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Research 31–60 of 1000+
- Hairless: A nuclear receptor corepressor essential for skin function
- Alopezien und Hypotrichosen im Kindesalter
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- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- Hair physiology and its disorders
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Congenital hypotrichosis due to short anagen
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Congenital hair loss disorders: Rare, but not too rare
- Line-Field Optical Coherence Tomography: Usefulness in the Non-Invasive Differential Diagnosis of Congenital Alopecia of Infancy
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Dermatopathology and molecular genetics
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Secondary cicatricial and other permanent alopecias
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Disorders of hair in children
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Morphological Approach to Hair Disorders
- Hairless is a nuclear receptor corepressor essential for skin function
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Hair follicles and their role in skin health
- Le gène<i>hairless</i>de la souris
- Differential diagnosis of alopetia in children and adolescents