ScholarLens Back to search
2003•Molecular CellOpen access

Basal Transcription Defect Discriminates between Xeroderma Pigmentosum and Trichothiodystrophy in XPD Patients

Sandy Dubaele, Luca Proietti‐De‐Santis, Rachelle J. Bienstock, Anne Keriel, Miria Stefanini, Bennett Van Houten, Jean‐Marc Egly

Open full text 201 citations

Abstract

This record does not include an abstract. Use the full-text link above if available.

Open-access reader

About this research paper

What this paper is about

An abstract is not available in the OpenAlex record for this paper.

Why it matters

OpenAlex reports 201 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Key concepts: Xeroderma pigmentosum, Transcription factor II H, Biology, Genetics, Helicase, Transactivation, Nucleotide excision repair, Phenotype

Related papers

Related paper 1Related paper 2Related paper 3
Back to paper searchBrowse research topicsOriginal source
Basal Transcription Defect Discriminates between Xeroderma Pigmentosum and Trichothiodystrophy in XPD Patients — Research Paper | ScholarLens