Per Guldberg integrates Gene with Minisatellite in his research. Per Guldberg integrates Genetics with Mutant in his study. Per Guldberg merges Mutant with Gene in his research. His Phenylalanine study typically links adjacent topics like Biochemistry. He performs integrative Biochemistry and Amino acid research in his work. He incorporates Amino acid and Phenylalanine hydroxylase in his research. He integrates Phenylalanine hydroxylase and Hyperphenylalaninemia in his studies. He integrates Hyperphenylalaninemia and Phenylalanine in his research. In his papers, he integrates diverse fields, such as Allele and Locus (genetics).
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DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis
Jirina Bartkova;Zuzana Horejsí;Karen Koed;Alwin Krämer.
Demethylation of a hypermethylated P15/INK4B gene in patients with myelodysplastic syndrome by 5-Aza-2′-deoxycytidine (decitabine) treatment
Michael Daskalakis;Tudung T. Nguyen;Carvell Nguyen;Per Guldberg.
Disruption of the MMAC1/PTEN Gene by Deletion or Mutation Is a Frequent Event in Malignant Melanoma
P. Guldberg;P. Thor Straten;A. Birck;V. Ahrenkiel.
Cancer Research (1997)
Adult human mesenchymal stem cell as a target for neoplastic transformation.
Nedime Serakinci;Per Guldberg;Jorge S Burns;Basem Abdallah.
The p16-cyclin D/Cdk4-pRb Pathway as a Functional Unit Frequently Altered in Melanoma Pathogenesis
Jirina Bartkova;Jiri Lukas;Per Guldberg;Jan Alsner.
Cancer Research (1996)
In-tube DNA methylation profiling by fluorescence melting curve analysis.
Jesper Worm;Anni Aggerholm;Per Guldberg.
Clinical Chemistry (2001)
Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1.
N. Tommerup;W. Schempp;P. Meinecke;S. Pedersen.
Nature Genetics (1993)
DNA methylation analysis techniques
Christina Dahl;Per Guldberg.
Promoter hypermethylation of p15INK4B, HIC1, CDH1, and ER is frequent in myelodysplastic syndrome and predicts poor prognosis in early-stage patients.
Anni Aggerholm;Mette S. Holm;Per Guldberg;Lene H. Olesen.
European Journal of Haematology (2006)
Molecular Analysis of Phenylketonuria in Denmark: 99% of the Mutations Detected by Denaturing Gradient Gel Electrophoresis
Per Guldberg;Karen Friis Henriksen;Flemming Güttler.
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