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Research 331–360 of 1000+
- Alopecia Areata
- Endocrine-skin interactions
- Physiology and Medical Treatments for Alopecia
- The involvement of androgens in human hair growth
- Lipid nanocarriers as innovative strategies for hair regrowth
- Comparative Study That Evaluates the Effectiveness of Intradermotherapy with 0.5% Minoxidil Versus Topical Application of 5% Monoxidil Solution in the Treatment of Androgenetic Alopecia
- Management of androgenetic alopecia
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- Congenital atrichia associated with situs inversus and mesocardia
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Effect of Oral Minoxidil on Monilethrix
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- New clinico‐genetic classification of trichothiodystrophy
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- FGF5 is a crucial regulator of hair length in humans
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Discreet monilethrix: De novo mutation on the example of polish families
- A missense mutation in Lama3 causes androgen alopecia
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis