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Publications by Miria Stefanini
In Vivo Destabilization and Functional Defects of the Xeroderma Pigmentosum C Protein Caused by a Pathogenic Missense Mutation
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Development of a New Easy Complementation Assay for DNA Repair Deficient Human Syndromes Using Cloned Repair Genes
Carcinogenesis
Medicine
Cancer Research
Related publications
Xeroderma Pigmentosum
British Medical Journal
Medicine
P53 Dysfunction by Xeroderma Pigmentosum Group C Defects Enhance Lung Adenocarcinoma Metastasis via Increased Mmp1 Expression
Cancer Research
Cancer Research
Oncology
Molecular Mechanisms of DNA Repair Defects and Heterogeneity in Xeroderma Pigmentosum
Japanese journal of human genetics
Xeroderma Pigmentosum
Annals of King Edward Medical University
Xeroderma Pigmentosum
Kokubyo Gakkai zasshi. The Journal of the Stomatological Society, Japan
Medicine
Detection of Protein Folding Defects Caused by BRCA1-BRCT Truncation and Missense Mutations
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Xeroderma Pigmentosum
Aktuelle Dermatologie
Dermatology
Ocular Manifestations of Xeroderma Pigmentosum
Ophthalmology
Ophthalmology
Biochemical and Structural Domain Analysis of Xeroderma Pigmentosum Complementation Group C
