Per Guldberg

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Publications in SciGraph latest 50 shown

  • 2018-12 Adoptive cancer immunotherapy using DNA-demethylated T helper cells as antigen-presenting cells in NATURE COMMUNICATIONS
  • 2018-06 Adoptive T cell cancer therapy in NATURE MATERIALS
  • 2016-12 Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57 in BMC MEDICAL GENETICS
  • 2016-12 Experimental factors affecting the robustness of DNA methylation analysis in SCIENTIFIC REPORTS
  • 2015-12 S100A4-neutralizing antibody suppresses spontaneous tumor progression, pre-metastatic niche formation and alters T-cell polarization balance in BMC CANCER
  • 2015-12 DNA methylation and histone modifications regulate SOX11 expression in lymphoid and solid cancer cells in BMC CANCER
  • 2015-02 KIT Is a Frequent Target for Epigenetic Silencing in Cutaneous Melanoma in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2014-12 A short acidic motif in ARF guards against mitochondrial dysfunction and melanoma susceptibility in NATURE COMMUNICATIONS
  • 2014-12 Bioenergetic modulation with dichloroacetate reduces the growth of melanoma cells and potentiates their response to BRAFV600E inhibition in JOURNAL OF TRANSLATIONAL MEDICINE
  • 2009-10 Genetic risk factors for melanoma in HUMAN GENETICS
  • 2008-05 Frequent hypermethylation of DBC1 in malignant lymphoproliferative neoplasms in MODERN PATHOLOGY
  • 2008-02 Risk for contralateral breast cancer among carriers of the CHEK21100delCCHEK2*1100delC mutation in the WECARE Study in BRITISH JOURNAL OF CANCER
  • 2007-07 Genomic profiling of malignant melanoma using tiling-resolution arrayCGH in ONCOGENE
  • 2006-05 Identification of identical TCRs in primary melanoma lesions and tumor free corresponding sentinel lymph nodes in CANCER IMMUNOLOGY, IMMUNOTHERAPY
  • 2005-10 G2 chromosomal radiosensitivity in Danish survivors of childhood and adolescent cancer and their offspring in BRITISH JOURNAL OF CANCER
  • 2005-09 Growth factors rescue cutaneous melanoma cells from apoptosis induced by knockdown of mutated (V600E) B-RAF in ONCOGENE
  • 2005-04 DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis in NATURE
  • 2005 The Tumor Suppressor Gene PTEN Plays a Role in Cell Cycle Regulation and Apoptosis in Prostate Cancer Cell Lines in HORMONAL CARCINOGENESIS IV
  • 2004-11 Aberrations of the Chk2 tumour suppressor in advanced urinary bladder cancer in ONCOGENE
  • 2004-08 Loss of heterozygosity at 9q33 and hypermethylation of the DBCCR1 gene in oral squamous cell carcinoma in BRITISH JOURNAL OF CANCER
  • 2004-07 Genetic and epigenetic alterations of the APC gene in malignant melanoma in ONCOGENE
  • 2004-06 Adult human mesenchymal stem cell as a target for neoplastic transformation in ONCOGENE
  • 2003-08 DNA methylation analysis techniques in BIOGERONTOLOGY
  • 2001-10-10 Mutational Analysis of Oncogenes and Tumor Suppressor Genes in Human Cancer Using Denaturing Gradient Gel Electrophoresis in MOLECULAR ANALYSIS OF CANCER
  • 2001-06-01 T-Cell Receptor Clonotype Mapping Using Denaturing Gradient Gel Electrophoresis: Analysis of Clonal T-Cell Responses in Melanoma in MELANOMA TECHNIQUES AND PROTOCOLS
  • 2001-05 Congenital Heart Disease in Maternal Phenylketonuria: Report from the Maternal PKU Collaborative Study in PEDIATRIC RESEARCH
  • 2001-04 Normal Clinical Outcome in Untreated Subjects with Mild Hyperphenylalaninemia in PEDIATRIC RESEARCH
  • 2000-12 Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE) in HUMAN GENETICS
  • 2000-10 Aberrant p27Kip1 promoter methylation in malignant melanoma in ONCOGENE
  • 2000-10 Concurrent disruption of p16INK4a and the ARF-p53 pathway predicts poor prognosis in aggressive non-Hodgkin's lymphoma in LEUKEMIA
  • 2000-09 Comparative delineation of T cell clonotypes in coexisting syngeneic B16 melanoma in CANCER IMMUNOLOGY, IMMUNOTHERAPY
  • 2000-09 Mutation analysis anticipates dietary requirements in phenylketonuria in EUROPEAN JOURNAL OF PEDIATRICS
  • 2000-04 Anti-Melanocyte T Cell Responses – Methodology Versus Biology in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2000-03 Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients in BREAST CANCER RESEARCH
  • 2000-02 Mutation and Allelic Loss of the PTEN/MMAC1 gene in Primary and Metastatic Melanoma Biopsies in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2000-02 Brain phenylalanine concentration in the management of adults with phenylketonuria in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1999-12 Accumulation of Identical T Cells in Melanoma and Vitiligo-Like Leukoderma in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 1999-09 In situ T cells in melanoma in CANCER IMMUNOLOGY, IMMUNOTHERAPY
  • 1999-03 Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma in ONCOGENE
  • 1998-08 Concurrent disruption of cell cycle associated genes in mantle cell lymphoma: a genotypic and phenotypic study of cyclin D1, p16, p15, p53 and pRb in LEUKEMIA
  • 1998-06 Aberrant phenylalanine metabolism in phenylketonuria heterozygotes in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1997-11 Large deletions in the phenylalanine hydroxylase gene as a cause of phenylketonuria in India in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1996-06 Phenotyping of phenylketonuric patients by oral phenylalanine loading in EUROPEAN JOURNAL OF PEDIATRICS
  • 1996-01 PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian population in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1996-01 The influence of mutations on enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiency in EUROPEAN JOURNAL OF PEDIATRICS
  • 1995-07 In vivo assessment of mutations in the phenylalanine hydroxylase gene by phenylalanine loading: Characterization of seven common mutations in EUROPEAN JOURNAL OF PEDIATRICS
  • 1995-05 Phenylketonuric patients decades after diet in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1994-11 Mutation analysis in families with discordant phenotypes of phenylalanine hydroxylase deficiency. Inheritance and expression of the hyperphenylalaninaemias in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1994-09 Brain magnetic resonance imaging in children with optimally controlled hyperphenylalaninaemia in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1994-05 Genotype-phenotype correlation in 11 Romanian PKU families in JOURNAL OF INHERITED METABOLIC DISEASE
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