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- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Molecular basis of congenital atrichia in humans and mice.
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Auditory Threshold Variability in the SAMP8 Mouse Model of Age-Related Hearing Loss: Functional Loss and Phenotypic Change Precede Outer Hair Cell Loss
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
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