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Experimental Dermatology|March 8, 2026
A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic DisordersMaddison N Salois, Saiphone Webb, Isaiah A Proctor, et al.
Biorxiv : the Preprint Server for Biology|May 19, 2023
Effects of TP63 Mutations on Keratinocyte Adhesion and MigrationMaddison N Salois, Jessica A Gugger, Saiphone Webb, et al.
Experimental Dermatology|July 11, 2023
Effects of TP63 mutations on keratinocyte adhesion and migrationMaddison N Salois, Jessica A Gugger, Saiphone Webb, et al.
Frontiers in Genetics|August 23, 2021
Rare Genetic Disorders: Novel Treatment Strategies and Insights Into Human BiologyPeter J Koch, Maranke I Koster
American Journal of Medical Genetics. Part A|October 15, 2025
Complex Wounds in Ectodermal Dysplasias: Translating Discovery to TherapyMary Fete, Becky M Abbott, Maddison N Salois, et al.
Cell Communication & Adhesion|January 28, 2014
Integrating animal models and in vitro tissue models to elucidate the role of desmosomal proteins in diseasesMaranke I Koster, Jason Dinella, Jiangli Chen, et al.
American Journal of Medical Genetics. Part A|December 19, 2022
Rare diseases of ectoderm: Translating discovery to therapyJohn Timothy Wright, Becky M Abbott, Maddison N Salois, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
Modeling AEC-New approaches to study rare genetic disordersPeter J Koch, Jason Dinella, Mary Fete, et al.
Molecular Carcinogenesis|June 18, 2011
Loss of Desmocollin 3 in skin tumor development and progressionJiangli Chen, Charlene O'Shea, James E Fitzpatrick, et al.
The Journal of Investigative Dermatology|April 14, 2012
Building models for keratin disordersMaranke I Koster
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