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Publications by Cristina Has
APOBEC Mutation Drives Early-Onset Squamous Cell Carcinomas in Recessive Dystrophic Epidermolysis Bullosa
Science Translational Medicine
Medicine
Altered Notch Signaling in Dowling-Degos Disease: Additional Mutations in POGLUT1 and Further Insights Into Disease Pathogenesis
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Absence of the Integrin Α3 Subunit Induces an Activated Phenotype in Human Keratinocytes
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Molecular Heterogeneity of Epidermolysis Bullosa Simplex: Contribution of EXPH5 Mutations
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Amlexanox Enhances Premature Termination Codon Read-Through in COL7A1 and Expression of Full Length Type VII Collagen: Potential Therapy for Recessive Dystrophic Epidermolysis Bullosa
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Laminin 332 in Junctional Epidermolysis Bullosa
Cell Adhesion and Migration
Molecular Neuroscience
Cell Biology
Cellular
Assessment of the Risk and Characterization of Non-Melanoma Skin Cancer in Kindler Syndrome: Study of a Series of 91 Patients
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Junctional Epidermolysis Bullosa: Allelic Heterogeneity and Mutation Stratification for Precision Medicine
Frontiers in Medicine
Medicine
Molecular Therapeutics in Development for Epidermolysis Bullosa: Update 2020
Molecular Diagnosis and Therapy
Medicine
Molecular Medicine
Genetics
Pharmacology
A Plakophilin-1 Gene Mutation in an Egyptian Family With Ectodermal Dysplasia-Skin Fragility Syndrome
Molecular Syndromology
Genetics
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