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P Guldberg

Showing results (91-100 of 101) with videos related to

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Blood|October 27, 1998
Somatic Fas mutations in non-Hodgkin's lymphoma: association with extranodal disease and autoimmunityK Grønbaek, P T Straten, E Ralfkiaer, et al.
Leukemia|August 11, 1998
Concurrent disruption of cell cycle associated genes in mantle cell lymphoma: a genotypic and phenotypic study of cyclin D1, p16, p15, p53 and pRbK Grønbaek, T Nedergaard, M K Andersen, et al.
American Journal of Human Genetics|July 1, 1996
Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative StudyP Guldberg, H L Levy, W B Hanley, et al.
Pediatrics|August 3, 1999
Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative StudyF Güttler, C Azen, P Guldberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 10, 1996
Spontaneous human squamous cell carcinomas are killed by a human cytotoxic T lymphocyte clone recognizing a wild-type p53-derived peptideM Röpke, J Hald, P Guldberg, et al.
Pediatric Research|May 1, 2001
Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative StudyH L Levy, P Guldberg, F Güttler, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian populationV Romano, P Guldberg, F Güttler, et al.
Pediatric Research|March 27, 2001
Normal clinical outcome in untreated subjects with mild hyperphenylalaninemiaJ Weglage, M Pietsch, R Feldmann, et al.
American Journal of Human Genetics|June 23, 1998
A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotypeP Guldberg, F Rey, J Zschocke, et al.
British Journal of Cancer|October 20, 2005
G(2) chromosomal radiosensitivity in Danish survivors of childhood and adolescent cancer and their offspringG B Curwen, J F Winther, E J Tawn, et al.
Pageof 11

Showing results (91-100 of 101) with videos related to

Sort By:
Pageof 11
Blood|October 27, 1998
Somatic Fas mutations in non-Hodgkin's lymphoma: association with extranodal disease and autoimmunityK Grønbaek, P T Straten, E Ralfkiaer, et al.
Leukemia|August 11, 1998
Concurrent disruption of cell cycle associated genes in mantle cell lymphoma: a genotypic and phenotypic study of cyclin D1, p16, p15, p53 and pRbK Grønbaek, T Nedergaard, M K Andersen, et al.
American Journal of Human Genetics|July 1, 1996
Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative StudyP Guldberg, H L Levy, W B Hanley, et al.
Pediatrics|August 3, 1999
Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative StudyF Güttler, C Azen, P Guldberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 10, 1996
Spontaneous human squamous cell carcinomas are killed by a human cytotoxic T lymphocyte clone recognizing a wild-type p53-derived peptideM Röpke, J Hald, P Guldberg, et al.
Pediatric Research|May 1, 2001
Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative StudyH L Levy, P Guldberg, F Güttler, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian populationV Romano, P Guldberg, F Güttler, et al.
Pediatric Research|March 27, 2001
Normal clinical outcome in untreated subjects with mild hyperphenylalaninemiaJ Weglage, M Pietsch, R Feldmann, et al.
American Journal of Human Genetics|June 23, 1998
A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotypeP Guldberg, F Rey, J Zschocke, et al.
British Journal of Cancer|October 20, 2005
G(2) chromosomal radiosensitivity in Danish survivors of childhood and adolescent cancer and their offspringG B Curwen, J F Winther, E J Tawn, et al.
Pageof 11