylalanine hydroxylase gene as a cause of phenylketonuria in IndiaP Guldberg, K F Henriksen, K C Mammen, et al.
Scandinavian Journal of Gastroenterology|April 13, 2004
Screening for dysplasia and TP53 mutations in closed rectal stumps of patients with ulcerative colitis or Crohn diseaseK V Winther, E Bruun, B Federspiel, et al.
Journal of Medical Genetics|December 1, 1995
Phenylketonuria in a low incidence population: molecular characterisation of mutations in FinlandP Guldberg, K F Henriksen, I Sipilä, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Molecular basis for the phenotypical diversity of phenylketonuria and related hyperphenylalaninaemiasF Güttler, P Guldberg, K F Henriksen, et al.
Biotechniques|August 26, 1998
Detection and characterization of alpha-beta-T-cell clonality by denaturing gradient gel electrophoresis (DGGE)P thor Straten, A Barfoed, T Seremet, et al.
Oncogene|April 20, 1999
Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanomaP Guldberg, P thor Straten, V Ahrenkiel, et al.
Pageof 11

Showing results (41-50 of 101) with videos related to

Sort By:
Pageof 11
European Journal of Pediatrics|July 1, 1995
In vivo assessment of mutations in the phenylalanine hydroxylase gene by phenylalanine loading: characterization of seven common mutationsP Guldberg, I Mikkelsen, K F Henriksen, et al.
Experimental Cell Research|April 25, 2000
Cell cycle arrest by the PTEN tumor suppressor is target cell specific and may require protein phosphatase activityA Hlobilkova, P Guldberg, M Thullberg, et al.
Human Mutation|January 1, 1996
Clinically applicable mutation screening in familial hypercholesterolemiaH Nissen, P Guldberg, A B Hansen, et al.
The Journal of Investigative Dermatology|December 14, 1999
Accumulation of identical T cells in melanoma and vitiligo-like leukodermaJ C Becker, P Guldberg, J Zeuthen, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
Large deletions in the phenylalanine hydroxylase gene as a cause of phenylketonuria in IndiaP Guldberg, K F Henriksen, K C Mammen, et al.
Scandinavian Journal of Gastroenterology|April 13, 2004
Screening for dysplasia and TP53 mutations in closed rectal stumps of patients with ulcerative colitis or Crohn diseaseK V Winther, E Bruun, B Federspiel, et al.
Journal of Medical Genetics|December 1, 1995
Phenylketonuria in a low incidence population: molecular characterisation of mutations in FinlandP Guldberg, K F Henriksen, I Sipilä, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Molecular basis for the phenotypical diversity of phenylketonuria and related hyperphenylalaninaemiasF Güttler, P Guldberg, K F Henriksen, et al.
Biotechniques|August 26, 1998
Detection and characterization of alpha-beta-T-cell clonality by denaturing gradient gel electrophoresis (DGGE)P thor Straten, A Barfoed, T Seremet, et al.
Oncogene|April 20, 1999
Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanomaP Guldberg, P thor Straten, V Ahrenkiel, et al.
Pageof 11