Torben Gjetting

PhiC31 integrase induces a DNA damage response and chromosomal rearrangements in human adult fibroblasts (2009)

Liu, Jian, Skjørringe, Tina, Gjetting, Torben, Jensen, Thomas G

Abstract Background PhiC31 integrase facilitates efficient integration of transgenes into human and mouse genomes and is considered for clinical gene therapy. However recent studies have shown that...

A Lesion-Mimic Syntaxin Double Mutant in Arabidopsis Reveals Novel Complexity of Pathogen Defense Signaling (2008)

Zhang, Ziguo, Lenk, Andrea, Andersson, Mats X., Gjetting, Torben, Pedersen, Carsten, Nielsen, Mads E., ...

The lesion-mimic Arabidopsis mutant, syp121 syp122, constitutively expresses the salicylic acid (SA) signaling pathway and has low penetration resistance to powdery mildew fungi. Genetic analyses of...

Differential gene expression in individual papilla-resistant and powdery mildew-infected barley epidermal cells (2004)

Gjetting, Torben, Carver, Timothy L. W., Skøt, Leif, Lyngkjær, Michael F.

Resistance and susceptibility in barley to the powdery mildew fungus (Blumeria graminis f. sp. hordei) is determined at the single-cell level. Even in genetically compatible interactions, attacked...

Missense Mutations in the N-Terminal Domain of Human Phenylalanine Hydroxylase Interfere with Binding of Regulatory Phenylalanine

Gjetting, Torben, Petersen, Marie, Guldberg, Per, Güttler, Flemming

Hyperphenylalaninemia due to a deficiency of phenylalanine hydroxylase (PAH) is an autosomal recessive disorder caused by >400 mutations in the PAH gene. Recent work has suggested that the majority...

Missense Mutations in the N-Terminal Domain of Human Phenylalanine Hydroxylase Interfere with Binding of Regulatory Phenylalanine

Gjetting, Torben, Petersen, Marie, Guldberg, Per, Güttler, Flemming

Hyperphenylalaninemia due to a deficiency of phenylalanine hydroxylase (PAH) is an autosomal recessive disorder caused by >400 mutations in the PAH gene. Recent work has suggested that the majority...