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- 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
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Le gène<i>hairless</i>de la souris
- Skin Cyst: A Pathological Dead-End With a New Twist of Morphogenetic Potentials in Organoid Cultures
- Insertional mutation of the hairless locus on mouse Chromosome 14
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Biology and Genetics of Hair
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
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- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Dermatologic Features of Classic Movie Villains
- Alopecia Areata
- Morphological Approach to Hair Disorders
- Clinical Management in Psychodermatology
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Animal and in vitro Models for the Study of Hair Follicles
- Genetic Hair Disorders: A Review
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Molecular basis of congenital atrichia in humans and mice.
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Hairless is a nuclear receptor corepressor essential for skin function