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Research 151–180 of 1000+
- Alopecia Areata
- Endocrine-skin interactions
- Acquired scalp alopecia. Part II: A review
- Atlas of Geriatric Dermatology
- Hair Disorders
- Lipid nanocarriers as innovative strategies for hair regrowth
- The involvement of androgens in human hair growth
- Management of androgenetic alopecia
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Effect of Oral Minoxidil on Monilethrix
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- New clinico‐genetic classification of trichothiodystrophy
- FGF5 is a crucial regulator of hair length in humans
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Molecular Genetics of Human Hair Diseases
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Keratins: the hair shaft's backbone revealed
- A missense mutation in Lama3 causes androgen alopecia
- Steatocystoma Multiplex
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Inherited ichthyoses/generalized Mendelian disorders of cornification