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Research 271–300 of 1000+
- Ectodermal Dysplasia: Variable Expressions
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Fibroblast bioelectric signaling drives hair growth
- Natural phenylethanoid glycoside forsythoside A alleviates androgenetic alopecia by selectively inhibiting TRPV3 channels in mice
- Risk associated with the use of 5-alpha reductase inhibitors with minoxidil in treatment of male androgenetic alopecia – literature review
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- Poliosis circumscripta: Overview and underlying causes
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Disorders of hair in infants and children other than alopecia
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- First Symposium of Ichthyosis Experts
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Pathogenesis of androgenetic alopecia
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Monilethrix – Case report of a rare disease
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Alopecia Areata: An Updated Review for 2023
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Pseudofolliculitis barbae; current treatment options
- Female pattern hair loss—An update