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Research 331–360 of 1000+
- Edar Signaling in the Control of Hair Follicle Development
- Anagen effluvium
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Cutaneous manifestations of HIV infection other than Kaposi's sarcoma: Clinical and histologic aspects
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Dynamic expression of Runx1 in skin affects hair structure
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Keratosis Follicularis Spinulosa Decalvans Associated with Acne Keloidalis Nuchae and Tufted Hair Folliculitis
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Alopecia Areata
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Cicatricial alopecia
- Secondary cicatricial and other permanent alopecias
- Keratins: the hair shaft's backbone revealed
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- A counter gradient of Activin A and follistatin instructs the timing of hair cell differentiation in the murine cochlea
- Hair shaft disorders in children – An update
- A rare case of woolly hair with unusual associations
- Pilot Study of 15 Patients Receiving a New Treatment Regimen for Androgenic Alopecia: The Effects of Atopy on AGA
- Hair follicles modulate skin barrier function
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Alopecia areata incognita in Cronkhite-Canada syndrome
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Discovery and Functional Analysis of Secondary Hair Follicle miRNAs during Annual Cashmere Growth
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children