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Research 31–60 of 382
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Efficacy of 0.1% adapalene in a non-inflammatory Kyoto Rhino Rat acne model
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Current Genetics in Hair Diseases
- Towards Defining the Pathogenesis of the Hairless Phenotype
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Disruption of the hedgehog signaling pathway contributes to the hair follicle cycling deficiency in Vdr knockout mice
- Endogenous Skin Fluorescence is a Good Marker for Objective Evaluation of Comedolysis
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Genetics of Structural Hair Disorders
- Le gène<i>hairless</i>de la souris
- Biology and Genetics of Hair
- Morphological Approach to Hair Disorders
- Hairless is a nuclear receptor corepressor essential for skin function
- Alopecia areata in a rhesus monkey (Macaca mulatta)
- Australasian Society for Dermatology Research Meeting, May 2006
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Skin morphology of the mutant hairless USP mouse
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
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- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Genetic Hair Disorders: A Review
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Androgenetic Alopecia: In Vivo Models
- Alopecia Areata
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Development and homeostasis of the sebaceous gland