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Research 511–540 of 1000+
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- Werner′s syndrome
- GAPO syndrome – Report of a rare case and review
- First Symposium of Ichthyosis Experts
- Hair promotion effect of Beta vulgaris L. fruit extracts; physicochemical, and analytical evaluation
- Relative Efficacy of Conventional Monotherapies and Select Nonconventional, Over‐the‐Counter Products for Male Androgenetic Alopecia: A Network Meta‐Analysis Study
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- 284 Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Skin manifestations of celiac disease
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The analysis of genetics and associated autoimmune diseases in Chinese vitiligo patients
- Causes and Management of Hypertrichosis
- Keratosis Follicularis Spinulosa Decalvans
- Serum elevation of dehydroepiandrosterone sulfate associated with male pattern baldness in young men
- Association between the D19S884 marker at the insulin receptor gene locus and polycystic ovary syndrome
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Metabolic syndrome in androgenic alopecia
- Development and Maintenance of Epidermal Stem Cells in Skin Adnexa
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome