Mark Berneburg

Six Genes Associated with the Clinical Phenotypes of Individuals with Deficient and Proficient DNA Repair (2008)

Tobias Gremmel, Susanne Wild, Winfried Schuller, Viola Kürten, Klaus Dietz, Jean Krutmann, ...

Xeroderma pigmentosum (XP) is a genetic disorder characterised by hypo-/hyperpigmentation, increased sensitivity to ultraviolet (UV)-radiation and an up to 2000-fold increased skin cancer risk. Cells...

Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene (2001)

Broughton, Bernard C., Berneburg, Mark, Fawcett, Heather, Taylor, Elaine M., Arlett, Colin F., Nardo, Tiziana, ...

The xeroderma pigmentosum group D (XPD) protein is a subunit of transcription factor TFIIH with DNA helicase activity. TFIIH has two functions, in basal transcription and nucleotide excision repair....

Photocarcinogenesis and inhibition of intercellular adhesion molecule 1 expression in cells of DNA-repair-defective individuals

Ahrens, Constanze, Grewe, Markus, Berneburg, Mark, Grether-Beck, Susanne, Quilliet, Xavier, Mezzina, Mauro, ...

Cells from patients with xeroderma pigmentosum complementation group D (XP-D) and most patients with trichothiodystrophy (TTD) are deficient in excision repair of ultraviolet (UV) radiation-induced...

UV damage causes uncontrolled DNA breakage in cells from patients with combined features of XP-D and Cockayne syndrome

Berneburg, Mark, Lowe, Jillian E., Nardo, Tiziana, Araújo, Sofia, Fousteri, Maria I., Green, Michael H.L., ...

Nucleotide excision repair (NER) removes damage from DNA in a tightly regulated multiprotein process. Defects in NER result in three different human disorders, xeroderma pigmentosum (XP),...

Photocarcinogenesis and inhibition of intercellular adhesion molecule 1 expression in cells of DNA-repair-defective individuals

Ahrens, Constanze, Grewe, Markus, Berneburg, Mark, Grether-Beck, Susanne, Quilliet, Xavier, Mezzina, Mauro, ...

Cells from patients with xeroderma pigmentosum complementation group D (XP-D) and most patients with trichothiodystrophy (TTD) are deficient in excision repair of ultraviolet (UV) radiation-induced...

UV damage causes uncontrolled DNA breakage in cells from patients with combined features of XP-D and Cockayne syndrome

Berneburg, Mark, Lowe, Jillian E., Nardo, Tiziana, Araújo, Sofia, Fousteri, Maria I., Green, Michael H.L., ...

Nucleotide excision repair (NER) removes damage from DNA in a tightly regulated multiprotein process. Defects in NER result in three different human disorders, xeroderma pigmentosum (XP),...

Dissecting the Impact of Chemotherapy on the Human Hair Follicle : A Pragmatic in Vitro Assay for Studying the Pathogenesis and Potential Management of Hair Follicle Dystrophy

Bodó, Enikő, Tobin, Desmond J., Kamenisch, York, Bíró, Tamás, Berneburg, Mark, Funk, Wolfgang, ...

Chemotherapy-induced alopecia represents one of the major unresolved problems of clinical oncology. The underlying molecular pathogenesis in humans is virtually unknown because of the lack of...