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Research 30 of 343
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- Differential activity of 2-methylene-19-nor vitamin D analogs on growth factor gene expression in rhino mouse skin and comparison to all-trans retinoic acid
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- Molecular basis of congenital atrichia in humans and mice.
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- Meibomian gland changes in the rhino (hrrhhrrh) mouse.
- Insertional mutation of the hairless locus on mouse Chromosome 14
- 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
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- Disruption of the hedgehog signaling pathway contributes to the hair follicle cycling deficiency in Vdr knockout mice
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Endogenous Skin Fluorescence is a Good Marker for Objective Evaluation of Comedolysis
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- IL-17a induces age-related olfactory dysfunction by impairing regeneration and promoting respiratory metaplasia in mice
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- The Rhino Mouse: Retinoid Effects on a Model of Keratin Accumulation
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- Alopecia Areata
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Eclipta alba extract with potential for hair growth promoting activity
- Mice lacking the epidermal retinol dehydrogenases SDR16C5 and SDR16C6 display accelerated hair growth and enlarged meibomian glands
- Relation of Skin Polyamines to the Hairless Phenotype in Transgenic Mice Overexpressing Spermidine/Spermine N1-Acetyltransferase
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression