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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
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Human Fetal Scalp Dermal Papilla Enriched Genes and the Role of R-Spondin-1 in the Restoration of Hair Neogenesis in Adult Mouse Cells
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- Relation of Skin Polyamines to the Hairless Phenotype in Transgenic Mice Overexpressing Spermidine/Spermine N1-Acetyltransferase
- Towards Defining the Pathogenesis of the Hairless Phenotype
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Skin morphology of the mutant hairless USP mouse
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- IL-17a induces age-related olfactory dysfunction by impairing regeneration and promoting respiratory metaplasia in mice
- KCNQ4 K+ channels tune mechanoreceptors for normal touch sensation in mouse and man
- TCF/Lef1 activity controls establishment of diverse stem and progenitor cell compartments in mouse epidermis
- Development and homeostasis of the sebaceous gland
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