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Research 961–990 of 1000+
- Hirsutism
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Types I and II Keratin Intermediate Filaments
- Short-Chain Fatty Acids from <i>Cutibacterium acnes</i> Activate Both a Canonical and Epigenetic Inflammatory Response in Human Sebocytes
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Atlas of Geriatric Dermatology
- Highlights from the Field of Pediatric Dermatology Research from the 2023 PeDRA Annual Conference
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Fundamental Concepts and Novel Aspects of Polycystic Ovarian Syndrome: Expert Consensus Resolutions
- Edar Signaling in the Control of Hair Follicle Development
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Pathomechanisms of immune-mediated alopecia
- Ethnobotanical, Phytochemical, Toxicological, and Pharmacological Properties of Ziziphus lotus (L.) Lam.: A Comprehensive Review
- Microarray analysis of androgenetic and senescent alopecia: Comparison of gene expression shows two distinct profiles
- Immunology of alopecia areata
- Association of Sensorineural Hearing Loss in Patients With Alopecia Areata
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Valproate-acid-induced cutaneous leukocytoclastic vasculitis.
- Taiwanese Dermatological Association consensus on the diagnosis and management of alopecia areata
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Uveodermatological syndrome associated with alopecia areata in a one‐year‐old female spayed Cavalier King Charles Spaniel dog
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Current Protocols: Alopecia Areata Mouse Models for Drug Efficacy and Mechanism Studies
- Uncombable hair in a case of Zellweger syndrome – A new association
- Cutaneous Adverse Events of Tyrosine Kinase Inhibitors in Endocrine Tumors: Clinical Features, Mechanisms, and Management Strategies